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Description: Z-IETD-FMK (also known as Z-IE(OMe)TD(OMe)-FMK) is a novel, specific, selective, irreversible and cell permeable Caspase-8/9 inhibitor. Z-IETD-FMK acts by inhibiting T cell proliferation induced by PHA or anti-CD3 plus anti-CD28 without toxicity of resting T cells. 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-kappaB activation when the concentration is 100uM. 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.
References: Toxicol Appl Pharmacol. 2012 Nov 15; 265(1):103-12; Cancer Res. 2000 Nov 15; 60(22):6259-65.
Synonym: Z-IE(OMe)TD(OMe)-FMK; Granzyme B Inhibitor III; Z-IETD-FMK; Z-Ile-Glu(OMe)-Thr-Asp(OMe)-CH?F.
Chemical Name: (5S, 8S, 11S, 14S)-5-((S)-sec-butyl)-8-(2-carboxyethyl)-14-(2-fluoroacetyl)-11-((R)-1-hydroxyethyl)-3, 6, 9, 12-tetraoxo-1-phenyl-2-oxa-4, 7, 10, 13-tetraazahexadecan-16-oic acid
InChi Key: CTXDBLYOEUERAT-VUVYEONESA-N
InChi Code: InChI=1S/C28H39FN4O11/c1-4-15(2)23(33-28(43)44-14-17-8-6-5-7-9-17)26(41)30-18(10-11-21(36)37)25(40)32-24(16(3)34)27(42)31-19(12-22(38)39)20(35)13-29/h5-9, 15-16, 18-19, 23-24, 34H, 4, 10-14H2, 1-3H3, (H, 30, 41)(H, 31, 42)(H, 32, 40)(H, 33, 43)(H, 36, 37)(H, 38, 39)/t15-, 16+, 18-, 19-, 23-, 24-/m0/s1
SMILES Code: O=C(O)C[CH](C(CF)=O)NC([CH]([CH](O)C)NC([CH](CCC(O)=O)NC([CH]([CH](C)CC)NC(OCC1=CC=CC=C1)=O)=O)=O)=O
Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.
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