cycloheterophyllin
cycloheterphyllin
Identification
| Name | cycloheterophyllin |
| CAS Number | 36545-53-6 |
| FDA UNII | Search |
| Molecular Formula | C30 H30 O7 |
| Molecular Weight | 502.56350000 |
| Nikkaji Number | J17.414I |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 741.40 °C. @ 760.00 mm Hg (est) |
| Flash Point | 475.00 °F. TCC ( 246.30 °C. ) (est) |
| logP (o/w) | 8.120 (est) |
| Soluble in | water, 0.0001147 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | natural substances and extractives |
| Recommendation for cycloheterophyllin usage levels up to | not for fragrance use. |
| Recommendation for cycloheterophyllin flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
cycloheterphyllin
6H,7H,11H-
pyrano[3',2':6,7][1]benzopyrano[3,2-c][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)-
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
(+)-2,3,8-
trihydroxy-11,11-dimethyl-13-(3-methyl-2-butenyl)-6-(2-methyl-1-propenyl)-6H,7H,11H-bis(1)benzopyrano(4,3-b'':6',7'-E)pyran-7-one
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
PubMed:
Effect of prenylated flavonoids and chalcones isolated from Artocarpus species on platelet aggregation in human whole blood.
PubMed:
Scavenger and antioxidant properties of prenylflavones isolated from Artocarpus heterophyllus.
PubMed:
Blockade of protein kinase C is involved in the inhibition by cycloheterophyllin of neutrophil superoxide anion generation.
PubMed:
Novel antiplatelet constituents from formosan moraceous plants.