PARP Inhibitor III; DPQ

Code: 300270-1MG D2-231

Biochem/physiol Actions

Cell permeable: no

Reversible: no

Product does not compete with ATP.

General description

A potent and selecti...


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Your Price
€174.00 1MG
€214.02 inc. VAT

Biochem/physiol Actions

Cell permeable: no

Reversible: no

Product does not compete with ATP.

General description

A potent and selective inhibitor of poly(ADP-ribose) polymerase (PARP; IC50 = 40 nM). Significantly reduces infarcet volume in rat focual cerebrale ischemia model.

A very potent and selective poly(ADP-ribose)polymerase (PARP) inhibitor (IC50 = 40 nM). Significantly reduces infarcet volume in rat focual cerebrale ischemia model.

Legal Information

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

Other Notes

Eliasson, M.J., et al. 1997. Nat. Med. 3, 1089.Takahashi, K., et al. 1997. J. Cereb. Blood Flow Metabl. 17, 1137.Suto, M.J., et al. 1991. Anticancer Drug Des. 6, 107.

Packaging

1 mg in Plastic ampoule

Warning

Toxicity: Harmful (C)

assay≥90% (HPLC)
coloroff-white
formsolid
manufacturer/tradenameCalbiochem®
potency40 nM IC50
Quality Level100
shipped inambient
solubilityDMSO: 5 mg/mL
storage conditionOK to freeze
storage temp.−20°C
Cas Number129075-73-6
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