Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 00:37:40 UTC

Update Date

2021-09-26 22:57:24 UTC

HMDB ID

HMDB0247624

Secondary Accession Numbers

None

Metabolite Identification

Common Name

9,12,15,18,21-Tetracosapentaenoic acid

Description

9,12,15,18,21-Tetracosapentaenoic acid belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms. Based on a literature review very few articles have been published on 9,12,15,18,21-Tetracosapentaenoic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). 9,12,15,18,21-tetracosapentaenoic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 9,12,15,18,21-Tetracosapentaenoic acid is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv1652309112102372D          

 26 25  0  0  0  0            999 V2000
   -2.0033    3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7177    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7177    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4322    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4322    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7177    0.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7177    0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0033   -0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2888    0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5743   -0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    0.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9980    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8559    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7138    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  4  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  4  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
M  END

HMDB0247624
     RDKit          3D
9,12,15,18,21-Tetracosapentaenoic acid
 64 63  0  0  0  0  0  0  0  0999 V2000
    9.5832   -2.5485   -0.7897 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9553   -1.2396   -1.4469 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2697   -0.0862   -0.8126 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4546   -0.3021    0.2020 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7624    0.8385    0.8461 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2930    0.6014    0.7090 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4896    0.4895    1.7329 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0390    0.2537    1.5350 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7709    0.1784    0.0891 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9780    0.9832   -0.5418 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2219    2.0771    0.0153 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7202    1.7887   -0.2021 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3843    0.6811   -0.7710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8927    0.1351   -1.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1354    0.7947   -0.8439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5778    1.8802   -0.3310 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0043    2.2606   -0.2043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9375    1.1939   -0.6232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8515    0.0268    0.3161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7301   -1.0921   -0.1590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1709   -0.6797   -0.2274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0086   -1.8671   -0.6849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4648   -1.5779   -0.7946 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1194   -1.1800    0.4618 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3090   -0.7908    0.4483 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4340   -1.2338    1.6533 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0207   -3.4136   -1.3563 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4767   -2.7102   -0.8744 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8387   -2.5747    0.2701 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0578   -1.1164   -1.2841 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7028   -1.2311   -2.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4106    0.9347   -1.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2782   -1.3237    0.5823 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0505    0.9273    1.9136 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0839    1.7683    0.3455 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9225    0.5286   -0.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8695    0.5668    2.7302 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7306   -0.7137    2.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4710    1.0609    2.0241 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3012   -0.6431   -0.4506 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8843    0.8371   -1.6540 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3293    2.1910    1.1021 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4369    3.0686   -0.4738 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809    2.5717    0.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2868   -0.0081   -1.0459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9087   -0.9153   -0.5936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8298   -0.1807   -2.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0074    0.1444   -1.2846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9035    2.6371    0.0646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1450    2.5049    0.8974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2092    3.2494   -0.6943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7391    0.8841   -1.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0017    1.5840   -0.6660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8535   -0.2641    0.6425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3165    0.3808    1.3341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4100   -1.3022   -1.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5784   -1.9930    0.4769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2732    0.1546   -0.9827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5278   -0.3698    0.7622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6470   -2.1193   -1.7123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7958   -2.7508   -0.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6750   -0.7820   -1.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9538   -2.4950   -1.2355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7436   -0.6726    2.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  2  3
 10 11  1  0
 11 12  1  0
 12 13  2  3
 13 14  1  0
 14 15  1  0
 15 16  2  3
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  0
 17 51  1  0
 18 52  1  0
 18 53  1  0
 19 54  1  0
 19 55  1  0
 20 56  1  0
 20 57  1  0
 21 58  1  0
 21 59  1  0
 22 60  1  0
 22 61  1  0
 23 62  1  0
 23 63  1  0
 26 64  1  0
M  END


  Mrv1652309112102372D          

 26 25  0  0  0  0            999 V2000
   -2.0033    3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7177    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7177    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4322    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4322    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7177    0.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7177    0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0033   -0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2888    0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5743   -0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    0.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9980    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8559    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7138    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  4  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  4  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0247624

