chalepin acetate
rutamarin
Identification
| Name | chalepin acetate |
| CAS Number | 14882-94-1 |
| FDA UNII | Search |
| Molecular Formula | C21 H24 O5 |
| Molecular Weight | 356.41828000 |
| Nikkaji Number | J13.449J |
| Beilstein | 1400300 |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 0.2393 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 chalepin acetate usage levels up to | not for fragrance use. |
| Recommendation for chalepin acetate flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
2-(1-
acetyloxy-1-methylethyl)-6-(1,1-dimethyl-2-propenyl)-2,3-dihydro-7H-furo(3,2-g)(1)benzopyran-7-one
7H-
furo(3,2-g)(1)benzopyran-7-one, 2-(1-(acetyloxy)-1-methylethyl)-6-(1,1-dimethyl-2-propenyl)-2,3-dihydro-
2-[6-(2-
methylbut-3-en-2-yl)-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]propan-2-yl acetate
rutamarin
PubMed:
Rutamarin, an Active Constituent from
Ruta angustifolia
Pers., Induced Apoptotic Cell Death in the HT29 Colon Adenocarcinoma Cell Line.
PubMed:
Semisynthesis of (-)-Rutamarin Derivatives and Their Inhibitory Activity on Epstein-Barr Virus Lytic Replication.
PubMed:
Chalepin: isolated from Ruta angustifolia L. Pers induces mitochondrial mediated apoptosis in lung carcinoma cells.
PubMed:
Phytochemicals from Ruta graveolens Activate TAS2R Bitter Taste Receptors and TRP Channels Involved in Gustation and Nociception.
PubMed:
Antiviral activity of topoisomerase II catalytic inhibitors against Epstein-Barr virus.
PubMed:
Antiviral activity of (+)-rutamarin against Kaposi's sarcoma-associated herpesvirus by inhibition of the catalytic activity of human topoisomerase II.
PubMed:
(+)-Rutamarin as a dual inducer of both GLUT4 translocation and expression efficiently ameliorates glucose homeostasis in insulin-resistant mice.
PubMed:
In silico target fishing for rationalized ligand discovery exemplified on constituents of Ruta graveolens.
PubMed:
Application of chitin and chitosan as elicitors of coumarins and fluoroquinolone alkaloids in Ruta graveolens L. (common rue).
PubMed:
Identification of Ruta graveolens L. metabolites accumulated in the presence of abiotic elicitors.
PubMed:
Effective biotic elicitation of Ruta graveolens L. shoot cultures by lysates from Pectobacterium atrosepticum and Bacillus sp.
PubMed:
Bioactive coumarins from Boenninghausenia sessilicarpa.
PubMed:
[Studies on lactone constituents from Boennighausenia sessilicarpa Lévl].
PubMed:
Antispasmogenic effect of rutamarin and arborinine on isolated smooth muscle organs.
PubMed:
[Rutamarin, coumarin derivative of Ruta graveolens].