Publication: Allahabadolactones A and B from the endophytic fungus, Aspergillus allahabadii BCC45335
dc.contributor.author | Karoon Sadorn | en_US |
dc.contributor.author | Siriporn Saepua | en_US |
dc.contributor.author | Nattawut Boonyuen | en_US |
dc.contributor.author | Pattiyaa Laksanacharoen | en_US |
dc.contributor.author | Pranee Rachtawee | en_US |
dc.contributor.author | Samran Prabpai | en_US |
dc.contributor.author | Palangpon Kongsaeree | en_US |
dc.contributor.author | Pattama Pittayakhajonwut | en_US |
dc.contributor.other | King Mongkut's Institute of Technology Ladkrabang | en_US |
dc.contributor.other | University of Phayao | en_US |
dc.contributor.other | Thailand National Center for Genetic Engineering and Biotechnology | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.date.accessioned | 2018-12-11T02:20:44Z | |
dc.date.accessioned | 2019-03-14T08:04:16Z | |
dc.date.available | 2018-12-11T02:20:44Z | |
dc.date.available | 2019-03-14T08:04:16Z | |
dc.date.issued | 2016-01-28 | en_US |
dc.description.abstract | © 2015 Elsevier Ltd. All rights reserved. Two new compounds, allahabadolactones A (1) and B (2), along with 10 known compounds including 16-amino-isopimar-7-en-19-oic acid (3), 16-α-d-glucopyranosyloxyisopimar-7-en-19-oic acid (4), 16-α-d-mannopyranosyloxyisopimar-7-en-19-oic acid (5), ergosterol, (22E)-5α,8α-epidioxyergosta-6,22-dien-3β-ol, cerevisterol, (R)-(-)-methoxycarbonylmellein, (-)-piliformic acid, 7-dechlorogriseofulvin, and cytochalasin D, were isolated from the endophytic fungus, Aspergillus allahabadii BCC45335. Their chemical structures were determined based on NMR spectroscopic and mass spectrometric analyses. The absolute stereochemistry of compound 1 was established by an X-ray crystallographic analysis and the reactions with Mosher's reagents. A plausible biosynthesis of allahabadolactones A (1) and B (2) was also proposed. Antibacterial activity against Bacillus cereus and cytotoxicity against MCF-7, KB, NCI-H187, and Vero cells of the isolated compounds were also evaluated. | en_US |
dc.identifier.citation | Tetrahedron. Vol.72, No.4 (2016), 489-495 | en_US |
dc.identifier.doi | 10.1016/j.tet.2015.11.056 | en_US |
dc.identifier.issn | 14645416 | en_US |
dc.identifier.issn | 00404020 | en_US |
dc.identifier.other | 2-s2.0-84952049950 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/43189 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84952049950&origin=inward | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Chemistry | en_US |
dc.title | Allahabadolactones A and B from the endophytic fungus, Aspergillus allahabadii BCC45335 | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84952049950&origin=inward | en_US |