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Molecular Diversity|June 1, 2022
Designing of disruptor molecules to restrain the protein-protein interaction network of VANG1/SCRIB/NOS1AP using fragment-based drug discovery techniquesSuchandra Roy Acharyya, Plaboni Sen, Thirukumaran Kandasamy, et al.Molecular Diversity|November 27, 2022
Molecular dynamics articulated multilevel virtual screening protocol to discover novel dual PPAR α/γ agonists for anti-diabetic and metabolic applicationsSubhankar Mandal, Syed Faizan, Nulgumnalli Manjunathaiah Raghavendra, et al.Molecular Diversity|November 29, 2022
Oncoinformatic screening of the gene clusters involved in the HER2-positive breast cancer formation along with the in silico pharmacodynamic profiling of selective long-chain omega-3 fatty acids as the metastatic antagonistsA K M Helal Morshed, Salauddin Al Azad, Md Abdur Rashid Mia, et al.Molecular Diversity|June 6, 2022
A diastereoselective three-component reaction for the assembly of succinimide and isatin hybrid molecules with potent anticancer activitiesHaoxuan Yuan, Yinfeng Guo, Zhijing Zhang, et al.Molecular Diversity|December 17, 2022
Quinolone: a versatile therapeutic compound classPhelelisiwe S Dube, Lesetja J Legoabe, Richard M BeteckMolecular Diversity|July 2, 2021
In silico analysis and identification of antiviral coumarin derivatives against 3-chymotrypsin-like main protease of the novel coronavirus SARS-CoV-2Rahman Abdizadeh, Farzin Hadizadeh, Tooba AbdizadehMolecular Diversity|June 19, 2022
PTSA-catalyzed selective synthesis and antibacterial evaluation of 1,2-disubstituted benzimidazolesJiaxu Fu, Yuandong Yue, Kejun Liu, et al.Molecular Diversity|July 6, 2021
Catalytic stereoselective Mannich-type reactions for construction of fluorinated compoundsMinoo Dabiri, Noushin Farajinia Lehi, Reza MohammadianMolecular Diversity|September 24, 2020
The evaluation of 1-tetralone and 4-chromanone derivatives as inhibitors of monoamine oxidaseStephanus J Cloete, Clarina I N'Da, Lesetja J Legoabe, et al.Molecular Diversity|October 13, 2020
Synthesis of 4-alkylaminoimidazo[1,2-a]pyridines linked to carbamate moiety as potent α-glucosidase inhibitorsMina Saeedi, Maryam Raeisi-Nafchi, Sepideh Sobhani, et al.Pageof 290