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Details

Stereochemistry ACHIRAL
Molecular Formula C6H5NO3
Molecular Weight 139.1088
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Oxiniacic Acid

SMILES

OC(=O)C1=CC=C[N+]([O-])=C1

InChI

InChIKey=FJCFFCXMEXZEIM-UHFFFAOYSA-N
InChI=1S/C6H5NO3/c8-6(9)5-2-1-3-7(10)4-5/h1-4H,(H,8,9)

HIDE SMILES / InChI
Oxiniacic Acid is a nicotinic acid derivative, that shows potent hypolipidemic activity.

Originator

Sources: Journal of the Chemical Society (1949), (Suppl. Issue, No. 1), S231-2

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Inhibition of liver glutathione S-transferase activity in rats by hypolipidemic drugs related or unrelated to clofibrate.
1986 May 15
Patents

Patents

Sample Use Guides

Rats were given a daily i.p. injection for 10 days of ethanolamine oxiniacate (500 mg/kg).
Route of Administration: Intraperitoneal
In Vitro Use Guide
Unknown
Name Type Language
Oxiniacic Acid
INN   MI  
INN  
Official Name English
OXINIACIC ACID [MI]
Common Name English
3-Pyridinecarboxylic acid, 1-oxide
Systematic Name English
Nicotinic acid, 1-oxide
Systematic Name English
oxiniacic acid [INN]
Common Name English
Nicotinic acid N-oxide
Systematic Name English
NSC-93890
Code English
Classification Tree Code System Code
NCI_THESAURUS C345
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
NCI_THESAURUS C98151
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
Code System Code Type Description
PUBCHEM
16976
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY
MERCK INDEX
m8310
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
Nicotinic acid N-oxide
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY
SMS_ID
100000083065
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY
DRUG CENTRAL
3410
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY
NCI_THESAURUS
C66269
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY
CAS
2398-81-4
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY
ChEMBL
CHEMBL1591725
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY
ECHA (EC/EINECS)
219-265-0
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY
EPA CompTox
DTXSID2046543
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY
NSC
93890
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY
EVMPD
SUB09533MIG
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY
FDA UNII
YY03Q39E6L
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY
INN
2768
Created by admin on Fri Dec 15 15:43:55 GMT 2023 , Edited by admin on Fri Dec 15 15:43:55 GMT 2023
PRIMARY