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
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
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/23176519Curator's Comment: Description was created based on several sources, including
http://www.selleckchem.com/products/vx-765.html
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23176519
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.
CNS Activity
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL4801 Sources: https://www.ncbi.nlm.nih.gov/pubmed/17289835 |
0.8 nM [Ki] | ||
Target ID: CHEMBL2226 Sources: https://www.ncbi.nlm.nih.gov/pubmed/17289835 |
|||
Target ID: CHEMBL1909490 |
0.67 µM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
(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 May |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT01048255
300mg Oral Tablet, 900mg TID
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/17289835
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.
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Q257O24H4J
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DTXSID00179169
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244133-31-1
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11443029
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ACTIVE MOIETY
PRODRUG (METABOLITE ACTIVE)