muricatacin
Identification
| Name | muricatacin |
| CAS Number | 134698-86-5 |
| FDA UNII | Search |
| Molecular Formula | C17 H32 O3 |
| Molecular Weight | 284.43964000 |
| Nikkaji Number | J549.805H |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 7.495 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 muricatacin usage levels up to | not for fragrance use. |
| Recommendation for muricatacin flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
2(3H)-
furanone, dihydro-5-(1-hydroxytridecyl)-, (R-(R*,R*))-
(5R)-5-[(1R)-1-
hydroxytridecyl]oxolan-2-one
PubMed:
Concise stereoselective total synthesis of (+)-muricatacin and (+)-epi-muricatacin.
PubMed:
A chiron approach to the total synthesis of cytotoxic (+)-muricatacin and (+)-5-epi-muricatacin from D-ribose.
PubMed:
Design, synthesis and antiproliferative activity of two new heteroannelated (-)-muricatacin mimics.
PubMed:
Synthesis of annonaceous acetogenins from muricatacin.
PubMed:
An efficient oxidative lactonization of 1,4-diols catalyzed by Cp*Ru(PN) complexes.
PubMed:
De novo asymmetric syntheses of muricatacin and its analogues via dihydroxylation of dienoates.
PubMed:
Synthesis and antitumour activity of new muricatacin and goniofufurone analogues.
PubMed:
Novel cytotoxic monotetrahydrofuranic Annonaceous acetogenins from Annona montana.
PubMed:
Concise total synthesis of (-)-muricatacin by tandem ring-closing/cross metathesis.
PubMed:
Total synthesis of (+)-muconin.
PubMed:
Synthesis of (--)-Muricatacin via alpha- and alpha'-C-H bond functionalization of tetrahydrofuran.
PubMed:
Unexpected stereochemistry in the lithium salt catalyzed ring expansion of nonracemic oxaspiropentanes. formal syntheses of (-)-(4R,5R)-muricatacin and the pheromone (R)-japonilure.
PubMed:
A novel constituent from Rollinia mucosa, rollicosin, and a new approach to develop annonaceous acetogenins as potential antitumor agents.
PubMed:
Syntheses and cytotoxicities of four stereoisomers of muricatacin from D-glucose.
PubMed:
Parallel, Stereoselective Syntheses of both Enantiomers of Muricatacin and Their Sulfur and Nitrogen Relatives Using the Silyloxy Diene-Based Methodology.
PubMed:
Synthesis of (-)-muricatacin.