| Record Information |
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| Version | 1.0 |
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| Created at | 2020-03-30 20:16:44 UTC |
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| Updated at | 2020-11-18 16:38:03 UTC |
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| CannabisDB ID | CDB003023 |
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| Secondary Accession Numbers | Not Available |
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| Cannabis Compound Identification |
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| Common Name | PA(18:0/18:0) |
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| Description | PA(18:0/18:0)is a phosphatidic acid. It is a glycerophospholipid in which a phosphate moiety occupies a glycerol substitution site. As is the case with diacylglycerols, phosphatidic acids can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PA(18:0/18:0), in particular, consists of two octadecanoyl chain at positions C-1 and C2. The oleic acid moiety is derived from vegetable oils, especially olive and canola oil, while the oleic acid moiety is derived from vegetable oils, especially olive and canola oil. Phosphatidic acids are quite rare but are extremely important as intermediates in the biosynthesis of triacylglycerols and phospholipids. This compound is expected to be in Cannabis as all living plants are known to produce and metabolize it. |
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| Structure | |
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| Synonyms | | Value | Source |
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| 1,2-Distearoyl-L-phosphatidic acid | ChEBI | | beta,gamma-Distearoyl-L-alpha-phosphatidic acid | ChEBI | | Distearoyl phosphatidic acid | ChEBI | | PA 18:0/18:0 | ChEBI | | 1,2-Distearoyl-L-phosphatidate | Generator | | b,g-Distearoyl-L-a-phosphatidate | Generator | | b,g-Distearoyl-L-a-phosphatidic acid | Generator | | beta,gamma-Distearoyl-L-alpha-phosphatidate | Generator | | Β,γ-distearoyl-L-α-phosphatidate | Generator | | Β,γ-distearoyl-L-α-phosphatidic acid | Generator | | Distearoyl phosphatidate | Generator |
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| Chemical Formula | C39H77O8P |
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| Average Molecular Weight | 705.01 |
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| Monoisotopic Molecular Weight | 704.5356 |
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| IUPAC Name | [(2R)-2,3-bis(octadecanoyloxy)propoxy]phosphonic acid |
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| Traditional Name | distearoyl phosphatidic acid |
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| CAS Registry Number | Not Available |
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| SMILES | [H][C@@](COC(=O)CCCCCCCCCCCCCCCCC)(COP(O)(O)=O)OC(=O)CCCCCCCCCCCCCCCCC |
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| InChI Identifier | InChI=1S/C39H77O8P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(40)45-35-37(36-46-48(42,43)44)47-39(41)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h37H,3-36H2,1-2H3,(H2,42,43,44)/t37-/m1/s1 |
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| InChI Key | YFWHNAWEOZTIPI-DIPNUNPCSA-N |
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| Chemical Taxonomy |
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| Description | Belongs to the class of organic compounds known as 1,2-diacylglycerol-3-phosphates. These are glycerol-3-phosphates in which the glycerol moiety is bonded to two aliphatic chains through ester linkages. |
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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 | Glycerophosphates |
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| Direct Parent | 1,2-diacylglycerol-3-phosphates |
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| Alternative Parents | |
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| Substituents | - 1,2-diacylglycerol-3-phosphate
- Fatty acid ester
- Monoalkyl phosphate
- Dicarboxylic acid or derivatives
- Fatty acyl
- Alkyl phosphate
- Phosphoric acid ester
- Organic phosphoric acid derivative
- Carboxylic acid ester
- Carboxylic acid derivative
- Hydrocarbon derivative
- Organic oxide
- Organic oxygen compound
- Carbonyl group
- Organooxygen compound
- Aliphatic acyclic compound
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| Molecular Framework | Aliphatic acyclic compounds |
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| External Descriptors | |
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| Ontology |
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|
Not Available | | Physical Properties |
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| State | Not Available |
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| Experimental 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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| Predicted Properties | [] |
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