PD-1/PD-L1-IN-9 |
| Catalog No.GC62387 |
PD-1/PD-L1-IN-9는 3.8nM의 IC50으로 PD-1/PD-L1 상호작용의 강력한 경구 활성 억제제입니다. PD-1/PD-L1-IN-9는 면역 세포에 의한 종양 세포의 사멸 활성을 향상시킬 수 있습니다. PD-1/PD-L1-IN-9는 또한 CT26 마우스 모델에서 상당한 생체내 항종양 활성을 나타낸다.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 2628506-54-5
Sample solution is provided at 25 µL, 10mM.
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PD-1/PD-L1-IN-9 is a potent and orally active inhibitor of PD-1/PD-L1 interaction, with an IC50 of 3.8 nM. PD-1/PD-L1-IN-9 can enhance the killing activity of tumor cells by immune cells. PD-1/PD-L1-IN-9 also exhibits significant in vivo antitumor activity in a CT26 mouse model[1].
PD-1/PD-L1-IN-9 (compound 24) (46.9-1500 nM; pretreated for 2 h) dose-dependently significantly activates the antitumor immunity of PBMCs to MDB-MB 231 cells, with an EC50 of ∼100 nM[1].
PD-1/PD-L1-IN-9 (compound 24) (40-80 mg/kg; p.o. once a day for 2 weeks) inhibits tumor growth in a dose-dependent manner and does not cause any body weight loss or mortality of mice[1].PD-1/PD-L1-IN-9 (3 mg/kg; a single i.v.) exhibits half-life (t1/2=4.2 h), plasma clearance (Cl=11.5 L/h/kg) and Cmax (1233 ng/mL) in rats[1].PD-1/PD-L1-IN-9 (25 mg/kg; a single p.o.) exhibits moderate oral bioavailability (F=22 %), half-life (t1/2=6.4 h) and Cmax (192 ng/mL) in rats[1].
[1]. Wang T, et, al. Novel Biphenyl Pyridines as Potent Small-Molecule Inhibitors Targeting the Programmed Cell Death-1/Programmed Cell Death-Ligand 1 Interaction. J Med Chem. 2021 May 30.
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