MGCD-265是一种有效的,多靶点,及ATP竞争性的c-Met和VEGFR1/2/3抑制剂,IC50分别为1 nM, 3 nM/3 nM/4 nM,也抑制Ron和Tie2。
MGCD-265 is a potent, multi-target and ATP-competitive inhibitor of c-Met and VEGFR1/2/3 with IC50 of 1 nM, 3 nM/3 nM/4 nM, respectively; also inhibits Ron and Tie2. Phase 1/2.
0-5 μM
20 mg/kg-60 mg/kg 口服处理
动物 A (mg/kg) = 动物 B (mg/kg)×动物 B的Km系数/动物 A的Km系数 | |
例如,已知某工具药用于小鼠的剂量为88 mg/kg , 则用于大鼠的剂量换算方法:将88 mg/kg 乘以小鼠的Km系数(3),再除以大鼠的Km系数(6),得到该药物用于大鼠的等效剂量44 mg/kg。
[1] Bonfils C. et al. AACR 2012 Annual Meeting, 2012. Abstract 1790.
分子式 C26H20FN5O2S2 |
分子量 517.6 |
CAS号 875337-44-3 |
储存方式 ﹣20 ℃冷藏长期储存。冰袋运输 |
溶剂(常温) |
DMSO 104 mg/mL |
Water <1 mg/mL |
Ethanol <1 mg/mL |
体内溶解度
NCT Number | Conditions | Interventions | Sponsor/Collaborators | Phases | Start Date | Last Updated |
NCT00975767 | Advanced Malignancies, Non-small Cell Lung Cancer | Drug: MGCD265+erlotinib|Drug: MGCD265+docetaxel | Mirati Therapeutics Inc. | Phase 1 | 2009-08-01 | 2015-01-06 |
NCT02544633 | Non-Small Cell Lung Cancer | Drug: MGCD265 | Mirati Therapeutics Inc. | Phase 2 | 2015-10-01 | 2017-01-11 |
NCT01930006 | Advanced Malignancies | Drug: MGCD265 | Mirati Therapeutics Inc. | Phase 1 | 2013-08-01 | 2015-01-06 |
NCT02117245 | Healthy | Mirati Therapeutics Inc. | 2011-12-01 | 2015-01-06 | ||
NCT00697632 | Advanced Cancer | Drug: MGCD265 | Mirati Therapeutics Inc. | Phase 1 | 2008-06-01 | 2017-01-17 |
NCT00679133 | Advanced Malignancies | Drug: MGCD265 | Mirati Therapeutics Inc. | Phase 1 | 2008-04-01 | 2015-01-06 |
NCT02954991 | Carcinoma, Non-Small-Cell Lung | Drug: Glesatinib|Drug: Sitravatinib|Drug: Mocetinostat|Drug: Nivolumab | Mirati Therapeutics Inc. | Phase 2 | 2016-11-01 | 2017-03-09 |
注:以上所有数据均来自公开文献,并不保证对所有实验均有效,数据仅供参考。
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