GW-559090

Investigational

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 Search

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 `Mon Mar 31 23:22:40 GMT 2025` Edited by `admin` on `Mon Mar 31 23:22:40 GMT 2025`
Record UNII	H9W4YH429K
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

GW-559090(FREE ACID)

Preferred Name

English

GW-559090

Code

English

L-TYROSINE, N-((2-METHYLPHENOXY)ACETYL)-L-LEUCYL-, 4-(AMINOCARBONYL)-1-PIPERIDINECARBOXYLATE (ESTER)

Systematic Name

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

GW559090X

Code

English

Code System Code Type Description

CAS

278598-52-0

Created by admin on Mon Mar 31 23:22:40 GMT 2025 , Edited by admin on Mon Mar 31 23:22:40 GMT 2025

PRIMARY

PUBCHEM

9809516

Created by admin on Mon Mar 31 23:22:40 GMT 2025 , Edited by admin on Mon Mar 31 23:22:40 GMT 2025

PRIMARY

FDA UNII

H9W4YH429K

Created by admin on Mon Mar 31 23:22:40 GMT 2025 , Edited by admin on Mon Mar 31 23:22:40 GMT 2025

PRIMARY

DRUG BANK

DB06508

Created by admin on Mon Mar 31 23:22:40 GMT 2025 , Edited by admin on Mon Mar 31 23:22:40 GMT 2025

PRIMARY

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ACTIVE MOIETY

Comments:

Class: Anti-asthmatic; Mechanism of Action: Integrin alpha4beta1 antagonists; Highest Development Phase: Discontinued for Allergic rhinitis and Asthma

Amount: