CASPASE-8 INHIBITOR II

CASPASE-8 INHIBITOR II
  • CAS No.:210344-98-2

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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CASPASE-8 INHIBITOR II Basic information
Product Name:CASPASE-8 INHIBITOR II
Synonyms:BENZYLOXYCARBONYL-ILE-GLU(OME)-THR-ASP(OME)-FLUOROMETHYLKETONE;GRANZYME B INHIBITOR III;CASPASE-8 INHIBITOR II;CASPASE-3 PROCESSING ENZYME INHIBITOR (FLUOROMETHYLKETONE);Z-IETD-FMK;Z-ILE-GLU(OME)-THR-ASP(OME)-FLUOROMETHYLKETONE;Z-ILE-GLU(OME)-THR-ASP(OME)-FMK;Z-ILE-GLU(OME)-THR-DL-ASP(OME)-FLUOROMETHYLKETONE
CAS:210344-98-2
MF:C30H43FN4O11
MW:654.68
EINECS:
Product Categories:Caspases/Apoptosis;Caspase/Related Products
Mol File:Mol File
CASPASE-8 INHIBITOR II Chemical Properties
Boiling point 925.7±65.0 °C(Predicted)
density 1.247±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Soluble in DMSO
pka11.12±0.46(Predicted)
Safety Information
MSDS Information
CASPASE-8 INHIBITOR II Usage And Synthesis
UsesA potent, cell-permeable, and irreversible inhibitor of caspase-8 and granzyme B. Effectively inhibits influenza virus-induced apoptosis in HeLa cells. Also inhibits granzyme B.
Biological Activityz-ietd-fmk is an inhibitor of caspase 8 [1].z-ietd-fmk inhibits t cell proliferation induced by pha or anti-cd3 plus anti-cd28 without toxicity of resting t cells. the mechanism of this inhibition of z-ietd-fmk has been proved not through the effect on il-2 secretion or ifn-γ production but the decrease of cd25 expression. experiments show that z-ietd-fmk has no effect on normal cell growth when there is no activation signal. z-ietd-fmk has also been found to significantly inhibit nf-κb activation when the concentration is 100μm [1].apart from the ability of inhibiting cell proliferation, z-ietd-fmk is reported to inhibit trail-mediated killing in cells. it protects the procaspases 9, 2, and 3, and protects parp to a similar extent in both hct116 and sw480 cells [2].
references[1] c.p. lawrence, s.c. chow. suppression of human t cell proliferation by the caspase inhibitors, z-vad-fmk and z-ietd-fmk is independent of their caspase inhibition properties. toxicology and applied pharmacology. 2012, 265: 103-112. [2] nesrin özören, kunhong kim, timothy f. burns, et al. the caspase 9 inhibitor z-lehd-fmk protects human liver cells while permitting death of cancer cells exposed to tumor necrosis factor-related apoptosis-inducing ligand. cancer research. 2000, 60: 6259-6265.
CASPASE-8 INHIBITOR II Preparation Products And Raw materials

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