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MC180295 is a highly potent and selective CDK9 inhibitor with preclinical in vitro and in vivo efficacy in cancer.
- Published in:
- Clinical Epigenetics, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13148-023-01617-3
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- Article
The Relationships of AMPK Allosteric Inhibitors with Their Activities against Breast Cancer in 2D and 3D Models.
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- ChemistrySelect, 2023, v. 8, n. 43, p. 1, doi. 10.1002/slct.202302979
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- Article
Liver Metabolomics and Inflammatory Profiles in Mouse Model of Fentanyl Overdose Treated with Beta-Lactams.
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- Metabolites (2218-1989), 2023, v. 13, n. 8, p. 965, doi. 10.3390/metabo13080965
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- Article
Nuclear Magnetic Resonance Structure of the Human Polyoma JC Virus Agnoprotein.
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- Journal of Cellular Biochemistry, 2017, v. 118, n. 10, p. 3268, doi. 10.1002/jcb.25977
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- Article
Emerging From the Unknown: Structural and Functional Features of Agnoprotein of Polyomaviruses.
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- Journal of Cellular Physiology, 2016, v. 231, n. 10, p. 2115, doi. 10.1002/jcp.25329
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- Article
Targeting neurodegenerative diseases: Drug discovery in a challenging arena.
- Published in:
- Pure & Applied Chemistry, 2012, v. 84, n. 7, p. 1543, doi. 10.1351/PAC-CON-11-11-09
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- Article
P2-337: Characterization of the affinity of GSI-953 for binding to gamma-secretase and comparison to benchmark gamma-secretase inhibitors
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- 2008
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- Abstract
P2-481: Small molecule BACE-1 inhibitors are potent, selective and orally active
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- 2008
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- Abstract
WAY-131256 is an orally active, efficacious, and in vivo functionally selective M<sub>1</sub> agonist.
- Published in:
- Drug Development Research, 1997, v. 40, n. 2, p. 185, doi. 10.1002/(SICI)1098-2299(199702)40:2<185::AID-DDR8>3.0.CO;2-H
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- Article
Preclinical profile of Wy-49,051: A new H<sub>1</sub>-antagonist.
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- Drug Development Research, 1990, v. 21, n. 1, p. 63, doi. 10.1002/ddr.430210108
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- Article
Behavioral pharmacology of the gamma carboline Wy 47,384: A potential antipsychotic agent.
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- Drug Development Research, 1988, v. 13, n. 1, p. 11, doi. 10.1002/ddr.430130103
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- Article