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Refinado por: assunto: Chemistry remover assunto: Pharmacology & Pharmacy remover Chemistry, Organic remover
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1
Design and evaluation of ‘Linkerless’ hydroxamic acids as selective HDAC8 inhibitors
Design and evaluation of ‘Linkerless’ hydroxamic acids as selective HDAC8 inhibitors
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Design and evaluation of ‘Linkerless’ hydroxamic acids as selective HDAC8 inhibitors

KrennHrubec, Keris ; Marshall, Brett L. ; Hedglin, Mark ; Verdin, Eric ; Ulrich, Scott M.

Bioorganic & medicinal chemistry letters, 2007-05, Vol.17 (10), p.2874-2878 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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2
Photosensitive GFP mutants containing an azobenzene unnatural amino acid
Photosensitive GFP mutants containing an azobenzene unnatural amino acid
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Photosensitive GFP mutants containing an azobenzene unnatural amino acid

Padilla, Marshall S. ; Young, Douglas D.

Bioorganic & medicinal chemistry letters, 2015-02, Vol.25 (3), p.470-473 [Periódico revisado por pares]

England: Elsevier Ltd

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3
Novel broad-spectrum inhibitors of bacterial methionine aminopeptidase
Novel broad-spectrum inhibitors of bacterial methionine aminopeptidase
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Novel broad-spectrum inhibitors of bacterial methionine aminopeptidase

Rose, Jonathan A. ; Lahiri, Sushmita D. ; McKinney, David C. ; Albert, Rob ; Morningstar, Marshall L. ; Shapiro, Adam B. ; Fisher, Stewart L. ; Fleming, Paul R.

Bioorganic & medicinal chemistry letters, 2015-08, Vol.25 (16), p.3301-3306 [Periódico revisado por pares]

England: Elsevier Ltd

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4
Structure-based drug design enables conversion of a DFG-in binding CSF-1R kinase inhibitor to a DFG-out binding mode
Structure-based drug design enables conversion of a DFG-in binding CSF-1R kinase inhibitor to a DFG-out binding mode
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Structure-based drug design enables conversion of a DFG-in binding CSF-1R kinase inhibitor to a DFG-out binding mode

Meyers, Marvin J. ; Pelc, Matthew ; Kamtekar, Satwik ; Day, Jacqueline ; Poda, Gennadiy I. ; Hall, Molly K. ; Michener, Marshall L. ; Reitz, Beverly A. ; Mathis, Karl J. ; Pierce, Betsy S. ; Parikh, Mihir D. ; Mischke, Deborah A. ; Long, Scott A. ; Parlow, John J. ; Anderson, David R. ; Thorarensen, Atli

Bioorganic & medicinal chemistry letters, 2010-03, Vol.20 (5), p.1543-1547 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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5
Light induced drug release from a folic acid-drug conjugate
Light induced drug release from a folic acid-drug conjugate
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Light induced drug release from a folic acid-drug conjugate

Dcona, M. Michael ; Sheldon, Jonathon E. ; Mitra, Deboleena ; Hartman, Matthew C.T.

Bioorganic & medicinal chemistry letters, 2017-02, Vol.27 (3), p.466-469 [Periódico revisado por pares]

England: Elsevier Ltd

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6
DNA photocleavage and biological activity of a pyrene dihydrodioxin
DNA photocleavage and biological activity of a pyrene dihydrodioxin
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DNA photocleavage and biological activity of a pyrene dihydrodioxin

Mack, Eric T. ; Birzniece, Dagne ; Veach, Darren R. ; Coyle, William ; Wilson, R. Marshall

Bioorganic & medicinal chemistry letters, 2005-04, Vol.15 (8), p.2173-2176 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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7
Structural insights of SmKDAC8 inhibitors: Targeting Schistosoma epigenetics through a combined structure-based 3D QSAR, in vitro and synthesis strategy
Structural insights of SmKDAC8 inhibitors: Targeting Schistosoma epigenetics through a combined structure-based 3D QSAR, in vitro and synthesis strategy
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Structural insights of SmKDAC8 inhibitors: Targeting Schistosoma epigenetics through a combined structure-based 3D QSAR, in vitro and synthesis strategy

Ballante, Flavio ; Reddy, D. Rajasekhar ; Zhou, Nancy J. ; Marshall, Garland R.

Bioorganic & medicinal chemistry, 2017-04, Vol.25 (7), p.2105-2132 [Periódico revisado por pares]

England: Elsevier Ltd

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8
Discovery of 4-amino-5,6-biaryl-furo[2,3- d]pyrimidines as inhibitors of Lck: Development of an expedient and divergent synthetic route and preliminary SAR
Discovery of 4-amino-5,6-biaryl-furo[2,3- d]pyrimidines as inhibitors of Lck: Development of an expedient and divergent synthetic route and preliminary SAR
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Discovery of 4-amino-5,6-biaryl-furo[2,3- d]pyrimidines as inhibitors of Lck: Development of an expedient and divergent synthetic route and preliminary SAR

DiMauro, Erin F. ; Newcomb, John ; Nunes, Joseph J. ; Bemis, Jean E. ; Boucher, Christina ; Buchanan, John L. ; Buckner, William H. ; Cheng, Alan ; Faust, Theodore ; Hsieh, Faye ; Huang, Xin ; Lee, Josie H. ; Marshall, Teresa L. ; Martin, Matthew W. ; McGowan, David C. ; Schneider, Stephen ; Turci, Susan M. ; White, Ryan D. ; Zhu, Xiaotian

Bioorganic & medicinal chemistry letters, 2007-04, Vol.17 (8), p.2305-2309 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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9
Design, synthesis, X-ray studies, and biological evaluation of novel macrocyclic HIV-1 protease inhibitors involving the P1′-P2′ ligands
Design, synthesis, X-ray studies, and biological evaluation of novel macrocyclic HIV-1 protease inhibitors involving the P1′-P2′ ligands
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Design, synthesis, X-ray studies, and biological evaluation of novel macrocyclic HIV-1 protease inhibitors involving the P1′-P2′ ligands

Ghosh, Arun K. ; Sean Fyvie, W. ; Brindisi, Margherita ; Steffey, Melinda ; Agniswamy, Johnson ; Wang, Yuan-Fang ; Aoki, Manabu ; Amano, Masayuki ; Weber, Irene T. ; Mitsuya, Hiroaki

Bioorganic & medicinal chemistry letters, 2017-11, Vol.27 (21), p.4925-4931 [Periódico revisado por pares]

England: Elsevier Ltd

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10
Potent and selective inhibitors of Helicobacter pylori glutamate racemase (MurI): Pyridodiazepine amines
Potent and selective inhibitors of Helicobacter pylori glutamate racemase (MurI): Pyridodiazepine amines
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Potent and selective inhibitors of Helicobacter pylori glutamate racemase (MurI): Pyridodiazepine amines

Geng, Bolin ; Basarab, Gregory ; Comita-Prevoir, Janelle ; Gowravaram, Madhusudhan ; Hill, Pamela ; Kiely, Andrew ; Loch, James ; MacPherson, Lawrence ; Morningstar, Marshall ; Mullen, George ; Osimboni, Ekundayo ; Satz, Alexander ; Eyermann, Charles ; Lundqvist, Tomas

Bioorganic & medicinal chemistry letters, 2009-02, Vol.19 (3), p.930-936 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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