6 results for "Additional 5-HT3 Receptor Compounds" in 产品

Additional 5-HT3 Receptor Compounds

Serotonin 5-HT3 receptors, are ligand-gated ion channels of the Cys-loop family. The receptor consists of 4-transmembrane domains that form an intrinsic cation-selective channel. So far five human 5-HT3 receptor subtypes have been identified (5-HT3A-E).

The 5-HT3B-E subtypes do not form functional homo-oligomeric complexes like the 5-HT3A subtypes, but co-assemble with 5-HT3A to influence its functional expression.

Tryptophan hydroxylase inhibitor

Purity: ≥99%
Tryptophan hydroxylase inhibitor
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Selective MAO-B inhibitor

Alternate Names: Ro 19-6327
Chemical Name: N-(2-Aminoethyl)-5-chloro-2-pyridinecarboxamide hydrochloride
Purity: ≥98%
Selective MAO-B inhibitor
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5-HT reuptake inhibitor; also stimulates 5-HT release

Alternate Names: (+)-Fenfluramine
Chemical Name: (S)-N-Ethyl-α-methyl-3-(trifluoromethyl)benzeneethanamine hydrochloride
Purity: ≥95%
5-HT reuptake inhibitor; also stimulates 5-HT release
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Selective and irreversible MAO-B inhibitor

Chemical Name: (1R)-2,3-Dihydro-N-2-propynyl-1H-inden-1-amine methanesulfonate
Purity: ≥98%
Selective and irreversible MAO-B inhibitor
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Reversible MAO-A inhibitor

Chemical Name: 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide
Purity: ≥98%
Reversible MAO-A inhibitor
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Induces dopamine, 5-HT and noradrenalin release; also α7 nAChR antagonist

Alternate Names: Dextroamphetamine sulfate
Chemical Name: (+)-α-Methylphenethylamine hemisulfate salt
Purity: ≥98%
Induces dopamine, 5-HT and noradrenalin release; also α7 nAChR antagonist
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