Sie suchten nach: 1-Ethyl-1H-imidazole-5-carbaldehyde+hydrochloride

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1-Ethyl-1H-imidazole-5-carbaldehyde hydrochloride 95%

Lieferant: Apollo Scientific

Beschreibung: 1-Ethyl-1H-imidazole-5-carbaldehyde hydrochloride 95%

1-Ethyl-1H-imidazole-2-carbaldehyde 95%

Lieferant: Apollo Scientific

Beschreibung: 1-Ethyl-1H-imidazole-2-carbaldehyde 95%

2-Ethyl-4-methyl-1H-imidazole-5-carbaldehyde

Lieferant: Apollo Scientific

Beschreibung: 2-Ethyl-4-methyl-1H-imidazole-5-carbaldehyde

Ethyl-4-amino-1-methyl-1H-imidazole-2-carboxylate hydrochloride

Artikel-Nr: (APOSOR52510-1G)

Lieferant: Apollo Scientific

Beschreibung: Ethyl-4-amino-1-methyl-1H-imidazole-2-carboxylate hydrochloride

VE: 1 * 1 g

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Dexmedetomidine hydrochloride

Lieferant: Thermo Scientific

Beschreibung: Dexmedetomidine hydrochloride

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.

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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