A new ent-kaurane diterpene from stems of Alibertia macrophylla K. Schum. (Rubiaceae)


Autoria(s): Da Silva, Viviane Cândida; Faria, Andréia de Oliveira; Bolzani, Vanderlan da Silva; Lopes, Márcia Nasser
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

27/05/2014

27/05/2014

11/10/2007

Resumo

Phytochemical investigations of the stems of a specimen of Alibertia macrophylla led to the isolation and characterization of the new diterpene ent-kaurane-2β,3α,16α-triol (1), along with triterpenes 2-8, iridoids 9-12, and phenolic acids 13-15. The structure of 1 was established based on spectroscopic studies (1H- and 13C-NMR, IR, and HR-ESI-MS). This is the first report of the isolation of a diterpene from the Alibertia genus in Rubiaceae. © 2007 Verlag Helvetica Chimica Acta AG.

Formato

1781-1785

Identificador

http://dx.doi.org/10.1002/hlca.200790187

Helvetica Chimica Acta, v. 90, n. 9, p. 1781-1785, 2007.

0018-019X

http://hdl.handle.net/11449/69936

10.1002/hlca.200790187

WOS:000249941300017

2-s2.0-34948816558

Idioma(s)

eng

Relação

Helvetica Chimica Acta

Direitos

closedAccess

Palavras-Chave #Alibertia macrophylla #Kaurane diterpene #Phytochemical investigations #Nuclear magnetic resonance spectroscopy #Phenols #Plants (botany) #Spectroscopic analysis #Olefins #6beta hydroxygeniposide #alpha amirenone #beta amirenone #caffeic acid #ent kaurane 2beta,3alpha,16alpha triol #ent kaurane diterpene #gardenoside #germanicone #iridoid #kaurane derivative #lupenone #lupeol #oleanolic acid #phenol #plant extract #protocatechuic acid #shanziside methyl ester #sitosterol #steroid #stigmasterol #triterpene derivative #unclassified drug #ursolic acid #vanillic acid #drug isolation #drug structure #electrospray mass spectrometry #infrared spectroscopy #nuclear magnetic resonance spectroscopy #plant stem #priority journal #Rubiaceae
Tipo

info:eu-repo/semantics/article