Found: 7
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Discovery of Rogaratinib (BAY 1163877): a pan‐FGFR Inhibitor.
- Published in:
- ChemMedChem, 2018, v. 13, n. 5, p. 437, doi. 10.1002/cmdc.201700718
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- Article
Prediction of a potentially effective dose in humans for BAY 60-5521, a potent inhibitor of cholesteryl ester transfer protein (CETP) by allometric species scaling and combined pharmacodynamic and physiologically-based pharmacokinetic modelling.
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- British Journal of Clinical Pharmacology, 2012, v. 73, n. 2, p. 219, doi. 10.1111/j.1365-2125.2011.04064.x
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- Article
Chronic inhibition of phosphodiesterase 5 does not prevent pressure-overload-induced right-ventricular remodelling.
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- Cardiovascular Research, 2009, v. 82, n. 1, p. 30, doi. 10.1093/cvr/cvp002
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- Article
Rogaratinib: A potent and selective pan‐FGFR inhibitor with broad antitumor activity in FGFR‐overexpressing preclinical cancer models.
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- International Journal of Cancer, 2019, v. 145, n. 5, p. 1346, doi. 10.1002/ijc.32224
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- Article
Potent and Selective Human Neutrophil Elastase Inhibitors with Novel Equatorial Ring Topology: in vivo Efficacy of the Polar Pyrimidopyridazine BAY-8040 in a Pulmonary Arterial Hypertension Rat Model.
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- ChemMedChem, 2016, v. 11, n. 2, p. 199, doi. 10.1002/cmdc.201500269
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- Article
Cover Picture: Freezing the Bioactive Conformation to Boost Potency: The Identification of BAY 85-8501, a Selective and Potent Inhibitor of Human Neutrophil Elastase for Pulmonary Diseases (ChemMedChem 7/2015).
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- ChemMedChem, 2015, v. 10, n. 7, p. 1117, doi. 10.1002/cmdc.201590019
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- Article
Freezing the Bioactive Conformation to Boost Potency: The Identification of BAY 85-8501, a Selective and Potent Inhibitor of Human Neutrophil Elastase for Pulmonary Diseases.
- Published in:
- ChemMedChem, 2015, v. 10, n. 7, p. 1163, doi. 10.1002/cmdc.201500131
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- Article