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首页-小分子抑制剂&激动剂-Others-Other Targets-LH1753
LH1753

Chemical Structure : LH1753

CAS No.: 2650492-10-5

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LH1753 (LH 1753)

货号: PC-22695Not For Human Use, Lab Use Only.

LH1753 is an orally bioavailable inhibitor of L-cystine crystallization for cystinuria, prevents stone formation effectively in the Slc3a1-knockout mouse model.

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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

LH1753 is an orally bioavailable inhibitor of L-cystine crystallization for cystinuria, prevents stone formation effectively in the Slc3a1-knockout mouse model.

物理化学性质&存储条件

分子量 630.57
分子式 C22H40N6O2S2.4ClH
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

(2R,2'R)-3,3'-disulfanediylbis(2-amino-1-(1,8-diazaspiro[4.5]decan-8-yl)propan-1-one) hydrochloride

参考文献

1. Hu L, et al. ACS Med Chem Lett. 2024 Jun 6;15(7):1026-1031.

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