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LGB321 monohydrochloride 是一种高效、选择性、可口服的ATP竞争性小分子抑制剂,能抑制全部三种PIM激酶。在多种来源于血液恶性肿瘤的细胞系中,LGB321 monohydrochloride 能抑制细胞增殖、mTOR-C1信号通路及BAD磷酸化。LGB321 monohydrochloride 可用于血液恶性肿瘤的相关研究。

LGB321 monohydrochloride 是一种高效、选择性、可口服的ATP竞争性小分子抑制剂,能抑制全部三种PIM激酶。在多种来源于血液恶性肿瘤的细胞系中,LGB321 monohydrochloride 能抑制细胞增殖、mTOR-C1信号通路及BAD磷酸化。LGB321 monohydrochloride 可用于血液恶性肿瘤的相关研究。

LGB321 monohydrochloride 相关产品
| 产品描述 | LGB321 monohydrochloride is an effective, selective, and orally active ATP-competitive small molecule inhibitor that targets all three PIM kinases. It inhibits proliferation, the mTOR-C1 signaling pathway, and BAD phosphorylation in various blood cancer-derived cell lines. LGB321 monohydrochloride is suitable for research on hematological malignancies. |
| 分子量 | N(C(=O)C=1N=C(C(F)=CC1)C2=C(F)C=CC=C2F)C=3C(=CC=NC3)N4C[C@H](C)[C@@H](O)[C@H](N)C4.Cl |
| 分子式 | C23H23ClF3N5O2 |
| CAS No. | 1469925-36-7 |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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