VX-765

CAS No. 273404-37-8

VX-765( Belnacasan | VX765 | VX 765 )

Catalog No. M13836 CAS No. 273404-37-8

VX-765 (Belnacasan) is an orally absorbed prodrug of VRT-043198, which is a potent and selective inhibitor of interleukin-converting enzyme/caspase-1 with Ki of 0.8 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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10MG 70 In Stock
25MG 156 In Stock
50MG 222 In Stock
100MG 397 In Stock
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Biological Information

  • Product Name
    VX-765
  • Note
    Research use only, not for human use.
  • Brief Description
    VX-765 (Belnacasan) is an orally absorbed prodrug of VRT-043198, which is a potent and selective inhibitor of interleukin-converting enzyme/caspase-1 with Ki of 0.8 nM.
  • Description
    VX-765 (Belnacasan) is an orally absorbed prodrug of VRT-043198, which is a potent and selective inhibitor of interleukin-converting enzyme/caspase-1 with Ki of 0.8 nM; VRT-043198 exhibits 100- to 10,000-fold selectivity against other caspase-3 and -6 to -9, VX-765 is converted rapidly to VRT-043198 under the action of plasma and liver esterases; inhibits LPS-induced IL-1β production, reduces disease severity and the expression of inflammatory mediators in models of rheumatoid arthritis and skin inflammation.Epilepsy Phase 2 Discontinued(In Vivo):Belnacasan reduces inflammatory response in murine models of inflammatory disease.Belnacasan (50-200 mg/kg) significantly reduces serum IL-1β levels by as much as 60%. It is noteworthy that the effect of Belnacasan on the release of IL-1β induced by LPS reached a plateau at 100 mg/kg. Belnacasan (25-100 mg/kg × 2) significantly reduces ear edema. Belnacasan also dose-dependently reduces the concentrations of cytokines, chemokines, and inflammatory mediators in the ear biopsy samples.Belnacasan (25-200 mg/kg) significantly delays the time to seizure onset by 1.5- to twofold (p<0.01), reduces the number of seizures by 40% (p<0.01) and the total time spent in EEG seizure activity by 30 to 50% (p<0.01).
  • In Vitro
    ——
  • In Vivo
    Belnacasan reduces inflammatory response in murine models of inflammatory disease.Belnacasan (50-200 mg/kg) significantly reduces serum IL-1β levels by as much as 60%. It is noteworthy that the effect of Belnacasan on the release of IL-1β induced by LPS reached a plateau at 100 mg/kg. Belnacasan (25-100 mg/kg × 2) significantly reduces ear edema. Belnacasan also dose-dependently reduces the concentrations of cytokines, chemokines, and inflammatory mediators in the ear biopsy samples. Belnacasan (25-200 mg/kg) significantly delays the time to seizure onset by 1.5- to twofold (p<0.01), reduces the number of seizures by 40% (p<0.01) and the total time spent in EEG seizure activity by 30 to 50% (p<0.01).
  • Synonyms
    Belnacasan | VX765 | VX 765
  • Pathway
    Apoptosis
  • Target
    Caspase
  • Recptor
    Caspase-1|Caspase-4
  • Research Area
    Neurological Disease
  • Indication
    Epilepsy

Chemical Information

  • CAS Number
    273404-37-8
  • Formula Weight
    508.995
  • Molecular Formula
    C24H33ClN4O6
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 27 mg/mL
  • SMILES
    O=C([C@H]1N(C([C@@H](NC(C2=CC=C(N)C(Cl)=C2)=O)C(C)(C)C)=O)CCC1)N[C@@H](C3)[C@H](OCC)OC3=O
  • Chemical Name
    L-Prolinamide, N-(4-amino-3-chlorobenzoyl)-3-methyl-L-valyl-N-[(2R,3S)-2-ethoxytetrahydro-5-oxo-3-furanyl]-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Stack JH, et al. J Immunol. 2005 Aug 15;175(4):2630-4. 2. Wannamaker W, et al. J Pharmacol Exp Ther. 2007 May;321(2):509-16. 3. Bialer M, et al. Epilepsy Res. 2013 Jan;103(1):2-30. 4. Wang W, et al. Proc Natl Acad Sci U S A. 2016 Aug 23;113(34):9587-92.
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