(+)-Bicuculline

• CAT Number: I003708
• CAS Number: 485-49-4
• Molecular Formula: C20H17NO6
• Molecular Weight: 367.4
• Purity: ≥95%
• Synonyms: NSC 32192
• Target: Membrane Transporter/Ion Channel
• Solubility: DMSO: ≥ 36 mg/mL
• Storage: 3 years -20℃ powder
• IUPAC Name: (6R)-6-[(5S)-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]-6H-furo[3,4-g][1,3]benzodioxol-8-one
• InChI: InChI=1S/C20H17NO6/c1-21-5-4-10-6-14-15(25-8-24-14)7-12(10)17(21)18-11-2-3-13-19(26-9-23-13)16(11)20(22)27-18/h2-3,6-7,17-18H,4-5,8-9H2,1H3/t17-,18+/m0/s1
• InChIKey: IYGYMKDQCDOMRE-ZWKOTPCHSA-N
• SMILES: CN1CCC2=CC3=C(C=C2[C@H]1[C@H]4C5=C(C6=C(C=C5)OCO6)C(=O)O4)OCO3

(+)-Bicuculline (Cat.No:I003708) is a natural alkaloid compound found in certain plants, including the seeds of the plant Adlumia fungosa. It is a potent antagonist of the neurotransmitter gamma-aminobutyric acid (GABA) and has been studied for its potential applications in neuroscience research. (+)-Bicuculline has shown to block the effects of GABA in preclinical studies. It is also used as a tool compound to study GABA receptor function.

Reference

[1]. Zahm DS, et al. Comparison of the locomotor-activating effects of bicuculline infusions into the preoptic area and ventral pallidum. Brain Struct Funct. 2014 Mar;219(2):511-26.
[2]. Johnston GA. Advantages of an antagonist: bicuculline and other GABA antagonists. Br J Pharmacol. 2013 May;169(2):328-36.
[3]. Graham AR Johnston. Advantages of an antagonist: bicuculline and other GABA antagonists. Br J Pharmacol. 2013 May; 169(2): 328–336.