> <DATABASE_NAME>
hmdb

> <SMILES>
CCC=CCC=CCC=CCC=CCC=CCCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H38O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(25)26/h3-4,6-7,9-10,12-13,15-16H,2,5,8,11,14,17-23H2,1H3,(H,25,26)

> <INCHI_KEY>
NPTIBOCVSPURCS-UHFFFAOYSA-N

> <FORMULA>
C24H38O2

> <MOLECULAR_WEIGHT>
358.566

> <EXACT_MASS>
358.287180464

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
44.601976081866795

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
tetracosa-9,12,15,18,21-pentaenoic acid

> <ALOGPS_LOGP>
7.59

> <JCHEM_LOGP>
8.003523814333333

> <ALOGPS_LOGS>
-6.80

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.988167283903808

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
119.4746

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.64e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
tetracosa-9,12,15,18,21-pentaenoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0247624
     RDKit          3D
9,12,15,18,21-Tetracosapentaenoic acid
 64 63  0  0  0  0  0  0  0  0999 V2000
    9.5832   -2.5485   -0.7897 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9553   -1.2396   -1.4469 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2697   -0.0862   -0.8126 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4546   -0.3021    0.2020 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7624    0.8385    0.8461 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2930    0.6014    0.7090 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4896    0.4895    1.7329 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0390    0.2537    1.5350 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7709    0.1784    0.0891 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9780    0.9832   -0.5418 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2219    2.0771    0.0153 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7202    1.7887   -0.2021 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3843    0.6811   -0.7710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8927    0.1351   -1.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1354    0.7947   -0.8439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5778    1.8802   -0.3310 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0043    2.2606   -0.2043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9375    1.1939   -0.6232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8515    0.0268    0.3161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7301   -1.0921   -0.1590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1709   -0.6797   -0.2274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0086   -1.8671   -0.6849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4648   -1.5779   -0.7946 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1194   -1.1800    0.4618 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3090   -0.7908    0.4483 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4340   -1.2338    1.6533 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0207   -3.4136   -1.3563 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4767   -2.7102   -0.8744 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8387   -2.5747    0.2701 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0578   -1.1164   -1.2841 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7028   -1.2311   -2.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4106    0.9347   -1.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2782   -1.3237    0.5823 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0505    0.9273    1.9136 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0839    1.7683    0.3455 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9225    0.5286   -0.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8695    0.5668    2.7302 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7306   -0.7137    2.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4710    1.0609    2.0241 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3012   -0.6431   -0.4506 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8843    0.8371   -1.6540 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3293    2.1910    1.1021 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4369    3.0686   -0.4738 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809    2.5717    0.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2868   -0.0081   -1.0459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9087   -0.9153   -0.5936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8298   -0.1807   -2.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0074    0.1444   -1.2846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9035    2.6371    0.0646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1450    2.5049    0.8974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2092    3.2494   -0.6943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7391    0.8841   -1.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0017    1.5840   -0.6660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8535   -0.2641    0.6425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3165    0.3808    1.3341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4100   -1.3022   -1.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5784   -1.9930    0.4769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2732    0.1546   -0.9827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5278   -0.3698    0.7622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6470   -2.1193   -1.7123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7958   -2.7508   -0.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6750   -0.7820   -1.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9538   -2.4950   -1.2355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7436   -0.6726    2.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  2  3
 10 11  1  0
 11 12  1  0
 12 13  2  3
 13 14  1  0
 14 15  1  0
 15 16  2  3
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  0
 17 51  1  0
 18 52  1  0
 18 53  1  0
 19 54  1  0
 19 55  1  0
 20 56  1  0
 20 57  1  0
 21 58  1  0
 21 59  1  0
 22 60  1  0
 22 61  1  0
 23 62  1  0
 23 63  1  0
 26 64  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0      -3.739   7.081   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.073   6.311   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.073   4.771   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.407   4.001   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.407   2.461   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.073   1.691   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.073   0.151   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.739  -0.619   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.406   0.151   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.072  -0.619   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.262   0.151   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.262   1.691   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.595   2.461   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.595   4.001   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.929   4.771   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.263   4.001   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.596   4.771   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.264   4.771   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.597   4.001   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.931   4.771   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.265   4.001   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.598   4.771   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.932   4.001   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      16.266   4.771   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      14.932   2.461   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   50    0
END

