CHLORURE DE CHXIMYTHRINE

Code: 220285-5mg D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Biochem/physiol Actions

Reversible: no

Product does not compete with ATP.

Primary TargetPKC

Cell permeable: yes

General description

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Non disponible en dehors du Royaume-Uni et de l'Irlande

Biochem/physiol Actions

Reversible: no

Product does not compete with ATP.

Primary TargetPKC

Cell permeable: yes

General description

Naturally occurring alkaloid. Cell-permeable, selective inhibitor of protein kinase C (IC50 = 660 nM). Acts on the catalytic domain irrespective of the attachment of the regulatory domain. Material is a competitive inhibitor with respect to the phosphate acceptor and a non-competitive inhibitor with respect to ATP. Over ten-fold more potent than H-7, HCl (Cat. No. 371955). Inhibits thromboxane formation and phosphoinositide metabolism in platelets. Also induces apoptotic DNA fragmentation and cell death in HL-60 human promyelocytic leukemia cells.

Naturally-occurring alkaloid. Potent, selective, and cell-permeable inhibitor of protein kinase C (IC50 = 660 nM). Acts on the catalytic domain of PKC. A competitive inhibitor with respect to the phosphate acceptor and a non-competitive inhibitor with respect to ATP. Over ten-fold more potent than H-7, HCl (Cat. No. 371955). Inhibits thromboxane formation and phosphoinositide metabolism in platelets. Also induces apoptotic DNA fragmentation and cell death in HL-60 human promyelocytic leukemia cells.

Legal Information

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

Other Notes

Kandasamy, R.A., et al. 1995. J. Biol. Chem.270 29209.Jarvis, W.D., et al. 1994. Cancer Res.54, 1707.Barg, J., et al. 1992. J. Neurochem.59, 1145.Herbert, J.M., et al. 1990. Biochem. Biophys. Res. Commun.172, 993.Ko, F., et al. 1990. Biochim. Biophys. Acta1052, 360.Walterova, D., et al. J. Med. Chem.24, 1100.

Packaging

5 mg in Plastic ampoule

Preparation Note

Heating to 40-50°C with gentle agitation may be necessary to achieve complete solubilization. Further dilute with buffer just prior to use.

Reconstitution

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.

Warning

Toxicity: Harmful (C)

assay≥97% (HPLC)
colorlight yellow to yellow
formsolid
InChI keyWEEFNMFMNMASJY-UHFFFAOYSA-M
InChI1S/C21H18NO4.ClH/c1-22-10-16-13(6-7-17(23-2)21(16)24-3)14-5-4-12-8-18-19(26-11-25-18)9-15(12)20(14)22;/h4-10H,11H2,1-3H3;1H/q+1;/p-1
manufacturer/tradenameCalbiochem®
potency660 nM IC50
Quality Level100
shipped inambient
solubilityDMSO: 10 mg/mL, water: 1 mg/mL
storage conditionOK to freeze
storage temp.−20°C
Cas Number3895-92-9
Ce produit répond aux critères suivants pour être admissible aux récompenses suivantes :



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