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Chemical Biology & Drug Design|December 24, 2009
Reduction and recombination of fingerprints of different design increase compound recall and the structural diversity of hitsBritta Nisius, Jürgen Bajorath
Chemical Biology & Drug Design|December 24, 2009
The aromatic amino acid residues of tumor necrosis factor receptor-1-derived peptide are important for promoting differentiation of neural stem cellsKazumi Kajiwara, Shin-ich Ogata, Masao Tanihara
Chemical Biology & Drug Design|December 24, 2009
In vitro studies on the antioxidant and protective effect of 2-substituted -8-hydroxyquinoline derivatives against H(2)O(2)-induced oxidative stress in BMSCsTing-Ting Wang, Gong-Chang Zeng, Xi-Can Li, et al.
Chemical Biology & Drug Design|January 28, 2010
Microwave-assisted solvent-free synthesis of Bis(dihydropyrimidinone)benzenes and evaluation of their cytotoxic activityJavad Azizian, Mohammad K Mohammadi, Omidreza Firuzi, et al.
Chemical Biology & Drug Design|January 28, 2010
Magnetic resonance imaging of human glioma cells by means of an interleukin-6 receptor-targeted contrast agentAlexander Sturzu, Stefan Heckl
Chemical Biology & Drug Design|October 17, 2017
Selective inhibition of TRPM2 channel by two novel synthesized ADPR analoguesXiao Luo, Meng Li, Kaiyu Zhan, et al.
Chemical Biology & Drug Design|November 16, 2017
Allosteric mechanism of quinoline inhibitors for HIV RT-associated RNase with MD simulation and dynamics fluctuation networkYi Cai, Hao Liu, Haifeng Chen
Chemical Biology & Drug Design|November 8, 2017
Design, synthesis, biological evaluation, and docking study of 4-isochromanone hybrids bearing N-benzyl pyridinium moiety as dual binding site acetylcholinesterase inhibitors (part II)Jia Wang, Chaolei Wang, Zheng Wu, et al.
Chemical Biology & Drug Design|November 10, 2017
Discovery of a novel class of pyridine derivatives that selectively inhibits mutant isocitrate dehydrogenase 2Fangying Wang, Zhuoling Li, Tao Zhang, et al.
Chemical Biology & Drug Design|March 16, 2018
Identification of NQO1 and ferrochelatase as interaction partners for neuroprotective N-{[2-(4-phenyl-piperazin-1-yl)-ethyl]-phenyl}-arylamidesSladjana-Kostic Rajacic, Gerhard Schwall, Jelena Penjisevic, et al.
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