| Literature DB >> 16835095 |
Micah Reynolds1, V S Prakash Chaturvedula, Fidisoa Ratovoson, Rabodo Andriantsiferana, Vincent E Rasamison, Rebecca C Guza, David G I Kingston.
Abstract
Bioassay-directed fractionation of an extract of the root and bark of Podocarpus madagascariensis resulted in the isolation of a new totarol diterpenoid (1) in addition to the three known cytotoxic diterpenoids 19-hydroxytotarol (2), totaradiol (3), and 4beta-carboxy-19-nor-totarol (4). The structure of the new compound 1 was established as methyl-13-hydroxy-14-isopropyl-9(11),12,14(8)-podocarpatriene-19-oate on the basis of 1D and 2D NMR spectroscopic interpretation and methylation of 4. All the compounds exhibited cytotoxic activity against the A2780 ovarian cancer cell line.Entities:
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Year: 2006 PMID: 16835095 DOI: 10.1080/14786410500249315
Source DB: PubMed Journal: Nat Prod Res ISSN: 1478-6419 Impact factor: 2.861