Search Results - "Boggs, Jason W."

Discovery of Selective 4‑Amino-pyridopyrimidine Inhibitors of MAP4K4 Using Fragment-Based Lead Identification and Optimization

Crawford, Terry D., Ndubaku, Chudi O., Chen, Huifen, Boggs, Jason W., Bravo, Brandon J., DeLaTorre, Kelly, Giannetti, Anthony M., Gould, Stephen E., Harris, Seth F., Magnuson, Steven R., McNamara, Erin, Murray, Lesley J., Nonomiya, Jim, Sambrone, Amy, Schmidt, Stephen, Smyczek, Tanya, Stanley, Mark, Vitorino, Philip, Wang, Lan, West, Kristina, Wu, Ping, Ye, Weilan

Assessment of the Hepatic CYP Reductase Null Mouse Model and Its Potential Application in Drug Discovery

Boggs, Jason W.^aff1d1, Hop, Cornelis E. C. A.^aff1d1, McNamara, Erin^aff1d2, Deng, Yuzhong^aff1d1, Messick, Kirsten^aff1d3, West, Kristina^aff1d2, Choo, Edna F.^aff1d1

Potent and Selective Aminopyrimidine-Based B-Raf Inhibitors with Favorable Physicochemical and Pharmacokinetic Properties

Mathieu, Simon^aff1, Gradl, Stefan N.^aff1, Ren, Li^aff2, Wen, Zhaoyang^aff1, Aliagas, Ignacio^aff1, Gunzner-Toste, Janet^aff1, Lee, Wendy^aff1, Pulk, Rebecca^aff1, Zhao, Guiling^aff1, Alicke, Bruno^aff1, Boggs, Jason W.^aff1, Buckmelter, Alex J.^aff2, Choo, Edna F.^aff1, Dinkel, Victoria^aff2, Gloor, Susan L.^aff2, Gould, Stephen E.^aff1, Hansen, Joshua D.^aff2, Hastings, Gregg^aff2, Hatzivassiliou, Georgia^aff1, Laird, Ellen R.^aff2, Moreno, David^aff2, Ran, Yingqing^aff1, Voegtli, Walter C.^aff2, Wenglowsky, Steve^aff2, Grina, Jonas^aff2, Rudolph, Joachim^aff1

Structure-Based Design of GNE-495, a Potent and Selective MAP4K4 Inhibitor with Efficacy in Retinal Angiogenesis

Ndubaku, Chudi O.^aff1, Crawford, Terry D.^aff1, Chen, Huifen^aff1, Boggs, Jason W.^aff1, Drobnick, Joy^aff1, Harris, Seth F.^aff1, Jesudason, Rajiv^aff1, McNamara, Erin^aff1, Nonomiya, Jim^aff1, Sambrone, Amy^aff1, Schmidt, Stephen^aff1, Smyczek, Tanya^aff1, Vitorino, Philip^aff1, Wang, Lan^aff1, Wu, Ping^aff1, Yeung, Stacey^aff1, Chen, Jinhua^aff2, Chen, Kevin^aff2, Ding, Charles Z.^aff2, Wang, Tao^aff2, Xu, Zijin^aff2, Gould, Stephen E.^aff1, Murray, Lesley J.^aff1, Ye, Weilan^aff1

Fragment-based identification and optimization of a class of potent pyrrolo[2,1-f][1,2,4]triazine MAP4K4 inhibitors

Wang, Lan, Stanley, Mark, Boggs, Jason W., Crawford, Terry D., Bravo, Brandon J., Giannetti, Anthony M., Harris, Seth F., Magnuson, Steven R., Nonomiya, Jim, Schmidt, Stephen, Wu, Ping, Ye, Weilan, Gould, Stephen E., Murray, Lesley J., Ndubaku, Chudi O., Chen, Huifen

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Discovery of Selective 4-Amino-pyridopyrimidineInhibitors of MAP4K4 Using Fragment-Based Lead Identification andOptimization.

Crawford, Terry D.¹, Ndubaku, Chudi O.¹, Chen, Huifen¹, Boggs, Jason W.¹, Bravo, Brandon J.¹, De La Torre, Kelly¹, Giannetti, Anthony M.¹, Gould, Stephen E.¹, Harris, Seth F.¹, Magnuson, Steven R.¹, McNamara, Erin¹, Murray, Lesley J.¹, Nonomiya, Jim¹, Sambrone, Amy¹, Schmidt, Stephen¹, Smyczek, Tanya¹, Stanley, Mark¹, Vitorino, Philip¹, Wang, Lan¹, West, Kristina¹

Potent and Selective Aminopyrimidine-BasedB-Raf Inhibitorswith Favorable Physicochemical and Pharmacokinetic Properties.

Mathieu, Simon¹, Gradl, Stefan N.¹, Ren, Li¹, Wen, Zhaoyang¹, Aliagas, Ignacio¹, Gunzner-Toste, Janet¹, Lee, Wendy¹, Pulk, Rebecca¹, Zhao, Guiling¹, Alicke, Bruno¹, Boggs, Jason W.¹, Buckmelter, Alex J.¹, Choo, Edna F.¹, Dinkel, Victoria¹, Gloor, Susan L.¹, Gould, Stephen E.¹, Hansen, Joshua D.¹, Hastings, Gregg¹, Hatzivassiliou, Georgia¹, Laird, Ellen R.¹

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