Works matching IS 18607179 AND DT 2017 AND VI 12 AND IP 9
Results: 9
Cover Picture: Synthesis of T-705-Ribonucleoside and T-705-Ribonucleotide and Studies of Chemical Stability (ChemMedChem 9/2017).
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- ChemMedChem, 2017, v. 12, n. 9, p. 621, doi. 10.1002/cmdc.201700255
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Design and Synthesis of C3-Substituted β-Carboline-Based Histone Deacetylase Inhibitors with Potent Antitumor Activities.
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- ChemMedChem, 2017, v. 12, n. 9, p. 646, doi. 10.1002/cmdc.201700133
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- Article
Corrigendum: Characterization of a Cell-Penetrating Peptide with Potential Anticancer Activity.
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- ChemMedChem, 2017, v. 12, n. 9, p. 712, doi. 10.1002/cmdc.201700206
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Structure-Based Target-Specific Screening Leads to Small-Molecule CaMKII Inhibitors.
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- ChemMedChem, 2017, v. 12, n. 9, p. 660, doi. 10.1002/cmdc.201600636
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Biological Evaluation of Dipyrromethanes in Cancer Cell Lines: Antiproliferative and Pro-apoptotic Properties.
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- ChemMedChem, 2017, v. 12, n. 9, p. 701, doi. 10.1002/cmdc.201700152
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- Article
Rafoxanide and Closantel Inhibit SPAK and OSR1 Kinases by Binding to a Highly Conserved Allosteric Site on Their C-terminal Domains.
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- ChemMedChem, 2017, v. 12, n. 9, p. 639, doi. 10.1002/cmdc.201700077
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Design, Synthesis, and in vitro and in vivo Evaluations of ( Z)-3,4,5-Trimethoxystyrylbenzenesulfonamides/sulfonates as Highly Potent Tubulin Polymerization Inhibitors.
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- ChemMedChem, 2017, v. 12, n. 9, p. 678, doi. 10.1002/cmdc.201600643
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- Article
Molecular Hybridization Tools in the Development of Furoxan-Based NO-Donor Prodrugs.
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- ChemMedChem, 2017, v. 12, n. 9, p. 622, doi. 10.1002/cmdc.201700113
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- Article
Synthesis of T-705-Ribonucleoside and T-705-Ribonucleotide and Studies of Chemical Stability.
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- ChemMedChem, 2017, v. 12, n. 9, p. 652, doi. 10.1002/cmdc.201700116
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- Article