Literature DB >> 15390028

Spectral assignments of new diterpenes from Hyptis martiusii Benth.

Edigênia Cavalcante da Cruz Araújo1, Mary Anne Sousa Lima, Edilberto Rocha Silveira.   

Abstract

The structural characterization of two new abietanes and a new spiro-fused tricyclic diterpene isolated from the roots of Hyptis martiusii is described. The first member of a new class of rearranged abietane diterpenoids designated martiusane was characterized by the use of 1D NMR and several 2D shift correlated NMR pulse sequences (1H,1H-COSY, HMQC, HMBC and NOESY). Unambiguous 1H and 13C chemical shift assignments for all compounds are reported. Copyright 2004 John Wiley & Sons, Ltd.

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Year:  2004        PMID: 15390028     DOI: 10.1002/mrc.1489

Source DB:  PubMed          Journal:  Magn Reson Chem        ISSN: 0749-1581            Impact factor:   2.447


  2 in total

1.  Decandrinin, an unprecedented C9-spiro-fused 7,8-seco-ent-abietane from the Godavari mangrove Ceriops decandra.

Authors:  Hui Wang; Min-Yi Li; Félix Zongwe Katele; Tirumani Satyanandamurty; Jun Wu; Gerhard Bringmann
Journal:  Beilstein J Org Chem       Date:  2014-01-27       Impact factor: 2.883

Review 2.  Subtribe Hyptidinae (Lamiaceae): A promising source of bioactive metabolites.

Authors:  Henrique Bridi; Gabriela de Carvalho Meirelles; Gilsane Lino von Poser
Journal:  J Ethnopharmacol       Date:  2020-08-05       Impact factor: 4.360

  2 in total

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