Highly potent dipeptidyl peptidase IV inhibitors derived from Alogliptin through pharmacophore hybridization and lead optimization | |
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 |
2013 | |
卷号 | 68 |
ISSN号 | 0223-5234 |
学科主题 | Pharmacology & Pharmacy |
语种 | 英语 |
内容类型 | 期刊论文 |
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). |
个性服务 |
查看访问统计 |
相关权益政策 |
暂无数据 |
收藏/分享 |
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。
修改评论