Search Results - "Kikelj, Danijel"
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Dual Inhibitors of Human DNA Topoisomerase II and Other Cancer-Related Targets
Published in Journal of medicinal chemistry (13-02-2020)“…Human DNA topoisomerase II is an important target in anticancer therapy. Despite the clinical success of drugs that target topoisomerase II, the development of…”
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ATP-competitive DNA gyrase and topoisomerase IV inhibitors as antibacterial agents
Published in Expert opinion on therapeutic patents (04-03-2019)“…The bacterial topoisomerases DNA gyrase and topoisomerase IV are validated targets for development of novel antibacterial agents. Fluoroquinolones inhibit the…”
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3
Rational design of balanced dual-targeting antibiotics with limited resistance
Published in PLoS biology (05-10-2020)“…Antibiotics that inhibit multiple bacterial targets offer a promising therapeutic strategy against resistance evolution, but developing such antibiotics is…”
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Antibacterial and Antibiofilm Potentials of Marine Pyrrole-2-Aminoimidazole Alkaloids and their Synthetic Analogs
Published in Mini reviews in medicinal chemistry (01-01-2018)“…Pyrrole-2-aminoimidazole compounds are found in marine organisms, mainly as secondary metabolites in various marine sponges. Studies of natural…”
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5
Cathepsin X promotes 6-hydroxydopamine-induced apoptosis of PC12 and SH-SY5Y cells
Published in Neuropharmacology (01-07-2014)“…The cysteine carboxypeptidase cathepsin X is an important player in degenerative processes under normal ageing and pathological conditions. In the present…”
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6
Isoform selective voltage-gated sodium channel modulators and the therapy of pain
Published in Current medicinal chemistry (01-01-2014)“…Voltage-gated sodium channels are large transmembrane protein complexes responsible for the propagation and transmission of electrical impulses through nerve,…”
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2-Aminoimidazoles in medicinal chemistry
Published in Mini reviews in medicinal chemistry (01-11-2013)“…2-Aminoimidazole skeleton represents a unique building block which is often used in the design of modulators of different targets and small molecule drugs…”
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Synthesis and Evaluation of Spumigin Analogues Library with Thrombin Inhibitory Activity
Published in Marine drugs (27-10-2018)“…Spumigins are marine natural products derived from cyanobacteria , which mimics the structure of the d-Phe-Pro-Arg sequence and is crucial for binding to the…”
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Recent advances in the synthesis of 2H-1,4-benzoxazin-3-(4H)-ones and 3,4-dihydro-2H-1,4-benzoxazines
Published in Tetrahedron (01-08-2005)Get full text
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10
The application of Freidinger lactams and their analogs in the design of conformationally constrained peptidomimetics
Published in Current medicinal chemistry (01-06-2006)“…Peptides exist in solution as an equilibrium mixture of conformers. The backbone conformational constraints are of interest as a means of limiting degrees of…”
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Characterization of Endogenous Sodium Channels in the ND7-23 Neuroblastoma Cell Line: Implications for Use as a Heterologous Ion Channel Expression System Suitable for Automated Patch Clamp Screening
Published in Assay and drug development technologies (01-03-2016)“…The rodent neuroblastoma cell line, ND7-23, is used to express voltage-dependent sodium (Nav) and other neuronal ion channels resistant to heterologous…”
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Hybrid Inhibitors of DNA Gyrase A and B: Design, Synthesis and Evaluation
Published in Pharmaceutics (22-12-2020)“…The discovery of multi-targeting ligands of bacterial enzymes is an important strategy to combat rapidly spreading antimicrobial resistance. Bacterial DNA…”
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13
Multitarget antithrombotic drugs
Published in Current topics in medicinal chemistry (01-11-2011)“…Thromboembolic disorders are still the leading causes of morbidity and mortality in developed societies. Therefore, prophylaxis and treatment of arterial and…”
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Efficient Synthesis of Hydroxy-Substituted 2‑Aminobenzo[d]thiazole-6-carboxylic Acid Derivatives as New Building Blocks in Drug Discovery
Published in ACS omega (14-04-2020)“…Benzo[d]thiazole is widely used in synthetic and medicinal chemistry, and it is a component of many compounds and drugs that have several different…”
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Novel 2-thioxothiazolidin-4-one inhibitors of bacterial MurD ligase targeting d-Glu- and diphosphate-binding sites
Published in European journal of medicinal chemistry (01-09-2011)“…Mur ligases are involved in cytoplasmic steps of bacterial peptidoglycan biosynthesis and are viable targets for antibacterial drug discovery. We have designed…”
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Practical Synthesis and Application of Halogen-Doped Pyrrole Building Blocks
Published in ACS omega (13-04-2021)“…A practical access to four new halogen-substituted pyrrole building blocks was realized in two to five synthetic steps from commercially available starting…”
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Novel Potent and Selective Thrombin Inhibitors Based on a Central 1,4-Benzoxazin-3(4H)-one Scaffold
Published in Journal of medicinal chemistry (08-05-2008)“…Novel thrombin inhibitors with the central 1,4-benzoxazine-3(4H)-one scaffold, benzamidine P1 arginine side chain mimetic and various P3 moieties are…”
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Dual Inhibitor of MurD and MurE Ligases from Escherichia coli and Staphylococcus aureus
Published in ACS medicinal chemistry letters (09-08-2012)“…MurD and MurE ligases, consecutive enzymes participating in the intracellular steps of bacterial peptidoglycan biosynthesis, are important targets for…”
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Synthesis and biological evaluation of new glutamic acid-based inhibitors of MurD ligase
Published in Bioorganic & medicinal chemistry letters (2009)“…Mur ligases catalyze the biosynthesis of the UDP-MurNAc-pentapeptide precursor of peptidoglycan, an essential polymer of bacterial cell-wall. They constitute…”
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Synthesis of ethyl 3-(hydroxyphenoxy)benzyl butylphosphonates as potential antigen 85C inhibitors
Published in Tetrahedron (22-10-2007)“…All three isomers of ethyl 3-(hydroxyphenoxy)benzyl butylphosphonates as potential antigen 85C inhibitors were synthesized from 3-bromobenzoic acid using…”
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