AKT-IN-3

目录号：SY-109319

AKT-IN-3 is a potent, orally active low hERG blocking Akt inhibitor (IC50: 1.4 nM, 1.2 nM, and 1.7 nM for Akt1, Akt2, and Akt3). AKT-IN-3 (compound E22) also exhibits good inhibitory activity against other AGC family kinases, such as PKA, PKC, ROCK1, RSK1

¥2618.00

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2-Fluoropalmitic acid

目录号：SY-109717

2-Fluoropalmitic acid(2-氟代十六烷醇)是一种含有氟原子的脂肪酸，可作为胶质母细胞瘤(GBM)的潜在治疗剂，抑制胶质瘤干细胞（GSC）的活力、增殖和茎样表型，抑制磷酸化erk、CD133和SOX-2的表达，导致MMP-2活性降低和MGMT启动子甲基化增加。

¥1874.00

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TX2-121-1

目录号：SY-109294

TX2-121-1 targets HER3 for proteasome-mediated degradation to inhibit HER3-dependent signalling and growth.

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Cepeginterferon alfa-2b

目录号：SY-109839

Cepeginterferon alfa-2b是一种聚乙二醇化干扰素, 其聚乙二醇基由分子量为20 kDa的PEG构成。该化合物广泛应用于丙型肝炎病毒(HCV)、真性红细胞增多症(PV)和原发性血小板增多症(ET)等疾病的研究中。

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SIAIS178

目录号：SY-109431

SIAIS178是一种靶向BCR-ABL的选择性PROTAC降解剂，IC50=24 nM，通过募集VHL E3 泛素连接酶来降解BCR-ABL蛋白，在体外抑制白血病细胞生长和导致K562异种移植肿瘤消退。

¥1540.00

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α2β1 Integrin Ligand Peptide

目录号：SY-109798

The Asp-Gly-Glu-Ala (DGEA) amino acid domain of type I collagen interacts with the α2β1 integrin receptor on the cell membrane and mediates extracellular signals into cells. It is a potential antagonist of collagen receptors.

¥418.00

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