Nalmefene hydrochloride dihydrate

Sodium tetrachloroaurate(III) dihydrate (NaAuCl 4 &#1832H 2 O) is the least expensive gold catalyst that is widely used in many organic transformations such as nucleophilic addition to multiple bonds, nonsymmetrical etherization, and nucleophilic

Application Telenzepine dihydrochloride hydrate was used to study M 1 muscarinic receptor-mediated signaling in juvenile rat hippocampus and rat urinary bladder. Biochem/physiol Actions Telenzepine is an analog of pirenzepine and inhibits the

Application Telenzepine dihydrochloride hydrate was used to study M 1 muscarinic receptor-mediated signaling in juvenile rat hippocampus and rat urinary bladder. Biochem/physiol Actions Telenzepine is an analog of pirenzepine and inhibits the

Application Telenzepine dihydrochloride hydrate was used to study M 1 muscarinic receptor-mediated signaling in juvenile rat hippocampus and rat urinary bladder. Biochem/physiol Actions Telenzepine is an analog of pirenzepine and inhibits the

Application Uridine 5&#8242-diphosphate disodium salt hydrate has been used: as a standard for quantification of metabolite levels in murine tumor interstitial fluid by liquid chromatography-mass spectrometry (LC/MS) as a UDP standard for

Application Uridine 5&#8242-diphosphate disodium salt hydrate has been used: as a standard for quantification of metabolite levels in murine tumor interstitial fluid by liquid chromatography-mass spectrometry (LC/MS) as a UDP standard for

InformationVardenafil HCl Trihydrate (BAY38-9456) is a new type PDE inhibitor with IC50 of 0.7 and 180 nM for PDE5 and PDE1, respectively.In vitroVardenafil specifically inhibits the hydrolysis of cGMP by PDE5 with an IC50 of 0.7 nM (6.6 nM).

Biochem/physiol Actions YM-244769 hydrochloride is a potent and selective inhibitor of Na+/Ca2+ exchange (NCX) acting preferentially at NCX3. It inhibits the Ca2+ entry mode of NCX more potently than the Ca2+ exit mode.

Biochem/physiol Actions YM-244769 hydrochloride is a potent and selective inhibitor of Na+/Ca2+ exchange (NCX) acting preferentially at NCX3. It inhibits the Ca2+ entry mode of NCX more potently than the Ca2+ exit mode.