Du sökte efter: 1-Ethyl-1H-imidazole-5-carbaldehyde+hydrochloride

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

Leverantör: Apollo Scientific

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

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

Leverantör: Apollo Scientific

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

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

Leverantör: Apollo Scientific

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

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

Artikel nummer : (APOSOR52510-1G)

Leverantör: Apollo Scientific

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

UOM: 1 * 1 g

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Dexmedetomidine hydrochloride

Leverantör: Thermo Scientific

Beskrivning: Dexmedetomidine hydrochloride

Dexmedetomidine hydrochloride ≥98.0% (by HPLC, titration analysis)

Leverantör: TCI EUROPE

Beskrivning: Dexmedetomidine hydrochloride ≥98.0% (by HPLC, titration analysis)

SKF-96365 hydrochloride ≥98%

Artikel nummer : (TCIAK0066-50MG)

Leverantör: TCI EUROPE

Beskrivning: SKF-96365 hydrochloride ≥98%

UOM: 1 * 50 mg

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Dexmedetomidine hydrochloride ≥99%

Leverantör: Cayman Chemical

Beskrivning: 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.

Atipamezole hydrochloride ≥98.0% (by HPLC, titration analysis)

Leverantör: TCI EUROPE

Beskrivning: Atipamezole hydrochloride ≥98.0% (by HPLC, titration analysis)

SKF-96365 hydrochloride ≥98%

Leverantör: ENZO LIFE SCIENCES AG

Beskrivning: 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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