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Details

Stereochemistry ABSOLUTE
Molecular Formula C31H40N4O8
Molecular Weight 596.6713
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GW-559090

SMILES

CC(C)C[C@H](NC(=O)COC1=C(C)C=CC=C1)C(=O)N[C@@H](CC2=CC=C(OC(=O)N3CCC(CC3)C(N)=O)C=C2)C(O)=O

InChI

InChIKey=RZMCXMNNXGCFQG-DQEYMECFSA-N
InChI=1S/C31H40N4O8/c1-19(2)16-24(33-27(36)18-42-26-7-5-4-6-20(26)3)29(38)34-25(30(39)40)17-21-8-10-23(11-9-21)43-31(41)35-14-12-22(13-15-35)28(32)37/h4-11,19,22,24-25H,12-18H2,1-3H3,(H2,32,37)(H,33,36)(H,34,38)(H,39,40)/t24-,25-/m0/s1

HIDE SMILES / InChI

Molecular Formula C31H40N4O8
Molecular Weight 596.6713
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 10:39:53 GMT 2023
Edited
by admin
on Sat Dec 16 10:39:53 GMT 2023
Record UNII
H9W4YH429K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GW-559090
Code English
L-TYROSINE, N-((2-METHYLPHENOXY)ACETYL)-L-LEUCYL-, 4-(AMINOCARBONYL)-1-PIPERIDINECARBOXYLATE (ESTER)
Systematic Name English
GW-559090(FREE ACID)
Code English
(2S)-3-(4-(4-CARBAMOYLPIPERIDINE-1-CARBONYL)OXYPHENYL)-2-(((2S)-4-METHYL-2-((2-(2-METHYLPHENOXY)ACETYL)AMINO)PENTANOYL)AMINO)PROPANOIC ACID
Systematic Name English
Code System Code Type Description
CAS
278598-52-0
Created by admin on Sat Dec 16 10:39:53 GMT 2023 , Edited by admin on Sat Dec 16 10:39:53 GMT 2023
PRIMARY
PUBCHEM
9809516
Created by admin on Sat Dec 16 10:39:53 GMT 2023 , Edited by admin on Sat Dec 16 10:39:53 GMT 2023
PRIMARY
FDA UNII
H9W4YH429K
Created by admin on Sat Dec 16 10:39:53 GMT 2023 , Edited by admin on Sat Dec 16 10:39:53 GMT 2023
PRIMARY
DRUG BANK
DB06508
Created by admin on Sat Dec 16 10:39:53 GMT 2023 , Edited by admin on Sat Dec 16 10:39:53 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY
Class: Anti-asthmatic; Mechanism of Action: Integrin alpha4beta1 antagonists; Highest Development Phase: Discontinued for Allergic rhinitis and Asthma