化合物PD-1/PD-L1-IN-10 T9616
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
10 mg | 2487550-41-2 | ¥1,730.00 | 询底价 |
25 mg | 2487550-41-2 | ¥3,460.00 | 询底价 |
1 mL | 2487550-41-2 | ¥1,160.00 | 询底价 |
1 mg | 2487550-41-2 | ¥456.00 | 询底价 |
100 mg | 2487550-41-2 | ¥7,230.00 | 询底价 |
50 mg | 2487550-41-2 | ¥4,970.00 | 询底价 |
5 mg | 2487550-41-2 | ¥996.00 | 询底价 |
Product Introduction
Bioactivity
英文名: PD-1/PD-L1-IN-10
描述: PD-1/PD-L1-IN-10 是一种口服有效的PD-1/PD-L1抑制剂 (IC50of 2.7 nM),显示出抗肿瘤活性。
体外活性: PD-1/PD-L1-IN-10 (compound B2) significantly promotes interferongamma secretion in a dose-dependent manner in vitro even at the low concentration of 1 nM[1].PD-1/PD-L1-IN-10 (compound B2) does not affect cell viability of LLC cells and lymph node T-cells[1].PD-1/PD-L1-IN-10 (compound B2, 0-100 nM) stabilizes the PD-L1 protein in mouse Lewis lung carcinoma (LLC) cells. Especially, PD-1/PD-L1-IN-10 (compound B2) maintains the PD-L1 stability in a dose-dependent manner at 58 °C. Suggesting that PD-1/PD-L1-IN-10 (compound B2) could enter LLC cells and then directly binds to the PD-L1 protein[1].
体内活性: PD-1/PD-L1-IN-10在LLC携带的同种异体移植小鼠模型中展现出强大的体内抗癌效果。PD-1/PD-L1-IN-10有效阻止肿瘤细胞的增殖,并在LLC肿瘤组织中诱导凋亡。[1]
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 100 mg/mL (171.93 mM)
关键字: Lewis | T-lymphocyte | tumor | IFN-γ | Inhibitor | PD-1/PD-L1-IN-10 | lung | LLC | inhibit | Apoptosis | PD1/PDL1IN10 | PD 1/PD L1 IN 10 | carcinoma | PD-1/PD-L-1-IN-10
相关产品: CAY10678 | PDL-1 cpd 10 | PD-1/PD-L1-IN-34 | BMS-1166 | Human PD-L1 inhibitor V | PD-L1-IN-3 | Feladilimab | Sasanlimab | LSD1-IN-24 | Peresolimab
相关库: Anti-Liver Cancer Compound Library | Anti-Cancer Compound Library | Immuno-Oncology Compound Library | Bioactive Compounds Library Max | Anti-Ovarian Cancer Compound Library | Inhibitor Library | Anti-Cancer Active Compound Library | PPI Inhibitor Library | Orally Active Compound Library | Bioactive Compound Library
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