COMPND    HMDB0247624
HETATM    1  C1  UNL     1       9.583  -2.548  -0.790  1.00  0.00           C  
HETATM    2  C2  UNL     1       9.955  -1.240  -1.447  1.00  0.00           C  
HETATM    3  C3  UNL     1       9.270  -0.086  -0.813  1.00  0.00           C  
HETATM    4  C4  UNL     1       8.455  -0.302   0.202  1.00  0.00           C  
HETATM    5  C5  UNL     1       7.762   0.839   0.846  1.00  0.00           C  
HETATM    6  C6  UNL     1       6.293   0.601   0.709  1.00  0.00           C  
HETATM    7  C7  UNL     1       5.490   0.489   1.733  1.00  0.00           C  
HETATM    8  C8  UNL     1       4.039   0.254   1.535  1.00  0.00           C  
HETATM    9  C9  UNL     1       3.771   0.178   0.089  1.00  0.00           C  
HETATM   10  C10 UNL     1       2.978   0.983  -0.542  1.00  0.00           C  
HETATM   11  C11 UNL     1       2.222   2.077   0.015  1.00  0.00           C  
HETATM   12  C12 UNL     1       0.720   1.789  -0.202  1.00  0.00           C  
HETATM   13  C13 UNL     1       0.384   0.681  -0.771  1.00  0.00           C  
HETATM   14  C14 UNL     1      -0.893   0.135  -1.108  1.00  0.00           C  
HETATM   15  C15 UNL     1      -2.135   0.795  -0.844  1.00  0.00           C  
HETATM   16  C16 UNL     1      -2.578   1.880  -0.331  1.00  0.00           C  
HETATM   17  C17 UNL     1      -4.004   2.261  -0.204  1.00  0.00           C  
HETATM   18  C18 UNL     1      -4.937   1.194  -0.623  1.00  0.00           C  
HETATM   19  C19 UNL     1      -4.852   0.027   0.316  1.00  0.00           C  
HETATM   20  C20 UNL     1      -5.730  -1.092  -0.159  1.00  0.00           C  
HETATM   21  C21 UNL     1      -7.171  -0.680  -0.227  1.00  0.00           C  
HETATM   22  C22 UNL     1      -8.009  -1.867  -0.685  1.00  0.00           C  
HETATM   23  C23 UNL     1      -9.465  -1.578  -0.795  1.00  0.00           C  
HETATM   24  C24 UNL     1     -10.119  -1.180   0.462  1.00  0.00           C  
HETATM   25  O1  UNL     1     -11.309  -0.791   0.448  1.00  0.00           O  
HETATM   26  O2  UNL     1      -9.434  -1.234   1.653  1.00  0.00           O  
HETATM   27  H1  UNL     1      10.021  -3.414  -1.356  1.00  0.00           H  
HETATM   28  H2  UNL     1       8.477  -2.710  -0.874  1.00  0.00           H  
HETATM   29  H3  UNL     1       9.839  -2.575   0.270  1.00  0.00           H  
HETATM   30  H4  UNL     1      11.058  -1.116  -1.284  1.00  0.00           H  
HETATM   31  H5  UNL     1       9.703  -1.231  -2.526  1.00  0.00           H  
HETATM   32  H6  UNL     1       9.411   0.935  -1.149  1.00  0.00           H  
HETATM   33  H7  UNL     1       8.278  -1.324   0.582  1.00  0.00           H  
HETATM   34  H8  UNL     1       8.051   0.927   1.914  1.00  0.00           H  
HETATM   35  H9  UNL     1       8.084   1.768   0.345  1.00  0.00           H  
HETATM   36  H10 UNL     1       5.922   0.529  -0.307  1.00  0.00           H  
