Toad Alkaloid for Pesticide Discovery: Dehydrobufotenine Derivatives as Novel Agents against Plant Virus and Fungi.
暂无分享,去创建一个
Qingmin Wang | Jin Kang | Ziwen Wang | Ancai Liao | A. Lu | Yongyue Gao | Zhaoyong Tian | Qingmin Wang
[1] X. Hao,et al. Natural product sciences: an integrative approach to the innovations of plant natural products , 2020, Science China Life Sciences.
[2] Yuxiu Liu,et al. Luotonin A and Its Derivatives as Novel Antiviral and Antiphytopathogenic Fungus Agents. , 2020, Journal of agricultural and food chemistry.
[3] Dejun Ma,et al. Streptindole and Its Derivatives as Novel Antiviral and Anti-phytopathogenic-fungus Agents. , 2020, Journal of agricultural and food chemistry.
[4] Yuxiu Liu,et al. Discovery of Tryptanthrins as Novel Antiviral and Anti-phytopathogenic-fungus Agents. , 2020, Journal of agricultural and food chemistry.
[5] Qing X. Li,et al. Enantioselective Synthesis and Antifungal Activity of C18 Polyacetylenes. , 2020, Journal of agricultural and food chemistry.
[6] T. França,et al. Synthesis and biological activity of hydrazones and derivatives: A review. , 2020, Mini reviews in medicinal chemistry.
[7] Shanyan Yang,et al. Discovery, Structural Optimization and Mode of Action of Essramycin Alkaloid and Its Derivatives as Anti-Tobacco Mosaic Virus (TMV) and Anti-phytopathogenic-Fungus Agents. , 2019, Journal of agricultural and food chemistry.
[8] Shengzheng Wang,et al. Structural Simplification of Natural Products. , 2019, Chemical reviews.
[9] Neil McRoberts,et al. The global burden of pathogens and pests on major food crops , 2019, Nature Ecology & Evolution.
[10] L. M. Lima,et al. N-Acylhydrazones as drugs. , 2018, Bioorganic & medicinal chemistry letters.
[11] S. Sang,et al. Avenanthramide Aglycones and Glucosides in Oat Bran: Chemical Profile, Levels in Commercial Oat Products, and Cytotoxicity to Human Colon Cancer Cells. , 2018, Journal of agricultural and food chemistry.
[12] Qing X. Li,et al. Synthesis and fungicidal activities of sanguinarine derivatives. , 2017, Pesticide biochemistry and physiology.
[13] Petra Schneider,et al. Counting on natural products for drug design. , 2016, Nature chemistry.
[14] Valérie Nicaise,et al. Crop immunity against viruses: outcomes and future challenges , 2014, Front. Plant Sci..
[15] Xiao-jiang Hao,et al. The limonoids and their antitobacco mosaic virus (TMV) activities from Munronia unifoliolata Oliv. , 2012, Journal of agricultural and food chemistry.
[16] B. Song. Environment-Friendly Antiviral Agents for Plants , 2010 .
[17] D. Clive,et al. Synthesis of 4-haloserotonin derivatives and synthesis of the toad alkaloid dehydrobufotenine , 2010 .
[18] S. Robinson,et al. Food Security: The Challenge of Feeding 9 Billion People , 2010, Science.
[19] Arthur J. Olson,et al. AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading , 2009, J. Comput. Chem..
[20] D L Caspar,et al. Refined atomic model of the four-layer aggregate of the tobacco mosaic virus coat protein at 2.4-A resolution. , 1998, Biophysical journal.
[21] S. Buchwald,et al. Novel Syntheses of Tetrahydropyrroloquinolines: Applications to Alkaloid Synthesis , 1996 .
[22] P. Butler,et al. The current picture of the structure and assembly of tobacco mosaic virus. , 1984, The Journal of general virology.
[23] J. Daly,et al. The synthesis of O-methylnordehydrobufotenine, a new psychoactive indole. , 1969, Journal of medicinal chemistry.
[24] J. Daly,et al. The synthesis of dehydrobufotenine. , 1967, Tetrahedron letters.
[25] H. Wieland,et al. Abbauversuche am Isonitroso-brucin. Über Strychnos-Alkaloide. XIX , 1937 .