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Bioorganic Chemistry|July 1, 2019
Extraction, isolation and in vitro evaluation of affinisine from Tabernaemontana catharinensis in human melanoma cellsPauline Fagundes Rosales, Adriana Gower, Martha Lucia Ruiz Benitez, et al.
Bioorganic Chemistry|October 12, 2019
Extending the γ-class carbonic anhydrases inhibition profiles with phenolic compoundsAlessio Nocentini, Sameh M Osman, Sonia Del Prete, et al.
Bioorganic Chemistry|October 13, 2019
Adapalene inhibits ovarian cancer ES-2 cells growth by targeting glutamic-oxaloacetic transaminase 1Qiqi Wang, Qingzhe Zhang, Shanshan Luan, et al.
Bioorganic Chemistry|October 14, 2019
Design, synthesis and biological evaluation of oxygenated chalcones as potent and selective MAO-B inhibitorsDella Grace Thomas Parambi, Jong Min Oh, Seung Cheol Baek, et al.
Bioorganic Chemistry|September 25, 2018
Coumarin-dithiocarbamate hybrids as novel multitarget AChE and MAO-B inhibitors against Alzheimer's disease: Design, synthesis and biological evaluationQi He, Jing Liu, Jin-Shuai Lan, et al.
Bioorganic Chemistry|September 25, 2018
Synthesis, antiproliferative activity and molecular docking of thiocolchicine urethanesUrszula Majcher, Alicja Urbaniak, Ewa Maj, et al.
Bioorganic Chemistry|September 25, 2018
Synthesis, antimicrobial activity and molecular modeling study of 3-(5-amino-(2H)-1,2,4-triazol-3-yl]-naphthyridinones as potential DNA-gyrase inhibitorsNoha G Mohamed, Mahmoud M Sheha, Hoda Y Hassan, et al.
Bioorganic Chemistry|September 26, 2018
1,2,4-Triazole-based benzothiazole/benzoxazole derivatives: Design, synthesis, p38α MAP kinase inhibition, anti-inflammatory activity and molecular docking studiesSana Tariq, Payal Kamboj, Ozair Alam, et al.
Bioorganic Chemistry|September 26, 2018
Synthesis of different thio-scaffolds bearing sulfonamide with subnanomolar carbonic anhydrase II and IX inhibitory properties and X-ray investigations for their inhibitory mechanismAndrea Angeli, Damiano Tanini, Antonella Capperucci, et al.
Bioorganic Chemistry|June 21, 2019
Exploiting the 7-methylimidazo[1,5-a]pyrazin-8(7H)-one scaffold for the development of novel chemical inhibitors for Bromodomain and Extraterminal Domain (BET) familyYifei Yang, Pan Chen, Leilei Zhao, et al.
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