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Showing metabocard for 2,6,10,14-tetramethylpentadecanoyl-CoA (HMDB0300699)

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IdentificationTaxonomyOntologyPhysical propertiesSpectraBiological propertiesConcentrationsLinksReferencesXML
Record Information
Version5.0
StatusPredicted
Creation Date2021-09-21 18:03:48 UTC
Update Date2021-10-01 16:50:10 UTC
HMDB IDHMDB0300699
Secondary Accession NumbersNone
Metabolite Identification
Common Name2,6,10,14-tetramethylpentadecanoyl-CoA
Description2,6,10,14-tetramethylpentadecanoyl-coa is an acyl-CoA or acyl-coenzyme A. More specifically, it is a 2_6_10_14-tetramethylpentadecanoic acid thioester of coenzyme A. 2,6,10,14-tetramethylpentadecanoyl-coa is an acyl-CoA with 15 fatty acid group as the acyl moiety attached to coenzyme A. Coenzyme A was discovered in 1946 by Fritz Lipmann (Journal of Biological Chemistry (1946) 162 (3): 743–744) and its structure was determined in the early 1950s at the Lister Institute in London. Coenzyme A is a complex, thiol-containing molecule that is naturally synthesized from pantothenate (vitamin B5), which is found in various foods such as meat, vegetables, cereal grains, legumes, eggs, and milk. More specifically, coenzyme A (CoASH or CoA) consists of a beta-mercaptoethylamine group linked to the vitamin pantothenic acid (B5) through an amide linkage and 3'-phosphorylated ADP. Coenzyme A is synthesized in a five-step process that requires four molecules of ATP, pantothenate and cysteine. It is believed that there are more than 1100 types of acyl-CoA’s in the human body, which also corresponds to the number of acylcarnitines in the human body. Acyl-CoAs exists in all living species, ranging from bacteria to plants to humans. The general role of acyl-CoA’s is to assist in transferring fatty acids from the cytoplasm to mitochondria. This process facilitates the production of fatty acids in cells, which are essential in cell membrane structure. Acyl-CoA's are also susceptible to beta oxidation, forming, ultimately, acetyl-CoA. Acetyl-CoA can enter the citric acid cycle, eventually forming several equivalents of ATP. In this way, fats are converted to ATP -- or biochemical energy. Acyl-CoAs can be classified into 9 different categories depending on the size of their acyl-group: 1) short-chain acyl-CoAs; 2) medium-chain acyl-CoAs; 3) long-chain acyl-CoAs; and 4) very long-chain acyl-CoAs; 5) hydroxy acyl-CoAs; 6) branched chain acyl-CoAs; 7) unsaturated acyl-CoAs; 8) dicarboxylic acyl-CoAs and 9) miscellaneous acyl-CoAs. Short-chain acyl-CoAs have acyl-groups with two to four carbons (C2-C4), medium-chain acyl-CoAs have acyl-groups with five to eleven carbons (C5-C11), long-chain acyl-CoAs have acyl-groups with twelve to twenty carbons (C12-C20) while very long-chain acyl-CoAs have acyl groups with more than 20 carbons. 2,6,10,14-tetramethylpentadecanoyl-coa is therefore classified as a long chain acyl-CoA. The oxidative degradation of fatty acids is a two-step process, catalyzed by acyl-CoA synthetase/synthase. Fatty acids are first converted to their acyl phosphate, the precursor to acyl-CoA. The latter conversion is mediated by acyl-CoA synthase. Three types of acyl-CoA synthases are employed, depending on the chain length of the fatty acid. 2,6,10,14-tetramethylpentadecanoyl-coa, being a long chain acyl-CoA is a substrate for long chain acyl-CoA synthase. The second step of fatty acid degradation is beta oxidation. Beta oxidation occurs in mitochondria and, in the case of very long chain acyl-CoAs, the peroxisome. After its formation in the cytosol, 2,6,10,14-tetramethylpentadecanoyl-CoA is transported into the mitochondria, the locus of beta oxidation. Transport of 2,6,10,14-tetramethylpentadecanoyl-CoA into the mitochondria requires carnitine palmitoyltransferase 1 (CPT1), which converts 2,6,10,14-tetramethylpentadecanoyl-CoA into 2_6_10_14-tetramethylpentadecanoylcarnitine, which gets transported into the mitochondrial matrix. Once in the matrix, 2_6_10_14-tetramethylpentadecanoylcarnitine is converted back to 2,6,10,14-tetramethylpentadecanoyl-CoA by CPT2, whereupon beta-oxidation can begin. Beta oxidation of 2,6,10,14-tetramethylpentadecanoyl-CoA occurs in four steps. First, since 2,6,10,14-tetramethylpentadecanoyl-CoA is a long chain acyl-CoA it is the substrate for a long chain acyl-CoA dehydrogenase, which catalyzes dehydrogenation of 2,6,10,14-tetramethylpentadecanoyl-CoA, creating a double bond between the alpha and beta carbons. FAD is the hydrogen acceptor, yielding FADH2. Second, Enoyl-CoA hydrase catalyzes the addition of water across the newly formed double bond to make an alcohol. Third, 3-hydroxyacyl-CoA dehydrogenase oxidizes the alcohol group to a ketone and NADH is produced from NAD+. Finally, Thiolase cleaves between the alpha carbon and ketone to release one molecule of acetyl-CoA and a new acyl-CoA which is now 2 carbons shorter. This four-step process repeats until 2,6,10,14-tetramethylpentadecanoyl-CoA has had all its carbons removed from the chain, leaving only acetyl-CoA. Beta oxidation, as well as alpha-oxidation, also occurs in the peroxisome. The peroxisome handles beta oxidation of fatty acids that have more than 20 carbons in their chain because the peroxisome contains very-long-chain Acyl-CoA synthetases and dehydrogenases. The heart primarily metabolizes fat for energy and Acyl-CoA metabolism has been identified as a critical molecule in early-stage heart muscle pump failure. Cellular acyl-CoA content also correlates with insulin resistance, suggesting that it can mediate lipotoxicity in non-adipose tissues. Acyl-CoA: diacylglycerol acyltransferase (DGAT) plays an important role in energy metabolism on account of key enzyme in triglyceride biosynthesis. The study of acyl-CoAs is an active area of research and it is likely that many novel acyl-CoAs will be discovered in the coming years. It is also likely that many novel roles in health and disease will be uncovered for these molecules.
Structure
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MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0300699 (2,6,10,14-tetramethylpentadecanoyl-CoA)


