英文名 | (1Z,4S,5Z,11aR,14S,14aR,15S,15aR,16aS,16bR)-14-(1H-Indol-3-ylmethyl)-4,6,15,15a-tetramethyl-9,10,14,14a,15,15a,16a,16b-octahydro-3H-cyclotrideca[d]oxireno[f]isoindole-7,8,11,12(4H,13H)-tetrone |
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英文别名 |
3H-Cyclotridec[d]oxireno[f]isoindole-7,8,11,12(4H,13H)-tetrone, 9,10,14,14a,15,15a,16a,16b-octahydro-14-(1H-indol-3-ylmethyl)-4,6,15,15a-tetramethyl-, (1Z,4S,5Z,11aR,14S,14aR,15S,15aR,16aS,16bR)-
(1Z,4S,5Z,11aR,14S,14aR,15S,15aR,16aS,16bR)-14-(1H-Indol-3-ylmethyl)-4,6,15,15a-tetramethyl-9,10,14,14a,15,15a,16a,16b-octahydro-3H-cyclotrideca[d]oxireno[f]isoindole-7,8,11,12(4H,13H)-tetrone |
描述 | Cochliodone A 能从深海衍生真菌 Chaetomium sp. 的培养物中提取得到活性化合物,具有抗细菌和抗癌活性。Cochliodone A 对多种细菌具有毒性,MICs 分别为 15.3 μg/mL (V. vulnificus),32.7 μg/mL (V. rotiferianus),15.9 μg/mL (S. aureus ATCC 43300),16.3 μg/mL (S. aureus CGMCC 1.12409)。Cochliodone A 也抑制多种癌细胞系,IC50s 分别为 28.1 μM (A549),20.7 μM (HeLa),23.2 μM (Hep G2)。 |
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相关类别 | |
参考文献 |
密度 | 1.3±0.1 g/cm3 |
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沸点 | 774.1±60.0 °C at 760 mmHg |
分子式 | C34H38O12 |
分子量 | 638.66 |
闪点 | 421.9±32.9 °C |
精确质量 | 528.262451 |
LogP | 3.45 |
蒸汽压 | 0.0±2.7 mmHg at 25°C |
折射率 | 1.633 |