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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H29ClN4O6
Molecular Weight 480.942
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of O-DESETHYL-BELNACASAN

SMILES

CC(C)(C)[C@H](NC(=O)C1=CC=C(N)C(Cl)=C1)C(=O)N2CCC[C@H]2C(=O)N[C@@H](CC(O)=O)C=O

InChI

InChIKey=SOZONDBMOYWSRW-QANKJYHBSA-N
InChI=1S/C22H29ClN4O6/c1-22(2,3)18(26-19(31)12-6-7-15(24)14(23)9-12)21(33)27-8-4-5-16(27)20(32)25-13(11-28)10-17(29)30/h6-7,9,11,13,16,18H,4-5,8,10,24H2,1-3H3,(H,25,32)(H,26,31)(H,29,30)/t13-,16-,18+/m0/s1

HIDE SMILES / InChI

Molecular Formula C22H29ClN4O6
Molecular Weight 480.942
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: Description was created based on several sources, including http://www.selleckchem.com/products/vx-765.html

Belnacasan (VX-765), and its active metabolite VRT- 043198, is a novel and irreversible IL-converting enzyme/ caspase-1 inhibitor. VRT-043198 exhibits 100- to 10,000-fold selectivity against other caspase-3, -6 and -9. It exhibited potent inhibition against ICE/caspase-1 and caspase-4 with Ki of 0.8 nM and less than 0.6 nM, respectively. And VRT-043198 also inhibits IL-1β release from both PBMCs and whole blood with IC50 of 0.67 uM and 1.9 uM, respectively. Belnacasan inhibits the release of IL-1, IL-18 and IL-33. Belnacasan has shown to inhibit acute partial seizures in preclinical models and has shown activity in preclinical models of chronic partial epilepsy that do not respond to currently available compounds for epilepsy. In addition, it seems to reduce disease severity and the expression of inflammatory mediators in models of rheumatoid arthritis and skin inflammation. Belnacasan had been in phase II clinical trials by Vertex for the treatment of epilepsy. However, this study has been terminated later.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.8 nM [Ki]
0.67 µM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
0.78 μg/mL
84 mg/kg single, oral
dose: 84 mg/kg
route of administration: Oral
experiment type: SINGLE
co-administered:
BELNACASAN plasma
Mus musculus
population: HEALTHY
age: ADOLESCENT
sex: MALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
2.06 μg × h/mL
84 mg/kg single, oral
dose: 84 mg/kg
route of administration: Oral
experiment type: SINGLE
co-administered:
BELNACASAN plasma
Mus musculus
population: HEALTHY
age: ADOLESCENT
sex: MALE
food status: UNKNOWN
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
(S)-1-((S)-2-{[1-(4-amino-3-chloro-phenyl)-methanoyl]-amino}-3,3-dimethyl-butanoyl)-pyrrolidine-2-carboxylic acid ((2R,3S)-2-ethoxy-5-oxo-tetrahydro-furan-3-yl)-amide (VX-765), an orally available selective interleukin (IL)-converting enzyme/caspase-1 inhibitor, exhibits potent anti-inflammatory activities by inhibiting the release of IL-1beta and IL-18.
2007-05
Patents

Patents

Sample Use Guides

300mg Oral Tablet, 900mg TID
Route of Administration: Oral
VRT-043198, active moiety of BELNACASAN, inhibited IL-1beta release from both human PBMCs and whole blood with IC50 values of 0.67  and 1.9 uM, respectively.
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:26:22 GMT 2025
Edited
by admin
on Mon Mar 31 21:26:22 GMT 2025
Record UNII
Q257O24H4J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VRT-043198
Preferred Name English
O-DESETHYL-BELNACASAN
Common Name English
L-PROLINAMIDE, N-(4-AMINO-3-CHLOROBENZOYL)-3-METHYL-L-VALYL-N-((1S)-2-CARBOXY-1-FORMYLETHYL)-
Systematic Name English
VRT043198
Code English
Code System Code Type Description
FDA UNII
Q257O24H4J
Created by admin on Mon Mar 31 21:26:22 GMT 2025 , Edited by admin on Mon Mar 31 21:26:22 GMT 2025
PRIMARY
EPA CompTox
DTXSID00179169
Created by admin on Mon Mar 31 21:26:22 GMT 2025 , Edited by admin on Mon Mar 31 21:26:22 GMT 2025
PRIMARY
CAS
244133-31-1
Created by admin on Mon Mar 31 21:26:22 GMT 2025 , Edited by admin on Mon Mar 31 21:26:22 GMT 2025
PRIMARY
PUBCHEM
11443029
Created by admin on Mon Mar 31 21:26:22 GMT 2025 , Edited by admin on Mon Mar 31 21:26:22 GMT 2025
PRIMARY
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