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Details

Stereochemistry ACHIRAL
Molecular Formula C34H43N3O3
Molecular Weight 541.7235
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Omesdafexor

SMILES

COC1=CC=C(C=C1C)[C@H]2CC[C@H](CN(C(=O)[C@H]3CC[C@H](O)CC3)C4=CC=CC(=C4)C5=CN(N=C5)C6CC6)CC2

InChI

InChIKey=RPBNLMPTFCTXRQ-RYYHSFPWSA-N
InChI=1S/C34H43N3O3/c1-23-18-28(12-17-33(23)40-2)25-8-6-24(7-9-25)21-36(34(39)26-10-15-32(38)16-11-26)31-5-3-4-27(19-31)29-20-35-37(22-29)30-13-14-30/h3-5,12,17-20,22,24-26,30,32,38H,6-11,13-16,21H2,1-2H3/t24-,25-,26-,32-

HIDE SMILES / InChI

Molecular Formula C34H43N3O3
Molecular Weight 541.7235
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 14:54:21 GMT 2023
Edited
by admin
on Sat Dec 16 14:54:21 GMT 2023
Record UNII
E05WEZ4XLE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Omesdafexor
INN  
Official Name English
Cyclohexanecarboxamide, N-[3-(1-cyclopropyl-1H-pyrazol-4-yl)phenyl]-4-hydroxy-N-[[trans-4-(4-methoxy-3-methylphenyl)cyclohexyl]methyl]-, trans-
Systematic Name English
omesdafexor [INN]
Common Name English
trans-N-[3-(1-Cyclopropyl-1H-pyrazol-4-yl)phenyl]-4-hydroxy-N-[[trans-4-(4-methoxy-3-methylphenyl)cyclohexyl]methyl]cyclohexanecarboxamide
Systematic Name English
trans-N-[3-(1-cyclopropyl-1H-pyrazol-4-yl)phenyl]-4- hydroxy-N-{[trans-4-(4-methoxy-3- methylphenyl)cyclohexyl]methyl}cyclohexane-1- carboxamide
Systematic Name English
Code System Code Type Description
FDA UNII
E05WEZ4XLE
Created by admin on Sat Dec 16 14:54:21 GMT 2023 , Edited by admin on Sat Dec 16 14:54:21 GMT 2023
PRIMARY
INN
12154
Created by admin on Sat Dec 16 14:54:21 GMT 2023 , Edited by admin on Sat Dec 16 14:54:21 GMT 2023
PRIMARY
NCI_THESAURUS
C190434
Created by admin on Sat Dec 16 14:54:21 GMT 2023 , Edited by admin on Sat Dec 16 14:54:21 GMT 2023
PRIMARY
CAS
2244440-85-3
Created by admin on Sat Dec 16 14:54:21 GMT 2023 , Edited by admin on Sat Dec 16 14:54:21 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
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ACTIVE MOIETY