37 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Solution-phase microwave assisted parallel synthesis, biological evaluation and in silico docking studies of N,N'-disubstituted thioureas derived from 3-chlorobenzoic acid.
Quaid-I-Azam University
Synthesis of potent urease inhibitors based on disulfide scaffold and their molecular docking studies.
Universiti Teknologi Mara (Uitm)
Discovery of indole-based tetraarylimidazoles as potent inhibitors of urease with low antilipoxygenase activity.
University of The Punjab
Design and synthesis of new barbituric- and thiobarbituric acid derivatives as potent urease inhibitors: Structure activity relationship and molecular modeling studies.
The Islamia University of Bahawalpur
Synthesis of novel derivatives of oxindole, their urease inhibition and molecular docking studies.
Universiti Teknologi Mara Puncak Alam Campus
Implications of N-capped urea/thiourea and C-capped 3-(1-piperazinyl)-1,2-benzisothiazole with bridging Gly-Val/Phe-Gly-Val-Pro as therapeutic targets.
University of Mysore
Synthesis and in vitro urease inhibitory activity of N,N'-disubstituted thioureas.
University Karachi
Solution-phase microwave assisted parallel synthesis of N,N'-disubstituted thioureas derived from benzoic acid: biological evaluation and molecular docking studies.
Quaid-I-Azam University
3D-QSAR CoMFA studies on bis-coumarine analogues as urease inhibitors: a strategic design in anti-urease agents.
University of Karachi
Synthesis, biological assay in vitro and molecular docking studies of new Schiff base derivatives as potential urease inhibitors.
Comsats Institute of Information Technology
Synthesis, antioxidant activities and urease inhibition of some new 1,2,4-triazole and 1,3,4-thiadiazole derivatives.
Quaid-I-Azam University
Facile one-pot synthesis of thio and selenourea derivatives: a new class of potent urease inhibitors.
Institute of Science
Insights into the recent progress in the medicinal chemistry of pyranopyrimidine analogs.
Mansoura University
Developing new hybrid scaffold for urease inhibition based on carbazole-chalcone conjugates: Synthesis, assessment of therapeutic potential and computational docking analysis.
Quaid-I-Azam University
Synthesis and urease inhibitory potential of benzophenone sulfonamide hybrid in vitro and in silico.
University of Karachi
1,2,3-Triazole-containing hybrids as leads in medicinal chemistry: A recent overview.
Chinese Academy of Sciences
Rational approaches, design strategies, structure activity relationship and mechanistic insights for therapeutic coumarin hybrids.
Guru Nanak Dev University
Design, synthesis and biological activities of some 7-aminocephalosporanic acid derivatives.
Karadeniz Technical University
Microwave assisted synthesis of some hybrid molecules derived from norfloxacin and investigation of their biological activities.
Karadeniz Technical University
Bisindolylmethane thiosemicarbazides as potential inhibitors of urease: Synthesis and molecular modeling studies.
Imam Abdulrahman Bin Faisal University
Synthesis and molecular docking study of some 5,6-dichloro-2-cyclopropyl-1H-benzimidazole derivatives bearing triazole, oxadiazole, and imine functionalities as potent inhibitors of urease.
Recep Tayyip Erdogan University
Non-peptide macrocyclic histone deacetylese (HDAC) inhibitors and methods of making and using thereof
Georgia Tech Research
Pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use
F. Hoffmann-La Roche
Functional selectivity of dopamine receptor agonists. I. Selective activation of postsynaptic dopamine D2 receptors linked to adenylate cyclase.
University of North Carolina
Synthesis and in vitro opioid activity profiles of DALDA analogues.
Clinical Research Institute of Montreal
Behaviroal, pharmacological, and molecular characterization of an amphibian cannabinoid receptor.
Oregon State University