Z-VDVAD-FMK

Modify Date: 2024-01-09 11:23:30

Z-VDVAD-FMK Structure
Z-VDVAD-FMK structure
Common Name Z-VDVAD-FMK
CAS Number 210344-92-6 Molecular Weight 695.73
Density N/A Boiling Point N/A
Molecular Formula C32H46FN5O11 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Z-VDVAD-FMK


Z-VDVAD-FMK is a special inhibitor of caspase-2. Z-VDVAD-FMK produces a reduction in Lovastatin-induced apoptosis[1][3][3].

 Names

Name methyl 5-fluoro-3-[2-[[2-[[4-methoxy-2-[[3-methyl-2-(phenylmethoxycarbonylamino)butanoyl]amino]-4-oxobutanoyl]amino]-3-methylbutanoyl]amino]propanoylamino]-4-oxopentanoate
Synonym More Synonyms

 Z-VDVAD-FMK Biological Activity

Description Z-VDVAD-FMK is a special inhibitor of caspase-2. Z-VDVAD-FMK produces a reduction in Lovastatin-induced apoptosis[1][3][3].
Related Catalog
Target

Caspase-2

In Vitro "Cotreatment of cells with the caspase inhibitors Ac-DEVD-CHO, Z-VDVAD-FMK (100μM), Z-IETD-fmk, and Z-LEHD-fmk alone or in combination, or overexpression of CrmA, prevents many morphological features of apoptosis but not loss of mitochondrial membrane potential (DCm), phospatidilserine exposure, and cell death[1]. Z-VDVAD-FMK (2 μM) greatly inhibits the Rho-kinase activity in HMEC-1 cells stimulated by Thrombin and displays no effect on control cells[2].  Z-VDVAD-FMK (zVDVAD-fmk) produces a reduction in Lovastatin-induced apoptosis. Z-VDVAD-FMK (100 μM) significantly reduces Lovastatin-induced loss of DNA by 19.1±8.3%[3]." Cell Viability Assay[1] Cell Line: The human T-cell leukemia Jurkat (Clone E6.1, ATCC TIB-152) Concentration: 100 μM Incubation Time: 22 hours Result: Prevented Doxorubicin (1 μM)-induced nuclear apoptosis, but not cell death.
References

[1]. S Gamen, et al. Doxorubicin treatment activates a Z-VAD-sensitive caspase, which causes deltapsim loss, caspase-9 activity, and apoptosis in Jurkat cells. Exp Cell Res. 2000 Jul 10;258(1):223-35.

[2]. Cédric Sapet, et al. Thrombin-induced endothelial microparticle generation: identification of a novel pathway involving ROCK-II activation by caspase-2. Blood. 2006 Sep 15;108(6):1868-76.

[3]. Simon W Rabkin, et al. Lovastatin-induced cardiac toxicity involves both oncotic and apoptotic cell death with the apoptotic component blunted by both caspase-2 and caspase-3 inhibitors. Toxicol Appl Pharmacol. 2003 Dec 15;193(3):346-55.

 Chemical & Physical Properties

Molecular Formula C32H46FN5O11
Molecular Weight 695.73
Exact Mass 695.31800
PSA 241.85000
LogP 3.78290

 Synonyms

Z-Val-Asp(OMe)-Val-Ala-Asp(OMe)-Fluoromethylketone
FK016
Z-Val-Asp(OMe)-Val-Ala-Asp(OMe)-FMK
Z-VD(OMe)VAD(OMe)-FMK
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