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Trichodermaerin: a diterpene lactone from Trichoderma asperellum.


ABSTRACT: The title compound, C20H28O3, known as 'trichodermaerin' [systematic name: (4E)-4,9,15,16,16-penta-methyl-6-oxa-tetra-cyclo-[10.3.1.0(1,10).0(5,9)]hexa-dec-4-ene-7,13-dione], is a diterpene lactone which was isolated from Trichoderma asperellum. The structure has a tetra-cycic 6-5-7-5 ring system, with the cyclo-hexa-none ring adopting a twisted half-chair conformation and the cyclo-pentane ring adopting a half-chair conformation, whereas the cyclo-heptene and tetra-hydro-furan-anone rings are in chair and envelope (with the methyl-substituted C atom as the flap) conformations, respectively. The three-dimensional architecture is stabilized by C-H?O inter-actions.

SUBMITTER: Chantrapromma S 

PROVIDER: S-EPMC3998585 | biostudies-literature | 2014 Apr

REPOSITORIES: biostudies-literature

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Trichodermaerin: a diterpene lactone from Trichoderma asperellum.

Chantrapromma Suchada S   Jeerapong Chotika C   Phupong Worrapong W   Quah Ching Kheng CK   Fun Hoong-Kun HK  

Acta crystallographica. Section E, Structure reports online 20140308 Pt 4


The title compound, C20H28O3, known as 'trichodermaerin' [systematic name: (4E)-4,9,15,16,16-penta-methyl-6-oxa-tetra-cyclo-[10.3.1.0(1,10).0(5,9)]hexa-dec-4-ene-7,13-dione], is a diterpene lactone which was isolated from Trichoderma asperellum. The structure has a tetra-cycic 6-5-7-5 ring system, with the cyclo-hexa-none ring adopting a twisted half-chair conformation and the cyclo-pentane ring adopting a half-chair conformation, whereas the cyclo-heptene and tetra-hydro-furan-anone rings are i  ...[more]

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