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Bioorganic Chemistry|December 30, 2019
Novel N,N-dimethylbarbituric-pyridinium derivatives as potent urease inhibitors: Synthesis, in vitro, and in silico studiesMahmood Biglar, Roghieh Mirzazadeh, Mehdi Asadi, et al.Bioorganic Chemistry|December 30, 2019
Preparation and in vitro antioxidant activity of some novel flavone analogues bearing piperazine moietyPaweł Berczyński, Aleksandra Kładna, Oya Bozdağ Dündar, et al.Bioorganic Chemistry|March 14, 2018
Caged xanthones displaying protein tyrosine phosphatase 1B (PTP1B) inhibition from Cratoxylum cochinchinenseZuo Peng Li, Hyeong-Hwan Lee, Zia Uddin, et al.Bioorganic Chemistry|March 14, 2018
Synthesis, molecular docking study and in vitro thymidine phosphorylase inhibitory potential of oxadiazole derivativesHayat Ullah, Fazal Rahim, Muhammad Taha, et al.Bioorganic Chemistry|February 24, 2018
Non-acidic 1,3,4-trisubstituted-pyrazole derivatives as lonazolac analogs with promising COX-2 selectivity, anti-inflammatory activity and gastric safety profileKhaled R A Abdellatif, Wael A A Fadaly, Yaseen A M M Elshaier, et al.Bioorganic Chemistry|February 25, 2018
Synthesis, α-glucosidase inhibition and molecular docking study of coumarin based derivativesMuhammad Taha, Syed Adnan Ali Shah, Muhammad Afifi, et al.Bioorganic Chemistry|March 19, 2018
Design, synthesis, analgesic, anti-inflammatory activity of novel pyrazolones possessing aminosulfonyl pharmacophore as inhibitors of COX-2/5-LOX enzymes: Histopathological and docking studiesMohamed A Abdelgawad, Madlen B Labib, Waleed A M Ali, et al.Bioorganic Chemistry|March 19, 2018
Synthesis of some novel orcinol based coumarin triazole hybrids with capabilities to inhibit RANKL-induced osteoclastogenesis through NF-κB signaling pathwayBoddu Rama Krishna, Dinesh Thummuri, V G M Naidu, et al.Bioorganic Chemistry|February 18, 2018
8-Chrysoeriol, as a potential BCL-2 inhibitor triggers apoptosis of SW1990 pancreatic cancer cellsYiwen Zhang, Zhimei Li, Qiuxia Min, et al.Bioorganic Chemistry|February 18, 2018
Probing the β-pocket of the active site of human liver glycogen phosphorylase with 3-(C-β-d-glucopyranosyl)-5-(4-substituted-phenyl)-1, 2, 4-triazole inhibitorsEfthimios Kyriakis, Theodora G A Solovou, Sándor Kun, et al.Pageof 864