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Details

Stereochemistry ACHIRAL
Molecular Formula C18H33NO4
Molecular Weight 327.4589
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CXA-10

SMILES

CCCCCCCC\C(=C/CCCCCCCC(O)=O)[N+]([O-])=O

InChI

InChIKey=WRADPCFZZWXOTI-BMRADRMJSA-N
InChI=1S/C18H33NO4/c1-2-3-4-5-8-11-14-17(19(22)23)15-12-9-6-7-10-13-16-18(20)21/h15H,2-14,16H2,1H3,(H,20,21)/b17-15+

HIDE SMILES / InChI

Approval Year

Name Type Language
CXA-10
Code English
9-OCTADECENOIC ACID, 10-NITRO-, (9E)-
Systematic Name English
10-NITROOLEIC ACID
Systematic Name English
OA-NO2
Common Name English
E-10-NO2-18:1
Common Name English
10-NITRO-9(E)-OCTADEC-9-ENOIC ACID
Systematic Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 701019
Created by admin on Sat Dec 16 01:55:13 GMT 2023 , Edited by admin on Sat Dec 16 01:55:13 GMT 2023
Code System Code Type Description
DRUG BANK
DB15026
Created by admin on Sat Dec 16 01:55:13 GMT 2023 , Edited by admin on Sat Dec 16 01:55:13 GMT 2023
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FDA UNII
1N19AGY57Y
Created by admin on Sat Dec 16 01:55:13 GMT 2023 , Edited by admin on Sat Dec 16 01:55:13 GMT 2023
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CAS
875685-46-4
Created by admin on Sat Dec 16 01:55:13 GMT 2023 , Edited by admin on Sat Dec 16 01:55:13 GMT 2023
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SMS_ID
300000020411
Created by admin on Sat Dec 16 01:55:13 GMT 2023 , Edited by admin on Sat Dec 16 01:55:13 GMT 2023
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MANUFACTURER PRODUCT INFORMATION
CXA-10
Created by admin on Sat Dec 16 01:55:13 GMT 2023 , Edited by admin on Sat Dec 16 01:55:13 GMT 2023
PRIMARY 10-Nitrooleate: Item NO. 10008043, CAS NO. 875685-46-4Description: Synonyms - (1)10-Nitrooleic Acid, (2)10-nitro-9-trans-Octadecenoic AcidNitrated unsaturated fatty acids, such as 10- and 12-nitrolinoleate (LNO2Item No. 10037), cholesteryl nitrolinoleate, and nitrohydroxylinoleate, represent a new class of endogenous lipid-derived signalling molecules. LNO2 isomers serve as potent endogenous ligands for PPAR.GAMMA. and can also decompose or be metabolized to release nitric oxide. 10-Nitrooleate is one of two regioisomers of nitrooleate, the other being 9-nitrooleate (Item No. 10008042) (OA-NO2, used for the mixture of isomers), which are formed by nitration of oleic acid in approximately equal proportions in vivo. Peroxynitrite, acidified nitrite, and myeloperoxidase in the presence of H2O2 and nitrite, all mediate the nitration of oleic acid. OA-NO2 is found in human plasma as the free acid and esterified in phospholipids at concentrations of 619 +/- 52 nM and 302 +/- 369 nM, respectively. OA-NO2 activates PPAR.GAMMA. approximately 7-fold at a concentration of 1 uM. and effectively promotes differentiation 3T3-L1 preadipocytes to adipocytes at 3 uM.
PUBCHEM
24836820
Created by admin on Sat Dec 16 01:55:13 GMT 2023 , Edited by admin on Sat Dec 16 01:55:13 GMT 2023
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