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

Details

Stereochemistry ABSOLUTE
Molecular Formula C34H30N2O5
Molecular Weight 546.6124
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FARGLITAZAR

SMILES

CC1=C(CCOC2=CC=C(C[C@H](NC3=CC=CC=C3C(=O)C4=CC=CC=C4)C(O)=O)C=C2)N=C(O1)C5=CC=CC=C5

InChI

InChIKey=ZZCHHVUQYRMYLW-HKBQPEDESA-N
InChI=1S/C34H30N2O5/c1-23-29(36-33(41-23)26-12-6-3-7-13-26)20-21-40-27-18-16-24(17-19-27)22-31(34(38)39)35-30-15-9-8-14-28(30)32(37)25-10-4-2-5-11-25/h2-19,31,35H,20-22H2,1H3,(H,38,39)/t31-/m0/s1

HIDE SMILES / InChI

Molecular Formula C34H30N2O5
Molecular Weight 546.6124
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Farglitazar is a non-thiazolidinedione insulin sensitizer and agonist of peroxisome proliferator-activated receptor-gamma. GlaxoSmithKline was developing farglitazar for the treatment of liver fibrosis and Type 2 diabetes mellitus.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P37231|||Q15179
Gene ID: 5468.0
Gene Symbol: PPARG
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
N-(2-Benzoylphenyl)-L-tyrosine PPARgamma agonists. 1. Discovery of a novel series of potent antihyperglycemic and antihyperlipidemic agents.
1998 Dec 3
The PPARs: from orphan receptors to drug discovery.
2000 Feb 24
Asymmetry in the PPARgamma/RXRalpha crystal structure reveals the molecular basis of heterodimerization among nuclear receptors.
2000 Mar
Synthesis of a high-affinity fluorescent PPARgamma ligand for high-throughput fluorescence polarization assays.
2003 Oct 1
Binding analyses between Human PPARgamma-LBD and ligands.
2004 Jan
GI262570, a peroxisome proliferator-activated receptor {gamma} agonist, changes electrolytes and water reabsorption from the distal nephron in rats.
2005 Feb
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:02:43 GMT 2023
Edited
by admin
on Sat Dec 16 16:02:43 GMT 2023
Record UNII
3433GY7132
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FARGLITAZAR
INN   USAN   WHO-DD  
INN   USAN  
Official Name English
Farglitazar [WHO-DD]
Common Name English
GI-262570X
Code English
N-(O-BENZOYLPHENYL)-O-(2-(5-METHYL-2-PHENYL-4-OXAZOLYL)ETHYL)-L-TYROSINE
Common Name English
farglitazar [INN]
Common Name English
GI-262570
Code English
L-TYROSINE, N-(2-BENZOYLPHENYL)-O-(2-(5-METHYL-2-PHENYL-4-OXAZOLYL)ETHYL)-
Systematic Name English
GI262570X
Code English
G1-262570
Code English
FARGLITAZAR [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C98233
Created by admin on Sat Dec 16 16:02:44 GMT 2023 , Edited by admin on Sat Dec 16 16:02:44 GMT 2023
Code System Code Type Description
FDA UNII
3433GY7132
Created by admin on Sat Dec 16 16:02:44 GMT 2023 , Edited by admin on Sat Dec 16 16:02:44 GMT 2023
PRIMARY
MESH
C422415
Created by admin on Sat Dec 16 16:02:44 GMT 2023 , Edited by admin on Sat Dec 16 16:02:44 GMT 2023
PRIMARY
CAS
274687-78-4
Created by admin on Sat Dec 16 16:02:44 GMT 2023 , Edited by admin on Sat Dec 16 16:02:44 GMT 2023
SUPERSEDED
PUBCHEM
170364
Created by admin on Sat Dec 16 16:02:44 GMT 2023 , Edited by admin on Sat Dec 16 16:02:44 GMT 2023
PRIMARY
NCI_THESAURUS
C81693
Created by admin on Sat Dec 16 16:02:44 GMT 2023 , Edited by admin on Sat Dec 16 16:02:44 GMT 2023
PRIMARY
WIKIPEDIA
FARGLITAZAR
Created by admin on Sat Dec 16 16:02:44 GMT 2023 , Edited by admin on Sat Dec 16 16:02:44 GMT 2023
PRIMARY
EPA CompTox
DTXSID1047310
Created by admin on Sat Dec 16 16:02:44 GMT 2023 , Edited by admin on Sat Dec 16 16:02:44 GMT 2023
PRIMARY
INN
8064
Created by admin on Sat Dec 16 16:02:44 GMT 2023 , Edited by admin on Sat Dec 16 16:02:44 GMT 2023
PRIMARY
ChEMBL
CHEMBL107367
Created by admin on Sat Dec 16 16:02:44 GMT 2023 , Edited by admin on Sat Dec 16 16:02:44 GMT 2023
PRIMARY
SMS_ID
100000177891
Created by admin on Sat Dec 16 16:02:44 GMT 2023 , Edited by admin on Sat Dec 16 16:02:44 GMT 2023
PRIMARY
USAN
LL-82
Created by admin on Sat Dec 16 16:02:44 GMT 2023 , Edited by admin on Sat Dec 16 16:02:44 GMT 2023
PRIMARY
CAS
196808-45-4
Created by admin on Sat Dec 16 16:02:44 GMT 2023 , Edited by admin on Sat Dec 16 16:02:44 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY