prmt5in1

PRMT5-IN-1 is a covalent inhibitor of protein arginine methyltransferase 5 (PRMT5)(IC50 of 11 nM for PRMT5/MEP50).

PRMT5-IN-14 is a PRMT5 inhibitor to treat cancer, sickle cell, and hereditary persistence of foetal hemoglobin (HPFH) mutations.

PRMT5-IN-13 is a selective inhibitor of protein arginine methyltransferase 5 (prmt5) .

PRMT5-IN-15 is a PRMT5 inhibitor with an IC 50 value of 0.84 nM.

PRMT5-IN-11 demonstrates potent structure-dependent inhibition against the protein methyltransferase PRMT5:MEP50 complex at submicromolar concentrations.

PRMT5-IN-12 shows remarkable inhibitory activity on PRMT5 .

PRMT5-IN-10 对蛋白甲基转移酶 PRMT5:MEP50复合物表现出良好的结构依赖性抑制作用。

PRMT5-IN-19 (Compound 41) is a potent orally active PRMT5 inhibitor, exhibiting selectivity towards the SAM-binding pocket of PRMT5 with IC50 values of 23.9 nM (radioactive biochemical assay) and 47 nM (AlphaLISA assay). It effectively blocks methyltransferase activity and demonstrates high specificity against other PRMTs and PKMTs. PRMT5-IN-19 exerts anti-proliferative effects through the induction of apoptosis and holds potential in cancer-related research [1].

PRMT5 IN-1 hydrochloride (compound 9) 是一种半缩醛胺，是一种选择性蛋白精氨酸甲基转移酶5 (PRMT5) 的有效抑制剂，对 PRMT5/MEP50 具有抑制作用 (IC50: 11 nM)。PRMT5 IN-1 hydrochloride 在生理条件下可以转化为醛，并与 C449 反应，形成共价加合物。

PRMT5-IN-17 (Compound 6) 是一种 PRMT5 抑制剂，表现出抗肿瘤活性。其中 PRMT5 是一种蛋白质精氨酸甲基转移酶，是新型的与表观遗传修饰相关的抗肿瘤靶点。

PRMT5-IN-16 (Compound 20) 是一种 PRMT5 抑制剂，具有抗肿瘤作用。其中 PRMT5 是一种蛋白质精氨酸甲基转移酶，是新型的与表观遗传修饰相关的抗肿瘤靶点。

PRMT5-IN-18 (Compound 002) 是 PRMT5 的有效抑制剂，能够用于由 PRMT5 介导的疾病（如肿瘤）的研究。