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The potent AMPK inhibitor BAY-3827 shows strong efficacy in androgen-dependent prostate cancer models.
- Published in:
- Cellular Oncology (2211-3428), 2021, v. 44, n. 3, p. 581, doi. 10.1007/s13402-020-00584-8
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- Article
Prioritizing Small Sets of Molecules for Synthesis through in‐silico Tools: A Comparison of Common Ranking Methods.
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- ChemMedChem, 2023, v. 18, n. 1, p. 1, doi. 10.1002/cmdc.202200425
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- Article
Front Cover: Computationally Empowered Workflow Identifies Novel Covalent Allosteric Binders for KRAS<sup>G12C</sup> (ChemMedChem 10/2020).
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- ChemMedChem, 2020, v. 15, n. 10, p. 808, doi. 10.1002/cmdc.202000297
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- Article
Computationally Empowered Workflow Identifies Novel Covalent Allosteric Binders for KRAS<sup>G12C</sup>.
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- ChemMedChem, 2020, v. 15, n. 10, p. 827, doi. 10.1002/cmdc.201900727
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- Article
Computational Macrocyclization: From de novo Macrocycle Generation to Binding Affinity Estimation.
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- ChemMedChem, 2017, v. 12, n. 22, p. 1866, doi. 10.1002/cmdc.201700478
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- Article
Identification of Atuveciclib (BAY 1143572), the First Highly Selective, Clinical PTEFb/CDK9 Inhibitor for the Treatment of Cancer.
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- ChemMedChem, 2017, v. 12, n. 21, p. 1776, doi. 10.1002/cmdc.201700447
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- Article
Galileo: Three-dimensional searching in large combinatorial fragment spaces on the example of pharmacophores.
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- Journal of Computer-Aided Molecular Design, 2023, v. 37, n. 1, p. 1, doi. 10.1007/s10822-022-00485-y
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- Article
Substantial improvements in large-scale redocking and screening using the novel HYDE scoring function.
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- Journal of Computer-Aided Molecular Design, 2012, v. 26, n. 6, p. 701, doi. 10.1007/s10822-011-9531-0
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- Article
Ultrafast de novo docking combining pharmacophores and combinatorics.
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- Journal of Computer-Aided Molecular Design, 2006, v. 20, n. 12, p. 717, doi. 10.1007/s10822-006-9091-x
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- Article
Mono- and multimeric PSMA-targeting small molecule-thorium-227 conjugates for optimized efficacy and biodistribution in preclinical models.
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- European Journal of Nuclear Medicine & Molecular Imaging, 2024, v. 51, n. 3, p. 669, doi. 10.1007/s00259-023-06474-z
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- Article
The Lab Oddity Prevails: Discovery of Pan-CDK Inhibitor ( R)- S-Cyclopropyl- S-(4-{[4-{[(1 R,2 R)-2-hydroxy-1-methylpropyl]oxy}-5-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)sulfoximide (BAY 1000394) for the Treatment of Cancer.
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- ChemMedChem, 2013, v. 8, n. 7, p. 1067, doi. 10.1002/cmdc.201300096
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- Article
Cover Picture: The Lab Oddity Prevails: Discovery of Pan-CDK Inhibitor ( R)- S-Cyclopropyl- S-(4-{[4-{[(1 R,2 R)-2-hydroxy-1-methylpropyl]oxy}-5-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)sulfoximide (BAY 1000394) for the Treatment of Cancer (ChemMedChem 7/2013)
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- ChemMedChem, 2013, v. 8, n. 7, p. 1021, doi. 10.1002/cmdc.201390025
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- Article
Macrocyclic Aminopyrimidines as Multitarget CDK and VEGF-R Inhibitors with Potent Antiproliferative Activities.
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- ChemMedChem, 2007, v. 2, n. 1, p. 63, doi. 10.1002/cmdc.200600199
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- Article
From the Insoluble Dye Indirubin towards Highly Active, Soluble CDK2-Inhibitors.
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- ChemBioChem, 2005, v. 6, n. 3, p. 531, doi. 10.1002/cbic.200400108
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- Article
Classifying “Kinase Inhibitor-Likeness” by Using Machine-Learning Methods.
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- ChemBioChem, 2005, v. 6, n. 3, p. 558, doi. 10.1002/cbic.200400109
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- Article