Z-VAD-FMK

Z-VAD-FMK

1 mg
€105,00

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Z-VAD-FMK

Z-VAD-FMK

Product ID: 3188

Carbobenzoxy- L-valyl- L-alanyl- β-Methyl- L-aspart-1-yl- Fluoromethane

€105,00
excl. 19% VAT
Quantity
Description

M.W. 467.49

C22H30N3O7F

187389-52-2

Carbobenzoxy- L-valyl- L-alanyl- β-Methyl- L-aspart-1-yl- Fluoromethane

Inhibitor for Caspases (specific pan Caspase inhibitor) Z-VAD-FMK (Z-VAD(OMe)-FMK) is a cell permeable, non seletive inhibitor for caspase-1 and caspase-3 enzymes which shows no cytotoxic effects. The benzyloxycarbonyl protected tripeptide is commonly used as inhibitor for T cell apoptosis, staunosporin induced cell death and Fas-mediate apoptosis. Our Pan Caspase inhibitor is commonly used for inflammation and apoptose studies. The chemically manufactured methylester of Z-VAD-FMK is soluble in DMSO and other organic solvents, but insoluble in water. We will ship a product specific vial instruction sheet together with the peptide.Z-VAD-FMK blocks caspases irreversible, but less selective, where as our inhibitor Ac-YVAD-CMK is specific for Caspase-1. We offer additionally the reversible Caspase-1 inhibitor Ac-YVAD-CHO. Our caspase inhibitors are manufactured in Japan by Peptide Institute Inc. and are usually available for prompt delivery ex stock Sandhausen.The related Caspase-1 substrate Ac-YVAD-AMC and Caspase-2 substrate Ac-VDVAD-AMC with the VAD Sequence is available from stock within short time .

Synthetic Product

Shipping | Storage | Stability Our product Z-VAD-FMK will be shipped at room temperature. Information about product specific storage conditions will be found on the vial. Stock solutions should be stored at -20°C. Please avoid repeated freezing and thawing by preparing aliquots.

4. Intracellular nicotinamide adenine dinucleotide promotes TNF-induced necroptosis in a sirtuin-dependent manner

References:

1. E.A. Slee, H. Zhu, S.C. Chow, M. MacFarlane, D.W. Nicholson and G.M. Cohen, Biochem. J., 315, 21 (1996) 2. H. Zhu, H.O. Fearnhead and G.M. Cohen, FEBS Lett., 3740, 303 (1995) 3. D. Leung, G. Abbenante and D.P. Fairlie, J. Med. Chem., 43, 305 (2000)

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