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551476

Sigma-Aldrich

Q-VD-OPh, Non-O-methylated

≥90% (HPLC), liquid, Caspase inhibitor, Calbiochem®

Sinonimo/i:

InSolution Q-VD-OPh, Non-O-methylated, N-(2-Quinolyl)valyl-aspartyl-(2,6-difluorophenoxy)methyl Ketone

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1 MG
CHF 289.00
5 MG
CHF 934.00

CHF 289.00


Spedizione prevista il16 maggio 2025



Scegli un formato

Cambia visualizzazione
1 MG
CHF 289.00
5 MG
CHF 934.00

About This Item

Formula empirica (notazione di Hill):
C26H25F2N3O6
Peso molecolare:
513.49
Codice UNSPSC:
12352200
NACRES:
NA.77

CHF 289.00


Spedizione prevista il16 maggio 2025


Nome del prodotto

Q-VD-OPh, Non-O-methylated, InSolution, ≥90%, irreversible broad-spectrum inhibitor of caspases

Livello qualitativo

Saggio

≥90% (HPLC)

Stato

liquid

Produttore/marchio commerciale

Calbiochem®

Condizioni di stoccaggio

OK to freeze
desiccated (hygroscopic)
protect from light

Condizioni di spedizione

wet ice

Temperatura di conservazione

−20°C

Descrizione generale

A cell-permeable, irreversible, broad-spectrum caspase inhibitor (IC50 = 50, 100, 430, and <25 nM for caspase-1,-8, -9, and -3, respectively) with effective antiapoptotic properties against all major caspase-mediated cellular apoptosis pathways. Exhibits no cytotoxic effects even at extremely high concentrations. Shown to reduce ischemic brain damage and stroke-induced programmed cell death in thymus and spleen.

Azioni biochim/fisiol

Cell permeable: yes
Primary Target
caspase-1
Product does not compete with ATP.
Reversible: no
Target IC50: 50, 100, 430, and <25 nM for caspase-1,-8, -9, and -3, respectively

Confezionamento

Packaged under inert gas

Attenzione

Toxicity: Irritant (B)

Sequenza

Q-Val-Asp-CH₂-OPh

Stato fisico

Supplied as a 10 mM (1 mg/195 µl) solution in DMSO.

Ricostituzione

Following initial thaw, aliquot and freeze (-20°C).

Altre note

Braun, J.S., et al. 2007. Exp. Neurol.206, 183.
Caserta, T.M., et al. 2003. Apoptosis8, 345.
Rebbaa, A., et al. 2003. Oncogene22, 2805.

Note legali

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

188.6 °F - closed cup - (Dimethylsulfoxide)

Punto d’infiammabilità (°C)

87 °C - closed cup - (Dimethylsulfoxide)


Certificati d'analisi (COA)

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Joshua D Bryant et al.
Current protocols, 2(2), e372-e372 (2022-02-18)
Mitochondria have emerged as key drivers of mammalian innate immune responses, functioning as signaling hubs to trigger inflammation and orchestrating metabolic switches required for phagocyte activation. Mitochondria also contain damage-associated molecular patterns (DAMPs), molecules that share similarity with pathogen-associated molecular
Sara H Small et al.
Science signaling, 14(714), eaba2611-eaba2611 (2021-12-22)
Cytokine production is a critical component of cell-extrinsic responses to DNA damage and cellular senescence. Here, we demonstrated that expression of the gene encoding interleukin-19 (IL-19) was enhanced by DNA damage through pathways mediated by c-Jun amino-terminal kinase (JNK) and
Javier Chicote et al.
Frontiers in pharmacology, 11, 580343-580343 (2020-11-13)
Macroautophagy (hereafter autophagy) is a multistep intracellular catabolic process with pleiotropic implications in cell fate. Attending to its activation, autophagy can be classified into inducible or constitutive. Constitutive, or basal autophagy, unfolds under nutrient-replete conditions to maintain the cellular homeostasis.
Yuanjiu Lei et al.
Cell, 186(14), 3013-3032 (2023-06-24)
Mitochondrial DNA (mtDNA) is a potent agonist of the innate immune system; however, the exact immunostimulatory features of mtDNA and the kinetics of detection by cytosolic nucleic acid sensors remain poorly defined. Here, we show that mitochondrial genome instability promotes

Questions

  1. Is Q-VD-OPh, Non-O-methylated and Bcl-2 Inhibitor VI, ABT-737 – CAS 852808-04-9-Calbiochem (197333, reconstituted in DMSO) stable in cell culture media at 37C for cell-based assays?

    1 answer
    1. The stability of this inhibitor in cell culture media has not been evaluated in-house and is expected to vary from one cell culture model system to another. The required frequency of refreshing culture medium containing this inhibitor should be determined empirically for the specific model system. Published literature may be used as a guide.

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