Record Information |
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Version | 5.0 |
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Status | Expected but not Quantified |
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Creation Date | 2006-05-22 14:17:38 UTC |
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Update Date | 2021-09-14 15:44:56 UTC |
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HMDB ID | HMDB0002148 |
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Secondary Accession Numbers | |
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Metabolite Identification |
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Common Name | 5-Methyltetrahydropteroylpentaglutamate |
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Description | 5-Methyltetrahydropteroylpentaglutamate belongs to the class of organic compounds known as tetrahydrofolic acids and derivatives. These are heterocyclic compounds based on the 5,6,7,8-tetrahydropteroic acid skeleton conjugated with at least one L-glutamic acid unit (or a derivative thereof) . 5-Methyltetrahydropteroylpentaglutamate has been detected, but not quantified in, a few different foods, such as anatidaes (Anatidae), chickens (Gallus gallus), and domestic pigs (Sus scrofa domestica). This could make 5-methyltetrahydropteroylpentaglutamate a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 5-Methyltetrahydropteroylpentaglutamate. |
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Structure | CN1C(CNC2=CC=C(C=C2)C(=O)N(C(=O)CC[C@H](N)C(O)=O)[C@](C(CC(O)=O)C(=O)CC[C@H](N)C(O)=O)(C(=O)CC[C@H](N)C(O)=O)C(=O)OC(=O)CC[C@H](N)C(O)=O)CNC2=C1C(=O)N=C(N)N2 InChI=1S/C40H53N11O18/c1-50-19(16-47-31-30(50)32(58)49-39(45)48-31)15-46-18-4-2-17(3-5-18)33(59)51(27(54)12-8-23(43)36(64)65)40(26(53)11-7-22(42)35(62)63,38(68)69-29(57)13-9-24(44)37(66)67)20(14-28(55)56)25(52)10-6-21(41)34(60)61/h2-5,19-24,46H,6-16,41-44H2,1H3,(H,55,56)(H,60,61)(H,62,63)(H,64,65)(H,66,67)(H4,45,47,48,49,58)/t19?,20?,21-,22-,23-,24-,40+/m0/s1 |
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Synonyms | Value | Source |
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5-Methyltetrahydropteroylpentaglutamic acid | Generator | 5-Me-THF(glu)5 | HMDB, MeSH | (2S,6R,11S)-2,11-Diamino-6-{n-[(4S)-4-amino-4-carboxybutanoyl]-1-(4-{[(4-hydroxy-2-imino-5-methyl-1,2,5,6,7,8-hexahydropteridin-6-yl)methyl]amino}phenyl)formamido}-6-({[(4S)-4-amino-4-carboxybutanoyl]oxy}carbonyl)-7-(carboxymethyl)-5,8-dioxododecanedioate | Generator, HMDB | 5-Methyltetrahydropteroylpentaglutamate | MeSH |
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Chemical Formula | C40H53N11O18 |
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Average Molecular Weight | 975.9117 |
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Monoisotopic Molecular Weight | 975.357003947 |
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IUPAC Name | (2S,6R,11S)-2,11-diamino-6-{N-[(4S)-4-amino-4-carboxybutanoyl]-1-(4-{[(2-amino-5-methyl-4-oxo-1,4,5,6,7,8-hexahydropteridin-6-yl)methyl]amino}phenyl)formamido}-6-({[(4S)-4-amino-4-carboxybutanoyl]oxy}carbonyl)-7-(carboxymethyl)-5,8-dioxododecanedioic acid |
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Traditional Name | (2S,6R,11S)-2,11-diamino-6-{N-[(4S)-4-amino-4-carboxybutanoyl]-1-(4-{[(2-amino-5-methyl-4-oxo-1,6,7,8-tetrahydropteridin-6-yl)methyl]amino}phenyl)formamido}-6-({[(4S)-4-amino-4-carboxybutanoyl]oxy}carbonyl)-7-(carboxymethyl)-5,8-dioxododecanedioic acid |
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CAS Registry Number | 39555-46-9 |
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SMILES | CN1C(CNC2=CC=C(C=C2)C(=O)N(C(=O)CC[C@H](N)C(O)=O)[C@](C(CC(O)=O)C(=O)CC[C@H](N)C(O)=O)(C(=O)CC[C@H](N)C(O)=O)C(=O)OC(=O)CC[C@H](N)C(O)=O)CNC2=C1C(=O)N=C(N)N2 |
