Medicinal Chemistry Driven by the Development of System Biology & Cheminformatics

Author(s): Guo-Ping Zhou, Jianyong Li.

Journal Name: Medicinal Chemistry

Volume 15 , Issue 5 , 2019

Become EABM
Become Reviewer

Zhou, G.P. Current progress in structural bioinformatics of protein-biomolecule interactions. Med. Chem., 2015, 11(3), 216-217.
Zhou, G.P. Impacts of computational biology to medicinal chemistry. Med. Chem., 2017, 13(6), 504-505.
Zhou, G.P. Impacts of biological science to medicinal chemistry. Curr. Top. Med. Chem., 2017, 17, 2335-2336.
Zhou, G.P. Modulations and their biological functions of protein-biomolecule interactions. Curr. Top. Med. Chem., 2016, 16, 579-580.
Zhou, G.P.; Zhong, W.Z. Perspectives in the medicinal chemistry. Curr. Top. Med. Chem., 2016, 16, 381-382.
Qiu-Xing, J. Structural variability in the RLR-MAVS pathway and sensitive detection of viral RNAs. Med. Chem., 2019, 15(5), 443-458.
Chen, W.; Liang, X.; Nong, Z.; Li, Y.; Pan, X.; Chen, C.; Huang, L. The multiple applications and possible mechanisms of the hyperbaric oxygenation therapy. Med. Chem., 2019, 15, 459-471.
Chou, K.C. Advance in predicting subcellular localization of multi-label proteins and its implication for developing multi-target drugs. Curr. Med. Chem., 2019. [Epub ahead of print].
Cheng, X.; Xiao, X.; Chou, K.C. pLoc-mEuk: Predict subcellular localization of multi-label eukaryotic proteins by extracting the key GO information into general PseAAC. Genomics, 2018, 110, 50-58.
Kuo-Chen, C.; Xiang, C.; Xuan, X. pLoc_bal-mEuk: Predict subcellular localization of eukaryotic proteins by general PseAAC and Quasi-balancing training dataset. Med. Chem., 2019, 15, 472-485.
Huang, R.B.; Cheng, D.; Lu, B.; Liao, S.M.; Troy, F.A.; Zhou, G.P. The intrinsic relationship between structure and function of the sialyltransferase ST8Sia family members. Curr. Top. Med. Chem., 2017, 17, 2359-2369.
Zhou, G.P.; Huang, R.B.; Troy, F.A. 3D structural conformation and functional domains of polysialyltransferase ST8Sia IV required for polysialylation of neural cell adhesion molecules. Protein Pept. Lett., 2015, 22, 137-148.
Li-Xin, P.; Xue-Hui, L.; Bo, L.; Si-Ming, L.; Feng, Z.; Ji-Min, H.; Dong, C.; Frederic, A.; Troy, I.I.; Guo-Ping, Z.; Ri-Bo, H. The inhibition of polysialyltranseferase ST8SiaIV through heparin binding to polysialyltransferase domain (PSTD). Med. Chem., 2019, 15, 486-495.
Xuan, X.; Xiang, C.; Genqiang, C.; Qi, M.; Kuo-Chen, C. pLoc_bal-mVirus: Predict subcellular localization of multi-label virus proteins by Chou’s general PseAAC and IHTS treatment to balance training dataset. Med. Chem., 2019, 15, 496-509.
Cheng, X.; Xiao, X.; Chou, K.C. pLoc-mHum: Predict subcellular localization of multi-location human proteins via general PseAAC to winnow out the crucial GO information. Bioinformatics, 2018, 34, 1448-1456.
Liao, S.M.; Shen, N.K.; Liang, G.; Lu, B.; Lu, Z.L.; Peng, L.X.; Zhou, F.; Du, L.Q.; Wei, Y.T.; Zhou, G.P.; Huang, R.B. Inhibition of α-amylase activity by Zn2+: Insights from spectroscopy and molecular dynamics simulations. Med. Chem., 2019, 15, 510-520.

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2019
Page: [441 - 442]
Pages: 2
DOI: 10.2174/157340641505190506125340

Article Metrics

PDF: 21