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首页-小分子抑制剂&激动剂-GPCR-5-HT Receptor-Bexicaserin
Bexicaserin

Chemical Structure : Bexicaserin

CAS No.: 2035818-24-5

Bexicaserin (LP352, LP-352)

货号: PC-21971Not For Human Use, Lab Use Only.

Bexicaserin (LP352) is a potent, highly selective, oral and centrally acting 5-HT2C receptor agonist with EC50 of 42 nM (Emax=112%), and Ki of 39 nM.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

Bexicaserin (LP352) is a potent, highly selective, oral and centrally acting 5-HT2C receptor agonist with EC50 of 42 nM (Emax=112%), and Ki of 39 nM.
Bexicaserin (LP352) shows no detected activity at the 5-HT2B and 5-HT2A receptor subtypes.
Bexicaserin (LP352) displays excellent oral bioavailability, good central nervous system partitioning, and decreased renal clearance in vivo.
Bexicaserin (LP352) also is a potent inhibitor of acute refeeding in the fasted rat, suggesting on-target effects.

物理化学性质&存储条件

分子量 295.33
分子式 C15H19F2N3O
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(3R)-N-(2,2-difluoroethyl)-3-methyl-1,10-diazatricyclo[6.4.1.04,13]trideca-4,6,8(13)-triene-5-carboxamide

参考文献

1. Ren A, et al. J Med Chem. 2025 May 14. doi: 10.1021/acs.jmedchem.4c02923.

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