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Sesquiterpenes and alkaloids from Lindera chunii and their inhibitory activities against HIV-1 integrase.

Authors :
Zhang CF
Nakamura N
Tewtrakul S
Hattori M
Sun QS
Wang ZT
Fujiwara T
Source :
Chemical & pharmaceutical bulletin [Chem Pharm Bull (Tokyo)] 2002 Sep; Vol. 50 (9), pp. 1195-200.
Publication Year :
2002

Abstract

Three new eudesmane type sesquiterpenoid lindenanolides E (1), F (2) and G (3), and two new aporphine alkaloid lindechunines A (18) and B (20) were isolated from roots of Lindera chunii MERR., together with seven known sesquiterpenes including a new naturally-occurring lindenanolide H (4) and eight known aporphine alkaloids. The structures of these compounds were determined by spectroscopic means. Of the isolated compounds, hernandonine (14), laurolistine (16), 7-oxohernangerine (17) and lindechunine A (18) showed significant anti-human immunodeficiency virus type 1 (HIV-1) integrase activity with IC(50) values of 16.3, 7.7, 18.2 and 21.1 microM, respectively. The major alkaloids presented in the roots of L. chunii were quantitatively analyzed by an HPLC method.

Details

Language :
English
ISSN :
0009-2363
Volume :
50
Issue :
9
Database :
MEDLINE
Journal :
Chemical & pharmaceutical bulletin
Publication Type :
Academic Journal
Accession number :
12237535
Full Text :
https://doi.org/10.1248/cpb.50.1195