A new antimycobacterial, 3β-acetoxy-15α,22-dihydroxyhopane, from the insect pathogenic fungus Aschersonia tubulata
Bioassay-guided fractionation of the cell extract of the insect pathogenic fungus Aschersonia tubulata BCC 1785 led to the isolation of dustanin (1), 3β,15α,22-trihydroxyhopane (3), 5α,8α-epidioxy-24(R)-methylcholesta-6,22-diene-3β-ol (6), together with the new 3β-acetoxy-15α,22-dihydroxyhopane (4)....
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th-mahidol.264652018-09-07T16:53:40Z A new antimycobacterial, 3β-acetoxy-15α,22-dihydroxyhopane, from the insect pathogenic fungus Aschersonia tubulata S. Boonphong P. Kittakoop M. Isaka P. Palittapongarnpim A. Jaturapat K. Danwisetkanjana M. Tanticharoen Y. Thebtaranonth Naresuan University Thailand National Center for Genetic Engineering and Biotechnology Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Medicine Pharmacology, Toxicology and Pharmaceutics Bioassay-guided fractionation of the cell extract of the insect pathogenic fungus Aschersonia tubulata BCC 1785 led to the isolation of dustanin (1), 3β,15α,22-trihydroxyhopane (3), 5α,8α-epidioxy-24(R)-methylcholesta-6,22-diene-3β-ol (6), together with the new 3β-acetoxy-15α,22-dihydroxyhopane (4). Chemical structures of these compounds were elucidated by spectral analyses as well as chemical transformation. Compounds I and 4 exhibited antimycobacterial activity with the minimum inhibitory concentration (MIC) of 12:5 μg/ml. 2018-09-07T09:38:11Z 2018-09-07T09:38:11Z 2001-04-26 Article Planta Medica. Vol.67, No.3 (2001), 279-281 10.1055/s-2001-11997 00320943 2-s2.0-0035053787 https://repository.li.mahidol.ac.th/handle/123456789/26465 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0035053787&origin=inward |
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Biochemistry, Genetics and Molecular Biology Chemistry Medicine Pharmacology, Toxicology and Pharmaceutics S. Boonphong P. Kittakoop M. Isaka P. Palittapongarnpim A. Jaturapat K. Danwisetkanjana M. Tanticharoen Y. Thebtaranonth A new antimycobacterial, 3β-acetoxy-15α,22-dihydroxyhopane, from the insect pathogenic fungus Aschersonia tubulata |
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Bioassay-guided fractionation of the cell extract of the insect pathogenic fungus Aschersonia tubulata BCC 1785 led to the isolation of dustanin (1), 3β,15α,22-trihydroxyhopane (3), 5α,8α-epidioxy-24(R)-methylcholesta-6,22-diene-3β-ol (6), together with the new 3β-acetoxy-15α,22-dihydroxyhopane (4). Chemical structures of these compounds were elucidated by spectral analyses as well as chemical transformation. Compounds I and 4 exhibited antimycobacterial activity with the minimum inhibitory concentration (MIC) of 12:5 μg/ml. |
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Naresuan University |
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Naresuan University S. Boonphong P. Kittakoop M. Isaka P. Palittapongarnpim A. Jaturapat K. Danwisetkanjana M. Tanticharoen Y. Thebtaranonth |
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Article |
author |
S. Boonphong P. Kittakoop M. Isaka P. Palittapongarnpim A. Jaturapat K. Danwisetkanjana M. Tanticharoen Y. Thebtaranonth |
author_sort |
S. Boonphong |
title |
A new antimycobacterial, 3β-acetoxy-15α,22-dihydroxyhopane, from the insect pathogenic fungus Aschersonia tubulata |
title_short |
A new antimycobacterial, 3β-acetoxy-15α,22-dihydroxyhopane, from the insect pathogenic fungus Aschersonia tubulata |
title_full |
A new antimycobacterial, 3β-acetoxy-15α,22-dihydroxyhopane, from the insect pathogenic fungus Aschersonia tubulata |
title_fullStr |
A new antimycobacterial, 3β-acetoxy-15α,22-dihydroxyhopane, from the insect pathogenic fungus Aschersonia tubulata |
title_full_unstemmed |
A new antimycobacterial, 3β-acetoxy-15α,22-dihydroxyhopane, from the insect pathogenic fungus Aschersonia tubulata |
title_sort |
new antimycobacterial, 3β-acetoxy-15α,22-dihydroxyhopane, from the insect pathogenic fungus aschersonia tubulata |
publishDate |
2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/26465 |
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1763496351518162944 |