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

Details

Stereochemistry ABSOLUTE
Molecular Formula C30H32Cl3N3O4.ClH
Molecular Weight 641.413
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VALATEGRAST HYDROCHLORIDE

SMILES

Cl.CCN(CC)CCOC(=O)[C@H](CC1=CC=C(NC(=O)C2=C(Cl)C=CC=C2Cl)C=C1)NC(=O)C3=C(C)C=CC=C3Cl

InChI

InChIKey=CNNHYZRRGXZIIA-UQIIZPHYSA-N
InChI=1S/C30H32Cl3N3O4.ClH/c1-4-36(5-2)16-17-40-30(39)25(35-28(37)26-19(3)8-6-9-22(26)31)18-20-12-14-21(15-13-20)34-29(38)27-23(32)10-7-11-24(27)33;/h6-15,25H,4-5,16-18H2,1-3H3,(H,34,38)(H,35,37);1H/t25-;/m0./s1

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C30H32Cl3N3O4
Molecular Weight 604.952
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Valategrast (R-411) is a dual-acting α4/β1 - α4/β7 integrin antagonist which underwent clinical development with Roche for the treatment of multiple sclerosis (MS) and asthma. Phase I and II studies have been conducted. It had shown good efficacy in animal disease models. Following oral administration, R-411 was rapidly and completely biotransformed into its active metabolite, RO-0270608, most of which was eliminated by biliary excretion. R-411 had shown acceptable pharmacokinetics and good safety in healthy volunteers. R-411 inhibited eosinophil and T H 2 cell excitation and survival, and inhibited eosinophil migration from blood to pulmonary tissues. The idea of combining R-411 with montelukast (leukotriene antagonist) in the pharmaceutical dosage forms, therefore, provided a therapeutic treatment that had the combined effect of reducing circulating eosinophil counts and reducing eosinophil egress into pulmonary tissues, thereby providing an early onset of bronchodilation as well as sustained anti-inflammatory effects. Valategrast had been in phase II clinical trials by Roche for the treatment of asthma and in phase I clinical trials for the treatment of multiple sclerosis (MS). However, the study had been discontinued. Development of Valategrast was discontinued for the treatment of asthma after clarification of the regulatory framework for that class of compounds.

Approval Year

PubMed

PubMed

TitleDatePubMed
Discontinued drugs in 2006: pulmonary-allergy, dermatological, gastrointestinal and arthritis drugs.
2007 Sep
Cell adhesion antagonists: therapeutic potential in asthma and chronic obstructive pulmonary disease.
2008
Small Macrocycles As Highly Active Integrin α2β1 Antagonists.
2014 Feb 13
Patents

Sample Use Guides

To test drug interactions, a single daily dose of Valategrast (R-411) 300 mg in tablet form was given for 8 consecutive days to 12 healthy volunteers and it was shown that it did not affect major CYP isoform activities, thus indicating a low potential for drug interactions.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:04:14 GMT 2023
Edited
by admin
on Fri Dec 15 16:04:14 GMT 2023
Record UNII
XN95730F0N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VALATEGRAST HYDROCHLORIDE
USAN  
USAN  
Official Name English
RO-272441002
Code English
RO0272441/002
Code English
2-(DIETHYLAMINO)ETHYL(2S)-2-((2-CHLORO-6-METHYLBENZOYL)AMINO)-3-(4-((2,6-DICHLOROBENZOYL)AMINO)PHENYL)PROPANOATE HYDROCHLORIDE
Systematic Name English
RO27-2441/002
Code English
RO-0272441/002
Code English
L-PHENYLALANINE, N-(2-CHLORO-6-METHYLBENZOYL)-4-((2,6-DICHLOROBENZOYL)AMINO-, 2-(DIETHYLAMINO)ETHYL ESTER, MONOHYDROCHLORIDE
Common Name English
VALATEGRAST HCL
Common Name English
RO-02724411002
Code English
VALATEGRAST HYDROCHLORIDE [USAN]
Common Name English
RO-27-2441/002
Code English
R-411
Code English
Classification Tree Code System Code
NCI_THESAURUS C29712
Created by admin on Fri Dec 15 16:04:14 GMT 2023 , Edited by admin on Fri Dec 15 16:04:14 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C75971
Created by admin on Fri Dec 15 16:04:14 GMT 2023 , Edited by admin on Fri Dec 15 16:04:14 GMT 2023
PRIMARY
USAN
RR-72
Created by admin on Fri Dec 15 16:04:14 GMT 2023 , Edited by admin on Fri Dec 15 16:04:14 GMT 2023
PRIMARY
SMS_ID
100000126342
Created by admin on Fri Dec 15 16:04:14 GMT 2023 , Edited by admin on Fri Dec 15 16:04:14 GMT 2023
PRIMARY
EPA CompTox
DTXSID701002935
Created by admin on Fri Dec 15 16:04:14 GMT 2023 , Edited by admin on Fri Dec 15 16:04:14 GMT 2023
PRIMARY
CAS
828271-96-1
Created by admin on Fri Dec 15 16:04:14 GMT 2023 , Edited by admin on Fri Dec 15 16:04:14 GMT 2023
PRIMARY
FDA UNII
XN95730F0N
Created by admin on Fri Dec 15 16:04:14 GMT 2023 , Edited by admin on Fri Dec 15 16:04:14 GMT 2023
PRIMARY
EVMPD
SUB32888
Created by admin on Fri Dec 15 16:04:14 GMT 2023 , Edited by admin on Fri Dec 15 16:04:14 GMT 2023
PRIMARY
PUBCHEM
11563635
Created by admin on Fri Dec 15 16:04:14 GMT 2023 , Edited by admin on Fri Dec 15 16:04:14 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107792
Created by admin on Fri Dec 15 16:04:14 GMT 2023 , Edited by admin on Fri Dec 15 16:04:14 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY