![3-[(2,3-Dihydro-1H-inden-5-yloxy)methyl]piperidinehydrochloride - chemical structure image](https://media.scbt.com/product/3--2-3-dihydro-1h-inden-5-yloxy-methylpiperidinehydrochloride-structure_22_81_b_228197.jpg)
![3-[(2,3-Dihydro-1H-inden-5-yloxy)methyl]piperidinehydrochloride - chemical structure image](https://media.scbt.com/product/3--2-3-dihydro-1h-inden-5-yloxy-methylpiperidinehydrochloride-structure_22_81_t_228197.jpg "Molecular structure of 3-[(2,3-Dihydro-1H-inden-5-yloxy)methyl]piperidinehydrochloride")
Molecular structure of 3-[(2,3-Dihydro-1H-inden-5-yloxy)methyl]piperidinehydrochloride
3-[(2,3-Dihydro-1H-inden-5-yloxy)methyl]piperidinehydrochloride
Molecular Weight:
267.8
Molecular Formula:
C15H22ClNO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Z-VAD(OMe)-FMK is an irreversible and cell permeable broad-spectrum Caspase Inhibitor displaying an IC50 of 5.8 nM in HepG2 cells. Z-VAD(OMe)-FMK may act to inhibit caspase-1 and caspase-3. Z-VAD(OMe)-FMK also been shown to inhibit Fas-mediated apoptosis in Jurkat T cells and apoptosis in THP.1 cells induced by diverse stimuli (including cycloheximide, thapsigargin, etoposide and staurosporine). Furthermore, anti-CD95-induced hepatocyte apoptosis was prevented in a concentration-dependent manner by inhibitor Z-VAD-FMK (IC50 = 1.5 nM). Additionally, Z-VAD(OMe)-FMK has been shown that pretreatment of MDA-MB-231 and HL-60 cells with Z-VAD(OMe)-FMK also inhibits apoptosis.
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-[(2,3-Dihydro-1H-inden-5-yloxy)methyl]piperidinehydrochloride, 500 mg | sc-312032 | 500 mg | $259.00 |