Name | Cycloheterophyllin |
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Synonyms |
Acylated oxime isatin derivative,18
2,3,8-Trihydroxy-11,11-dimethyl-13-(3-methyl-2-buten-1-yl)-6-(2-methyl-1-propen-1-yl)-6H,7H,11H-chromeno[4,3-b]pyrano[3,2-g]chromen-7-one 6H,7H,11H-[1]Benzopyrano[3',4':5,6]pyrano[3,2-g][1]benzopyran-7-one, 2,3,8-trihydroxy-11,11-dimethyl-13-(3-methyl-2-buten-1-yl)-6-(2-methyl-1-propen-1-yl)- 6H,7H,11H-Bis(1)benzopyrano(4,3-b'':6',7'-e)pyran-7-one, 2,3,8-trihydroxy-11,11-dimethyl-13-(3-methyl-2-butenyl)-6-(2-methyl-1-propenyl)-, (+)- HMS2269P06 2,3,8-Trihydroxy-11,11-dimethyl-13-(3-methylbut-2-en-1-yl)-6-(2-methylprop-1-en-1-yl)-6H,7H,11H-chromeno[4,3-b]pyrano[3,2-g]chromen-7-one 6H,7H,11H-[1]benzopyrano[4,3-b]pyrano[3,2-g][1]benzopyran-7-one, 2,3,8-trihydroxy-11,11-dimethyl-13-(3-methyl-2-buten-1-yl)-6-(2-methyl-1-propen-1-yl)- cycloheterphyllin |
Description | Cycloheterophyllin is a flavonoid, that can be isolated from Artocarpus communis and A. heterophyllus. Cycloheterophyllin shows antiinflammatory activity[1]. |
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Related Catalog | |
References |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 741.4±60.0 °C at 760 mmHg |
Molecular Formula | C30H30O7 |
Molecular Weight | 502.56 |
Flash Point | 246.3±26.4 °C |
Exact Mass | 502.199158 |
PSA | 109.36000 |
LogP | 8.12 |
Vapour Pressure | 0.0±2.5 mmHg at 25°C |
Index of Refraction | 1.680 |
Hazard Codes | Xi |
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