CAS NO: | 129298-91-5 |
生物活性 | TNP-470 is amethionine aminopeptidase-2inhibitor and also anangiogenesisinhibitor. | ||||||||||||||||
IC50& Target | methionine aminopeptidase-2[1], angiogenesis[2] | ||||||||||||||||
体外研究 (In Vitro) | No significant difference of apoptotic cell numbers is observed between cells treated with TNP-470 and the controls. The IC50s of TNP-470 are 16.86±0.9 μg/mL, 3.16±0.6 μg/mL and 1.78±0.8 μg/mL for KKU-M213 cells at 24, 48 and 72 h, respectively. The results show that TNP-470 significantly reduces the number of migrated cells and invaded cells as compare with the vehicle treated group. TNP-470 decreases the migrated cells of KKU-M213 to 26% and of KKU-M214 to 11% (P<0.01). Similarly, TNP-470 also significantly affects cell invasion, the number of invaded cells is reduced to 25% in KKU-M213 (P<0.01) and to 15% in KKU-M214 (P<0.01). The relative expressions ofMMP2,MMP9andc-MYCin TNP-470 treated cells are significantly suppressed compare to the vehicle treated cells[1]. | ||||||||||||||||
体内研究 (In Vivo) | Treatment with TNP-470 attenuates (P<0.05) liver lipid accumulation compare to high fat fed (HFF) mice. By day 5, TNP-470 treated mice consume significantly less grams of high fat food than vehicle treated HFF mice. By day 15 of treatment, TNP-470 mice are consuming an equivalent number of calories to that of chow fed mice, despite the provision of high fat diet. Treatment with TNP-470 increases (P<0.05) expression of adipose tissue LPL mRNA, compare to chow-fed and high-fat fed controls. TNP-470 decreases energy intake and increases energy expenditure[2]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 401.88 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C19H28ClNO6 | ||||||||||||||||
CAS 号 | 129298-91-5 | ||||||||||||||||
中文名称 | 夫马菌素醇;夫马吉欣 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | -20°C, stored under nitrogen *In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 100 mg/mL(248.83 mM;Need ultrasonic) 配制储备液
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