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Record Information |
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| Version |
1.0 |
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| Update Date |
1/22/2018 11:54:54 AM |
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Metabolite ID | PAMDB001710 |
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Identification |
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| Name: |
Acyl phosphatidylglycerol (N-C18:1) |
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| Description: | Phosphatidylglycerol is a glycerophospholipid. The general structure of phosphatidylglycerol consists of a L-glycerol 3-phosphate backbone ester-bonded to either saturated or unsaturated fatty acids on carbons 1 and 2. The head group substituent glycerol is bonded through a phosphomonoester. Phosphatidylglycerol is important as an intermediate for biosynthesis of other lipids, including cardiolipins. |
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Structure |
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| Synonyms: | Not Available |
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Chemical Formula: |
C60H110O11P |
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| Average Molecular Weight: |
1038.4826 |
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| Monoisotopic Molecular
Weight: |
1037.778575874 |
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| InChI Key: |
MNEWMEXDRDMOEP-IKVQWSBMSA-M |
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| InChI: | InChI=1S/C60H111O11P/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-46-49-58(62)67-52-56(61)53-69-72(65,66)70-55-57(71-60(64)51-48-45-42-39-36-33-30-27-24-21-18-15-12-9-6-3)54-68-59(63)50-47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h19-24,56-57,61H,4-18,25-55H2,1-3H3,(H,65,66)/p-1/b22-19+,23-20+,24-21+ |
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| CAS
number: |
Not Available |
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| IUPAC Name: | 3-({2,3-bis[(11E)-octadec-11-enoyloxy]propyl phosphonato}oxy)-2-hydroxypropyl (11E)-octadec-11-enoate |
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Traditional IUPAC Name: |
3-({2,3-bis[(11E)-octadec-11-enoyloxy]propyl phosphonato}oxy)-2-hydroxypropyl (11E)-octadec-11-enoate |
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| SMILES: | [H]\C(CCCCCC)=C(\[H])CCCCCCCCCC(=O)OCC(O)COP([O-])(=O)OCC(COC(=O)CCCCCCCCC\C([H])=C(/[H])CCCCCC)OC(=O)CCCCCCCCC\C([H])=C(/[H])CCCCCC |
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Chemical Taxonomy |
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Taxonomy Description | This compound belongs to the class of organic compounds known as semilysobisphosphatidic acids. These are bisphosphatidic acid analogues with three moles of fatty acid per mole of lipid. |
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Kingdom |
Organic compounds |
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| Super Class | Lipids and lipid-like molecules |
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Class |
Glycerophospholipids |
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| Sub Class | Semilysobisphosphatidic acids |
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Direct Parent |
Semilysobisphosphatidic acids |
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| Alternative Parents |
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| Substituents |
- Semilysobisphosphatidic acid
- Tricarboxylic acid or derivatives
- Dialkyl phosphate
- Fatty acid ester
- Fatty acyl
- Alkyl phosphate
- Phosphoric acid ester
- Organic phosphoric acid derivative
- Organic phosphate
- Secondary alcohol
- Carboxylic acid ester
- Carboxylic acid derivative
- Hydrocarbon derivative
- Organooxygen compound
- Carbonyl group
- Alcohol
- Organic anion
- Aliphatic acyclic compound
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| Molecular Framework |
Aliphatic acyclic compounds |
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| External Descriptors |
Not Available |
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Physical Properties |
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| State: |
Not Available |
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| Charge: | -1 |
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Melting point: |
Not Available |
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| Experimental Properties: |
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| Predicted Properties |
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Biological Properties |
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| Cellular Locations: |
Membrane |
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| Reactions: | |
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Pathways: |
Not Available |
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Spectra |
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| Spectra: |
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References |
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| References: |
- Yurtsever D. (2007). Fatty acid methyl ester profiling of Enterococcus and Esherichia coli for microbial source tracking. M.sc. Thesis. Villanova University: U.S.A
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| Synthesis Reference: |
Not Available |
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| Material Safety Data Sheet (MSDS) |
Not Available |
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Links |
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| External Links: |
| Resource | Link |
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| CHEBI ID | Not Available | | HMDB ID | Not Available | | Pubchem Compound ID | Not Available | | Kegg ID | Not Available | | ChemSpider ID | Not Available | | Wikipedia ID | Not Available | | BioCyc ID | CPD0-2179 | | EcoCyc ID | CPD0-2179 |
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