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Quinoline-Val-Asp-Difluorophenoxymethylketone_Molecular_structure_CAS_)
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Quinoline-Val-Asp-Difluorophenoxymethylketone

Catalog No. 03OPH109 Name MP Biomedicals
CAS Number Website http://www.mpbio.com
M. F. C26H25F2N3O6 Telephone
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Storage Chembase ID: 106601

SYNONYMS

IUPAC name
(3S)-5-(2,6-difluorophenoxy)-3-[(2S)-3-methyl-2-(quinolin-2-ylformamido)butanamido]-4-oxopentanoic acid
IUPAC Traditional name
(3S)-5-(2,6-difluorophenoxy)-3-[(2S)-3-methyl-2-(quinolin-2-ylformamido)butanamido]-4-oxopentanoic acid
Synonyms
Q-VD-OPH
Q-Val-Asp-OPH

DATABASE IDS

PROPERTIES

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DETAILS

Description (English)
An broad spectrum Caspase inhibitor for in vivo research. The novel Q-VD-OPH compound synthesized using proprietary technology is an irreversible caspase inhibitor specifically designed for in-vivo research.
The Q-VD-OPH irreversibily binds to activated Caspases to block apoptosis. Apoptosis is a physiological for of cell death, which plays important role in embryogenesis, cellular homoestasis, tissue atrophy , and removal damaged and mutated cells. Caspases, which acts as molecular chainsaw are the central components of apoptosis response. Caspases are Cysteine proteases that cleave after aspartate residue in their substrates. At least 7 of 14 known mammalian caspases have important role in apoptosis.
The OPH trap with its superior potency, proven cell permeability and minimal toxicity provides an exceptional alternative to the Fluoromethylketone family of inhibitors.
Caserta, T. M.; et al. Apoptosis, 2003, 8, 345-352.
Renolleau, S. et al. Journal of Neurochemistry, 2007, 100, 1062-1071.

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