Drug Information
Drug General Information | |||||
---|---|---|---|---|---|
Drug ID |
D0HK3N
|
||||
Former ID |
DIB009085
|
||||
Drug Name |
Belnacasan
|
||||
Synonyms |
Second generation ICE inhibitors, Vertex; VRT-043198; VRT-43198; VX-765; VX-765)
|
||||
Drug Type |
Small molecular drug
|
||||
Indication | Epilepsy [ICD10:G40] | Phase 2 | [526728] | ||
Company |
MedKoo Biosciences; vertex pharmaceuticals
|
||||
Structure |
Download2D MOL |
||||
Formula |
C24H33ClN4O6
|
||||
Canonical SMILES |
C1C(=O)O[C@H]([C@H]1NC(=O)[C@@H]1CCCN1C(=O)[C@@H](NC(=O<br />)c1cc(c(cc1)N)Cl)C(C)(C)C)OCC
|
||||
PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Interleukin-1 beta convertase | Target Info | Inhibitor | [527677], [528662] | |
Pathway Interaction Database | IL1-mediated signaling events | ||||
Direct p53 effectors | |||||
IFN-gamma pathway | |||||
Cellular roles of Anthrax toxin | |||||
References | |||||
Ref 527677 | IL-converting enzyme/caspase-1 inhibitor VX-765 blocks the hypersensitive response to an inflammatory stimulus in monocytes from familial cold autoinflammatory syndrome patients. J Immunol. 2005 Aug 15;175(4):2630-4. | ||||
Ref 528662 | (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. J Pharmacol Exp Ther. 2007 May;321(2):509-16. Epub 2007 Feb 8. |
If You Find Any Error in Data or Bug in Web Service, Please Kindly Report It to Dr. Zhou and Dr. Zhang.