Cywin, Charles L.
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5

Substituted 2H-isoquinolin-1-one as potent Rho-Kinase inhib..:

Wu, Frank ; Büttner, Frank H. ; Chen, Rhonda...
Bioorganic & Medicinal Chemistry Letters.  20 (2010)  11 - p. 3235-3239 , 2010
 
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6

Rapid synthesis of an array of trisubstituted urea-based so..:

Kowalski, Jennifer A. ; Swinamer, Alan D. ; Muegge, Ingo...
Bioorganic & Medicinal Chemistry Letters.  20 (2010)  12 - p. 3703-3707 , 2010
 
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7

Substituted 2H-isoquinolin-1-ones as potent Rho-kinase inhi..:

Ginn, John D. ; Bosanac, Todd ; Chen, Rhonda...
Bioorganic & Medicinal Chemistry Letters.  20 (2010)  17 - p. 5153-5156 , 2010
 
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9

The discovery of thienopyridine analogues as potent IκB kin..:

Wu, Jiang-Ping ; Fleck, Roman ; Brickwood, Janice...
Bioorganic & Medicinal Chemistry Letters.  19 (2009)  19 - p. 5547-5551 , 2009
 
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10

Hit to Lead Account of the Discovery of a New Class of Inhi..:

Qian, Kevin ; Wang, Lian ; Cywin, Charles L....
Journal of Medicinal Chemistry.  52 (2009)  7 - p. 1814-1827 , 2009
 
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11

5-Aminomethyl-1H-benzimidazoles as orally active inhibitors..:

Winters, Michael P. ; Robinson, Darius J. ; Khine, Hnin Hnin...
Bioorganic & Medicinal Chemistry Letters.  18 (2008)  20 - p. 5541-5544 , 2008
 
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12

Discovery of potent and selective PKC-θ inhibitors:

Cywin, Charles L. ; Dahmann, Georg ; Prokopowicz III, Anthony S....
Bioorganic & Medicinal Chemistry Letters.  17 (2007)  1 - p. 225-230 , 2007
 
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13

Hit-to-lead studies on benzimidazole inhibitors of ITK: Dis..:

Snow, Roger J. ; Abeywardane, Asitha ; Campbell, Scot...
Bioorganic & Medicinal Chemistry Letters.  17 (2007)  13 - p. 3660-3665 , 2007
 
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14

Evolution of the Thienopyridine Class of Inhibitors of IκB ..:

Morwick, Tina ; Berry, Angela ; Brickwood, Janice...
Journal of Medicinal Chemistry.  49 (2006)  10 - p. 2898-2908 , 2006
 
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15

An orally active reversible inhibitor of cathepsin S inhibi..:

Desai, Sudha N. ; White, Della M. ; O'Shea, Kathryn M....
European Journal of Pharmacology.  538 (2006)  1-3 - p. 168-174 , 2006
 
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