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BGC 20-761 Sale

目录号 : GC15092

BGC 20-761 是一种选择性 5-HT6 和多巴胺受体拮抗剂(人受体 Ki 值:5-HT6 (20 nM)、5-HT2A (69 nM)、D2 (140 nM))。

BGC 20-761 Chemical Structure

Cas No.:17375-63-2

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10mg
¥2,636.00
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50mg
¥11,099.00
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Sample solution is provided at 25 µL, 10mM.

Description

BGC20-761 is a selective and high affinity antagonist of 5-HTC.

The 5-HT6 receptor, a G protein-coupled receptor (GPCR), is a subtype of 5-HT receptor which binds the endogenous neurotransmitter serotonin (5-hydroxytryptamine, 5-HT). This protein is expressed almost exclusively in the brain and mediates excitatory neurotransmission.

In cellular level, BGC20-761 (5-methoxy-2-phenyl-N,N-dimethyltryptamine) was shown to selectively blocked 5-HTC.

BGC20-761 was used to study the difference in drug- induced effects in memory consolidation in young and mature rats and human. In young mice, BGC20-761 treatment at doses of 5 mg/kg and 10 mg/kg i.p, dose-dependently reversed a deficit of social recognition induced by scopolamine, an anticholinergic drug that impairs memory at dosage of 0.4 mg/kg i.p. In mature rats (6 months), recognition of the novel object was improved following administration of BGC20-761. The difference in effects of BGC20-761 in young vs. mature rats may reflect the status of memory consolidation in these different age ranges 1.

Reference:
1.  Mitchell ES, Hoplight BJ, Lear SP, et al. BGC20-761, a novel tryptamine analog, enhances memory consolidation and reverses scopolamine-induced memory deficit in social and visuospatial memory tasks through a 5-HT6 receptor-mediated mechanism. Neuropharmacology. 2006;50(4):412-420.

化学性质

Cas No. 17375-63-2 SDF
化学名 2-(5-methoxy-2-phenyl-1H-indol-3-yl)-N,N-dimethylethanamine
Canonical SMILES COC1=CC2=C(NC(C3=CC=CC=C3)=C2CCN(C)C)C=C1
分子式 C19H22N2O 分子量 294.39
溶解度 <14.72mg/ml in ethanol; <29.44mg/ml in DMSO 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 3.3969 mL 16.9843 mL 33.9685 mL
5 mM 0.6794 mL 3.3969 mL 6.7937 mL
10 mM 0.3397 mL 1.6984 mL 3.3969 mL
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