Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Antony D. Buss"'
Publikováno v:
CHIMIA, Vol 61, Iss 6 (2007)
The screening of crude natural product extracts can be problematic, especially in enzyme/protein-based assays, due to promiscuous inhibitors and interference compounds, while high salt and lipid content can significantly dilute compounds of interest.
Externí odkaz:
https://doaj.org/article/862d02f6c6b74ebcbc361cead15578a9
Autor:
Mark S. Butler, Siewbee Ng, K. Yoganathan, Shugeng Cao, Antony D. Buss, Srinivasulu Aitipamula, Stephen R. Whitton, Sharon C. Crasta
Publikováno v:
Tetrahedron. 64:10181-10187
Bioassay-guided isolation using an MRSA whole cell assay yielded four novel benzophenone dimers, microsphaerins A-D (1-4), from two Singapore isolates of the soil anamorph Microsphaeropsis sp. The structures of 1-4 were elucidated on the basis of spe
Autor:
Jung-Rae Rho, Hyukjae Choi, Eun-Hee Kim, Sok Peng Ng, K. Yoganathan, Gurusamy Subramaniam, Siewbee Ng, Mark S. Butler, William H. Gerwick, Antony D. Buss
Gargantulide A (1), an extremely complex 52-membered macrolactone, was isolated from Streptomyces sp. A42983 and displayed moderate activity against MRSA. The planar structure of 1 was determined using 2D NMR, and its stereochemistry was partially es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5bcf9fb6f5abc0ab2dcb733e1f1be17
https://europepmc.org/articles/PMC5125438/
https://europepmc.org/articles/PMC5125438/
Autor:
Antony D. Buss, Mark S. Butler
Publikováno v:
Biochemical Pharmacology. 71:919-929
Natural products have played a pivotal role in antibiotic drug discovery with most antibacterial drugs being derived from a natural product or natural product lead. However, the rapid onset of resistance to most antibacterial drugs diminishes their e
Autor:
Shugeng Cao, Yicun Huang, and Antony D. Buss, K. Yoganathan, Christine Rossant, Siewbee Ng, Robert P. Glover, Jagadese J. Vittal, Mark S. Butler
Publikováno v:
Journal of Natural Products. 67:1681-1684
An extract from the fungus Emericella aurantiobrunnea was found to compete with macrophage inflammatory protein (MIP)-1alpha for binding to human CCR5 in a scintillation proximity assay (SPA). Bioassay-guided fractionation led to the isolation of var
Autor:
Antony D. Buss, Mark S. Butler
Publikováno v:
Drug Development Research. 62:362-370
Although combinatorial chemistry technology has enabled large libraries of compounds to be screened for biological activity and synthetic modifications to be effected rapidly, the reality is that quality leads and development candidates for many drug
Autor:
Antony D. Buss, Alex S. Y. Lee, Victor C. Yu, Doel D. Soejarto, Lay-Kien Yang, Shing Leng Chan, Mei Chin Lee, Mark S. Butler, Nai Yang Fu, Horst Flotow, Kuan Onn Tan
Publikováno v:
Journal of Biological Chemistry. 278:20453-20456
The identification of small molecule inhibitors of antiapoptotic Bcl-2 family members has opened up new therapeutic opportunities, while the vast diversity of chemical structures and biological activities of natural products are yet to be systematica
Publikováno v:
SLAS Discovery. 7:367-371
Despite decades of research, malaria remains the world's most deadly parasitic disease. New treatments with novel mechanisms of action are urgently needed. Plasmepsin II is an aspartyl protease that has been validated as an antimalarial therapeutic t
Autor:
Philip J. Sidebottom, R. F. Middleton, Tracy C. Kennedy, Antony D. Buss, Oonagh S. Kinsman, Michael J. Dawson, Graham Webb, Richard J. P. Cannell, Nicholas L. Taylor
Publikováno v:
Europe PubMed Central
The isolation and structure determination of 6 analogues of the fungal protein synthesis inhibitor GR135402, from Graphium putredinis, is described. The relative potencies of the compounds as protein synthesis inhibitors and as in vitro antifungal ag
Autor:
Kia-Ngee Low, Shugeng Cao, Sharon C. Crasta, and Antony D. Buss, Robert P. Glover, Siewbee Ng, Mark S. Butler
Publikováno v:
Journal of Natural Products. 69:707-709
Bioassay-directed fractionation using a glucocorticoid receptor assay led to the isolation of two new, weakly active polyprenylated acylphloroglucinol derivatives, sundaicumones A (1) and B (2), from the leaves of Calophyllum sundaicum collected in S