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7ACC2

    
99%

7ACC2

源叶(MedMol)
S83441 一键复制产品信息
1472624-85-3
C18H15NO4
309.316
7-[苄基(甲基)氨基]-2-氧代-2H-苯并吡喃-3-羧酸
货号 规格 价格 上海 北京 武汉 南京 购买数量
S83441-2mg 99% ¥490.00 5 - - -
S83441-5mg 99% ¥740.00 6 - - -
S83441-10mg 99% ¥1230.00 5 - - -
S83441-50mg 99% ¥3500.00 3 - - -
S83441-100mg 99% ¥4900.00 货期:2-3天 - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品

产品介绍

7ACC2 is a potent monocarboxylate transporter (MCT) inhibitor with an IC50 of 11 nM for inhibition of [14C]-lactate influx. 7ACC2 is also a potent inhibitor of mitochondrial pyruvate transport. 7ACC2 is an anticancer agent through inhibition of lactate flux

产品描述: 7ACC2 is a potent monocarboxylate transporter (MCT) inhibitor with an IC50 of 11 nM for inhibition of [14C]-lactate influx. 7ACC2 is also a potent inhibitor of mitochondrial pyruvate transport. 7ACC2 is an anticancer agent through inhibition of lactate flux
靶点: IC50: 11 nM (Monocarboxylate transporter) Mitochondrial pyruvate transport;MitochondrialMetabolism; Monocarboxylatetransporter
体外研究: 7ACC2 (compound 19; 72 hours) inhibits SiHa cells proliferation in lactate-containing medium with an EC50 of 0.22 μM. In SiHa cells, lactate uptake primarily depends on the high affinity MCT1 transporter. 7ACC2 (compound 19) shows an excellent chemical stability in simulated gastric (SGF) and intestinal (SIF) fluids, a good apparent permeability coefficient (Papp) through Caco-2 monolayer and a high metabolic stability on mouse (MLM) and human liver microsomes (HLM) as well as on human hepatocytes. 7ACC2 is a potent inhibitor of mitochondrial pyruvate transport which consecutively blocks extracellular lactate uptake by promoting intracellular pyruvate accumulation
体内研究: 7ACC2 (3 mg/kg; intraperitoneal administration; daily; for 5 days or 10days) treatment significantly inhibits tumor growth in mice. 7ACC2 radiosensitizes tumor cells by reducing hypoxia in vivo. The intraperitoneal administration of 7ACC2 (compound 19; 3 mg/kg) to mice leads to a Cmax of 1246 ng/ml (4 μM) in a very short time (Tmax=10 min) associated with a plasma half-life of 4.5 h. Animal Model: 7-week-old female NMRI nude mice with radiotherapy administered[2] Dosage: 3 mg/kg Administration: Intraperitoneal administration; daily; for 5 days or 10days Result: A significant increase in tumor growth delay was observed.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.233 ml 16.165 ml 32.329 ml
5 mM 0.647 ml 3.233 ml 6.466 ml
10 mM 0.323 ml 1.616 ml 3.233 ml
50 mM 0.065 ml 0.323 ml 0.647 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

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