Bioorganic & Medicinal Chemistry Letters

Papers
(The H4-Index of Bioorganic & Medicinal Chemistry Letters is 24. 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 2022-06-01 to 2026-06-01.)
ArticleCitations
Editorial Board108
Pyrazolo-1-carbothioamides as EGR-1–DNA binding disruptors75
Discovery of TNG-6132, a potent, selective, and orally bioavailable USP1 inhibitor56
Armeniaspirol analogues disrupt the electrical potential (ΔΨ) of the proton motive force52
Graphical Abstract TOC44
Editorial Board39
Neuropilin 1-targeted near-infrared fluorescence probes for tumor diagnosis37
Contents continued34
Synthesis and biological evaluation of novel 1,2,3,4-tetrahydro-β-carboline derivatives as potential antibacterial agents33
Studies on in vitro modulatory effects to base excision repair enzymes induced by small molecule binding to Deaminated CAG repeat hairpin30
Design, synthesis and biological evaluation of alginate oligosaccharide derivatives30
Design and evaluation of anaplastic lymphoma kinase degraders using a covalent fumarate handle30
Discovery of multitargeting single agents as a novel route to the potential treatment of neurodegenerative diseases29
SARS-CoV-2 papain-like protease (PLpro) inhibitory and antiviral activity of small molecule derivatives for drug leads27
Design and synthesis of Tetrahydroindeno[4,5-c]chromen-4(3H)-one derivatives as antiproliferative agents for prostate Cancer cells27
Phytochemical investigation of Asarum sieboldii var. seoulense and the phenotypic profiles of its constituents against a Parkinson’s Disease olfactory cell line26
Discovery of DS-1093a: An oral hypoxia-inducible factor prolyl hydroxylase inhibitor for the treatment of renal anemia26
Epigallocatechin and epigallocatechin-3-gallate are not inhibitors of tyrosinase26
Improved synthesis and anticancer activity of a potent neuronal nitric oxide synthase inhibitor25
Revisiting the dipeptidyl carboxypeptidase inhibitor captopril as a source of pan anti-trypanosomatid agents25
New class of fused [3,2-b][1,2,4]triazolothiazoles for targeting glioma in vitro24
Discovery of structural diverse reversible BTK inhibitors utilized to develop a novel in vivo CD69 and CD86 PK/PD mouse model24
Synthesis and evaluation of novel oxanthrene scaffold-derived oxazolidinone antibiotics with potent antitubercular activity and low cellular toxicity24
Green synthesis and anti-biofilm activities of 3,5-disubstituted isoxazoline/isoxazole-linked secondary sulfonamide derivatives on Pseudomonas aeruginosa24
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