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Details

Stereochemistry RACEMIC
Molecular Formula C36H29FN2O4
Molecular Weight 572.6249
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARFLOGLITAZAR

SMILES

OC(=O)C(CC1=CC=C(OCCN2C3=C(C=CC=C3)C4=C2C=CC=C4)C=C1)NC5=C(C=CC=C5)C(=O)C6=CC=C(F)C=C6

InChI

InChIKey=QNLWMPLUWMWDMQ-UHFFFAOYSA-N
InChI=1S/C36H29FN2O4/c37-26-17-15-25(16-18-26)35(40)30-9-1-4-10-31(30)38-32(36(41)42)23-24-13-19-27(20-14-24)43-22-21-39-33-11-5-2-7-28(33)29-8-3-6-12-34(29)39/h1-20,32,38H,21-23H2,(H,41,42)

HIDE SMILES / InChI

Molecular Formula C36H29FN2O4
Molecular Weight 572.6249
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:05:37 UTC 2023
Edited
by admin
on Sat Dec 16 16:05:37 UTC 2023
Record UNII
8WE94VAO6U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARFLOGLITAZAR
INN  
Official Name English
O-(2-(9H-CARBAZOL-9-YL)ETHYL)-N-(2-(4-FLUOROBENZOYL)PHENYL)TYROSINE
Systematic Name English
O-(2-(9H-CARBAZOL-9-YL)ETHYL)-N-(2-(4-FLUOROBENZOYL)PHENYL)-DL-TYROSINE
Systematic Name English
TYROSINE, O-(2-(9H-CARBAZOL-9-YL)ETHYL)-N-(2-(4-FLUOROBENZOYL)PHENYL)-
Systematic Name English
CHIGLITAZAR, (±)-
Common Name English
Carfloglitazar [WHO-DD]
Common Name English
carfloglitazar [INN]
Common Name English
Code System Code Type Description
NCI_THESAURUS
C175753
Created by admin on Sat Dec 16 16:05:38 UTC 2023 , Edited by admin on Sat Dec 16 16:05:38 UTC 2023
PRIMARY
INN
11349
Created by admin on Sat Dec 16 16:05:38 UTC 2023 , Edited by admin on Sat Dec 16 16:05:38 UTC 2023
PRIMARY
PUBCHEM
9938010
Created by admin on Sat Dec 16 16:05:38 UTC 2023 , Edited by admin on Sat Dec 16 16:05:38 UTC 2023
PRIMARY
SMS_ID
300000027591
Created by admin on Sat Dec 16 16:05:38 UTC 2023 , Edited by admin on Sat Dec 16 16:05:38 UTC 2023
PRIMARY
FDA UNII
8WE94VAO6U
Created by admin on Sat Dec 16 16:05:38 UTC 2023 , Edited by admin on Sat Dec 16 16:05:38 UTC 2023
PRIMARY
CAS
2213406-75-6
Created by admin on Sat Dec 16 16:05:38 UTC 2023 , Edited by admin on Sat Dec 16 16:05:38 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
SALT/SOLVATE -> PARENT
TARGET -> AGONIST
ACTIVE ENANTIOMER->RACEMATE
TARGET -> AGONIST
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY