Name | 3,5,7-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxychromen-4-one |
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Synonyms |
Limocitrin
3,5,7,4'-tetrahydroxy-8,3'-dimethoxyflavone 3,5,7,4'-Tetrahydroxy-3',8-dimethoxy-flavon 8,3'-dimethoxy gossypetin gossypetin 8,3'-dimethyl ether |
Description | Limocitrin is a natural product that can be isolated from the buds of P. acerifolia and P. orientalis. Limocitrin suppresses estradiol-dependent proliferation of MCF7 cells weakly but estradiol-induced AlkP (alkaline phosphatase) expression only marginally[1]. |
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Related Catalog | |
References |
Density | 1.591g/cm3 |
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Boiling Point | 621.2ºC at 760 mmHg |
Molecular Formula | C17H14O8 |
Molecular Weight | 346.28800 |
Flash Point | 231.4ºC |
Exact Mass | 346.06900 |
PSA | 129.59000 |
LogP | 2.29960 |
Vapour Pressure | 5.03E-16mmHg at 25°C |
Index of Refraction | 1.707 |
~85% 489-33-8 |
Literature: Horie; Tsukayama; Kawamura; Seno; Yamamoto Bulletin of the Chemical Society of Japan, 1988 , vol. 61, # 2 p. 441-447 |
~% 489-33-8 |
Literature: Horie; Tsukayama; Kawamura; Seno; Yamamoto Bulletin of the Chemical Society of Japan, 1988 , vol. 61, # 2 p. 441-447 |
~% 489-33-8 |
Literature: Horie; Tsukayama; Kawamura; Seno; Yamamoto Bulletin of the Chemical Society of Japan, 1988 , vol. 61, # 2 p. 441-447 |
~% 489-33-8 |
Literature: Yuldashev Chemistry of Natural Compounds, 2001 , vol. 37, # 3 p. 288 - 289 |
Precursor 1 | |
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DownStream 0 |