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

Details

Stereochemistry ACHIRAL
Molecular Formula C19H14N2O4
Molecular Weight 334.3255
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of C-286

SMILES

CC1=C2OC(=CC2=C(C)C=C1)C3=NC(=NO3)C4=CC=C(C=C4)C(O)=O

InChI

InChIKey=AVCXUODHLRZJJP-UHFFFAOYSA-N
InChI=1S/C19H14N2O4/c1-10-3-4-11(2)16-14(10)9-15(24-16)18-20-17(21-25-18)12-5-7-13(8-6-12)19(22)23/h3-9H,1-2H3,(H,22,23)

HIDE SMILES / InChI

Molecular Formula C19H14N2O4
Molecular Weight 334.3255
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 18:21:31 GMT 2023
Edited
by admin
on Sat Dec 16 18:21:31 GMT 2023
Record UNII
N8LRS5GBB6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
C-286
Code English
RAR.BETA. AGONIST COMPOUND 10
Common Name English
BHBA001
Code English
BENZOIC ACID, 4-(5-(4,7-DIMETHYL-2-BENZOFURANYL)-1,2,4-OXADIAZOL-3-YL)-
Systematic Name English
BHBA-001
Code English
C286
Code English
4-(5-(4,7-DIMETHYLBENZOFURAN-2-YL)-1,2,4-OXADIAZOL-3-YL) BENZOIC ACID
Systematic Name English
4-(5-(4,7-DIMETHYL-2-BENZOFURANYL)-1,2,4-OXADIAZOL-3-YL)BENZOIC ACID
Systematic Name English
Code System Code Type Description
WIKIPEDIA
C286
Created by admin on Sat Dec 16 18:21:31 GMT 2023 , Edited by admin on Sat Dec 16 18:21:31 GMT 2023
PRIMARY
PUBCHEM
121414283
Created by admin on Sat Dec 16 18:21:31 GMT 2023 , Edited by admin on Sat Dec 16 18:21:31 GMT 2023
PRIMARY
EPA CompTox
DTXSID401336569
Created by admin on Sat Dec 16 18:21:31 GMT 2023 , Edited by admin on Sat Dec 16 18:21:31 GMT 2023
PRIMARY
FDA UNII
N8LRS5GBB6
Created by admin on Sat Dec 16 18:21:31 GMT 2023 , Edited by admin on Sat Dec 16 18:21:31 GMT 2023
PRIMARY
CAS
1952276-71-9
Created by admin on Sat Dec 16 18:21:31 GMT 2023 , Edited by admin on Sat Dec 16 18:21:31 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY