Found: 17
Select item for more details and to access through your institution.
Unsymmetrically substituted furoxans. Part 16.
- Published in:
- Journal of Heterocyclic Chemistry, 1996, v. 33, n. 2, p. 327, doi. 10.1002/jhet.5570330220
- By:
- Publication type:
- Article
Synthesis and Authentication of Iodoazidophenpyramine, a Photoaffinity Reporter Ligand Previously used for Histamine H<sub>1</sub>-Receptor Labelling.
- Published in:
- Archiv der Pharmazie, 1995, v. 328, n. 9, p. 677, doi. 10.1002/ardp.19953280909
- By:
- Publication type:
- Article
α<sub>1</sub>-Adrenoceptor Blocking Activity of Some Ring-open Analogues of Prazosin.
- Published in:
- Archiv der Pharmazie, 1994, v. 327, n. 10, p. 661, doi. 10.1002/ardp.19943271012
- By:
- Publication type:
- Article
Potential Histamine H<sub>2</sub>-Receptor Antagonists: Twin Compounds Containing Diaminofurazan Substructure.
- Published in:
- Archiv der Pharmazie, 1989, v. 322, n. 9, p. 579, doi. 10.1002/ardp.19893220914
- By:
- Publication type:
- Article
Potential Histamine H<sub>2</sub>-Receptor Antagonists: Analogues of Classical Antagonists Containing 4-Substituted-3-Aminofurazan Moieties.
- Published in:
- Archiv der Pharmazie, 1988, v. 321, n. 2, p. 77, doi. 10.1002/ardp.19883210207
- By:
- Publication type:
- Article
Potential Histamine H<sub>2</sub>-Receptor Antagonists: Ranitidine Analogues Containing 'Semicarbazono Equivalent' Groups.
- Published in:
- Archiv der Pharmazie, 1984, v. 317, n. 6, p. 496, doi. 10.1002/ardp.19843170604
- By:
- Publication type:
- Article
Synthesis and Pharmacological Characterization of New H<sub>2</sub>-Antagonists Containing NO-Donor Moieties, Endowed with Mixed Antisecretory and Gastroprotective Activities.
- Published in:
- Helvetica Chimica Acta, 2000, v. 83, n. 1, p. 287, doi. 10.1002/(SICI)1522-2675(20000119)83:1<287::AID-HLCA287>3.0.CO;2-2
- By:
- Publication type:
- Article
Click chemistry reactions in medicinal chemistry: Applications of the 1,3-dipolar cycloaddition between azides and alkynes.
- Published in:
- Medicinal Research Reviews, 2008, v. 28, n. 2, p. 278, doi. 10.1002/med.20107
- By:
- Publication type:
- Article
The Guareschi Pyridine Scaffold as a Valuable Platform for the Identification of Selective PI3K Inhibitors.
- Published in:
- Molecules, 2015, v. 20, n. 9, p. 17275, doi. 10.3390/molecules200917275
- By:
- Publication type:
- Article
Identification of a Potent Phosphoinositide 3-Kinase Pan Inhibitor Displaying a Strategic Carboxylic Acid Group and Development of Its Prodrugs.
- Published in:
- ChemMedChem, 2017, v. 12, n. 18, p. 1542, doi. 10.1002/cmdc.201700340
- By:
- Publication type:
- Article
Are 1,4- and 1,5-Disubstituted 1,2,3-Triazoles Good Pharmacophoric Groups?
- Published in:
- ChemMedChem, 2014, v. 9, n. 11, p. 2497, doi. 10.1002/cmdc.201402233
- By:
- Publication type:
- Article
A Concise Synthesis of Pyrazole Analogues of Combretastatin A1 as Potent Anti-Tubulin Agents.
- Published in:
- ChemMedChem, 2013, v. 8, n. 4, p. 633, doi. 10.1002/cmdc.201200561
- By:
- Publication type:
- Article
The Tubulin Colchicine Domain: a Molecular Modeling Perspective.
- Published in:
- ChemMedChem, 2012, v. 7, n. 1, p. 33, doi. 10.1002/cmdc.201100361
- By:
- Publication type:
- Article
Synthesis and Biological Evaluation of Isosteric Analogues of FK866, an Inhibitor of NAD Salvage.
- Published in:
- ChemMedChem, 2008, v. 3, n. 5, p. 771, doi. 10.1002/cmdc.200700311
- By:
- Publication type:
- Article
Estrogenic Analogues Synthesized by Click Chemistry.
- Published in:
- ChemMedChem, 2007, v. 2, n. 4, p. 437, doi. 10.1002/cmdc.200600192
- By:
- Publication type:
- Article
A New Furoxan NO-Donor Rabeprazole Derivative and Related Compounds.
- Published in:
- ChemBioChem, 2003, v. 4, n. 9, p. 899, doi. 10.1002/cbic.200300617
- By:
- Publication type:
- Article
Synthesis and anti-Helicobacter pylori properties of NO-donor/metronidazole hybrids and related compounds.
- Published in:
- Drug Development Research, 2003, v. 60, n. 3, p. 225, doi. 10.1002/ddr.10284
- By:
- Publication type:
- Article