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

Details

Stereochemistry RACEMIC
Molecular Formula C16H16O2
Molecular Weight 240.297
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of XENBUCIN

SMILES

CCC(C(O)=O)C1=CC=C(C=C1)C2=CC=CC=C2

InChI

InChIKey=IYEPZNKOJZOGJG-UHFFFAOYSA-N
InChI=1S/C16H16O2/c1-2-15(16(17)18)14-10-8-13(9-11-14)12-6-4-3-5-7-12/h3-11,15H,2H2,1H3,(H,17,18)

HIDE SMILES / InChI

Molecular Formula C16H16O2
Molecular Weight 240.297
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Xenbucin is an antihyperlipidemic agent. Information about the current use of this agent is not available.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:58:10 GMT 2023
Edited
by admin
on Fri Dec 15 15:58:10 GMT 2023
Record UNII
R3U09W4H4I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
XENBUCIN
INN   MART.   MI   USAN  
USAN   INN  
Official Name English
4-BIPHENYLACETIC ACID, .ALPHA.-ETHYL-
Systematic Name English
xenbucin [INN]
Common Name English
XENBUCIN [USAN]
Common Name English
BUTYRIC ACID, 2-(4-BIPHENYLYL)-
Systematic Name English
.ALPHA.-(P-XENYL)BUTYRIC ACID
Common Name English
M.G. 1559
Code English
MG-1559
Code English
LIOSOL
Brand Name English
2-(4-BIPHENYLYL)BUTYRIC ACID
Systematic Name English
XENBUCIN [MART.]
Common Name English
(4-DIPHENYLYL)ETHYLACETIC ACID
Common Name English
(1,1'-BIPHENYL)-4-ACETIC ACID, .ALPHA.-ETHYL-
Systematic Name English
NSC-16316
Code English
LISOL
Brand Name English
XENBUCIN [MI]
Common Name English
W-1760
Code English
MAGGIONI-1559
Code English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
Code System Code Type Description
MERCK INDEX
m1268
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
213-492-9
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
PRIMARY
FDA UNII
R3U09W4H4I
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
PRIMARY
INN
3442
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105601
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
PRIMARY
DRUG CENTRAL
3656
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
PRIMARY
SMS_ID
100000079373
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
PRIMARY
EVMPD
SUB00102MIG
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
PRIMARY
EPA CompTox
DTXSID80862486
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
PRIMARY
PUBCHEM
13737
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
PRIMARY
NCI_THESAURUS
C66663
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
PRIMARY
CAS
959-10-4
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
PRIMARY
NSC
16316
Created by admin on Fri Dec 15 15:58:10 GMT 2023 , Edited by admin on Fri Dec 15 15:58:10 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY