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Z-DEVD-FMK

Basic information Safety Supplier Related

Z-DEVD-FMK Basic information

Product Name:
Z-DEVD-FMK
Synonyms:
  • Z-ASP-GLU-VAL-ASP-FLUOROMETHYLKETONE
  • Z-ASP(OME)-GLU(OME)-VAL-ASP(OME)-CH2F
  • Z-ASP(OME)-GLU(OME)-VAL-ASP(OME)-FLUOROMETHYLKETONE
  • Z-ASP(OME)-GLU(OME)-VAL-ASP(OME)-FMK
  • Z-ASP(OME)-GLU(OME)-VAL-DL-ASP(OME)-FLUOROMETHYLKETONE
  • Z-DEVD-FLUOROMETHYLKETONE
  • Z-DEVD-FMK
  • Z-D(OME)E(OME)VD(OME) FLUOROMETHYLKETONE
CAS:
210344-95-9
MF:
C30H41FN4O12
MW:
668.66
Product Categories:
  • Inhibitors
  • Apoptosis
  • Caspases/Apoptosis
  • peptide
  • peptides
  • API
  • Caspase/Related Products
  • Pepetides
Mol File:
Mol File
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Z-DEVD-FMK Chemical Properties

Boiling point:
914.2±65.0 °C(Predicted)
Density 
1.260±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
DMSO/DMF: ≥20 mM
form 
White to slightly brown solid
pka
10.26±0.46(Predicted)
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Safety Information

WGK Germany 
3

MSDS

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Z-DEVD-FMK Usage And Synthesis

Uses

Z-DEVD-FMK is an irrversible caspase-3 inhibitor used as an anaesthetic agent. In addition, it is proposed to increase the longevity of platelet storage.

Definition

ChEBI: Z-DEVD-FMK is a tetrapeptide consisting of Fmoc-L-aspartic acid 4-methyl ester, methyl L-alpha-glutamic acid 5-methyl ester, L-valine and the fluoromethyl ketone derived from the 1-carboxy group of L-aspartic acid 4-methyl ester coupled in sequence. It is a specific, irreversible caspase-3 inhibitor that also shows potent inhibition of caspase-6, caspase-7, caspase-8, and caspase-10. It has a role as an apoptosis inhibitor, an EC 3.4.22.56 (caspase-3) inhibitor and a neuroprotective agent.

General Description

A potent, cell-permeable, and irreversible inhibitor of caspase-3 as well as caspase-6, caspase-7, caspase-8, and caspase-10. When using with purified native or recombinant enzyme, pretreatment with an esterase is required. A 5 mM (250 μg/75 μl) solution of Z-DEVD-FMK (Cat. No. 264156) in DMSO is also available.

Biological Activity

Cell-permeable, irreversible inhibitor of caspase-3/CPP32; inhibits tumor cell apoptosis. Neuroprotective in rat hippocampus following seizures in vivo .

Biochem/physiol Actions

Cell permeable: yes

target

Caspase-3

References

1. garcia-calvo m, peterson ep, leiting b, ruel r, nicholson dw, thornberry na (1998) inhibition of human caspases by peptidebased and macromolecular inhibitors. j biol chem 273:32608–32613 2. thornberry na, rano ta, peterson ep, rasper dm, timkey t, garcia-calvo m, houtzager vm, nordstrom pa, roy s, vaillancourt jp, chapman kt, nicholson dw (1997) a combinatorial approach defines specificities of members of the caspase family and granzyme b. functional relationships established for key mediators of apoptosis. j biol chem 272:17907–17911 3. yakovlev ag, knoblach sm, fan l, fox gb, goodnight r, faden ai (1997) activation of cpp32-like caspases contributes to neuronal apoptosis and neurological dysfunction after traumatic brain injury. j neurosci 17:7415–7424 4. clark rs, kochanek pm, watkins sc, chen m, dixon ce, seidberg na, melick j, loeffert je, nathaniel pd, jin kl, graham sh (2000) caspase-3 mediated neuronal death after traumatic brain injury in rats. j neurochem 74:740–753 5. s. m. knoblach, d. a. alroy et al, caspase inhibitor z-devd-fmk attenuates calpain and necrotic cell death in vitro and after traumatic brain injury, journal of cerebral blood flow & metabolism 24:1119–1132.

Z-DEVD-FMKSupplier

Shanghai Zhengyi Pharmaceutical Co., Ltd Gold
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3B Pharmachem (Wuhan) International Co.,Ltd.
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