HETATM   37  H11 UNL     1       5.870   0.567   2.730  1.00  0.00           H  
HETATM   38  H12 UNL     1       3.731  -0.714   2.042  1.00  0.00           H  
HETATM   39  H13 UNL     1       3.471   1.061   2.024  1.00  0.00           H  
HETATM   40  H14 UNL     1       4.301  -0.643  -0.451  1.00  0.00           H  
HETATM   41  H15 UNL     1       2.884   0.837  -1.654  1.00  0.00           H  
HETATM   42  H16 UNL     1       2.329   2.191   1.102  1.00  0.00           H  
HETATM   43  H17 UNL     1       2.437   3.069  -0.474  1.00  0.00           H  
HETATM   44  H18 UNL     1       0.081   2.572   0.158  1.00  0.00           H  
HETATM   45  H19 UNL     1       1.287  -0.008  -1.046  1.00  0.00           H  
HETATM   46  H20 UNL     1      -0.909  -0.915  -0.594  1.00  0.00           H  
HETATM   47  H21 UNL     1      -0.830  -0.181  -2.226  1.00  0.00           H  
HETATM   48  H22 UNL     1      -3.007   0.144  -1.285  1.00  0.00           H  
HETATM   49  H23 UNL     1      -1.903   2.637   0.065  1.00  0.00           H  
HETATM   50  H24 UNL     1      -4.145   2.505   0.897  1.00  0.00           H  
HETATM   51  H25 UNL     1      -4.209   3.249  -0.694  1.00  0.00           H  
HETATM   52  H26 UNL     1      -4.739   0.884  -1.660  1.00  0.00           H  
HETATM   53  H27 UNL     1      -6.002   1.584  -0.666  1.00  0.00           H  
HETATM   54  H28 UNL     1      -3.853  -0.264   0.643  1.00  0.00           H  
HETATM   55  H29 UNL     1      -5.317   0.381   1.334  1.00  0.00           H  
HETATM   56  H30 UNL     1      -5.410  -1.302  -1.218  1.00  0.00           H  
HETATM   57  H31 UNL     1      -5.578  -1.993   0.477  1.00  0.00           H  
HETATM   58  H32 UNL     1      -7.273   0.155  -0.983  1.00  0.00           H  
HETATM   59  H33 UNL     1      -7.528  -0.370   0.762  1.00  0.00           H  
HETATM   60  H34 UNL     1      -7.647  -2.119  -1.712  1.00  0.00           H  
HETATM   61  H35 UNL     1      -7.796  -2.751  -0.060  1.00  0.00           H  
HETATM   62  H36 UNL     1      -9.675  -0.782  -1.572  1.00  0.00           H  
HETATM   63  H37 UNL     1      -9.954  -2.495  -1.236  1.00  0.00           H  
HETATM   64  H38 UNL     1      -9.744  -0.673   2.442  1.00  0.00           H  
CONECT    1    2   27   28   29
CONECT    2    3   30   31
CONECT    3    4    4   32
CONECT    4    5   33
CONECT    5    6   34   35
CONECT    6    7    7   36
CONECT    7    8   37
CONECT    8    9   38   39
CONECT    9   10   10   40
CONECT   10   11   41
CONECT   11   12   42   43
CONECT   12   13   13   44
CONECT   13   14   45
CONECT   14   15   46   47
CONECT   15   16   16   48
CONECT   16   17   49
CONECT   17   18   50   51
CONECT   18   19   52   53
CONECT   19   20   54   55
CONECT   20   21   56   57
CONECT   21   22   58   59
CONECT   22   23   60   61
CONECT   23   24   62   63
CONECT   24   25   25   26
CONECT   26   64
END

