A new ent-kaurane diterpene from stems of Alibertia macrophylla K. Schum. (Rubiaceae)
Contribuinte(s) |
Universidade Estadual Paulista (UNESP) |
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Data(s) |
27/05/2014
27/05/2014
11/10/2007
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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 |