macrocarpal C
Identification
| Name | macrocarpal C |
| CAS Number | 142628-53-3 |
| FDA UNII | Search |
| Molecular Formula | C28 H38 O5 |
| Molecular Weight | 454.60686000 |
| Nikkaji Number | J867.765D |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 1.42e-006 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 macrocarpal C usage levels up to | not for fragrance use. |
| Recommendation for macrocarpal C flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
5-[(1R)-1-[(1aR,4aR,7S,7aR,7bR)-1,1,7-
trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-yl]-3-methylbutyl]-2,4,6-trihydroxybenzene-1,3-dicarbaldehyde
5-((1R)-1-((11S)-3,3,11-
trimethyl-7-methylenetricyclo(6.3.0.0(2,4))undec-11-yl)-3-methylbutyl)-2,4,6-trihydroxybenzene-1,3-dicarbaldehyde
PubMed:
Macrocarpal C isolated from Eucalyptus globulus inhibits dipeptidyl peptidase 4 in an aggregated form.
PubMed:
Antifungal mode of action of macrocarpal C extracted from Eucalyptus globulus Labill (Lan An) towards the dermatophyte Trichophyton mentagrophytes.
PubMed:
Semisynthesis of macrocarpal C and analogues by selective dehydration of macrocarpal A or B.
PubMed:
Two antifungal components isolated from Fructus Psoraleae and Folium Eucalypti Globuli by bioassay-guided purification.
PubMed:
Intestinal permeability of antivirus constituents from the fruits of Eucalyptus globulus Labill. in Caco-2 Cell Model.