tirucallol
20-epi-euphol
Identification
| Name | tirucallol |
| CAS Number | 514-46-5 |
| FDA UNII | Search |
| Molecular Formula | C30 H50 O |
| Molecular Weight | 426.72770000 |
| Nikkaji Number | J13.991B |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 4.105e-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 tirucallol usage levels up to | not for fragrance use. |
| Recommendation for tirucallol flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
20-epi-
euphol
lanosta-8,24-dien-3-ol, (3beta,13alpha,14beta,17alpha,20S)-
(3S,5R,10S,13S,14S,17S)-4,4,10,13,14-
pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol
PubMed:
Topical anti-inflammatory effect of tirucallol, a triterpene isolated from Euphorbia lactea latex.
PubMed:
Chios mastic gum extract and isolated phytosterol tirucallol exhibit anti-inflammatory activity in human aortic endothelial cells.
PubMed:
An isopimarane diterpene from Euphorbia ebracteolata Hayata.
PubMed:
Studies in the Chemical Constituents of Azadirachta indica Part II: Isolation and Structure of the New Triterpenoid Azadirachtol.
PubMed:
Rotational isomerism about the 17(20)-bond of steroids and euphoids as shown by the crystal structures of euphol and tirucallol.
PubMed:
[Studies on the constituents of Chinese drug "kanzui." 8. KMnO4 oxidation of euphol, tirucallol and beta-euphorbol].