ChemicalBook > CAS DataBase List > Z-Vad-fmk, non-methylated
Z-Vad-fmk, non-methylated
Z-Vad-fmk, non-methylated
- CAS No.161401-82-7
- Chemical Name:Z-Vad-fmk, non-methylated
- CBNumber:CB42497499
- Molecular Formula:C21H28FN3O7
- Formula Weight:453.46
- MOL File:161401-82-7.mol
Z-Vad-fmk, non-methylated Property
- Boiling point 758.0±60.0 °C(Predicted)
- Density 1.260±0.06 g/cm3(Predicted)
- storage temp. -20°C
- solubility DMSO:5.0(Max Conc. mg/mL);11.0(Max Conc. mM)
- pka 3.91±0.19(Predicted)
- form Off-white solid
- color White to light yellow
- UNSPSC Code 12352209
- NACRES NA.77
-
Symbol(GHS)
- Signal wordWarning
- Hazard statements H302-H315-H319-H335
- Precautionary statements P261-P305+P351+P338
Z-Vad-fmk, non-methylated Price
More Price(2)
- Brand: Sigma-Aldrich(India)
- Product number: 219007
- Product name : Caspase Inhibitor VI - CAS 161401-82-7 - Calbiochem
- Purity: Z-VAD-FMK, CAS 161401-82-7, is an irreversible pan caspase inhibitor. Does not require pretreatment with esterase for in vitro studies.
- Packaging: 250μG
- Price: ₹10670
- Updated: 2022/06/14
- Buy: Buy
- Brand: Sigma-Aldrich(India)
- Product number: 219007
- Product name : Caspase Inhibitor VI - CAS 161401-82-7 - Calbiochem
- Purity: Z-VAD-FMK, CAS 161401-82-7, is an irreversible pan caspase inhibitor. Does not require pretreatment with esterase for in vitro studies.
- Packaging: 1MG
- Price: ₹31630.01
- Updated: 2022/06/14
- Buy: Buy
Z-Vad-fmk, non-methylated Chemical Properties,Usage,Production
-
Description
Z-
VAD(OH)- FMK is an irreversible tripeptide inhibitor of all caspases. This non- methylated form is useful in studies involving recombinant, isolated, or purified enzymes. Unlike the methylated form, Z- VAD(OMe)- FMK , this compound does not require pretreatment with esterases prior to in vitro use. - Uses Z-VAD-FMK (Z-VAD(OH)-FMK) is a well-know pan caspase inhibitor, which does not inhibit ubiquitin carboxy-terminal hydrolase L1 (UCHL1) activity even at concentrations as high as 440 μM[1].
- General Description An irreversible general caspase inhibitor. Useful for studies involving recombinant, isolated, and purified caspase enzymes. Unlike Caspase Inhibitor I (Cat. No. 627610), this inhibitor does not require pretreatment with esterase for in vitro studies. A 10 mM (1 mg/221 μl) solution of Caspase Inhibitor VI (Cat. No. 219011) in DMSO is also available.
- Biochem/physiol Actions Product does not compete with ATP.
- IC 50 Caspase
-
References
[1] Davies CW, et al. The co-crystal structure of ubiquitin carboxy-terminal hydrolase L1 (UCHL1) with a tripeptide fluoromethyl ketone (Z-VAE(OMe)-FMK). Bioorg Med Chem Lett. 2012 Jun 15;22(12):3900-4. DOI:10.1016/j.bmcl.2012.04.124
[2] Liu HR, et al. Antiproliferative activity of the total saponin of Solanum lyratum Thunb in Hela cells by inducing apoptosis. Pharmazie. 2008 Nov;63(11):836-42. PMID:19069247
Z-Vad-fmk, non-methylated Preparation Products And Raw materials
Raw materials
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