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Brian S Safina

Showing results (1-10 of 21) with videos related to

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Journal of the American Chemical Society|August 4, 2005
Total synthesis of thiostrepton. Assembly of key building blocks and completion of the synthesisK C Nicolaou, Mark Zak, Brian S Safina, et al.
Journal of the American Chemical Society|August 4, 2005
Total synthesis of thiostrepton. Retrosynthetic analysis and construction of key building blocksK C Nicolaou, Brian S Safina, Mark Zak, et al.
ACS Medicinal Chemistry Letters|September 27, 2017
Design of Selective Benzoxazepin PI3Kδ Inhibitors Through Control of Dihedral AnglesBrian S Safina, Richard L Elliott, Andrew K Forrest, et al.
Bioorganic & Medicinal Chemistry Letters|July 23, 2013
Identification of GNE-293, a potent and selective PI3Kδ inhibitor: navigating in vitro genotoxicity while improving potency and selectivityBrian S Safina, Zachary K Sweeney, Jun Li, et al.
Journal of Medicinal Chemistry|November 8, 2017
Pyrrolobenzodiazepine Dimer Antibody-Drug Conjugates: Synthesis and Evaluation of Noncleavable Drug-LinkersStephen J Gregson, Luke A Masterson, Binqing Wei, et al.
ACS Medicinal Chemistry Letters|March 18, 2016
Discovery of Aryl Sulfonamides as Isoform-Selective Inhibitors of NaV1.7 with Efficacy in Rodent Pain ModelsThilo Focken, Shifeng Liu, Navjot Chahal, et al.
Cell Reports|September 21, 2018
Selective Na<sub>V</sub>1.7 Antagonists with Long Residence Time Show Improved Efficacy against Inflammatory and Neuropathic PainGirish Bankar, Samuel J Goodchild, Sarah Howard, et al.
Journal of Medicinal Chemistry|March 30, 2018
Discovery of a Potent (4 R,5 S)-4-Fluoro-5-methylproline Sulfonamide Transient Receptor Potential Ankyrin 1 Antagonist and Its Methylene Phosphate Prodrug Guided by Molecular ModelingHuifen Chen, Matthew Volgraf, Steven Do, et al.
Journal of Medicinal Chemistry|September 1, 2012
Discovery and preclinical pharmacology of a selective ATP-competitive Akt inhibitor (GDC-0068) for the treatment of human tumorsJames F Blake, Rui Xu, Josef R Bencsik, et al.
Bioorganic & Medicinal Chemistry Letters|June 8, 2012
Potent and selective inhibitors of PI3Kδ: obtaining isoform selectivity from the affinity pocket and tryptophan shelfDaniel P Sutherlin, Stewart Baker, Angelina Bisconte, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Journal of the American Chemical Society|August 4, 2005
Total synthesis of thiostrepton. Assembly of key building blocks and completion of the synthesisK C Nicolaou, Mark Zak, Brian S Safina, et al.
Journal of the American Chemical Society|August 4, 2005
Total synthesis of thiostrepton. Retrosynthetic analysis and construction of key building blocksK C Nicolaou, Brian S Safina, Mark Zak, et al.
ACS Medicinal Chemistry Letters|September 27, 2017
Design of Selective Benzoxazepin PI3Kδ Inhibitors Through Control of Dihedral AnglesBrian S Safina, Richard L Elliott, Andrew K Forrest, et al.
Bioorganic & Medicinal Chemistry Letters|July 23, 2013
Identification of GNE-293, a potent and selective PI3Kδ inhibitor: navigating in vitro genotoxicity while improving potency and selectivityBrian S Safina, Zachary K Sweeney, Jun Li, et al.
Journal of Medicinal Chemistry|November 8, 2017
Pyrrolobenzodiazepine Dimer Antibody-Drug Conjugates: Synthesis and Evaluation of Noncleavable Drug-LinkersStephen J Gregson, Luke A Masterson, Binqing Wei, et al.
ACS Medicinal Chemistry Letters|March 18, 2016
Discovery of Aryl Sulfonamides as Isoform-Selective Inhibitors of NaV1.7 with Efficacy in Rodent Pain ModelsThilo Focken, Shifeng Liu, Navjot Chahal, et al.
Cell Reports|September 21, 2018
Selective Na<sub>V</sub>1.7 Antagonists with Long Residence Time Show Improved Efficacy against Inflammatory and Neuropathic PainGirish Bankar, Samuel J Goodchild, Sarah Howard, et al.
Journal of Medicinal Chemistry|March 30, 2018
Discovery of a Potent (4 R,5 S)-4-Fluoro-5-methylproline Sulfonamide Transient Receptor Potential Ankyrin 1 Antagonist and Its Methylene Phosphate Prodrug Guided by Molecular ModelingHuifen Chen, Matthew Volgraf, Steven Do, et al.
Journal of Medicinal Chemistry|September 1, 2012
Discovery and preclinical pharmacology of a selective ATP-competitive Akt inhibitor (GDC-0068) for the treatment of human tumorsJames F Blake, Rui Xu, Josef R Bencsik, et al.
Bioorganic & Medicinal Chemistry Letters|June 8, 2012
Potent and selective inhibitors of PI3Kδ: obtaining isoform selectivity from the affinity pocket and tryptophan shelfDaniel P Sutherlin, Stewart Baker, Angelina Bisconte, et al.
Pageof 3