  Mrv1652304092123112D          

 68 70  0  0  0  0            999 V2000
   38.3067    3.4429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
Download

3D MOL for HMDB0300699 (2,6,10,14-tetramethylpentadecanoyl-CoA)

HMDB0300699
     RDKit          3D
2,6,10,14-tetramethylpentadecanoyl-CoA
140142  0  0  0  0  0  0  0  0999 V2000
  -18.7011    0.0066    1.1650 C   0  0  0  0  0  0  0  0  0  0  0  0
  -18.0681   -0.7150    0.0021 C   0  0  0  0  0  0  0  0  0  0  0  0
  -18.3557   -2.2060    0.1980 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.6073   -0.4614   -0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.2596    0.9864   -0.3392 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.7426    1.1630   -0.4766 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.0240    0.7136    0.7316 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.4299    1.4661    1.9853 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5254    0.9211    0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9959    0.1410   -0.5327 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5399    0.1899   -0.8526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6535   -0.2601    0.2261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6574    0.5338    1.4786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1975   -0.5292   -0.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6011    0.6930   -0.8342 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0989    0.2758   -0.4950 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.8309    1.3474    0.5232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4728    1.3074    1.5592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6507    2.6544    0.3139 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4830    2.3491   -1.0273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5142    1.2403   -0.6691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5657    0.9412   -1.7044 N   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5988   -0.2058   -1.3564 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5694    0.5435   -0.1827 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5733    0.6426    0.5478 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8314    1.2982    0.2412 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9052   -0.1719    2.2460 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246    1.0226    1.4827 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0250   -0.8895    0.1873 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8364   -1.7460    0.9870 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2081   -3.1136    0.0361 P   0  0  0  0  0  5  0  0  0  0  0  0
    5.9545   -3.9910   -0.0634 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3940   -3.9993    0.8415 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7022   -2.6062   -1.4894 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3785   -2.8058   -1.6843 P   0  0  0  0  0  5  0  0  0  0  0  0
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    9.9119   -1.9571   -3.0563 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1280   -2.1923   -0.2959 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658   -0.9401   -0.5190 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3122   -0.4551    0.7585 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8541    0.8177    0.5550 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1728    0.5979    0.1538 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9588    1.7787    0.1741 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.5394    3.0301    0.3593 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6019    3.8832    0.3080 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.7061    3.1621    0.0879 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0511    3.4301   -0.0618 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4850    4.7715    0.0190 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.9453    2.4307   -0.2837 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.5300    1.1572   -0.3611 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2358    0.9126   -0.2158 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.2876    1.8433    0.0058 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
Download

3D SDF for HMDB0300699 (2,6,10,14-tetramethylpentadecanoyl-CoA)


  Mrv1652304092123112D          

 68 70  0  0  0  0            999 V2000
   38.3067    3.4429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   38.3067    2.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.5923    2.2054    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   36.8778    2.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.1633    2.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.4488    2.6179    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   34.7344    2.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.7344    1.3804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.0199    2.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.0199    3.4429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.3054    2.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.5910    2.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.8765    2.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.1620    2.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.1620    3.4429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.4475    2.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.7331    2.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.0186    2.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.3041    2.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.3041    3.4429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.5897    2.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.8752    2.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.1607    2.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.4463    2.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.7318    2.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.4463    3.4429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   39.0212    2.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   39.7357    2.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.4501    2.2054    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   41.1646    2.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.1646    3.4429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   41.8791    2.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.8791    1.3804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   42.5936    2.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   43.0061    1.9034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   42.1811    3.3323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   43.3080    3.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   44.0225    2.6179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   44.7370    3.0304    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   45.1495    2.3159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   45.4514    3.4429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   46.1659    3.0304    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   45.7534    2.3159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   46.8804    2.6179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   47.5949    3.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   48.3093    2.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   49.0630    2.9534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   49.6150    2.3403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   50.4355    2.4266    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   50.8480    3.1410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   51.6550    2.9695    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   51.7412    2.1490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   52.4087    1.6641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   52.3224    0.8436    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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   50.9013    0.9930    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   50.9875    1.8135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   53.1623    1.9997    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   49.2025    1.6259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   49.5381    0.8722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   48.3956    1.7974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   47.7825    1.2453    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   46.9978    1.5003    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   47.2528    2.2849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   46.7429    0.7157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   46.2132    1.7552    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
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 39 41  1  0  0  0  0
 39 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 43 45  1  0  0  0  0
 43 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  2  0  0  0  0
 56 57  1  0  0  0  0
 57 58  2  0  0  0  0
 58 59  1  0  0  0  0
 54 59  2  0  0  0  0
 51 59  1  0  0  0  0
 55 60  1  0  0  0  0
 50 61  1  0  0  0  0
 61 62  1  0  0  0  0
 61 63  1  0  0  0  0
 48 63  1  0  0  0  0
 63 64  1  0  0  0  0
 64 65  1  0  0  0  0
 65 66  2  0  0  0  0
 65 67  1  0  0  0  0
 65 68  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0300699

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)CCCC(C)CCCC(C)CCCC(C)C(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N

> <INCHI_IDENTIFIER>
InChI=1S/C40H72N7O17P3S/c1-25(2)11-8-12-26(3)13-9-14-27(4)15-10-16-28(5)39(52)68-20-19-42-30(48)17-18-43-37(51)34(50)40(6,7)22-61-67(58,59)64-66(56,57)60-21-29-33(63-65(53,54)55)32(49)38(62-29)47-24-46-31-35(41)44-23-45-36(31)47/h23-29,32-34,38,49-50H,8-22H2,1-7H3,(H,42,48)(H,43,51)(H,56,57)(H,58,59)(H2,41,44,45)(H2,53,54,55)

> <INCHI_KEY>
XYJPSQPVCBNZHT-UHFFFAOYSA-N

> <FORMULA>
C40H72N7O17P3S

> <MOLECULAR_WEIGHT>
1048.03

> <EXACT_MASS>
1047.391826054

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
140

> <JCHEM_AVERAGE_POLARIZABILITY>
106.01847843403284

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-({[hydroxy({[hydroxy(3-hydroxy-2,2-dimethyl-3-{[2-({2-[(2,6,10,14-tetramethylpentadecanoyl)sulfanyl]ethyl}carbamoyl)ethyl]carbamoyl}propoxy)phosphoryl]oxy})phosphoryl]oxy}methyl)oxolan-3-yl]oxy}phosphonic acid

> <ALOGPS_LOGP>
2.76

> <JCHEM_LOGP>
1.557784281185373

> <ALOGPS_LOGS>
-2.98

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-4

> <JCHEM_PKA>
1.900120734776186

> <JCHEM_PKA_STRONGEST_ACIDIC>
0.8209787813398193

> <JCHEM_PKA_STRONGEST_BASIC>
4.006053268556904

> <JCHEM_POLAR_SURFACE_AREA>
363.62999999999994

> <JCHEM_REFRACTIVITY>
250.26720000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
33

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.09e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[5-(6-aminopurin-9-yl)-4-hydroxy-2-({[hydroxy([hydroxy(3-hydroxy-2,2-dimethyl-3-{[2-({2-[(2,6,10,14-tetramethylpentadecanoyl)sulfanyl]ethyl}carbamoyl)ethyl]carbamoyl}propoxy)phosphoryl]oxy)phosphoryl]oxy}methyl)oxolan-3-yl]oxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0300699 (2,6,10,14-tetramethylpentadecanoyl-CoA)

HMDB0300699
     RDKit          3D
2,6,10,14-tetramethylpentadecanoyl-CoA
140142  0  0  0  0  0  0  0  0999 V2000
  -18.7011    0.0066    1.1650 C   0  0  0  0  0  0  0  0  0  0  0  0
  -18.0681   -0.7150    0.0021 C   0  0  0  0  0  0  0  0  0  0  0  0
  -18.3557   -2.2060    0.1980 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.6073   -0.4614   -0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.2596    0.9864   -0.3392 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.7426    1.1630   -0.4766 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.0240    0.7136    0.7316 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.4299    1.4661    1.9853 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5254    0.9211    0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9959    0.1410   -0.5327 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5399    0.1899   -0.8526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6535   -0.2601    0.2261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6574    0.5338    1.4786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1975   -0.5292   -0.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6011    0.6930   -0.8342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2310    0.6285   -1.3819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0989    0.2758   -0.4950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1917   -1.0708    0.1098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8309    1.3474    0.5232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4728    1.3074    1.5592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6507    2.6544    0.3139 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4830    2.3491   -1.0273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5142    1.2403   -0.6691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5657    0.9412   -1.7044 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4007   -0.0956   -1.4735 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3649   -0.7030   -0.3535 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3738   -0.4214   -2.4961 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6599   -1.0113   -2.0312 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5988   -0.2058   -1.3564 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5694    0.5435   -0.1827 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5733    0.6426    0.5478 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8314    1.2982    0.2412 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4374    2.3284    1.1226 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6767    0.3091    1.0113 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9052   -0.1719    2.2460 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246    1.0226    1.4827 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0250   -0.8895    0.1873 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8364   -1.7460    0.9870 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2081   -3.1136    0.0361 P   0  0  0  0  0  5  0  0  0  0  0  0
    5.9545   -3.9910   -0.0634 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3940   -3.9993    0.8415 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7022   -2.6062   -1.4894 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3785   -2.8058   -1.6843 P   0  0  0  0  0  5  0  0  0  0  0  0
    9.6515   -4.2819   -1.8100 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9119   -1.9571   -3.0563 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1280   -2.1923   -0.2959 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658   -0.9401   -0.5190 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3122   -0.4551    0.7585 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8541    0.8177    0.5550 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1728    0.5979    0.1538 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9588    1.7787    0.1741 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.5394    3.0301    0.3593 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6019    3.8832    0.3080 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.7061    3.1621    0.0879 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0511    3.4301   -0.0618 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4850    4.7715    0.0190 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.9453    2.4307   -0.2837 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.5300    1.1572   -0.3611 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2358    0.9126   -0.2158 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.2876    1.8433    0.0058 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6175   -0.3510    1.2452 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8042   -0.9936    0.9883 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.4333   -1.3371    1.2238 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6682   -2.3078    0.2698 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8952   -3.8357    0.9542 P   0  0  0  0  0  5  0  0  0  0  0  0
   13.0023   -3.7614    2.4569 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5519   -4.7845    0.5765 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2587   -4.5974    0.2820 O   0  0  0  0  0  0  0  0  0  0  0  0
  -19.5904   -0.5803    1.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
  -18.0404    0.0242    2.0650 H   0  0  0  0  0  0  0  0  0  0  0  0
  -19.0716    1.0195    0.9085 H   0  0  0  0  0  0  0  0  0  0  0  0
  -18.6421   -0.4333   -0.9112 H   0  0  0  0  0  0  0  0  0  0  0  0
  -17.6901   -2.5394    1.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
  -19.3891   -2.2794    0.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
  -18.1494   -2.7841   -0.7033 H   0  0  0  0  0  0  0  0  0  0  0  0
  -16.0972   -0.9000    0.7482 H   0  0  0  0  0  0  0  0  0  0  0  0
  -16.2543   -1.0632   -1.0165 H   0  0  0  0  0  0  0  0  0  0  0  0
  -16.6975    1.3321   -1.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
  -16.5927    1.6417    0.4588 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5635    2.2438   -0.6260 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.4324    0.5839   -1.3625 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.1260   -0.4036    0.9016 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.7506    0.7009    2.7369 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.1903    2.2337    1.8041 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.5732    1.9881    2.4699 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1284    0.4738    1.5572 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2769    2.0032    0.5665 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5874    0.4578   -1.4565 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2376   -0.9714   -0.4257 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4073   -0.5468   -1.7168 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2736    1.2159   -1.2429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9508   -1.3329    0.5618 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0936    1.5272    1.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5473    0.6795    1.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0568    0.0127    2.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1736   -1.3993   -0.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6390   -0.8391    0.6837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3014    1.0436   -1.6641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5893    1.5248   -0.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9888    1.6081   -1.9173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2013   -0.1177   -2.2436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1839    0.2700   -1.1641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1397   -1.5164    0.1158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4296   -0.9965    1.1914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8588   -1.7356   -0.4391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9996    2.1311   -1.9806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8953    3.2719   -1.1850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8850    1.5852    0.2207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0442    0.3511   -0.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5728    1.4558   -2.5976 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9274   -1.1425   -3.2587 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5980    0.4996   -3.1253 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1547   -1.5151   -2.9364 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4105   -1.9380   -1.3875 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5724   -0.1663   -1.9186 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2858    1.7099   -0.6251 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5106    2.6180    0.9639 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1060    0.5674    2.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4798   -1.1843    2.0705 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5936   -0.1914    3.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4954    0.3109    2.1221 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5269    1.3725    0.6296 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5916    1.8794    2.1178 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0608   -1.4346   -0.0208 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5879   -0.6282   -0.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1154   -4.0189    1.8087 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7879   -0.9862   -2.8171 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8431   -0.2297   -0.7490 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4336   -0.9336   -1.3196 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4878   -0.4120    1.5205 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.1913    0.0356   -0.8032 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.5365    3.3816    0.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.1234    5.4668   -0.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   18.1609    5.0636    0.7434 H   0  0  0  0  0  0  0  0  0  0  0  0
   18.2049    0.3266   -0.5361 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.6372    0.1277    2.2339 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.4244   -0.8994    1.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.2950   -1.7637    2.2413 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4221   -5.5493    1.1750 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.0630   -4.0267    0.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
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 12 13  1  0
 12 14  1  0
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 19 20  2  0
 19 21  1  0
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 23 24  1  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
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 32 34  1  0
 34 35  1  0
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 34 37  1  0
 37 38  1  0
 38 39  1  0
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 43 45  1  0
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 48 49  1  0
 49 50  1  0
 50 51  1  0
 51 52  1  0
 52 53  2  0
 53 54  1  0
 54 55  2  0
 55 56  1  0
 55 57  1  0
 57 58  2  0
 58 59  1  0
 59 60  2  0
 50 61  1  0
 61 62  1  0
 61 63  1  0
 63 64  1  0
 64 65  1  0
 65 66  2  0
 65 67  1  0
 65 68  1  0
 63 48  1  0
 60 51  1  0
 60 54  1  0
  1 69  1  0
  1 70  1  0
  1 71  1  0
  2 72  1  0
  3 73  1  0
  3 74  1  0
  3 75  1  0
  4 76  1  0
  4 77  1  0
  5 78  1  0
  5 79  1  0
  6 80  1  0
  6 81  1  0
  7 82  1  0
  8 83  1  0
  8 84  1  0
  8 85  1  0
  9 86  1  0
  9 87  1  0
 10 88  1  0
 10 89  1  0
 11 90  1  0
 11 91  1  0
 12 92  1  0
 13 93  1  0
 13 94  1  0
 13 95  1  0
 14 96  1  0
 14 97  1  0
 15 98  1  0
 15 99  1  0
 16100  1  0
 16101  1  0
 17102  1  0
 18103  1  0
 18104  1  0
 18105  1  0
 22106  1  0
 22107  1  0
 23108  1  0
 23109  1  0
 24110  1  0
 27111  1  0
 27112  1  0
 28113  1  0
 28114  1  0
 29115  1  0
 32116  1  0
 33117  1  0
 35118  1  0
 35119  1  0
 35120  1  0
 36121  1  0
 36122  1  0
 36123  1  0
 37124  1  0
 37125  1  0
 41126  1  0
 45127  1  0
 47128  1  0
 47129  1  0
 48130  1  0
 50131  1  0
 52132  1  0
 56133  1  0
 56134  1  0
 58135  1  0
 61136  1  0
 62137  1  0
 63138  1  0
 67139  1  0
 68140  1  0
M  END
Download

PDB for HMDB0300699 (2,6,10,14-tetramethylpentadecanoyl-CoA)

HEADER    PROTEIN                                 09-APR-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-APR-21         0                                  
HETATM    1  O   UNK     0      71.506   6.427   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      71.506   4.887   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      70.172   4.117   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      68.839   4.887   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      67.505   4.117   0.000  0.00  0.00           C+0
HETATM    6  S   UNK     0      66.171   4.887   0.000  0.00  0.00           S+0
HETATM    7  C   UNK     0      64.837   4.117   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      64.837   2.577   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      63.504   4.887   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      63.504   6.427   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      62.170   4.117   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      60.836   4.887   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      59.503   4.117   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      58.169   4.887   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      58.169   6.427   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      56.835   4.117   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      55.502   4.887   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      54.168   4.117   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      52.834   4.887   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      52.834   6.427   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      51.501   4.117   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      50.167   4.887   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      48.833   4.117   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      47.500   4.887   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      46.166   4.117   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      47.500   6.427   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      72.840   4.117   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      74.173   4.887   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0      75.507   4.117   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0      76.841   4.887   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      76.841   6.427   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      78.174   4.117   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      78.174   2.577   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      79.508   4.887   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      80.278   3.553   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      78.738   6.220   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      80.842   5.657   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      82.175   4.887   0.000  0.00  0.00           O+0
HETATM   39  P   UNK     0      83.509   5.657   0.000  0.00  0.00           P+0
HETATM   40  O   UNK     0      84.279   4.323   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      82.739   6.990   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      84.843   6.427   0.000  0.00  0.00           O+0
HETATM   43  P   UNK     0      86.176   5.657   0.000  0.00  0.00           P+0
HETATM   44  O   UNK     0      85.406   4.323   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0      86.946   6.990   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      87.510   4.887   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      88.844   5.657   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      90.177   4.887   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      91.584   5.513   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      92.615   4.369   0.000  0.00  0.00           C+0
HETATM   51  N   UNK     0      94.146   4.530   0.000  0.00  0.00           N+0
HETATM   52  C   UNK     0      94.916   5.863   0.000  0.00  0.00           C+0
HETATM   53  N   UNK     0      96.423   5.543   0.000  0.00  0.00           N+0
HETATM   54  C   UNK     0      96.584   4.012   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      97.829   3.106   0.000  0.00  0.00           C+0
HETATM   56  N   UNK     0      97.669   1.575   0.000  0.00  0.00           N+0
HETATM   57  C   UNK     0      96.262   0.948   0.000  0.00  0.00           C+0
HETATM   58  N   UNK     0      95.016   1.854   0.000  0.00  0.00           N+0
HETATM   59  C   UNK     0      95.177   3.385   0.000  0.00  0.00           C+0
HETATM   60  N   UNK     0      99.236   3.733   0.000  0.00  0.00           N+0
HETATM   61  C   UNK     0      91.845   3.035   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0      92.471   1.628   0.000  0.00  0.00           O+0
HETATM   63  C   UNK     0      90.338   3.355   0.000  0.00  0.00           C+0
HETATM   64  O   UNK     0      89.194   2.325   0.000  0.00  0.00           O+0
HETATM   65  P   UNK     0      87.729   2.801   0.000  0.00  0.00           P+0
HETATM   66  O   UNK     0      88.205   4.265   0.000  0.00  0.00           O+0
HETATM   67  O   UNK     0      87.253   1.336   0.000  0.00  0.00           O+0
HETATM   68  O   UNK     0      86.265   3.276   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   27                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27    2   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36   37                                             
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   34   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41   42                                             
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   39   43                                                       
CONECT   43   42   44   45   46                                             
CONECT   44   43                                                            
CONECT   45   43                                                            
CONECT   46   43   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49   63                                                  
CONECT   49   48   50                                                       
CONECT   50   49   51   61                                                  
CONECT   51   50   52   59                                                  
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55   59                                                  
CONECT   55   54   56   60                                                  
CONECT   56   55   57                                                       
CONECT   57   56   58                                                       
CONECT   58   57   59                                                       
CONECT   59   58   54   51                                                  
CONECT   60   55                                                            
CONECT   61   50   62   63                                                  
CONECT   62   61                                                            
CONECT   63   61   48   64                                                  
CONECT   64   63   65                                                       
CONECT   65   64   66   67   68                                             
CONECT   66   65                                                            
CONECT   67   65                                                            
CONECT   68   65                                                            
MASTER        0    0    0    0    0    0    0    0   68    0  140    0
END
Download

3D PDB for HMDB0300699 (2,6,10,14-tetramethylpentadecanoyl-CoA)

COMPND    HMDB0300699
HETATM    1  C1  UNL     1     -18.701   0.007   1.165  1.00  0.00           C  
HETATM    2  C2  UNL     1     -18.068  -0.715   0.002  1.00  0.00           C  
HETATM    3  C3  UNL     1     -18.356  -2.206   0.198  1.00  0.00           C  
HETATM    4  C4  UNL     1     -16.607  -0.461  -0.133  1.00  0.00           C  
HETATM    5  C5  UNL     1     -16.260   0.986  -0.339  1.00  0.00           C  
HETATM    6  C6  UNL     1     -14.743   1.163  -0.477  1.00  0.00           C  
HETATM    7  C7  UNL     1     -14.024   0.714   0.732  1.00  0.00           C  
HETATM    8  C8  UNL     1     -14.430   1.466   1.985  1.00  0.00           C  
HETATM    9  C9  UNL     1     -12.525   0.921   0.595  1.00  0.00           C  
HETATM   10  C10 UNL     1     -11.996   0.141  -0.533  1.00  0.00           C  
HETATM   11  C11 UNL     1     -10.540   0.190  -0.853  1.00  0.00           C  
HETATM   12  C12 UNL     1      -9.654  -0.260   0.226  1.00  0.00           C  
HETATM   13  C13 UNL     1      -9.657   0.534   1.479  1.00  0.00           C  
HETATM   14  C14 UNL     1      -8.198  -0.529  -0.254  1.00  0.00           C  
HETATM   15  C15 UNL     1      -7.601   0.693  -0.834  1.00  0.00           C  
HETATM   16  C16 UNL     1      -6.231   0.628  -1.382  1.00  0.00           C  
HETATM   17  C17 UNL     1      -5.099   0.276  -0.495  1.00  0.00           C  
HETATM   18  C18 UNL     1      -5.192  -1.071   0.110  1.00  0.00           C  
HETATM   19  C19 UNL     1      -4.831   1.347   0.523  1.00  0.00           C  
HETATM   20  O1  UNL     1      -5.473   1.307   1.559  1.00  0.00           O  
HETATM   21  S1  UNL     1      -3.651   2.654   0.314  1.00  0.00           S  
HETATM   22  C20 UNL     1      -2.483   2.349  -1.027  1.00  0.00           C  
HETATM   23  C21 UNL     1      -1.514   1.240  -0.669  1.00  0.00           C  
HETATM   24  N1  UNL     1      -0.566   0.941  -1.704  1.00  0.00           N  
HETATM   25  C22 UNL     1       0.401  -0.096  -1.473  1.00  0.00           C  
HETATM   26  O2  UNL     1       0.365  -0.703  -0.354  1.00  0.00           O  
HETATM   27  C23 UNL     1       1.374  -0.421  -2.496  1.00  0.00           C  
HETATM   28  C24 UNL     1       2.660  -1.011  -2.031  1.00  0.00           C  
HETATM   29  N2  UNL     1       3.599  -0.206  -1.356  1.00  0.00           N  
HETATM   30  C25 UNL     1       3.569   0.543  -0.183  1.00  0.00           C  
HETATM   31  O3  UNL     1       2.573   0.643   0.548  1.00  0.00           O  
HETATM   32  C26 UNL     1       4.831   1.298   0.241  1.00  0.00           C  
HETATM   33  O4  UNL     1       4.437   2.328   1.123  1.00  0.00           O  
HETATM   34  C27 UNL     1       5.677   0.309   1.011  1.00  0.00           C  
HETATM   35  C28 UNL     1       4.905  -0.172   2.246  1.00  0.00           C  
HETATM   36  C29 UNL     1       6.925   1.023   1.483  1.00  0.00           C  
HETATM   37  C30 UNL     1       6.025  -0.890   0.187  1.00  0.00           C  
HETATM   38  O5  UNL     1       6.836  -1.746   0.987  1.00  0.00           O  
HETATM   39  P1  UNL     1       7.208  -3.114   0.036  1.00  0.00           P  
HETATM   40  O6  UNL     1       5.955  -3.991  -0.063  1.00  0.00           O  
HETATM   41  O7  UNL     1       8.394  -3.999   0.842  1.00  0.00           O  
HETATM   42  O8  UNL     1       7.702  -2.606  -1.489  1.00  0.00           O  
HETATM   43  P2  UNL     1       9.378  -2.806  -1.684  1.00  0.00           P  
HETATM   44  O9  UNL     1       9.651  -4.282  -1.810  1.00  0.00           O  
HETATM   45  O10 UNL     1       9.912  -1.957  -3.056  1.00  0.00           O  
HETATM   46  O11 UNL     1      10.128  -2.192  -0.296  1.00  0.00           O  
HETATM   47  C31 UNL     1      10.666  -0.940  -0.519  1.00  0.00           C  
HETATM   48  C32 UNL     1      11.312  -0.455   0.759  1.00  0.00           C  
HETATM   49  O12 UNL     1      11.854   0.818   0.555  1.00  0.00           O  
HETATM   50  C33 UNL     1      13.173   0.598   0.154  1.00  0.00           C  
HETATM   51  N3  UNL     1      13.959   1.779   0.174  1.00  0.00           N  
HETATM   52  C34 UNL     1      13.539   3.030   0.359  1.00  0.00           C  
HETATM   53  N4  UNL     1      14.602   3.883   0.308  1.00  0.00           N  
