Carvedilol hydrochloride

Application (±)-CGP-12177A has been used as a &#946-Adrenergic receptor agonist: to evaluate the&nbspdissociation constant&nbsp(Kd) by frontal affinity chromatography to study its cardiostimulant effects on rat ventricular cardiomyocytes to

Application (±)-CGP-12177A has been used as a &#946-Adrenergic receptor agonist: to evaluate the&nbspdissociation constant&nbsp(Kd) by frontal affinity chromatography to study its cardiostimulant effects on rat ventricular cardiomyocytes to

BW 245C is a selective agonist for the DP1 receptor. The Ki of BW 245C for the inhibition of [3H]-PGD2 binding to isolated human platelet membranes is 0.

BW 245C is a selective agonist for the DP1 receptor. The Ki of BW 245C for the inhibition of [3H]-PGD2 binding to isolated human platelet membranes is 0.

BW 245C is a selective agonist for the DP1 receptor. The Ki of BW 245C for the inhibition of [3H]-PGD2 binding to isolated human platelet membranes is 0.

General description Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. Carvedilol

InformationCarvedilol (BM-14190, SKF 105517) is a non-selectivebeta blocker/alpha-1blocker, used to treat congestive heart failure (CHF) and high blood pressure.In vitroCarvedilol rapidly inhibits Fe(++)-initiated lipid peroxidation, measured as

A potent antagonist of the PAF receptor, inhibiting aggregation of rabbit and human platelets induced by PAF with IC₅₀ values of 75 and 170 nM, respectively prevents PAF-induced hypotension in rats, while not blocking hypotension

A potent antagonist of the PAF receptor, inhibiting aggregation of rabbit and human platelets induced by PAF with IC₅₀ values of 75 and 170 nM, respectively prevents PAF-induced hypotension in rats, while not blocking hypotension

A potent antagonist of the PAF receptor, inhibiting aggregation of rabbit and human platelets induced by PAF with IC₅₀ values of 75 and 170 nM, respectively prevents PAF-induced hypotension in rats, while not blocking hypotension

Synthetic (+)-cis isomer that acts as an L-type Ca 2+ channel antagonist. Similar in function to nifedipine and verapamil.

A prodrug of the &alpha1-adrenergic receptor agonist, DMAE (Kis= 2, 6.9, and 1.