HMDB0247624
     RDKit          3D
9,12,15,18,21-Tetracosapentaenoic acid
 64 63  0  0  0  0  0  0  0  0999 V2000
    9.5832   -2.5485   -0.7897 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9553   -1.2396   -1.4469 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2697   -0.0862   -0.8126 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4546   -0.3021    0.2020 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7624    0.8385    0.8461 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2930    0.6014    0.7090 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4896    0.4895    1.7329 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0390    0.2537    1.5350 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7709    0.1784    0.0891 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9780    0.9832   -0.5418 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2219    2.0771    0.0153 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7202    1.7887   -0.2021 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3843    0.6811   -0.7710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8927    0.1351   -1.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1354    0.7947   -0.8439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5778    1.8802   -0.3310 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0043    2.2606   -0.2043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9375    1.1939   -0.6232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8515    0.0268    0.3161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7301   -1.0921   -0.1590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1709   -0.6797   -0.2274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0086   -1.8671   -0.6849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4648   -1.5779   -0.7946 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1194   -1.1800    0.4618 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3090   -0.7908    0.4483 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4340   -1.2338    1.6533 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0207   -3.4136   -1.3563 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4767   -2.7102   -0.8744 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8387   -2.5747    0.2701 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0578   -1.1164   -1.2841 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7028   -1.2311   -2.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4106    0.9347   -1.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2782   -1.3237    0.5823 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0505    0.9273    1.9136 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0839    1.7683    0.3455 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9225    0.5286   -0.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8695    0.5668    2.7302 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7306   -0.7137    2.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4710    1.0609    2.0241 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3012   -0.6431   -0.4506 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8843    0.8371   -1.6540 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3293    2.1910    1.1021 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4369    3.0686   -0.4738 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809    2.5717    0.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2868   -0.0081   -1.0459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9087   -0.9153   -0.5936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8298   -0.1807   -2.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0074    0.1444   -1.2846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9035    2.6371    0.0646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1450    2.5049    0.8974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2092    3.2494   -0.6943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7391    0.8841   -1.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0017    1.5840   -0.6660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8535   -0.2641    0.6425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3165    0.3808    1.3341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4100   -1.3022   -1.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5784   -1.9930    0.4769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2732    0.1546   -0.9827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5278   -0.3698    0.7622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6470   -2.1193   -1.7123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7958   -2.7508   -0.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6750   -0.7820   -1.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9538   -2.4950   -1.2355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7436   -0.6726    2.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  2  3
 10 11  1  0
 11 12  1  0
 12 13  2  3
 13 14  1  0
 14 15  1  0
 15 16  2  3
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  0
 17 51  1  0
 18 52  1  0
 18 53  1  0
 19 54  1  0
 19 55  1  0
 20 56  1  0
 20 57  1  0
 21 58  1  0
 21 59  1  0
 22 60  1  0
 22 61  1  0
 23 62  1  0
 23 63  1  0
 26 64  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
9,12,15,18,21-Tetracosapentaenoate	Generator