HETATM   54  C35 UNL     1      15.706   3.162   0.088  1.00  0.00           C  
HETATM   55  C36 UNL     1      17.051   3.430  -0.062  1.00  0.00           C  
HETATM   56  N5  UNL     1      17.485   4.772   0.019  1.00  0.00           N  
HETATM   57  N6  UNL     1      17.945   2.431  -0.284  1.00  0.00           N  
HETATM   58  C37 UNL     1      17.530   1.157  -0.361  1.00  0.00           C  
HETATM   59  N7  UNL     1      16.236   0.913  -0.216  1.00  0.00           N  
HETATM   60  C38 UNL     1      15.288   1.843   0.006  1.00  0.00           C  
HETATM   61  C39 UNL     1      13.617  -0.351   1.245  1.00  0.00           C  
HETATM   62  O13 UNL     1      14.804  -0.994   0.988  1.00  0.00           O  
HETATM   63  C40 UNL     1      12.433  -1.337   1.224  1.00  0.00           C  
HETATM   64  O14 UNL     1      12.668  -2.308   0.270  1.00  0.00           O  
HETATM   65  P3  UNL     1      12.895  -3.836   0.954  1.00  0.00           P  
HETATM   66  O15 UNL     1      13.002  -3.761   2.457  1.00  0.00           O  
HETATM   67  O16 UNL     1      11.552  -4.785   0.576  1.00  0.00           O  
HETATM   68  O17 UNL     1      14.259  -4.597   0.282  1.00  0.00           O  
HETATM   69  H1  UNL     1     -19.590  -0.580   1.472  1.00  0.00           H  
HETATM   70  H2  UNL     1     -18.040   0.024   2.065  1.00  0.00           H  
HETATM   71  H3  UNL     1     -19.072   1.019   0.908  1.00  0.00           H  
HETATM   72  H4  UNL     1     -18.642  -0.433  -0.911  1.00  0.00           H  
HETATM   73  H5  UNL     1     -17.690  -2.539   1.029  1.00  0.00           H  
HETATM   74  H6  UNL     1     -19.389  -2.279   0.567  1.00  0.00           H  
HETATM   75  H7  UNL     1     -18.149  -2.784  -0.703  1.00  0.00           H  
HETATM   76  H8  UNL     1     -16.097  -0.900   0.748  1.00  0.00           H  
HETATM   77  H9  UNL     1     -16.254  -1.063  -1.016  1.00  0.00           H  
HETATM   78  H10 UNL     1     -16.698   1.332  -1.293  1.00  0.00           H  
HETATM   79  H11 UNL     1     -16.593   1.642   0.459  1.00  0.00           H  
HETATM   80  H12 UNL     1     -14.564   2.244  -0.626  1.00  0.00           H  
HETATM   81  H13 UNL     1     -14.432   0.584  -1.363  1.00  0.00           H  
HETATM   82  H14 UNL     1     -14.126  -0.404   0.902  1.00  0.00           H  
HETATM   83  H15 UNL     1     -14.751   0.701   2.737  1.00  0.00           H  
HETATM   84  H16 UNL     1     -15.190   2.234   1.804  1.00  0.00           H  
HETATM   85  H17 UNL     1     -13.573   1.988   2.470  1.00  0.00           H  
HETATM   86  H18 UNL     1     -12.128   0.474   1.557  1.00  0.00           H  
HETATM   87  H19 UNL     1     -12.277   2.003   0.566  1.00  0.00           H  
HETATM   88  H20 UNL     1     -12.587   0.458  -1.456  1.00  0.00           H  
HETATM   89  H21 UNL     1     -12.238  -0.971  -0.426  1.00  0.00           H  
HETATM   90  H22 UNL     1     -10.407  -0.547  -1.717  1.00  0.00           H  
HETATM   91  H23 UNL     1     -10.274   1.216  -1.243  1.00  0.00           H  
HETATM   92  H24 UNL     1      -9.951  -1.333   0.562  1.00  0.00           H  
HETATM   93  H25 UNL     1     -10.094   1.527   1.337  1.00  0.00           H  
HETATM   94  H26 UNL     1      -8.547   0.680   1.769  1.00  0.00           H  
HETATM   95  H27 UNL     1     -10.057   0.013   2.360  1.00  0.00           H  
HETATM   96  H28 UNL     1      -8.174  -1.399  -0.928  1.00  0.00           H  
HETATM   97  H29 UNL     1      -7.639  -0.839   0.684  1.00  0.00           H  
HETATM   98  H30 UNL     1      -8.301   1.044  -1.664  1.00  0.00           H  
HETATM   99  H31 UNL     1      -7.589   1.525  -0.054  1.00  0.00           H  
HETATM  100  H32 UNL     1      -5.989   1.608  -1.917  1.00  0.00           H  
HETATM  101  H33 UNL     1      -6.201  -0.118  -2.244  1.00  0.00           H  
HETATM  102  H34 UNL     1      -4.184   0.270  -1.164  1.00  0.00           H  
HETATM  103  H35 UNL     1      -4.140  -1.516   0.116  1.00  0.00           H  
HETATM  104  H36 UNL     1      -5.430  -0.996   1.191  1.00  0.00           H  
HETATM  105  H37 UNL     1      -5.859  -1.736  -0.439  1.00  0.00           H  
HETATM  106  H38 UNL     1      -3.000   2.131  -1.981  1.00  0.00           H  
