Weight | 354.358 g/mol |
---|---|
Formula | C20H18O6 |
Hydrogen Acceptors | 6 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
Asarinin
607-80-7, 7076-24-6, 133-04-0
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- CH Insertion Approach to the Synthesis of endo,exo-Furofuranones: Synthesis of ()-Asarinin, ()-Epimagnolin A, and ()-Fargesin (Journal of Organic Chemistry, 2001)
- The Epimerization of Sesamin and Asarinin (Journal of Natural Products, 2005)
- Diastereodivergent Chiral Synthesis of the Furofuran Lignans (+)-Sesamin and (-)-Asarinin. (Chemistry Letters, 1995)
- Inhibition of 5-desaturase in polyunsaturated fatty acid biosynthesis by ()-asarinin and ()-epiasarinin (Phytochemistry, 1992)
- Synthetic methods for (Exo,Exo)- and (Exo-,Endo)-2,6-Diarylbicycio [3:3:0] octane lignans: Syntheses of ()-aptosimon, ()- styraxin, ()- asarinin, and ()- pluviatilol (Tetrahedron Letters, 1986)
- Epiasarinin, a Diastereoisomer of Sesamin and Asarinin. Stereochemistry of 2,6-Diaryl-cis-3,7-dioxabicyclo [3.3.0]octane (Journal of the American Chemical Society, 1956)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6
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InChIKeyPEYUIKBAABKQKQ-UHFFFAOYSA-N
- Pubchem - Asarinin
- Wikipedia - asarinin
Sesamin is a lignan isolated from the bark of Fagara plants and from sesame oil. It has been used as a dietary fat-reduction supplement, although no controlled studies on this application have been performed. Its major metabolite is enterolactone, which has an elimination half life of less than 6 hours.
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