中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly potent dipeptidyl peptidase IV inhibitors derived from Alogliptin through pharmacophore hybridization and lead optimization

文献类型:期刊论文

作者Xu, Hongjiang; Xie, Hui; Zeng, Lili; Zeng, Shaogao; Lu, Xin; Zhao, Xin; Zhang, Guicheng; Tu, Zhengchao; Yang, Ling; Zhang, Xiquan
刊名EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
出版日期2013
卷号68
ISSN号0223-5234
学科主题Pharmacology & Pharmacy
语种英语
源URL[http://ir.foo.ac.cn/handle/2SETSVCV/820]  
专题中国科学院广州生物医药与健康研究院
推荐引用方式
GB/T 7714
Xu, Hongjiang,Xie, Hui,Zeng, Lili,et al. Highly potent dipeptidyl peptidase IV inhibitors derived from Alogliptin through pharmacophore hybridization and lead optimization[J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,2013,68.
APA Xu, Hongjiang.,Xie, Hui.,Zeng, Lili.,Zeng, Shaogao.,Lu, Xin.,...&Hu, Wenhui.(2013).Highly potent dipeptidyl peptidase IV inhibitors derived from Alogliptin through pharmacophore hybridization and lead optimization.EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,68.
MLA Xu, Hongjiang,et al."Highly potent dipeptidyl peptidase IV inhibitors derived from Alogliptin through pharmacophore hybridization and lead optimization".EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY 68(2013).

入库方式: OAI收割

来源:广州生物医药与健康研究院

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