camelliol C
Identification
| Name | camelliol C |
| CAS Number | 220359-76-2 |
| FDA UNII | Search |
| Molecular Formula | C30 H50 O |
| Molecular Weight | 426.72770000 |
| Nikkaji Number | J1.061.814B |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 1.59e-007 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 camelliol C usage levels up to | not for fragrance use. |
| Recommendation for camelliol C flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
(1S,5R)-4,6,6-
trimethyl-5-[(3E,7E,11E)-3,8,12,16-tetramethylheptadeca-3,7,11,15-tetraenyl]cyclohex-3-en-1-ol
PubMed:
Euphorbia tirucalli β-Amyrin Synthase: Critical Roles of Steric Sizes at Val483 and Met729 and the CH-Ï Interaction between Val483 and Trp534 for Catalytic Action.
PubMed:
Arabidopsis camelliol C synthase evolved from enzymes that make pentacycles.
PubMed:
Eupha-7,9(11),24-trien-3beta-ol ("antiquol C") and other triterpenes from Euphorbia antiquorum latex and their inhibitory effects on Epstein-Barr virus activation.
PubMed:
Steric bulk at cycloartenol synthase position 481 influences cyclization and deprotonation.
PubMed:
Acyclic and incompletely cyclized triterpene alcohols in the seed oils of theaceae and gramineae.