research use only

Z-VAD-FMK Caspase inhibitor

Cat.No.S7023

Z-VAD-FMK (Z-VAD(OMe)-FMK) is a cell-permeable, irreversible pan-caspase inhibitor, blocks all features of apoptosis in THP.1 and Jurkat T-cells.

Quality Control

Batch: Purity: 99.79%
99.79

Solubility in DMSO or Water

In vitro
Batch:

DMSO : 93 mg/mL (198.93 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 2 mg/mL

Water : Insoluble

The solubility data above are all experimental results (not literature values).

Molarity Calculator

Mass Concentration Volume Molecular Weight
Dilution Calculator Molecular Weight Calculator

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

mg/kg
g
μL

Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

% DMSO
%
% Tween 80
% ddH2O
% DMSO
+
%

Calculation results:

Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Read more about Z-VAD-FMK solubility in DMSO or water

Working Concentrations for Cell Culture Treatment

Step 1: Select a research area to find working concentrations, or search directly for a cell line

Read more about Z-VAD-FMK working concentrations for cell culture treatment

Working Concentrations for Animal Model Treatment

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Mechanism of Action

Information Z-VAD-FMK is a cell-permeant, irreversible pan-caspase inhibitor. It binds to the catalytic site of caspase proteases, blocking caspase-dependent apoptosis, pyroptosis, and related proteolytic signaling pathways. It is widely used to distinguish cell death mechanisms.

Read more about Z-VAD-FMK IC50 for cell-based and cell-free assays

Primary Applications and Mechanism of Action

Read more about Z-VAD-FMK Mechanism of Action

Chemical Information, Storage & Stability

Molecular Weight 467.49 Formula

C22H30FN3O7

Storage (From the date of receipt)
CAS No. 187389-52-2 Download SDF Storage of Stock Solutions

Synonyms Z-VAD(OMe)-FMK Smiles CC(C)C(C(=O)NC(C)C(=O)NC(CC(=O)OC)C(=O)CF)NC(=O)OCC1=CC=CC=C1

Read more about storage & stability

Z-VAD-FMK VS Q-VD-Oph|Belnacasan (VX-765)

Read more comparative analysis about Z-VAD-FMK

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Tech Support

Handling Instructions

Tel: +1-832-582-8158 Ext:3

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Frequently Asked Questions

Question 1:
Can you suggest an in vivo formulation of it for animal studies?

Answer:
For in vivo study of this compound, the IP formulation is 2% DMSO+35 % PEG 300+2% Tween 80+ddH2O up to 6 mg/ml. The gavage formula is 1%CMC-Na up to 30 mg/ml (suspensions).

Question 2:
What is the difference between S7023 & S8102?

Answer:
Unlike S7023, it does not require pretreatment with esterase for in vitro studies. This information was cited from the article: https://www.ncbi.nlm.nih.gov/pubmed/16973565.