Literature DB >> 17711345

Agladupols A-E, triterpenoids from Aglaia duperreana.

Bo-Jun Xie1, Sheng-Ping Yang, Hua-Dong Chen, Jian-Min Yue.   

Abstract

Three new apotirucallane-type triterpenoids, agladupols A-C (1- 3), and two new tirucallane-type triterpenoids, agladupols D and E (4 and 5), along with four known compounds, were isolated from the leaves and stems of Aglaia duperreana (Meliaceae). The structures of compounds 1- 5 were elucidated by spectroscopic data. A (13)C NMR-based general rule for assignment of the C-21 configuration in the side chain of apotirucallane- and tirucallane-type triterpenoids was proposed. According to this, the relative stereochemistry of 21- O-methyltoosendanpentol (1a), a known compound with the relative configurations of the stereocenters in the side chain undetermined, was completely assigned.

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Year:  2007        PMID: 17711345     DOI: 10.1021/np0702842

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  3 in total

1.  New cytotoxic apotirucallanes from the leaves of Walsura trichostemon.

Authors:  Jirapast Sichaem; Suttira Khumkratok; Pongpan Siripong; Santi Tip-pyang
Journal:  J Nat Med       Date:  2013-12-01       Impact factor: 2.343

Review 2.  Chemistry and biology of rocaglamides (= flavaglines) and related derivatives from aglaia species (meliaceae).

Authors:  Sherif S Ebada; Neil Lajkiewicz; John A Porco; Min Li-Weber; Peter Proksch
Journal:  Prog Chem Org Nat Prod       Date:  2011

Review 3.  Discovery of structurally diverse and bioactive compounds from plant resources in China.

Authors:  Sheng-Ping Yang; Jian-Min Yue
Journal:  Acta Pharmacol Sin       Date:  2012-09-03       Impact factor: 6.150

  3 in total

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