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Z-LEVD-FMK
🥰Excellent
Catalog No. T73096Cas No. 1135688-25-3
Z-LEVD-FMK is a cell-permeable caspase-4 inhibitor with potential anticancer activity, capable of eliminating LPS-induced GCLC protein degradation and inducing apoptosis in cancer cells.
Z-LEVD-FMK
🥰Excellent
Catalog No. T73096Cas No. 1135688-25-3
Z-LEVD-FMK is a cell-permeable caspase-4 inhibitor with potential anticancer activity, capable of eliminating LPS-induced GCLC protein degradation and inducing apoptosis in cancer cells.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $107 | - | In Stock | |
| 5 mg | $263 | - | In Stock | |
| 10 mg | $446 | - | In Stock | |
| 25 mg | $893 | - | In Stock | |
| 50 mg | $1,450 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $378 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
Bioactivity
Chemical Properties
| Description | Z-LEVD-FMK is a cell-permeable caspase-4 inhibitor with potential anticancer activity, capable of eliminating LPS-induced GCLC protein degradation and inducing apoptosis in cancer cells. |
| In vitro | Z-LEVD-FMK is a specific inhibitor of caspase-4. Z-LEVD-FMK (2 μM) completely eliminated IL-8 protein production in induced hRPE cells. [1] Z-LEVD-FMK was most active in blocking 17β-estradiol (E2) -induced apoptosis. In addition, z-LEVD-fmk completely blocked the cutting of ADP-ribose polymerase (PARP), and E2 inhibited growth and apoptotic morphology. [2] Z-LEVD-FMK (50 μM) treated for 72 hours only inhibited IL-17A-induced caspase-4 cleavage and N-terminal GSDMD up-regulation in CRC cells. There was no significant effect on the expression of NLRP3 inflammasome (NLRP3, ASC, caspase-1). [3] |
| Molecular Weight | 652.71 |
| Formula | C31H45FN4O10 |
| Cas No. | 1135688-25-3 |
| Smiles | [C@@H](NC([C@@H](NC(OCC1=CC=CC=C1)=O)CC(C)C)=O)(C(N[C@H](C(N[C@@H](CC(OC)=O)C(CF)=O)=O)C(C)C)=O)CCC(OC)=O |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 100 mg/mL (153.21 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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