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Q-VD-Oph pan-Caspase inhibitor

Cat.No.S7311

Q-VD-Oph (Quinoline-Val-Asp-Difluorophenoxymethylketone) is a potent pan-caspase inhibitor with IC50 ranged from 25 to 400 nM for caspases 1,3,8, and 9. Q-VD-OPh can inhibits HIV infection.
Q-VD-Oph Caspase inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 513.49

Quality Control

Products Often Used Together with Q-VD-Oph

Z-VAD-FMK

It inhibits caspase-3 activity and DNA fragmentation much more effectively than Z-VAD-FMK in JURL-MK1 cells.

Memantine HCl

It significantly decreases the number and percentage of apoptotic cells than the combined treatment of this compound and Memantine in vivo.

Necrostatin-1 (Nec-1)

The combination of this compound and Necrostatin-1 reduces the cell death induced by pep5-cpp in HeLa cells.

Cell Culture, Treatment & Working Concentration

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

Chemical Information, Storage & Stability

Molecular Weight 513.49 Formula
C26H25F2N3O6
Storage (From the date of receipt)
CAS No. 1135695-98-5 Download SDF Storage of Stock Solutions

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

Solubility

In vitro
Batch:

DMSO : 100 mg/mL (194.74 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 100 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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mg/kg g μL

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%DMSO %

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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.
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.

Mechanism of Action

Targets/IC50/Ki
Caspase-1 [1]
25 nM-400 nM
Caspase-3 [1]
25 nM-400 nM
Caspase-8 [1]
25 nM-400 nM
Caspase-9 [1]
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. [2] Q-VD-OPh protects cardiac myocytes from virus-induced apoptosis in vitro. [4]
In vivo
Q-VD-OPh inhibits caspase-1 activity, IL-18 protein expression, and neutrophil infiltration during ischemic ARF in mice. [3] In vivo, caspase inhibition by Q-VD-OPh provides protection from virus-induced myocardial injury, with a significant reduction in caspase-3 activity. [4] In TgCRND8 mice, Q-VD-OPh inhibits caspase-7 activation and limits the pathological changes associated with tau, including caspase cleavage. [5]
References
  • [4] https://pubmed.ncbi.nlm.nih.gov/15452224/
  • [5] https://pubmed.ncbi.nlm.nih.gov/20057974/

Applications

Methods Biomarkers Images PMID
Western blot pS-Akt / Akt / pS6 / LC3B S7311-WB1 24682219
Immunofluorescence LC3B S7311-IF1 24682219

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