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RASA:A Rapid Retrosynthesis-Based Scoring Method for the Assessment of Synthetic Accessibility of Dr
[会议论文] 作者：Qi Huang,Lin-Li Li,Sheng-Yong Yang,
来源：第九届IUPAC化学生物学国际研讨会暨第八届世界华人药物化学研讨会 年份：2012
In this account,a rapid retrosynthesis-based scoring method for the assessment of synthetic accessibility of drug-like molecules,called RASA(Retrosynthesis-based Assessment of Synthetic Accessibility)...
Random Walk Model with Non-uniform Grid and its Application on Brownian Particle Transport in Dissym
[会议论文] 作者：ZHANG Jian-Wen,CHEN Xu,ZHU Yu-Dan,HE Lin-Li,LI Zi-Rui,
来源：2016年大连国际微纳流体和微流控芯片大会(2016 International Conference of Micro 年份：2016
The analysis of the Brownian particle transport in the micro-/nano-scale porous media involves precise descriptions of geometrical and physiochemical properties of the channel wall, electrical and mec...
Discovery of Selective Protein Arginine Methyltransferase 5 (PRMT5) Inhibitors and Biological Evalua
[会议论文] 作者：Sen Ji,Shuang Ma,Wen-Jing Wang,Shen-Zhen Huang,Tian-qi Wang,Rong Xiang,Yi-Guo Hu,Qiang Chen,Lin-Li Li,
来源：第九届国际分子模拟与信息技术应用学术会议(ICMS&I2018) 年份：2018
PRMT5 is an important protein arginine methyltransferase that catalyzes the symmetric dimethylation of arginine resides on histones or non-histone substrate...
Discovery and Structure-Activity Relationship Analysis of 4-((5-nitropyrimidin-4-yl)amino)benzimidam
[会议论文] 作者：Xu-Ri Yu,Yun Tang,Wen-Jing Wang,Sen Ji,Lei Zhong,Chun-Hui Zhang,Jiao Yang,Xiao-Ai Wu,Sheng-Yong Yang,Lin-Li Li,
来源：2015年全国药物化学学术会议暨第五届中英药物化学学术会议 年份：2015
Protein arginine methyltransferase 1(PRMT1)is an important member of PRMT subfamily,which catalyzes the transfer of a methyl group from the co-factor S-adenosyl methionine(SAM)onto a specific arginine...
From Lead to Drug CandidateOptimization of 3-(Phenylethynyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine Der
[会议论文] 作者：Chun-Hui Zhang,Kai Chen,Yan Jiao,Lin-Li Li,Ya-Ping Li,Rong-Jie Zhang,Ming-Wu Zheng,Lei Zhong,Shen-Zhen,
来源：第九届国际分子模拟与信息技术应用学术会议(ICMS&I2018) 年份：2018
Herein we report the sophisticated process of structural optimization toward a previously disclosed Src inhibitor,compound 1,which showed high potency in th...
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