U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C19H39O7P
Molecular Weight 410.4825
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-PALMITOYL-SN-GLYCEROL 3-PHOSPHATE

SMILES

CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(O)(O)=O

InChI

InChIKey=YNDYKPRNFWPPFU-GOSISDBHSA-N
InChI=1S/C19H39O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19(21)25-16-18(20)17-26-27(22,23)24/h18,20H,2-17H2,1H3,(H2,22,23,24)/t18-/m1/s1

HIDE SMILES / InChI

Molecular Formula C19H39O7P
Molecular Weight 410.4825
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Specific phospholipids enhance the activity of beta-lactam antibiotics against Pseudomonas aeruginosa.
2000 Sep
Identification of p2y9/GPR23 as a novel G protein-coupled receptor for lysophosphatidic acid, structurally distant from the Edg family.
2003 Jul 11
Substance Class Chemical
Created
by admin
on Sat Dec 16 15:06:56 GMT 2023
Edited
by admin
on Sat Dec 16 15:06:56 GMT 2023
Record UNII
DJA0CXH1MJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-PALMITOYL-SN-GLYCEROL 3-PHOSPHATE
Common Name English
1-PALMITOYL-SN-GLYCERYL 3-PHOSPHATE
Common Name English
PALMITIN, 1-MONO-, 3-(DIHYDROGEN PHOSPHATE), L-
Common Name English
Code System Code Type Description
CAS
7220-34-0
Created by admin on Sat Dec 16 15:06:56 GMT 2023 , Edited by admin on Sat Dec 16 15:06:56 GMT 2023
PRIMARY
EPA CompTox
DTXSID401292133
Created by admin on Sat Dec 16 15:06:56 GMT 2023 , Edited by admin on Sat Dec 16 15:06:56 GMT 2023
PRIMARY
PUBCHEM
6419701
Created by admin on Sat Dec 16 15:06:56 GMT 2023 , Edited by admin on Sat Dec 16 15:06:56 GMT 2023
PRIMARY
FDA UNII
DJA0CXH1MJ
Created by admin on Sat Dec 16 15:06:56 GMT 2023 , Edited by admin on Sat Dec 16 15:06:56 GMT 2023
PRIMARY