Structural analysis of novel inhibitors through docking of homology modeled yeast α-glucosidase

被引:0
|
作者
Turner, Joshua [1 ]
Kennedy, Sarah [1 ]
机构
[1] Radford Univ, Chem, Radford, VA 24142 USA
来源
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2017年 / 253卷
关键词
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
724
引用
收藏
页数:1
相关论文
共 50 条
  • [1] Discovery of novel α-glucosidase inhibitors based on the virtual screening with the homology-modeled protein structure
    Park, Hwangseo
    Hwang, Kyo Yeol
    Oh, Kyung Hwan
    Kim, Young Hoon
    Lee, Jae Yeon
    Kim, Keun
    BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (01) : 284 - 292
  • [2] Toward the virtual screening of α-glucosidase inhibitors with the homology-modeled protein structure
    Department of Bioscience and Biotechnology, Sejong University, Seoul 143-747, Korea, Republic of
    Bull. Korean Chem. Soc., 2008, 5 (921-927): : 921 - 927
  • [3] Toward the virtual, screening of α-glucosidase inhibitors with the homology-modeled protein structure
    Park, Jung-Hum
    Ko, Sungmin
    Park, Hwangseo
    BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2008, 29 (05) : 921 - 927
  • [4] Understanding the activity of FAAH inhibitors through homology modeling and docking
    Macias, Alba T.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 243
  • [5] Docking and QSAR analysis of tetracyclic oxindole derivatives as α-glucosidase inhibitors
    Asadollahi-Baboli, M.
    Dehnavi, S.
    COMPUTATIONAL BIOLOGY AND CHEMISTRY, 2018, 76 : 283 - 292
  • [6] Molecular docking studies and synthesis of novel bisbenzimidazole derivatives as inhibitors of α-glucosidase
    Ozil, Musa
    Emirik, Mustafa
    Belduz, Ali
    Ulker, Serdar
    BIOORGANIC & MEDICINAL CHEMISTRY, 2016, 24 (21) : 5103 - 5114
  • [7] Discovery of Novel DUSP16 Phosphatase Inhibitors through Virtual Screening with Homology Modeled Protein Structure
    Park, Hwangseo
    Park, So Ya
    Nam, Sang-Won
    Ryu, Seong Eon
    JOURNAL OF BIOMOLECULAR SCREENING, 2014, 19 (10) : 1383 - 1390
  • [8] Novel thiosemicarbazide-oxadiazole hybrids as unprecedented inhibitors of yeast α-glucosidase and in silico binding analysis
    Taha, Muhammad
    Ismail, Nor Hadiani
    Imran, Syahrul
    Wadood, Abdul
    Ali, Muhammad
    Rahim, Fazal
    Khan, Aftab Ahmad
    Riaz, Muhammad
    RSC ADVANCES, 2016, 6 (40): : 33733 - 33742
  • [9] Design of novel PhMTNA inhibitors, targeting neurological disorder through homology modeling, molecular docking, and dynamics approaches
    Jayaprakash, Prajisha
    Biswal, Jayashree
    Kanagarajan, Sureka
    Prabhu, Dhamodharan
    Gogoi, Prerana
    Kanaujia, Shankar Prasad
    Jeyakanthan, Jeyaraman
    JOURNAL OF RECEPTORS AND SIGNAL TRANSDUCTION, 2019, 39 (01) : 28 - 38
  • [10] Design, synthesis and docking study of novel tetracyclic oxindole derivatives as α-glucosidase inhibitors
    Han, Kailin
    Li, Yashan
    Zhang, Yazhou
    Teng, Yuou
    Ma, Ying
    Wang, Meiyan
    Wang, Runling
    Xu, Weiren
    Yao, Qingwei
    Zhang, Yongmin
    Qin, Haijuan
    Sun, Hua
    Yu, Peng
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2015, 25 (07) : 1471 - 1475