research use only
Cat.No.S7023
| Related Targets | Bcl-2 PD-1/PD-L1 Ferroptosis p53 Apoptosis related Synthetic Lethality STAT TNF-alpha Ras KRas |
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| Other Caspase Inhibitors | Emricasan (IDN-6556) Q-VD-Oph Z-DEVD-FMK Belnacasan (VX-765) Z-IETD-FMK Ac-DEVD-CHO Z-LEHD-FMK TFA Z-VAD(OH)-FMK PAC-1 Z-YVAD-FMK |
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In vitro |
DMSO
: 93 mg/mL
(198.93 mM)
Ethanol : 2 mg/mL Water : Insoluble The solubility data above are all experimental results (not literature values). |
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
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.)
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 working concentrations for cell culture treatment
| 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. |
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Read more about Z-VAD-FMK IC50 for cell-based and cell-free assays |
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| Primary Applications and Mechanism of Action | |
| Molecular Weight | 467.49 | Formula | C22H30FN3O7 |
Storage (From the date of receipt) | |
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| CAS No. | 187389-52-2 | Download SDF | Storage of Stock Solutions |
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| 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 | ||
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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.