Bradley Condon - Lilly Biotechnol Ctr

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论文共 11 篇作者统计合作学者相似作者

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Structure-based, Multi-Targeted Drug Discovery Approach to Eicosanoid Inhibition: Dual Inhibitors of Mpges-1 and 5-Lipoxygenase Activating Protein (FLAP)

Joseph D. Ho,Matthew R. Lee,Charles T. Rauch, Kristen Aznavour, Jonathan S. Park,John G. Luz,Stephen Antonysamy,Bradley Condon,Milan Maletic,Aiping Zhang,Michael J. Hickey,Norman E. Hughes,Srinivasan Chandrasekhar,Ashley Sloan, Karen Gooding,Anita Harvey,Xiao-Peng Yu,Steven D. Kahl,Bryan H. Norman

Biochimica et Biophysica Acta (BBA) - General Subjects（2020）

引用14浏览0WOS引用

Discovery of Chiral Dihydropyridopyrimidinones As Potent, Selective and Orally Bioavailable Inhibitors of AKT

Saravanan Parthasarathy,Kenneth Henry,Huaxing Pei,Josh Clayton,Mark Rempala, Deidre Johns,Oscar De Frutos, Pablo Garcia,Carlos Mateos,Sehila Pleite,Yong Wang,Stephanie Stout,Bradley Condon,Sheela Ashok, Zhohai Lu, William Ehlhardt, Tom Raub,Mei Lai,Sandaruwan Geeganage,Timothy P. Burkholder

Bioorganic & Medicinal Chemistry Letters（2018）

引用10浏览0WOS引用

Crystal Structures of Mpges-1 Inhibitor Complexes Form a Basis for the Rational Design of Potent Analgesic and Anti-Inflammatory Therapeutics

John Gately Luz,Stephen Antonysamy,Steven L. Kuklish,Bradley Condon,Matthew R. Lee,Dagart Allison,Xiao-Peng Yu,Srinivasan Chandrasekhar,Ryan Backer,Aiping Zhang,Marijane Russell,Shawn S. Chang,Anita Harvey,Ashley V. Sloan,Matthew J. Fisher

openalex（2017）

引用60浏览0WOS引用

(1S,2R,3S,4S,5R,6R)‐2‐アミノ‐3‐[(3,4‐ジフルオロフェニル)スルファニルメチル]‐4‐ヒドロキシ‐ビシクロ[3.1.0]ヘキサン‐2,6‐ジカルボン酸塩酸塩(LY3020371HCl)の発見: 抗鬱様活性を持つ強力な向代謝性グルタミン酸2/3受容体アンタゴニスト

Journal of Medicinal Chemistryno. 24 (2016): 10993

引用0浏览0引用

Discovery of (1S,2r,3s,4s,5r,6r)-2-amino-3-[(3,4-difluorophenyl)sulfanylmethyl]-4-hydroxy-bicyclo[3.1.0]hexane-2,6-dicarboxylic Acid Hydrochloride (ly3020371·hcl): A Potent, Metabotropic Glutamate 2/3 Receptor Antagonist with Antidepressant-Like Activity

Journal of Medicinal Chemistry（2016）

引用30浏览0WOS引用

Correction to the 2.5 Å Crystal Structure of the SIRT1 Catalytic Domain Bound to Nicotinamide Adenine Dinucleotide (NAD+) and an Indole (EX527 Analogue) Reveals a Novel Mechanism of Histone Deacetylase Inhibition

Xun Zhao,Dagart Allison,Bradley Condon,Feiyu Zhang,Tarun Gheyi,Aiping Zhang,Sheela Ashok,Marijane Russell,Iain MacEwan,Yuewei Qian,James A. Jamison,John Gately Luz

Journal of medicinal chemistry（2016）

引用164浏览0WOS引用

164

The 2.5 Angstrom Crystal Structure Of The Sirt1 Catalytic Domain Bound To Nicotinamide Adenine Dinucleotide (Nad(+)) And An Indole (Ex527 Analogue) Reveals A Novel Mechanism Of Histone Deacetylase Inhibition (Vol 56, Pg 963, 2013)

Xun Zhao,Dagart Allison,Bradley Condon,Feiyu Zhang,Tarun Gheyi,Aiping Zhang,Sheela Ashok,Marijane Russell, Lain Macewan,Yuewei Qian,James A. Jamison,John Gately Luz

JOURNAL OF MEDICINAL CHEMISTRY（2016）

引用3浏览0引用

2‐アシルアミノイミダゾールミクロソームプロスタグランジンE合成酵素‐1阻害剤の発見と特徴分析

Journal of Medicinal Chemistryno. 1 (2016): 205

引用0浏览0引用

Indole Glucocorticoid Receptor Antagonists Active in a Model of Dyslipidemia Act Via a Unique Association with an Agonist Binding Site

John G. Luz, Matthew W. Carson,Bradley Condon,David Clawson,Anna Pustilnik, Daniel T. Kohlman,Robert J. Barr,James S. Bean,M. Joelle Dill,Dana K. Sindelar,Milan Maletic,Michael J. Coghlan

Journal of Medicinal Chemistry（2015）

引用30浏览0WOS引用

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