Chemical Formula

C₂₄H₃₈O₂

Average Molecular Weight

358.566

Monoisotopic Molecular Weight

358.287180464

IUPAC Name

tetracosa-9,12,15,18,21-pentaenoic acid

Traditional Name

tetracosa-9,12,15,18,21-pentaenoic acid

CAS Registry Number

Not Available

SMILES

CCC=CCC=CCC=CCC=CCC=CCCCCCCCC(O)=O

InChI Identifier

InChI=1S/C24H38O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(25)26/h3-4,6-7,9-10,12-13,15-16H,2,5,8,11,14,17-23H2,1H3,(H,25,26)

InChI Key

NPTIBOCVSPURCS-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Very long-chain fatty acids

Alternative Parents

Substituents

Very long-chain fatty acid
Unsaturated fatty acid
Straight chain fatty acid
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	7.59	ALOGPS
logP	8	ChemAxon
logS	-6.8	ALOGPS
pKa (Strongest Acidic)	4.99	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	119.47 m³·mol⁻¹	ChemAxon
Polarizability	44.6 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	188.06	30932474
DeepCCS	[M-H]-	185.702	30932474
DeepCCS	[M-2H]-	218.588	30932474
DeepCCS	[M+Na]+	194.153	30932474
AllCCS	[M+H]+	198.4	32859911
AllCCS	[M+H-H2O]+	195.8	32859911
AllCCS	[M+NH4]+	200.8	32859911
AllCCS	[M+Na]+	201.5	32859911
AllCCS	[M-H]-	198.7	32859911
AllCCS	[M+Na-2H]-	201.4	32859911
AllCCS	[M+HCOO]-	204.5	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Predicted by Siyang on May 30, 2022	31.0627 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.46 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	3662.3 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	734.9 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	304.7 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	565.7 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	882.5 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	1455.9 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	786.9 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	96.2 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	2874.5 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	952.7 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	2272.2 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	1102.0 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	650.6 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	554.1 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	702.8 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	9.3 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
9,12,15,18,21-Tetracosapentaenoic acid	CCC=CCC=CCC=CCC=CCC=CCCCCCCCC(O)=O	4061.8	Standard polar	33892256
9,12,15,18,21-Tetracosapentaenoic acid	CCC=CCC=CCC=CCC=CCC=CCCCCCCCC(O)=O	2479.5	Standard non polar	33892256
9,12,15,18,21-Tetracosapentaenoic acid	CCC=CCC=CCC=CCC=CCC=CCCCCCCCC(O)=O	2730.3	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 9,12,15,18,21-Tetracosapentaenoic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-0573-4291000000-6ea1ffbff016c500f881	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9,12,15,18,21-Tetracosapentaenoic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9,12,15,18,21-Tetracosapentaenoic acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 9,12,15,18,21-Tetracosapentaenoic acid GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 9,12,15,18,21-Tetracosapentaenoic acid 10V, Positive-QTOF	splash10-0a4l-1209000000-64c8332d7a4d08496bd0	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 9,12,15,18,21-Tetracosapentaenoic acid 20V, Positive-QTOF	splash10-001i-7935000000-24270d7686c4efb93ee9	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 9,12,15,18,21-Tetracosapentaenoic acid 40V, Positive-QTOF	splash10-001i-9700000000-31fdde5bd12aea13cb7d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 9,12,15,18,21-Tetracosapentaenoic acid 10V, Negative-QTOF	splash10-0a4i-0009000000-d0130aa56928ec01bd25	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 9,12,15,18,21-Tetracosapentaenoic acid 20V, Negative-QTOF	splash10-0a4r-1009000000-cdb09eaf51e739ac062b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 9,12,15,18,21-Tetracosapentaenoic acid 40V, Negative-QTOF	splash10-000f-9112000000-dedeae256c4d74390dfb	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

57561560

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54124086

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for 9,12,15,18,21-Tetracosapentaenoic acid (HMDB0247624)

MOL for HMDB0247624 (9,12,15,18,21-Tetracosapentaenoic acid)

3D MOL for HMDB0247624 (9,12,15,18,21-Tetracosapentaenoic acid)

3D SDF for HMDB0247624 (9,12,15,18,21-Tetracosapentaenoic acid)

3D-SDF for HMDB0247624 (9,12,15,18,21-Tetracosapentaenoic acid)

PDB for HMDB0247624 (9,12,15,18,21-Tetracosapentaenoic acid)

3D PDB for HMDB0247624 (9,12,15,18,21-Tetracosapentaenoic acid)

SMILES for HMDB0247624 (9,12,15,18,21-Tetracosapentaenoic acid)

INCHI for HMDB0247624 (9,12,15,18,21-Tetracosapentaenoic acid)

Structure for HMDB0247624 (9,12,15,18,21-Tetracosapentaenoic acid)

3D Structure for HMDB0247624 (9,12,15,18,21-Tetracosapentaenoic acid)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra