| Literature DB >> 15675882 |
Anthony R Carroll1, Edward Hyde, Jill Smith, Ronald J Quinn, Gordon Guymer, Paul I Forster.
Abstract
Bioassay-guided fractionation of the aqueous extract of the leaves of Alstonia actinophylla with use of a coupled enzyme assay, CPU/hippuricase, to detect carboxypeptidase U inhibitors led to the isolation of a novel indole alkaloid, actinophyllic acid (1). The structure of 1 was determined from detailed 2D NMR studies. Actinophyllic acid was found to be a potent inhibitor of the coupled enzyme assay with an IC(50) of 0.84 microM. Actinophyllic acid possesses a unique 2,3,6,7,9,13c-hexahydro-1H-1,7,8-(methanetriyloxymethano)pyrrolo[1',2':1,2]azocino[4,3-b]indole-8(5H)-carboxylic acid skeleton.Entities:
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Year: 2005 PMID: 15675882 DOI: 10.1021/jo048439n
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354