| Identification | Back Directory | [Name]
Z-VDVAD-FMK | [CAS]
210344-92-6 | [Synonyms]
Z-VDVAD-FMK
CASPASE-2 INHIBITOR I
Z-VD(OME)VAD(OME)-FMK
Z-VDVAD-FLUOROMETHYLKETONE
Z-VAL-ASP(OME)-VAL-ALA-ASP(OME)-FMK
Z-VD(OME)VAD(OME)-FLUOROMETHYLKETONE
Z-VAL-ASP-VAL-ALA-ASP-FLUOROMETHYLKETONE
Z-VAL-ASP(OME)-VAL-ALA-ASP(OME)-FLUOROMETHYLKETONE
Z-VAL-ASP(OME)-VAL-ALA-DL-ASP(OME)-FLUOROMETHYLKETONE
BENZYLOXYCARBONYL-VAL-ASP(OME)-VAL-ALA-ASP(OME)-FLUOROMETHYLKETONE
L-Alaninamide, N-[(phenylmethoxy)carbonyl]-L-valyl-L-α-aspartyl-L-valyl-N-[(1S)-3-fluoro-1-(2-methoxy-2-oxoethyl)-2-oxopropyl]-, methyl ester | [Molecular Formula]
C32H46FN5O11 | [MDL Number]
MFCD03452881 | [MOL File]
210344-92-6.mol | [Molecular Weight]
695.73 |
| Hazard Information | Back Directory | [Uses]
Z-VDVAD-FMK is a special inhibitor of caspase-2. Z-VDVAD-FMK produces a reduction in Lovastatin-induced apoptosis[1][2][3]. | [Biological Activity]
Irreversible caspase-2 inhibitor. Attenuates oxyhemoglobin-induced cleavage of PARP and apoptosis in endothelial cells. | [Biochem/physiol Actions]
A cell-permeable inhibitor of caspase-2, which exhibits competitive and irreversible inhibition. | [IC 50]
Caspase-2 | [References]
1. j. d. robertson, m. enoksson et al. caspase-2 acts upstream of mitochondria to promote cytochrome c release during etoposide-induced apoptosis. the journal of biological chemistry. 277, :29803–29809, 2002 2. t. meguro, b. chen et al. caspase inhibitors attenuate oxyhemoglobin-induced apoptosis in endothelial cells, stroke. 2001; 32:561-566. 3. talanian, r. v., quinlan, c., trautz, s., hackett, m. c., mankovich, j. a., banach, d., ghayur, t., brady, k. d., and wong, w. w. (1997). substrate speci?city of caspase family proteases. j. biol. chem. 272, 9677–9682. 4. gamen et al (2000) doxorubicin treatment activates a z-vad-sensitive caspase, which causes dym loss, caspase-9 activity, and apoptosis in jurkat cells. exp.cell res. 258 223. |
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