Bioorganic & Medicinal Chemistry Letters

Papers
(The H4-Index of Bioorganic & Medicinal Chemistry Letters is 30. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-05-01 to 2024-05-01.)
ArticleCitations
The SARS-CoV-2 main protease as drug target538
Main protease mutants of SARS-CoV-2 variants remain susceptible to nirmatrelvir126
Pyridones in drug discovery: Recent advances70
The relationship between the structure and toxicity of aminoglycoside antibiotics63
Structural hybridization as a facile approach to new drug candidates60
Synthesis, biological evaluation of benzothiazole derivatives bearing a 1,3,4-oxadiazole moiety as potential anti-oxidant and anti-inflammatory agents58
Recent advances in antibacterial agents53
New coumarin-benzotriazole based hybrid molecules as inhibitors of acetylcholinesterase and amyloid aggregation52
The expanding reaction toolkit for DNA-encoded libraries51
Cryo-EM as a powerful tool for drug discovery49
1,2,3-triazole-thiazole hybrids: Synthesis, in vitro antimicrobial activity and antibiofilm studies48
Design and synthesis, biological evaluation of bis-(1,2,3- and 1,2,4)-triazole derivatives as potential antimicrobial and antifungal agents47
Discovery of a novel series of substituted quinolines acting as anticancer agents and selective EGFR blocker: Molecular docking study44
Structure and bioactivity of colibactin44
Selective CDK6 degradation mediated by cereblon, VHL, and novel IAP-recruiting PROTACs41
Discovery and biological evaluation of proteolysis targeting chimeras (PROTACs) as an EGFR degraders based on osimertinib and lenalidomide37
Synthesis and biological evaluation of anti-tubercular activity of Schiff bases of 2-Amino thiazoles35
Design, synthesis, biological evaluation and molecular docking of new uracil analogs-1,2,4-oxadiazole hybrids as potential anticancer agents34
Aminopyrazole based CDK9 PROTAC sensitizes pancreatic cancer cells to venetoclax34
Unique para-aminobenzenesulfonyl oxadiazoles as novel structural potential membrane active antibacterial agents towards drug-resistant methicillin resistant Staphylococcus aureus33
Microwave assisted regioselective synthesis of quinoline appended triazoles as potent anti-tubercular and antifungal agents via copper (I) catalyzed cycloaddition33
Synthesis and biological evaluation of novel quinazoline-triazole hybrid compounds with potential use in Alzheimer’s disease33
Screening of chalcone analogs with anti-depressant, anti-inflammatory, analgesic, and COX-2-inhibiting effects32
New bis- and tetrakis-1,2,3-triazole derivatives: Synthesis, DNA cleavage, molecular docking, antimicrobial, antioxidant activity and acid dissociation constants32
Novel isoniazid embedded triazole derivatives: Synthesis, antitubercular and antimicrobial activity evaluation32
New vinyl-1,2,4-triazole derivatives as antimicrobial agents: Synthesis, biological evaluation and molecular docking studies31
Synthesis and anti-proliferative activity of a novel 1,2,3-triazole tethered chalcone acetamide derivatives31
Novel vanillin derivatives containing a 1,3,4-thiadiazole moiety as potential antibacterial agents31
Exploring the potential of novel phenolic compounds as potential therapeutic candidates against SARS-CoV-2, using quantum chemistry, molecular docking and dynamic studies30
Click synthesis of 1,2,3-triazole based imidazoles: Antitubercular evaluation, molecular docking and HSA binding studies30
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