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bicuculline methochloride

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Bicuculline methochloride
T7411238641-83-7
Bicuculline methochloride ((+)-Bicuculline; d-Bicuculline), a selective GABAA receptor antagonist, exhibits an IC50 of 3 μM. It induces tonic-clonic convulsions in mammals and blocks Ca2+ activated potassium channels, making it useful for studying epilepsy and related psychiatric disorders [1] [2].
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(-)-Bicuculline methochloride
l-Bicuculline methochloride
T1204453552-05-9
(-)-Bicuculline methochloride is a potent antagonist of GABAA receptor.
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8-10 weeks
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Bicuculline
d-Bicuculline, (+)-Bicuculline
T2850485-49-4
Bicuculline ((+)-Bicuculline) is a light-sensitive competitive antagonist of GABAA receptors, originally identified in 1932 from plant alkaloid extracts, and isolated from Dicentra cucullaria, Adlumia fungosa, Fumariaceae, and various Corydalis species.
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Bicuculline methobromide
d-Bicuculline methobromide, (+)-Bicuculline methobromide ; d-Bicuculline methobromide, (+)-Bicuculline methobromide
T7224666016-70-4
Bicuculline methobromide, a selective GABAA Receptor antagonist with an IC50 value of 3 μM, induces tonic-clonic convulsions in mammals and blocks Ca2+ activated potassium channels. It is applicable in researching epilepsy and related psychiatric disorders.
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8-10 weeks
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