Name | 6-hydroxy-9b-methyl-7-propan-2-yl-3,3b,4,5,10,11-hexahydronaphtho[2,1-e][2]benzofuran-1-one |
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Synonyms |
Triptophenolide
Phenanthro[1,2-c]furan-1(3H)-one, 3b,4,5,9b,10,11-hexahydro-6-hydroxy-9b-methyl-7-(1-methylethyl)-, (3bR,9bS)- 6-hydroxy-9b-methyl-7-propan-2-yl-3,3b,4,5,10,11-hexahydronaphtho[2,1-e]isobenzofuran-1-one (3bR,9bS)-6-Hydroxy-7-isopropyl-9b-methyl-3b,4,5,9b,10,11-hexahydrophenanthro[1,2-c]furan-1(3H)-one |
Description | Triptophenolide is a colorless crystalline plate isolated from ethyl acetate extracts of Tripterygium wilfordii. IC50 value:Target:In vitro: Triptophenolide can remarkably inhibit the delayed type hypersensitivity (DTH) reaction induced by DNCB and BSA; and diminished the peripheral blood ANAE+lymphocytes in rats and micc. Moreover, triptophenolide can dramatically increase the amount of total serum complement and significautly decrcase the serum antibody products (1gG ) of rats and mice. The phagocytosis of perioneal exudate macrophages in mice present double effects in vitro [1].In vivo: |
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Related Catalog | |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 490.0±45.0 °C at 760 mmHg |
Melting Point | 232-233ºC |
Molecular Formula | C20H24O3 |
Molecular Weight | 312.403 |
Flash Point | 202.4±21.5 °C |
Exact Mass | 312.172546 |
PSA | 46.53000 |
LogP | 3.92 |
Vapour Pressure | 0.0±1.3 mmHg at 25°C |
Index of Refraction | 1.603 |
Storage condition | -20°C |
~10% 74285-86-2 |
Literature: Journal of Organic Chemistry, , vol. 65, # 7 p. 2208 - 2217 |
~% 74285-86-2 |
Literature: Journal of Organic Chemistry, , vol. 65, # 7 p. 2208 - 2217 |
~% 74285-86-2 |
Literature: Journal of Organic Chemistry, , vol. 65, # 7 p. 2208 - 2217 |
~% 74285-86-2 |
Literature: Journal of Organic Chemistry, , vol. 65, # 7 p. 2208 - 2217 |
Precursor 4 | |
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DownStream 0 |