Z-VDVAD-FMK
- Product Name
- Z-VDVAD-FMK
- CAS No.
- 210344-92-6
- Chemical Name
- Z-VDVAD-FMK
- 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
- CBNumber
- CB6364843
- Molecular Formula
- C32H46FN5O11
- Formula Weight
- 695.73
- MOL File
- Mol file
Z-VDVAD-FMK Property
- storage temp.
- −20°C
- solubility
- DMSO/DMF: 20 mM
- form
- powder
- color
- white
- biological source
- synthetic (organic)
Safety
- WGK Germany
- 3
N-Bromosuccinimide Price
- Product number
- 218744
- Product name
- Caspase-2 Inhibitor I
- Purity
- The Caspase-2 Inhibitor I controls the biological activity of Caspase-2. This small molecule/inhibitor is primarily used for Cancer applications.
- Packaging
- 250μG
- Price
- $207
- Updated
- 2025/07/31
- Product number
- C1605
- Product name
- Z-Val-Asp(O-Me)-Val-Ala-Asp(O-Me) fluoromethyl ketone
- Purity
- powder, ≥95% (TLC)
- Packaging
- 1mg
- Price
- $547
- Updated
- 2025/07/31
- Product number
- 218744
- Product name
- Caspase-2 Inhibitor I
- Purity
- The Caspase-2 Inhibitor I controls the biological activity of Caspase-2. This small molecule/inhibitor is primarily used for Cancer applications.
- Packaging
- 1MG
- Price
- $577
- Updated
- 2025/07/31
- Product number
- 32785
- Product name
- Z-Val-Asp(OMe)-Val-Ala-DL-Asp(OMe)-fluoromethylketone
- Packaging
- 1MG
- Price
- $402.5
- Updated
- 2021/12/16
- Product number
- A1922
- Product name
- Z-VDVAD-FMK
- Packaging
- 10mg
- Price
- $500
- Updated
- 2021/12/16
Z-VDVAD-FMK Chemical Properties,Usage,Production
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 specificity 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.
Z-VDVAD-FMK Preparation Products And Raw materials
Raw materials
Preparation Products
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