trilobacin
Identification
| Name | trilobacin |
| CAS Number | 140224-67-5 |
| FDA UNII | Search |
| Molecular Formula | C37 H66 O7 |
| Molecular Weight | 622.92742000 |
| Nikkaji Number | J776.863J |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 7.216e-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 trilobacin usage levels up to | not for fragrance use. |
| Recommendation for trilobacin flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
(2S)-4-[(2R,13R)-2,13-
dihydroxy-13-[(2R,5R)-5-[(2S,5R)-5-[(1R)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]tridecyl]-2-methyl-2H-furan-5-one
2(5H)-
furanone, 3-(2,13-dihydroxy-13-(octahydro-5'-(1-hydroxyundecyl)(2,2'-bifuran)-5-yl)tridecyl)-5-methyl-
PubMed:
Acetogenins as Potential Anticancer Agents.
PubMed:
Asymmetric total synthesis of trilobacin via organoselenium-mediated oxonium ion formation/SiO2-promoted fragmentation.
PubMed:
Oxidative cyclization reactions of trienes and dienynes: total synthesis of membrarollin.
PubMed:
Additional bioactive annonaceous acetogenins from Asimina triloba (Annonaceae).
PubMed:
Toward Chemical Libraries of Annonaceous Acetogenins. Total Synthesis of Trilobacin.
PubMed:
Additional bioactive compounds and trilobacin, a novel highly cytotoxic acetogenin, from the bark of Asimina triloba.