N-substituted derivatives of EM 49 structure-activity relationships

Interface geometry and molecular junction conductance: geometric fluctuation and stochastic switching.

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Quantification of the various contributors to rate enhancement in nucleophilic strain releasing reactions.

The Journal of organic chemistry·2001

Phosphorus-containing inhibitors of HMG-CoA reductase. 2. Synthesis and biological activities of a series of substituted pyridines containing a hydroxyphosphinyl moiety.

Journal of medicinal chemistry·1991

The binding of substituted cis-Pt(II)-diammines to duplex DNA.

Biopolymers·1990

Theoretical studies of cis-Pt(II)-diammine binding to duplex DNA.

Biopolymers·1990

Structural relationships of angiotensin converting-enzyme inhibitors to pharmacologic activity.

Circulation·1988

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A N-methylated antimicrobial peptide targets the fructose transporter FruA of Staphylococcus aureus.

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Discovery of new α-pyrone derivative with α-glucosidase inhibitory activity from the fungus Acremonium persicinum.

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Organocatalytic stereoselective synthesis of amino acid-fused quinazolinone based triazacyclic new chemical entities.

Organic & biomolecular chemistry·2026

Stereoselective access to allenic sphingosine analogues as SphK inhibitors.

Organic & biomolecular chemistry·2026

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Future medicinal chemistry·2026

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Frontiers in toxicology·2026

Crystalline Mate Assists Structural Elucidation and Offline LC-SCXRD Analysis of Flavonoid Glycosides via Synergistic π-π Stacking and C-H···O Interactions.

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Fitoterapia·2026

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N-substituted derivatives of EM 49 structure-activity relationships

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Interface geometry and molecular junction conductance: geometric fluctuation and stochastic switching.

Quantification of the various contributors to rate enhancement in nucleophilic strain releasing reactions.

Phosphorus-containing inhibitors of HMG-CoA reductase. 2. Synthesis and biological activities of a series of substituted pyridines containing a hydroxyphosphinyl moiety.

The binding of substituted cis-Pt(II)-diammines to duplex DNA.

Theoretical studies of cis-Pt(II)-diammine binding to duplex DNA.

Structural relationships of angiotensin converting-enzyme inhibitors to pharmacologic activity.

Reimagining antimicrobial resistance: AI-driven predictive epidemiology and the C-AMRE framework for next-generation antibiotic discovery.

Comprehensive derivatization of thiostrepton via heterologous expression.

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A N-methylated antimicrobial peptide targets the fructose transporter FruA of Staphylococcus aureus.

Discovery of new α-pyrone derivative with α-glucosidase inhibitory activity from the fungus Acremonium persicinum.

Allantopyrone A promotes cross-linking of ubiquitin-specific protease 5 (USP5) and inhibits its deubiquitinase activity by targeting distinct domains.

Organocatalytic stereoselective synthesis of amino acid-fused quinazolinone based triazacyclic new chemical entities.

Stereoselective access to allenic sphingosine analogues as SphK inhibitors.

Design and development of 2,7-disubstituted 6-methoxyquinazolin-4 (3H)-ones as potential anti-cancer agents possibly through downregulation of Wnt/β-catenin/TCF4 signaling pathway.

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