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Cat.No.S7311
| Related Targets | Bcl-2 K-Ras PD-1/PD-L1 Ferroptosis p53 Apoptosis related Synthetic Lethality STAT TNF-alpha Ras |
|---|---|
| Other Caspase Inhibitors | Z-VAD-FMK Z-DEVD-FMK Emricasan (IDN-6556) Belnacasan (VX-765) Z-IETD-FMK Ac-DEVD-CHO Z-LEHD-FMK TFA Z-VAD(OH)-FMK PAC-1 Z-YVAD-FMK |
| Cell Lines | Assay Type | Concentration | Incubation Time | Formulation | Activity Description | PMID |
|---|---|---|---|---|---|---|
| JEG3 cells | Function assay | 50 μM | abrogation of caspase-8 cleavage from its 55 kDa proform to its 18 kDa active fragment | 28151467 | ||
| MV4-11 cells | Cell viability assay | 25 μM | 1 hour | protection cells from caspase-dependent cell death | 27956387 | |
| SH-SY5Y | Cytotoxicity assay | 5 μM | 48 h | Q-VD-OPh sensitizes SH-SY5Y cells to necrosis caused by cypermethrin | 27007526 | |
| MEFs | Function assay | 20 μM | exhibited characteristic stress-induced generation and rupture of nuclear bubbles | 25482068 | ||
| Click to View More Cell Line Experimental Data | ||||||
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In vitro |
DMSO
: 100 mg/mL
(194.74 mM)
Ethanol : 100 mg/mL Water : Insoluble |
|
In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
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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.
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| Molecular Weight | 513.49 | Formula | C26H25F2N3O6
|
Storage (From the date of receipt) | |
|---|---|---|---|---|---|
| CAS No. | 1135695-98-5 | Download SDF | Storage of Stock Solutions |
|
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| Synonyms | Quinoline-Val-Asp-Difluorophenoxymethylketone | Smiles | CC(C)C(C(=O)NC(CC(=O)O)C(=O)COC1=C(C=CC=C1F)F)NC(=O)C2=NC3=CC=CC=C3C=C2 | ||
| Targets/IC50/Ki |
Caspase-1
25 nM-400 nM
Caspase-3
25 nM-400 nM
Caspase-8
25 nM-400 nM
Caspase-9
25 nM-400 nM
|
|---|---|
| In vitro |
Q-VD-OPh (5-100 μM) potently inhibits Actinomycin D-induced DNA laddering and subsequent apoptosis with minimal toxicity in WEHI 231 cells. Q-VD-OPh prevents caspase mediated cleavage of PARP and activation of the major initiator and effector caspases. Q-VD-OPh protects cardiac myocytes from virus-induced apoptosis in vitro.
|
| In vivo |
Q-VD-OPh inhibits caspase-1 activity, IL-18 protein expression, and neutrophil infiltration during ischemic ARF in mice. In vivo, caspase inhibition by Q-VD-OPh provides protection from virus-induced myocardial injury, with a significant reduction in caspase-3 activity. In TgCRND8 mice, Q-VD-OPh inhibits caspase-7 activation and limits the pathological changes associated with tau, including caspase cleavage.
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References |
|
| Methods | Biomarkers | Images | PMID |
|---|---|---|---|
| Western blot | pS-Akt / Akt / pS6 / LC3B |
|
24682219 |
| Immunofluorescence | LC3B |
|
24682219 |
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