(-)-Bicuculline methochloride

Modify Date: 2024-01-09 23:24:58

(-)-Bicuculline methochloride Structure
(-)-Bicuculline methochloride structure
Common Name (-)-Bicuculline methochloride
CAS Number 53552-05-9 Molecular Weight 417.84000
Density N/A Boiling Point N/A
Molecular Formula C21H20ClNO6 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of (-)-Bicuculline methochloride


(-)-Bicuculline methochloride (l-Bicuculline methochloride) is a potent GABAA receptor antagonist. (-)-Bicuculline methochloride blocks afterhyperpolarizations (AHPs) mediated by Ca2+-activated K+ channels in various types of neurons[1].

 Names

Name 6-(6,6-dimethyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-6-ium-5-yl)-6H-furo[3,4-g][1,3]benzodioxol-8-one,chloride

 (-)-Bicuculline methochloride Biological Activity

Description (-)-Bicuculline methochloride (l-Bicuculline methochloride) is a potent GABAA receptor antagonist. (-)-Bicuculline methochloride blocks afterhyperpolarizations (AHPs) mediated by Ca2+-activated K+ channels in various types of neurons[1].
Related Catalog
Target

GABAA[1]

In Vivo (-)-Bicuculline methochloride (0.6 nmol/rat) attenuates the antiallodynic effect of Neurotropin[2]. Animal Model: Rat L5-SNL model[2] Dosage: 0.6 nmol/rat Administration: Intrathecal injection, 5 minutes before administration of Neurotropin (100 NU/kg, i.v.) Result: Attenuated the antiallodynic effect of Neurotropin.
References

[1]. Seutin V, et al. Recent advances in the pharmacology of quaternary salts of bicuculline. Trends Pharmacol Sci. 1999 Jul;20(7):268-70.

[2]. Okazaki R, et al. The antiallodynic effect of Neurotropin is mediated via activation of descending pain inhibitory systems in rats with spinal nerve ligation. Anesth Analg. 2008 Sep;107(3):1064-9.

 Chemical & Physical Properties

Molecular Formula C21H20ClNO6
Molecular Weight 417.84000
Exact Mass 417.09800
PSA 63.22000
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