Sie suchten nach: 1H-imidazole-2-boronic+acid+hydrochloride

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1-(4-Fluoro-benzyl)-2-piperidin-4-yl-1H-benzoimidazole hydrochloride

Artikel-Nr: (APOSPC408416-500MG)

Lieferant: Apollo Scientific

Beschreibung: 1-(4-Fluoro-benzyl)-2-piperidin-4-yl-1H-benzoimidazole hydrochloride

VE: 1 * 500 mg

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1H-Indazol-4-boronsäure Hydrochlorid

Lieferant: COMBI-BLOCKS

Beschreibung: 1H-Indazol-4-boronsäure Hydrochlorid

Dexmedetomidine hydrochloride ≥99%

Lieferant: Cayman Chemical

Beschreibung: Dexmedetomidine is the (S)-enantiomer of medetomidine, an imidazole compound that binds to α2-adrenoceptors (Ki = 1.08 nM) with high affinity and selectivity compared to that of α1-adrenoceptors (Ki = 1.8 μM). Dexmedetomidine produces analgesic, sedative, and anxiolytic effects through both presynaptic activation of α2-adrenoceptors, which inhibits norepinephrine release, and postsynaptic activation of α2-adrenoceptors, which inhibits sympathetic activity and decreases blood pressure and heart rate.

1-(3-Fluoro-benzyl)-2-(piperidin-3-ylmethoxy)-1H-benzoimidazole hydrochloride

Artikel-Nr: (APOSPC408408-500MG)

Lieferant: Apollo Scientific

Beschreibung: 1-(3-Fluoro-benzyl)-2-(piperidin-3-ylmethoxy)-1H-benzoimidazole hydrochloride

VE: 1 * 500 mg

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L(+)-Histidin Hydrochlorid, Sigma-Aldrich®

Lieferant: Merck

Beschreibung: L(+)-Histidin Hydrochlorid, Sigma-Aldrich®

SKF-96365 hydrochloride ≥98% (durch HPLC)

Lieferant: ENZO LIFE SCIENCES

Beschreibung: A novel, selective inhibitor of receptor-mediated calcium entry. It inhibits receptor-mediated calcium entry in stimulated platelets (IC50=8-12µM) neutrophils and endothelial cells at concentrations which do not affect internal Ca²⁺ release. Note, in some cells SK&F 96365 can activate a novel Ca²⁺ entry pathway. Blocks TRPC3 and TRPC6 activation. Inhibits the histamine-induced formation of nitric oxide in human endothelial cells.

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