Showing chemical card for 5-Hydroxycapsanthin-3,6-epoxide (CFc000333565)
| Record Information | |
|---|---|
| Version | 1.0 |
| Creation Date | |
| Update Date | 2022-09-14 05:13:46 UTC |
| Chemfont ID | CFc000333565 |
| Molecule Identification | |
| Common Name | 5-Hydroxycapsanthin-3,6-epoxide |
| Definition | 5-hydroxycapsanthin-3,6-epoxide is a member of the class of compounds known as xanthophylls. Xanthophylls are carotenoids containing an oxygenated carotene backbone. Carotenes are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Xanthophylls arise by oxygenation of the carotene backbone. Thus, 5-hydroxycapsanthin-3,6-epoxide is considered to be an isoprenoid lipid molecule. 5-hydroxycapsanthin-3,6-epoxide is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 5-hydroxycapsanthin-3,6-epoxide can be found in a number of food items such as yellow bell pepper, pepper (c. annuum), green bell pepper, and orange bell pepper, which makes 5-hydroxycapsanthin-3,6-epoxide a potential biomarker for the consumption of these food products. |
| Structure | |
| Synonyms | Not Available |
| Chemical Formula | |
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| IUPAC Name | |
| Traditional Name | |
| CAS Registry Number | Not Available |
| SMILES | Not Available |
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| Chemical Taxonomy | |
| Classification | Not classified |
| Functional Ontology | |
| Physiological effect | Not Available |
| Disposition | Source
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| Process | Not Available |
| Role | Not Available |
| Physical Properties | |
| Predicted Properties | Not Available |
| External Links | |
| External Links | Not Available |
| References | |
| Synthesis Reference | Not Available |