332372-09-5

332372-09-5 structure

Name: Strychnistenolide
Chemical 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
CAS Number: 332372-09-5
Molecular Formula: C₁₅H₁₈O₄
Molecular Weight: 262.301
Catalog: Research Areas Others
Create Date: 2018-06-26 08:39:47
Modify Date: 2025-08-25 18:09:29
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].

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
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)-

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	Research Areas >> Others Signaling Pathways >> Others >> Others
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.