Works matching IS 17470277 AND DT 2017 AND VI 89 AND IP 6
Results: 15
Synthesis, cytotoxic activity, and 2D- and 3D- QSAR studies of 19-carboxyl-modified novel isosteviol derivatives as potential anticancer agents.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 870, doi. 10.1111/cbdd.12910
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- Article
Protective effects of β-sheet breaker α/β-hybrid peptide against amyloid β-induced neuronal apoptosis in vitro.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 888, doi. 10.1111/cbdd.12912
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- Article
(Z)-2-(3-Chlorobenzylidene)-3,4-dihydro- N-(2-methoxyethyl)-3-oxo-2H-benzo[b][1,4]oxazine-6-carboxamide as GSK-3β inhibitor: Identification by virtual screening and its validation in enzyme- and cell-based assay.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 964, doi. 10.1111/cbdd.12913
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- Article
Design, synthesis and in vitro antiplasmodial activity of some bisquinolines against chloroquine-resistant strain.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 901, doi. 10.1111/cbdd.12914
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- Article
Fusion of Ssm6a with a protein scaffold retains selectivity on Na<sub>V</sub>1.7 and improves its therapeutic potential against chronic pain.
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- 2017
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- Publication type:
- Editorial
Structural insight into the antiprion compound inhibition mechanism of native prion folding over misfolding.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 907, doi. 10.1111/cbdd.12916
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- Article
Comparative molecular field analysis (CoMFA), topomer CoMFA, and hologram QSAR studies on a series of novel HIV-1 protease inhibitors.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 918, doi. 10.1111/cbdd.12917
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- Article
Reactivity of 9-aminoacridine drug quinacrine with glutathione limits its antiprion activity.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 932, doi. 10.1111/cbdd.12918
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- Article
Mapping of inhibitors and activity data to the human kinome and exploring promiscuity from a ligand and target perspective.
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- 2017
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- Publication type:
- Editorial
Theoretical studies on the selective mechanisms of GSK3β and CDK2 by molecular dynamics simulations and free energy calculations.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 846, doi. 10.1111/cbdd.12907
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- Article
1 H-1,2,3-triazole-tethered uracil-ferrocene and uracil-ferrocenylchalcone conjugates: Synthesis and antitubercular evaluation.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 856, doi. 10.1111/cbdd.12908
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- Article
Identification and structure-activity relationship of purine derivatives as novel MTH1 inhibitors.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 862, doi. 10.1111/cbdd.12909
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- Article
Issue Information.
- Published in:
- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 821, doi. 10.1111/cbdd.12854
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- Article
Mannich bases of 1,2,4-triazole-3-thione containing adamantane moiety: Synthesis, preliminary anticancer evaluation, and molecular modeling studies.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 943, doi. 10.1111/cbdd.12920
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- Article
Danazol has potential to cause PKC translocation, cell cycle dysregulation, and apoptosis in breast cancer cells.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 953, doi. 10.1111/cbdd.12921
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- Article