HETATM  107  H39 UNL     1      -1.895   3.272  -1.185  1.00  0.00           H  
HETATM  108  H40 UNL     1      -0.885   1.585   0.221  1.00  0.00           H  
HETATM  109  H41 UNL     1      -2.044   0.351  -0.287  1.00  0.00           H  
HETATM  110  H42 UNL     1      -0.573   1.456  -2.598  1.00  0.00           H  
HETATM  111  H43 UNL     1       0.927  -1.143  -3.259  1.00  0.00           H  
HETATM  112  H44 UNL     1       1.598   0.500  -3.125  1.00  0.00           H  
HETATM  113  H45 UNL     1       3.155  -1.515  -2.936  1.00  0.00           H  
HETATM  114  H46 UNL     1       2.411  -1.938  -1.387  1.00  0.00           H  
HETATM  115  H47 UNL     1       4.572  -0.166  -1.919  1.00  0.00           H  
HETATM  116  H48 UNL     1       5.286   1.710  -0.625  1.00  0.00           H  
HETATM  117  H49 UNL     1       3.511   2.618   0.964  1.00  0.00           H  
HETATM  118  H50 UNL     1       4.106   0.567   2.438  1.00  0.00           H  
HETATM  119  H51 UNL     1       4.480  -1.184   2.071  1.00  0.00           H  
HETATM  120  H52 UNL     1       5.594  -0.191   3.100  1.00  0.00           H  
HETATM  121  H53 UNL     1       7.495   0.311   2.122  1.00  0.00           H  
HETATM  122  H54 UNL     1       7.527   1.373   0.630  1.00  0.00           H  
HETATM  123  H55 UNL     1       6.592   1.879   2.118  1.00  0.00           H  
HETATM  124  H56 UNL     1       5.061  -1.435  -0.021  1.00  0.00           H  
HETATM  125  H57 UNL     1       6.588  -0.628  -0.707  1.00  0.00           H  
HETATM  126  H58 UNL     1       8.115  -4.019   1.809  1.00  0.00           H  
HETATM  127  H59 UNL     1       9.788  -0.986  -2.817  1.00  0.00           H  
HETATM  128  H60 UNL     1       9.843  -0.230  -0.749  1.00  0.00           H  
HETATM  129  H61 UNL     1      11.434  -0.934  -1.320  1.00  0.00           H  
HETATM  130  H62 UNL     1      10.488  -0.412   1.521  1.00  0.00           H  
HETATM  131  H63 UNL     1      13.191   0.036  -0.803  1.00  0.00           H  
HETATM  132  H64 UNL     1      12.537   3.382   0.528  1.00  0.00           H  
HETATM  133  H65 UNL     1      17.123   5.467  -0.653  1.00  0.00           H  
HETATM  134  H66 UNL     1      18.161   5.064   0.743  1.00  0.00           H  
HETATM  135  H67 UNL     1      18.205   0.327  -0.536  1.00  0.00           H  
HETATM  136  H68 UNL     1      13.637   0.128   2.234  1.00  0.00           H  
HETATM  137  H69 UNL     1      15.424  -0.899   1.769  1.00  0.00           H  
HETATM  138  H70 UNL     1      12.295  -1.764   2.241  1.00  0.00           H  
HETATM  139  H71 UNL     1      11.422  -5.549   1.175  1.00  0.00           H  
HETATM  140  H72 UNL     1      15.063  -4.027   0.357  1.00  0.00           H  
CONECT    1    2   69   70   71
CONECT    2    3    4   72
CONECT    3   73   74   75
CONECT    4    5   76   77
CONECT    5    6   78   79
CONECT    6    7   80   81
CONECT    7    8    9   82
CONECT    8   83   84   85
CONECT    9   10   86   87
CONECT   10   11   88   89
CONECT   11   12   90   91
CONECT   12   13   14   92
CONECT   13   93   94   95
CONECT   14   15   96   97
CONECT   15   16   98   99
CONECT   16   17  100  101
CONECT   17   18   19  102
CONECT   18  103  104  105
CONECT   19   20   20   21
CONECT   21   22
CONECT   22   23  106  107
CONECT   23   24  108  109
CONECT   24   25  110
CONECT   25   26   26   27
CONECT   27   28  111  112
CONECT   28   29  113  114
CONECT   29   30  115
CONECT   30   31   31   32
CONECT   32   33   34  116
CONECT   33  117
CONECT   34   35   36   37
CONECT   35  118  119  120
CONECT   36  121  122  123
CONECT   37   38  124  125
CONECT   38   39
CONECT   39   40   40   41   42
CONECT   41  126
CONECT   42   43
CONECT   43   44   44   45   46
CONECT   45  127
CONECT   46   47
CONECT   47   48  128  129
CONECT   48   49   63  130
CONECT   49   50
CONECT   50   51   61  131
CONECT   51   52   60
CONECT   52   53   53  132
CONECT   53   54
CONECT   54   55   55   60
CONECT   55   56   57
CONECT   56  133  134
CONECT   57   58   58
CONECT   58   59  135
CONECT   59   60   60
CONECT   61   62   63  136
CONECT   62  137
CONECT   63   64  138
CONECT   64   65
CONECT   65   66   66   67   68
CONECT   67  139
CONECT   68  140
END
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SMILES for HMDB0300699 (2,6,10,14-tetramethylpentadecanoyl-CoA)

