Chrysomycins, Anti-Tuberculosis C-Glycoside Polyketides from Streptomyces sp. MS751
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C. Liu | Huanqin Dai | Fuhang Song | L. Ouyang | Xiaoguang Lei | Guoliang Zhu | Jiansen Hu | Hongtao He | Nathan Yang | Hui Guo | Caixia Chen | Jiaming Yu | Jing Zhang | Fan Yang | Zexu Lin | Lixin Zhang
[1] Shaojiang Song,et al. [2 + 2]-Cycloaddition-derived cyclobutane natural products: structural diversity, sources, bioactivities, and biomimetic syntheses. , 2022, Natural product reports.
[2] Shanhong Zhang,et al. Chrysomycin A Inhibits the Proliferation, Migration and Invasion of U251 and U87-MG Glioblastoma Cells to Exert Its Anti-Cancer Effects , 2022, Molecules.
[3] Weiming Zhu,et al. Antibacterial Gilvocarcin-Type Aryl-C-Glycosides from a Soil-Derived Streptomyces Species. , 2022, Journal of natural products.
[4] Huawei Zhang,et al. Formulation of Chrysomycin A Cream for the Treatment of Skin Infections , 2022, Molecules.
[5] G. Du,et al. Chrysomycin A Attenuates Neuroinflammation by Down-Regulating NLRP3/Cleaved Caspase-1 Signaling Pathway in LPS-Stimulated Mice and BV2 Cells , 2021, International journal of molecular sciences.
[6] Huawei Zhang,et al. Mechanochemical preparation of chrysomycin A self-micelle solid dispersion with improved solubility and enhanced oral bioavailability , 2021, Journal of Nanobiotechnology.
[7] Xiaoguang Lei,et al. Chrysomycin A Derivatives for the Treatment of Multi-Drug-Resistant Tuberculosis , 2020, ACS central science.
[8] David J Newman,et al. Natural Products as Sources of New Drugs over the Nearly Four Decades from 01/1981 to 09/2019. , 2020, Journal of natural products.
[9] S. Dastager,et al. Anti-microbial activity of chrysomycin A produced by Streptomyces sp. against Mycobacterium tuberculosis , 2017 .
[10] J. Yue,et al. Attractive natural products with strained cyclopropane and/or cyclobutane ring systems , 2016, Science China Chemistry.
[11] T. Bach,et al. Recent Advances in the Synthesis of Cyclobutanes by Olefin [2 + 2] Photocycloaddition Reactions , 2016, Chemical reviews.
[12] G. Bloemberg,et al. Acquired Resistance to Bedaquiline and Delamanid in Therapy for Tuberculosis. , 2015, The New England journal of medicine.
[13] Z. Memish,et al. Emerging novel and antimicrobial-resistant respiratory tract infections: new drug development and therapeutic options , 2014, The Lancet Infectious Diseases.
[14] D. Tantillo,et al. How cyclobutanes are assembled in nature--insights from quantum chemistry. , 2014, Chemical Society reviews.
[15] Xiaolin Li,et al. Endophytic Streptomyces sp. Y3111 from traditional Chinese medicine produced antitubercular pluramycins , 2013, Applied Microbiology and Biotechnology.
[16] S. Bharate,et al. Chrysomycins A–C, antileukemic naphthocoumarins from Streptomyces sporoverrucosus , 2013 .
[17] Xueting Liu,et al. Three antimycobacterial metabolites identified from a marine-derived Streptomyces sp. MS100061 , 2013, Applied Microbiology and Biotechnology.
[18] Andrew M. Piggott,et al. Abyssomicins from the South China Sea Deep-Sea Sediment Verrucosispora sp.: Natural Thioether Michael Addition Adducts as Antitubercular Prodrugs , 2012, Angewandte Chemie.
[19] Andrew M. Piggott,et al. Brevianamides with antitubercular potential from a marine-derived isolate of Aspergillus versicolor. , 2012, Organic letters.
[20] J. Rohr,et al. Enzymatic total synthesis of defucogilvocarcin M and its implications for gilvocarcin biosynthesis. , 2012, Angewandte Chemie.
[21] R. Wallace,,et al. Susceptibility Testing of Mycobacteria, Nocardiae, and Other Aerobic Actinomycetes , 2011 .
[22] T. Bach,et al. Photochemical reactions as key steps in natural product synthesis. , 2011, Angewandte Chemie.
[23] J. Rohr,et al. Engineered Biosynthesis of Gilvocarcin Analogues with Altered Deoxyhexopyranose Moieties , 2010, Applied and Environmental Microbiology.
[24] M. Greaney,et al. Photocycloaddition in natural product synthesis , 2007 .
[25] J. Rohr,et al. The complete gene cluster of the antitumor agent gilvocarcin V and its implication for the biosynthesis of the gilvocarcins. , 2003, Journal of the American Chemical Society.
[26] E. Lee-Ruff,et al. Enantiomerically pure cyclobutane derivatives and their use in organic synthesis. , 2003, Chemical reviews.
[27] A. Müller,et al. A dimeric ArC2 compound from Peperomia pellucida. , 2000, Phytochemistry.
[28] M. Crimmins. Synthetic Applications of Intramolecular Enone-Olefin Photocycloadditions , 1988 .
[29] R. White,et al. The chemistry of the antibiotics chrysomycin A and B. Antitumor activity of chrysomycin A. , 1982, The Journal of antibiotics.
[30] F. Strelitz,et al. CHRYSOMYCIN: A NEW ANTIBIOTIC SUBSTANCE FOR BACTERIAL VIRUSES , 1955, Journal of bacteriology.
[31] P. Wayne. Reference method for broth dilution antifungal susceptibility testing of yeasts, Approved standard-second edition , 2002 .