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InChI Identifier | InChI=1S/C40H53N11O18/c1-50-19(16-47-31-30(50)32(58)49-39(45)48-31)15-46-18-4-2-17(3-5-18)33(59)51(27(54)12-8-23(43)36(64)65)40(26(53)11-7-22(42)35(62)63,38(68)69-29(57)13-9-24(44)37(66)67)20(14-28(55)56)25(52)10-6-21(41)34(60)61/h2-5,19-24,46H,6-16,41-44H2,1H3,(H,55,56)(H,60,61)(H,62,63)(H,64,65)(H,66,67)(H4,45,47,48,49,58)/t19?,20?,21-,22-,23-,24-,40+/m0/s1 |
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InChI Key | WNRFVFOPCUPRFK-JPUKBXPDSA-N |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as tetrahydrofolic acids and derivatives. These are heterocyclic compounds based on the 5,6,7,8-tetrahydropteroic acid skeleton conjugated with at least one L-glutamic acid unit (or a derivative thereof). |
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Kingdom | Organic compounds |
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Super Class | Organoheterocyclic compounds |
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Class | Pteridines and derivatives |
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Sub Class | Pterins and derivatives |
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Direct Parent | Tetrahydrofolic acids and derivatives |
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Alternative Parents | |
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Substituents | - Tetrahydrofolic acid or derivatives
- N-epsilon-acetyl-lysine
- Glutamic acid or derivatives
- Glutamine or derivatives
- Hippuric acid or derivatives
- Aminobenzamide
- Aminobenzoic acid or derivatives
- Alpha-amino acid
- L-alpha-amino acid
- Alpha-amino acid or derivatives
- Benzoic acid or derivatives
- Phenylalkylamine
- Aniline or substituted anilines
- Dialkylarylamine
- Gamma-keto acid
- Tertiary aliphatic/aromatic amine
- Benzoyl
- Beta-keto acid
- Secondary aliphatic/aromatic amine
- Amino fatty acid
- Aminopyrimidine
- Pyrimidone
- Monocyclic benzene moiety
- Fatty acyl
- Gamma-aminoketone
- Benzenoid
- Keto acid
- N-acyl-amine
- Carboxylic acid imide, n-substituted
- Pyrimidine
- Heteroaromatic compound
- Carboxylic acid anhydride
- Carboxylic acid imide
- Dicarboximide
- Vinylogous amide
- Amino acid
- Tertiary amine
- Ketone
- Amino acid or derivatives
- Carboxylic acid derivative
- Azacycle
- Secondary amine
- Carboxylic acid
- Primary amine
- Carbonyl group
- Organic oxygen compound
- Primary aliphatic amine
- Organic nitrogen compound
- Organic oxide
- Hydrocarbon derivative
- Organonitrogen compound
- Organopnictogen compound
- Organooxygen compound
- Amine
- Aromatic heteropolycyclic compound
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Molecular Framework | Aromatic heteropolycyclic compounds |
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External Descriptors | Not Available |
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Ontology |
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Physiological effect | Not Available |
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Disposition | |
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Process | Not Available |
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Role | Not Available |
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Physical Properties |
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State | Solid |
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Experimental Molecular Properties | Property | Value | Reference |
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Melting Point | Not Available | Not Available | Boiling Point | Not Available | Not Available | Water Solubility | Not Available | Not Available | LogP | Not Available | Not Available |
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Experimental Chromatographic Properties | Not Available |
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Predicted Molecular Properties | |
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Predicted Chromatographic Properties | Predicted Collision Cross SectionsPredicted Kovats Retention IndicesNot Available |
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