CC(C)CCCC(C)CCCC(C)CCCC(C)C(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
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INCHI for HMDB0300699 (2,6,10,14-tetramethylpentadecanoyl-CoA)

InChI=1S/C40H72N7O17P3S/c1-25(2)11-8-12-26(3)13-9-14-27(4)15-10-16-28(5)39(52)68-20-19-42-30(48)17-18-43-37(51)34(50)40(6,7)22-61-67(58,59)64-66(56,57)60-21-29-33(63-65(53,54)55)32(49)38(62-29)47-24-46-31-35(41)44-23-45-36(31)47/h23-29,32-34,38,49-50H,8-22H2,1-7H3,(H,42,48)(H,43,51)(H,56,57)(H,58,59)(H2,41,44,45)(H2,53,54,55)
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View in JSmolView Stereo Labels
Synonyms
ValueSource
4-({[({[5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-2-hydroxy-3,3-dimethyl-N-[2-({2-[(2,6,10,14-tetramethylpentadecanoyl)sulfanyl]ethyl}-C-hydroxycarbonimidoyl)ethyl]butanimidateGenerator
4-({[({[5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-2-hydroxy-3,3-dimethyl-N-[2-({2-[(2,6,10,14-tetramethylpentadecanoyl)sulphanyl]ethyl}-C-hydroxycarbonimidoyl)ethyl]butanimidateGenerator
4-({[({[5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-2-hydroxy-3,3-dimethyl-N-[2-({2-[(2,6,10,14-tetramethylpentadecanoyl)sulphanyl]ethyl}-C-hydroxycarbonimidoyl)ethyl]butanimidic acidGenerator
Chemical FormulaC40H72N7O17P3S
Average Molecular Weight1048.03
Monoisotopic Molecular Weight1047.391826054
IUPAC Name{[5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-({[hydroxy({[hydroxy(3-hydroxy-2,2-dimethyl-3-{[2-({2-[(2,6,10,14-tetramethylpentadecanoyl)sulfanyl]ethyl}carbamoyl)ethyl]carbamoyl}propoxy)phosphoryl]oxy})phosphoryl]oxy}methyl)oxolan-3-yl]oxy}phosphonic acid
Traditional Name[5-(6-aminopurin-9-yl)-4-hydroxy-2-({[hydroxy([hydroxy(3-hydroxy-2,2-dimethyl-3-{[2-({2-[(2,6,10,14-tetramethylpentadecanoyl)sulfanyl]ethyl}carbamoyl)ethyl]carbamoyl}propoxy)phosphoryl]oxy)phosphoryl]oxy}methyl)oxolan-3-yl]oxyphosphonic acid
CAS Registry NumberNot Available
SMILES
CC(C)CCCC(C)CCCC(C)CCCC(C)C(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
InChI Identifier
InChI=1S/C40H72N7O17P3S/c1-25(2)11-8-12-26(3)13-9-14-27(4)15-10-16-28(5)39(52)68-20-19-42-30(48)17-18-43-37(51)34(50)40(6,7)22-61-67(58,59)64-66(56,57)60-21-29-33(63-65(53,54)55)32(49)38(62-29)47-24-46-31-35(41)44-23-45-36(31)47/h23-29,32-34,38,49-50H,8-22H2,1-7H3,(H,42,48)(H,43,51)(H,56,57)(H,58,59)(H2,41,44,45)(H2,53,54,55)
InChI KeyXYJPSQPVCBNZHT-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as long-chain fatty acyl coas. These are acyl CoAs where the group acylated to the coenzyme A moiety is a long aliphatic chain of 13 to 21 carbon atoms.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassFatty acyl thioesters
Direct ParentLong-chain fatty acyl CoAs
Alternative Parents
Substituents
  • Coenzyme a or derivatives
  • Purine ribonucleoside 3',5'-bisphosphate
  • Purine ribonucleoside bisphosphate
  • Purine ribonucleoside diphosphate
  • Diterpenoid
  • Ribonucleoside 3'-phosphate
  • Pentose phosphate
  • Pentose-5-phosphate
  • Glycosyl compound
  • N-glycosyl compound
  • 6-aminopurine
  • Monosaccharide phosphate
  • Organic pyrophosphate
  • Pentose monosaccharide
  • Imidazopyrimidine
  • Purine
  • Monoalkyl phosphate
  • Aminopyrimidine
  • Monosaccharide
  • N-substituted imidazole
  • Organic phosphoric acid derivative
  • Alkyl phosphate
  • Imidolactam
  • Phosphoric acid ester
  • Pyrimidine
  • Heteroaromatic compound
  • Imidazole
  • Azole
  • Oxolane
  • Carbothioic s-ester
  • Secondary alcohol
  • Amino acid or derivatives
  • Thiocarboxylic acid ester
  • Azacycle
  • Sulfenyl compound
  • Thiocarboxylic acid or derivatives
  • Carboximidic acid
  • Carboxylic acid derivative
  • Carboximidic acid derivative
  • Organoheterocyclic compound
  • Oxacycle
  • Organic 1,3-dipolar compound
  • Propargyl-type 1,3-dipolar organic compound
  • Primary amine
  • Organic nitrogen compound
  • Organic oxygen compound
  • Alcohol
  • Organonitrogen compound
  • Carbonyl group
  • Organooxygen compound
  • Organosulfur compound
  • Organic oxide
  • Amine
  • Hydrocarbon derivative
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
DispositionNot Available
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
logP2.76ALOGPS
logP1.56ChemAxon
logS-3ALOGPS
pKa (Strongest Acidic)0.82ChemAxon
pKa (Strongest Basic)4.01ChemAxon
Physiological Charge-4ChemAxon
Hydrogen Acceptor Count17ChemAxon
Hydrogen Donor Count9ChemAxon
Polar Surface Area363.63 ŲChemAxon
Rotatable Bond Count33ChemAxon
Refractivity250.27 m³·mol⁻¹ChemAxon
Polarizability106.02 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
AllCCS[M+H]+306.99332859911
AllCCS[M+H-H2O]+307.42532859911
AllCCS[M+Na]+306.42932859911
AllCCS[M+NH4]+306.5632859911
AllCCS[M-H]-290.66532859911
AllCCS[M+Na-2H]-296.97632859911
AllCCS[M+HCOO]-303.81832859911
DeepCCS[M+H]+270.60830932474
DeepCCS[M-H]-267.49130932474
DeepCCS[M-2H]-303.15530932474
DeepCCS[M+Na]+278.05530932474

Predicted Kovats Retention Indices

Not Available
Spectra

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6,10,14-tetramethylpentadecanoyl-CoA 10V, Positive-QTOFsplash10-0002-9000000004-9464482b5e09b803e9ed2021-10-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6,10,14-tetramethylpentadecanoyl-CoA 20V, Positive-QTOFsplash10-053l-7200000309-c3110acf0e21da6ca42c2021-10-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6,10,14-tetramethylpentadecanoyl-CoA 40V, Positive-QTOFsplash10-0006-0000390000-2f55f68806036eff826c2021-10-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6,10,14-tetramethylpentadecanoyl-CoA 10V, Negative-QTOFsplash10-0002-9000000000-bd4d1369e432ebec189b2021-10-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6,10,14-tetramethylpentadecanoyl-CoA 20V, Negative-QTOFsplash10-002s-9010101100-79f2af7a225c5b69a3142021-10-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2,6,10,14-tetramethylpentadecanoyl-CoA 40V, Negative-QTOFsplash10-004r-9103503601-11b5471db09004e225612021-10-21Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem CompoundNot Available
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Abe T, Fujino T, Fukuyama R, Minoshima S, Shimizu N, Toh H, Suzuki H, Yamamoto T: Human long-chain acyl-CoA synthetase: structure and chromosomal location. J Biochem. 1992 Jan;111(1):123-8. [PubMed:1607358 ]
  2. Wishart DS, Li C, Marcu A, Badran H, Pon A, Budinski Z, Patron J, Lipton D, Cao X, Oler E, Li K, Paccoud M, Hong C, Guo AC, Chan C, Wei W, Ramirez-Gaona M: PathBank: a comprehensive pathway database for model organisms. Nucleic Acids Res. 2020 Jan 8;48(D1):D470-D478. doi: 10.1093/nar/gkz861. [PubMed:31602464 ]