Letters in Drug Design & Discovery
Volume 16, 12 Issues, 2019
ISSN: 1875-628X (Online)
ISSN: 1570-1808 (Print)
This journal supports open access
ISSN: 1875-628X (Online)
ISSN: 1570-1808 (Print)
This journal supports open access
Ranking and Category
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57th of 61 in
Chemistry, Medicinal
Contents
Letters in Drug Design & Discovery, Volume 12 - Number 10
Novel Derivatives of Benfluron and Dimefluron Synthesis and Anticancer activity
, 12(10): 787 - 801Lenka Sucha, Marek Kolenic, Jiri Kratochvil, Milan Pour, Milan Nobilis, Eva Cermakova, Martina Rezacova and Pavel Tomsik
DOI: 10.2174/1570180812666150529204508
Novel Derivatives of Benfluron and Dimefluron Synthesis and Anticancer activity
Synthesis, Cytoprotective and Anti-Tumor Activities of Isatin Schiff Bases
, 12(10): 802 - 805Gang Chen, Mei Meng, Yu Zhang, Xiaojiang Hao, Ye Wang and Shuzhen Mu
DOI: 10.2174/1570180812666150514234029
Synthesis, Cytoprotective and Anti-Tumor Activities of Isatin Schiff Bases
Synthesis and Cytotoxicities of 2-[4-hydroxy-(3,5-bis-aminomethyl)- benzylidene]-indan-1-ones
, 12(10): 806 - 812Mehtap Tugrak, Halise Inci Gul and Hiroshi Sakagami
DOI: 10.2174/1570180812666150430002002
Synthesis and Cytotoxicities of 2-[4-hydroxy-(3,5-bis-aminomethyl)- benzylidene]-indan-1-ones
Synthesis, Anti-tumor Activity and Odd–even Effect of Simple Isatin Derivatives
, 12(10): 813 - 818Gang Chen, Xiaojiang Hao, Ye Wang and Shuzhen Mu
DOI: 10.2174/157018081210151012120940
Synthesis, Anti-tumor Activity and Odd–even Effect of Simple Isatin Derivatives
Discovery of New Inhibitors of Urease Enzyme: A Study Using STD-NMR Spectroscopy
, 12(10): 819 - 827Jalaluddin A. J. Awllia, Ayesha Sara, Atia-tul- Wahab, Maryam AL-Ghamdi, Saima Rasheed, Etimad Huwait and M. Iqbal Choudhary
DOI: 10.2174/1570180812666150520001629
Discovery of New Inhibitors of Urease Enzyme: A Study Using STD-NMR Spectroscopy
Syntheses and Activity of Carbohydrate-Containing Chitinase Inhibitors
, 12(10): 828 - 832Gangliang Huang, Xinya Mei, Xin Chen and Xiaomei Wang
DOI: 10.2174/1570180812666150514234246
Syntheses and Activity of Carbohydrate-Containing Chitinase Inhibitors
Effect of Acute Administration of 8-(Trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine Hydrochloride (TC-2153) on Biogenic Amines Metabolism in Mouse Brain
, 12(10): 833 - 836Elizabeth A. Kulikova, Ekaterina Y. Bazhenova, Nina K. Popova, Tatyana M. Khomenko, Konstantin P. Volcho, Nariman F. Salakhutdinov and Alexander V. Kulikov
DOI: 10.2174/1570180812666150522221634
Effect of Acute Administration of 8-(Trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine Hydrochloride (TC-2153) on Biogenic Amines Metabolism in Mouse Brain
3D-QSAR and Molecular Docking Studies of Flavonoid Derivatives as Potent Acetylcholinesterase Inhibitors
, 12(10): 837 - 843An Zhou, Zeyu Wu, Ailing Hui, Bin Wang, Xianchun Duan, Haixiang Wang and Jian Pan
DOI: 10.2174/1570180812666150514233543
3D-QSAR and Molecular Docking Studies of Flavonoid Derivatives as Potent Acetylcholinesterase Inhibitors
An Insight into Patents of Fluoroquinolone Derivatives
, 12(10): 844 - 855Prabodh Chander Sharma, Mona Piplani and Harish Rajak
DOI: 10.2174/1570180812666150429234635
An Insight into Patents of Fluoroquinolone Derivatives
Computational Docking Studies of Novel Heterocyclic Carboxamides as Potential PI3Kα Inhibitors
, 12(10): 856 - 863Kamal Sweidan, Dima A. Sabbah, Jorn Engelmann, Heba Abdel-Halim and Ghassan Abu Sheikha
DOI: 10.2174/1570180812666150529205248
Computational Docking Studies of Novel Heterocyclic Carboxamides as Potential PI3Kα Inhibitors
Synthesis and Biological Evaluation of 2´-Hydroxy-4´,6´-Diprenyloxychal-Cone Derivatives as Potent CDC25B and PTP1B Inhibitors
, 12(10): 864 - 871Dong-Hai Zhao, JIan Zhang, Lei Zhang, Da-Peng Li, Zhou Peng and Li-Ping Guan
DOI: 10.2174/1570180812666150723002629
Synthesis and Biological Evaluation of 2´-Hydroxy-4´,6´-Diprenyloxychal-Cone Derivatives as Potent CDC25B and PTP1B Inhibitors
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Letters in Drug Design & Discovery was introduced in 2004 with the assistance of Dr. George Perry, who is the current Editor-in-Chief serving since 2004.
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