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https://doi.org/10.1039/c7ra06933b
Title: | Sumalactones A-D, four new curvularin-type macrolides from a marine deep sea fungus: Penicillium Sumatrense | Authors: | Wu, Y.-H Zhang, Z.-H Zhong, Y Huang, J.-J Li, X.-X Jiang, J.-Y Deng, Y.-Y Zhang, L.-H He, F |
Keywords: | Metabolites Nitric oxide Spectroscopic analysis Absolute configuration CD spectra Deep sea sediment IC50 value Inhibition activity Marine fungus Mosher's method Raw 264.7 macrophages Drug products |
Issue Date: | 2017 | Citation: | Wu, Y.-H, Zhang, Z.-H, Zhong, Y, Huang, J.-J, Li, X.-X, Jiang, J.-Y, Deng, Y.-Y, Zhang, L.-H, He, F (2017). Sumalactones A-D, four new curvularin-type macrolides from a marine deep sea fungus: Penicillium Sumatrense. RSC Advances 7 (63) : 40015-40019. ScholarBank@NUS Repository. https://doi.org/10.1039/c7ra06933b | Rights: | Attribution 4.0 International | Abstract: | Sumalactones A-D (1-4), four new curvularin-type macrolides, together with two known analogues, curvularin (5) and dehydrocurvularin (6), were isolated from Penicillium Sumatrense, a marine fungus isolated from deep-sea sediments. Sumalactones C (3) and D (4) are unprecedented curvularin-type macrolides bearing a rare 11-membered macrolide skeleton. Their structures were elucidated on the basis of intensive spectroscopic analysis. The absolute configurations of compounds 1-4 were determined by CD spectra and modified Mosher's method. Compound 6 showed significant inhibition activity towards LPS-induced nitric oxide production in RAW 264.7 macrophages with IC50 value of 0.91 ?M. © 2017 The Royal Society of Chemistry. | Source Title: | RSC Advances | URI: | https://scholarbank.nus.edu.sg/handle/10635/178722 | ISSN: | 20462069 | DOI: | 10.1039/c7ra06933b | Rights: | Attribution 4.0 International |
Appears in Collections: | Elements Staff Publications |
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