Strychnistenolide

Modify Date: 2025-08-25 18:09:29

Strychnistenolide Structure
Strychnistenolide structure
Common Name Strychnistenolide
CAS Number 332372-09-5 Molecular Weight 262.301
Density 1.4±0.1 g/cm3 Boiling Point 492.8±45.0 °C at 760 mmHg
Molecular Formula C15H18O4 Melting Point N/A
MSDS N/A Flash Point 190.0±22.2 °C

 Use of Strychnistenolide


Strychnistenolide is a sesquiterpene lactone that can be isolated from the roots of Lindera strychnifolia. Strychnistenolide exists as a single stereoisomer in CHCl3, but exomeric in pyridine[1].

 Names

Name (4R,4aS,5aS,6aR,6bS)-4,7a-Dihydroxy-3,6b-dimethyl-5-methylene-4a,5,5a,6,6a,6b,7,7a-octahydrocyclopropa[2,3]indeno[5,6-b]furan-2(4H)-one
Synonym More Synonyms

 Strychnistenolide Biological Activity

Description Strychnistenolide is a sesquiterpene lactone that can be isolated from the roots of Lindera strychnifolia. Strychnistenolide exists as a single stereoisomer in CHCl3, but exomeric in pyridine[1].
Related Catalog
References

[1]. Kouno I, et al. New eudesmane sesquiterpenes from the root of Lindera strychnifolia. J Nat Prod. 2001 Mar;64(3):286-8.  

[2]. Gan LS, et al. Sesquiterpene lactones from the root tubers of Lindera aggregata. J Nat Prod. 2009 Aug;72(8):1497-501.  

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Boiling Point 492.8±45.0 °C at 760 mmHg
Molecular Formula C15H18O4
Molecular Weight 262.301
Flash Point 190.0±22.2 °C
Exact Mass 262.120514
LogP 0.83
Vapour Pressure 0.0±2.8 mmHg at 25°C
Index of Refraction 1.623

 Synonyms

(4R,4aS,5aS,6aR,6bS)-4,7a-Dihydroxy-3,6b-dimethyl-5-methylene-4a,5,5a,6,6a,6b,7,7a-octahydrocyclopropa[2,3]indeno[5,6-b]furan-2(4H)-one
Cycloprop[2,3]indeno[5,6-b]furan-2(4H)-one, 4a,5,5a,6,6a,6b,7,7a-octahydro-4,7a-dihydroxy-3,6b-dimethyl-5-methylene-, (4R,4aS,5aS,6aR,6bS)-
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