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Bioorganic Chemistry|May 19, 2019
An efficient one-pot synthesis of polyphenolic amino acids and evaluation of their radical-scavenging activityLuís S Monteiro, Fátima Paiva-Martins, Sandra Oliveira, et al.Bioorganic Chemistry|May 19, 2019
Follow on-based optimization of the biphenyl-DAPYs as HIV-1 nonnucleoside reverse transcriptase inhibitors against the wild-type and mutant strainsYali Sang, Sheng Han, Shuwen Han, et al.Bioorganic Chemistry|May 19, 2019
Chiral β-lactam-based integrin ligands through Lipase-catalysed kinetic resolution and their enantioselective receptor responseGiulia Martelli, Paola Galletti, Monica Baiula, et al.Bioorganic Chemistry|May 20, 2019
Synthesis, molecular modeling and biological evaluation of new pyrazolo[3,4-b]pyridine analogs as potential antimicrobial, antiquorum-sensing and anticancer agentsN S El-Gohary, M T Gabr, M I ShaabanBioorganic Chemistry|May 22, 2019
Syntesis of thio- and seleno-acetamides bearing benzenesulfonamide as potent inhibitors of human carbonic anhydrase II and XIIDamiano Tanini, Antonella Capperucci, Martina Scopelliti, et al.Bioorganic Chemistry|May 28, 2019
Recent advancement in the discovery and development of COX-2 inhibitors: Insight into biological activities and SAR studies (2008-2019)Vrinda Sharma, Parth Bhatia, Ozair Alam, et al.Bioorganic Chemistry|May 28, 2019
Molecular docking and experimental investigation of new indole derivative cyclooxygenase inhibitor to probe its binding mechanism with bovine serum albuminTanveer A Wani, Ahmed H Bakheit, Seema Zargar, et al.Bioorganic Chemistry|May 28, 2019
Design, synthesis and evaluation of phenylfuroxan nitric oxide-donor phenols as potential anti-diabetic agentsYun-Dong Xie, Li-Hua Shao, Qiu-Tang Wang, et al.Bioorganic Chemistry|May 31, 2019
Targeting malaria and leishmaniasis: Synthesis and pharmacological evaluation of novel pyrazole-1,3,4-oxadiazole hybrids. Part IIGarima Verma, Mohemmed Faraz Khan, Lalit Mohan Nainwal, et al.Bioorganic Chemistry|August 1, 2018
Synthesis of novel isoindoline-1,3-dione-based oximes and benzenesulfonamide hydrazones as selective inhibitors of the tumor-associated carbonic anhydrase IXAlaa A-M Abdel-Aziz, Adel S El-Azab, Mohamed A Abu El-Enin, et al.Pageof 868