描述 |
9-Methoxycamptothecin (MCPT),是从Nothapodytes foetida 中分离得到的,通过抑制拓扑异构酶发挥抗肿瘤活性。9-Methoxycamptothecin (MCPT) 具有强效的诱导G2/M期细胞和癌细胞凋亡的作用。 |
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相关类别 |
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靶点 |
Topoisomerase[1]. Apoptosis[2].
|
SMILES |
CC[C@@]1(C2=C(COC1=O)C(N3C(C4=NC5=CC=CC(OC)=C5C=C4C3)=C2)=O)O |
参考文献 |
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密度 | 1.5±0.1 g/cm3 |
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沸点 | 773.1±60.0 °C at 760 mmHg |
熔点 | 223-225 ?C |
分子式 | C21H18N2O5 |
分子量 | 378.378 |
闪点 | 421.4±32.9 °C |
精确质量 | 378.121582 |
PSA | 90.65000 |
LogP | 2.00 |
蒸汽压 | 0.0±2.8 mmHg at 25°C |
折射率 | 1.723 |
水溶解性 | Slightly soluble (2.7 g/L) (25 ?C) |
~%
9-甲氧基喜树碱
39026-92-1
|
文献:Gao, Mingzhang; Miller, Kathy D.; Sledge, George W.; Zheng, Qi-Huang Bioorganic and Medicinal Chemistry Letters, 2005 , vol. 15, # 17 p. 3865 – 3869 |
~94%
9-甲氧基喜树碱
39026-92-1
|
文献:Sawada; Matsuoka; Nokata; Nagata; Furuta; Yokokura; Miyasaka Chemical and Pharmaceutical Bulletin, 1991 , vol. 39, # 12 p. 3183 – 3188 |
~%
9-甲氧基喜树碱
39026-92-1
|
文献:Gao, Mingzhang; Miller, Kathy D.; Sledge, George W.; Zheng, Qi-Huang Bioorganic and Medicinal Chemistry Letters, 2005 , vol. 15, # 17 p. 3865 – 3869 |
~%
9-甲氧基喜树碱
39026-92-1
|
文献:Gao, Mingzhang; Miller, Kathy D.; Sledge, George W.; Zheng, Qi-Huang Bioorganic and Medicinal Chemistry Letters, 2005 , vol. 15, # 17 p. 3865 – 3869 |
9-甲氧基喜树碱上游产品? 5 | |
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9-甲氧基喜树碱下游产品? 0 |
1H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4-ethyl-4-hydroxy-10-methoxy-, (4S)- |
10-methoxycamptothecin |
9-methoxycamtothecin |
(4S)-4-Ethyl-4-hydroxy-10-methoxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione |
Camptothecin,9-methoxy |