Name | (1R,2S,3E,5S,7S,8S,10R,13S)-2,7,13-Triacetoxy-10-hydroxy-8,12,15,15-tetramethyl-9-oxotricyclo[9.3.1.14,8]hexadeca-3,11-dien-5-yl (2E)-3-phenylacrylate |
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Synonyms |
(1R,2S,3E,5S,7S,8S,10R,13S)-2,7,13-Triacetoxy-10-hydroxy-8,12,15,15-tetramethyl-9-oxotricyclo[9.3.1.14,8]hexadeca-3,11-dien-5-yl (2E)-3-phenylacrylate
2-Propenoic acid, 3-phenyl-, (1R,2S,3E,5S,7S,8S,10R,13S)-2,7,13-tris(acetyloxy)-10-hydroxy-8,12,15,15-tetramethyl-9-oxotricyclo[9.3.1.14,8]hexadeca-3,11-dien-5-yl ester, (2E)- (1R,2S,3E,5S,7S,8S,10R,13S)-2,7,13-tris(acetyloxy)-10-hydroxy-8,12,15,15-tetramethyl-9-oxotricyclo[9.3.1.14,8]hexadeca-3,11-dien-5-yl (2E)-3-phenylprop-2-enoate |
Description | Taxuspine B is a natural product, that can be isolated from Japanese yew Taxus. Taxuspine B exhibits appreciable taxol-like activity to reduce CaCl2-induced depolymerixation of microtubules among the taxoids[1]. |
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Related Catalog | |
In Vitro | Taxuspine B 对小鼠淋巴瘤 L1210 (IC50=18 μg/mL) 和人表皮样癌 KB 细胞表现出较弱的细胞毒性,在 10 μg/mL 时抑制率分别为 42.3% 和 11.8% [1]。 |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 709.1±60.0 °C at 760 mmHg |
Molecular Formula | C35H42O10 |
Molecular Weight | 622.70 |
Flash Point | 216.8±26.4 °C |
Exact Mass | 622.277771 |
LogP | 5.14 |
Vapour Pressure | 0.0±2.4 mmHg at 25°C |
Index of Refraction | 1.573 |
Storage condition | 2-8℃ |
Hazard Codes | Xi |
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