AZD3965 is a potent, selective and orally available monocarboxylate transporter 1 (MCT1) inhibitor with a binding affinity of 1.6 nM.
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描述 | AZD3965 is engineered to selectively block Monocarboxylate Transporter-1 (MCT1), thus anticipated to affect lactate transport into and out of cells[1]. AZD3965 treatment leads to a 3.7-fold rise in intracellular lactate levels under hypoxic conditions in COR-L103 cells, and increases of 3.7-fold and 3.9-fold in NCI-H1048 cells under normoxic and hypoxic conditions, respectively. In all other scenarios, a less than 1.9-fold increase is observed. These results align with AZD3965's mechanism of blocking lactate transport in cells, reducing cell numbers, and indicate its action through MCT1 inhibition. Furthermore, overexpression of MCT1 in NCI-H1048 cells elevates the EC50 from 0.14 nM to 10.5 nM, supporting the action of AZD3965 via MCT1 inhibition[2]. |
Animal study | COR-L103 tumor-bearing mice receive 100 mg/kg AZD3965 or a vehicle BID for 21 days, with tumor volume tracked. Pharmacokinetic analysis reveals that 100 mg/kg AZD3965 BID achieves free AZD3965 concentrations predicted to block lactate transport. The treatment with AZD3965 significantly curtails COR-L103 tumor growth; however, tumor regression is not observed, aligning with the understanding that AZD3965 primarily targets the tumor's hypoxic fraction[2]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
1.94mL 0.39mL 0.19mL |
9.70mL 1.94mL 0.97mL |
19.40mL 3.88mL 1.94mL |
CAS号 | 1448671-31-5 |
分子式 | C21H24F3N5O5S |
分子量 | 515.51 |
SMILES Code | O=C1N(C(C)C)C2=C(C(C(N3OC[C@@](C)(O)C3)=O)=C(CC4=C(C)NN=C4C(F)(F)F)S2)C(N1C)=O |
MDL No. | MFCD28963899 |
别名 | |
运输 | 蓝冰 |
InChI Key | PRNXOFBDXNTIFG-FQEVSTJZSA-N |
Pubchem ID | 10369242 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Keep in dark place, sealed in dry, 2-8°C |
溶解方案 |
请根据您的动物给药指南选择适当的溶解方案。 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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动物实验配方 |
IP 2% DMSO+2% Tween80+40% PEG300+water 11 mg/mL clear PO 0.5% CMC-Na 30 mg/mL suspension |