中文名 | ONO-AE3-208 |
英文名 | ONO-AE3-208 |
别名 | 4-氰基-2-[[2-(4-氟-1-萘基)-1-氧代丙基]氨基]苯基丁酸 |
英文别名 | AE 3-208 ONO AE3 208 ONO-AE3-208 4-(4-cyano-2-(2-(4-fluoronaphthalen-1-yl)propanamido)phenyl)butanoic acid 4-Cyano-2-[[2-(4-fluoro-1-naphthalenyl)-1-oxopropyl]amino]Benzenebutanoic acid 4-{4-Cyano-2-[2-(4-fluoro-naphthalen-1-yl)-propionylamino]-phenyl}-butyric acid Benzenebutanoic acid, 4-cyano-2-[[2-(4-fluoro-1-naphthalenyl)-1-oxopropyl]amino]- |
CAS | 402473-54-5 |
化学式 | C24H21FN2O3 |
分子量 | 404.43 |
密度 | 1.30 |
沸点 | 662.4±55.0 °C(Predicted) |
酸度系数 | 4.69±0.10(Predicted) |
存储条件 | -20°C |
外观 | 粉末 |
颜色 | white to beige |
体外研究 | ONO-AE3-208 surpresses the in vitro cell invasion and migration in a dose-dependent manner without affecting cell proliferation. ONO-AE3-208 abolisheS CTGF in the presence of the EET synthesis inhibitor MS-PPOH. Arachidonic acid (AA) causeS dose-dependent dilation of the attached Af-Art, and this effect is blocked by ONO-AE3-208. |
体内研究 | ONO-AE3-208 surpresses the in vivo bone metastasis of PC3 cells in mice. The photon tumor burdens are significantly increased in a time-dependent manner in the control group in comparison with those in the ONO-AE3-208-treated group. The rate of metastasis formation is significantly higher in the former than in the latter. The median time of metastasis formation is 29 d in the ONO-AE3-208-treated animals as compared with 21 d in the controls. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.473 ml | 12.363 ml | 24.726 ml |
5 mM | 0.495 ml | 2.473 ml | 4.945 ml |
10 mM | 0.247 ml | 1.236 ml | 2.473 ml |
5 mM | 0.049 ml | 0.247 ml | 0.495 ml |
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