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Fitoterapia, v.135, 2019년, pp.5 - 8
Rao, Li (Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, and Tumour Targeted Therapy and Chemical Biology Research Center, School of Pharmaceutical Sciences, Chongqing University) , You, Yun-Xia (Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, and Tumour Targeted Therapy and Chemical Biology Research Center, School of Pharmaceutical Sciences, Chongqing University) , Su, Yu (Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, and Tumour Targeted Therapy and Chemical Biology Research Center, School of Pharmaceutical Sciences, Chongqing University) , Liu, Yu (Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, and Tumour Targeted Therapy and Chemical Biology Research Center, School of Pharmaceutical Sciences, Chongqing University) , He, Qian (Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, and Tumour Targeted Therapy and Chemica) , Fan, Yue , Hu, Feng , Xu, You-Kai , Zhang, Chuan-Rui
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Abstract Two new spiroketal derivatives with an unprecedented amino group, 2′-aminodechloromaldoxin (1) and 2′-aminodechlorogeodoxin (2), along with one known analogue dechloromaldoxin (3), were isolated from the plant endophytic fungus Pestalotiopsis flavidula. Their structures were el...
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