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编号化学名称Cas号纯度化学结构
24017AMG-1932790567-82-598.62%; EE 98.28%
AMG-193是安进公司开发的一种口服小分子甲硫腺苷协同PRMT5酶抑制剂
20638ATH434 mesylate2387898-69-1≧98.0%
ATH434 是一种口服药物,旨在抑制与神经变性有关的病理蛋白的聚
20633STX-4782883540-92-7≧98.0%
STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。
24084Iclepertin (BI-425809)1421936-85-7≧98.0%
Iclepertin(BI-425809)是一种口服的GlyT-1小分子抑制剂,用于治疗与
20471FHD-2862671128-05-3≧98.0%
FHD-286 is an oral, small-molecule, selective, allosteric inhibitor of BRG1 and BRM i
20657Zilurgisertib2173389-57-4≧98.0%
Zilurgisertib(之前称为 INCB 00928)是一种激活素受体样激酶 2(ALK2,
20549STC-152648257-56-9≧98.0%
STC-15 is a first-in-class inhibitor of RNA modification and is the first ever RNA me
23122601Navacaprant2244614-14-8≧98.0%
Navacaprant (NMRA-335140, BTRX-140) 是一种口服、选择性、可逆的 kappa 阿
171680Bexotegrast ( PLN-74809 )2376257-44-0≧98.0%
Bexotegrast(同义词:PLN-74809)是一种小分子、双重选择性 αVβ1 / α
1711225Fosgonimeton (ATH-1017) 2093305-05-4≧98.0%
Fosgonimeton (ATH-1017) 是一种小分子,旨在增强肝细胞生长因子 (HGF)
52013ONX-0914 ( PR-957 )960374-59-8≧95.0%
ONX-0914 是免疫蛋白酶体 LMP7 和 LMP2 亚基的抑制剂,在多种自身免疫
24067PBT434 氢溴酸盐1232841-78-9≧98.0%
PBT434, also known as ATH434 , is a novel, brain-penetrant, inhibitor of α-synuclein