Author

Erick R. R. Young

Observed names: E. R. R. Young, E.R.R. Young, ERICK R. R. YOUNG, Erick R. Young, Erick R.R. Young, Erick Young, Erick R. R. Young

Institution: Boehringer Ingelheim (United States)

Observed institutions: Pennsylvania State University, Boehringer Ingelheim (United States), The Ohio State University, Colorado State University

OpenAlex ID: A5113876597

Novel cross-talk within the IKK family controls innate immunity

2011 · Kristopher Clark, Mark Peggie, et al. · Biochemical Journal · 326

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Photochemical Cycloaromatization Reactions ofortho-Dialkynylarenes: A New Class of DNA Photocleaving Agents

1996 · Raymond L. Funk, Erick R. R. Young, et al. · Journal of the American Chemical Society · 80

Discovery of potent and selective PKC-θ inhibitors

2006 · Charles L. Cywin, Georg Dahmann, et al. · Bioorganic & Medicinal Chemistry Letters · 71

Temporal Regulation of the Bacterial Metabolite Deoxycholate during Colonic Repair Is Critical for Crypt Regeneration

2018 · Umang Jain, Chin-Wen Lai, et al. · Cell Host & Microbe · 68

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Substituted 2H-isoquinolin-1-ones as potent Rho-kinase inhibitors: Part 3, aryl substituted pyrrolidines

2010 · Todd Bosanac, Eugene R. Hickey, et al. · Bioorganic & Medicinal Chemistry Letters · 50

Essential Role for IKKβ in Production of Type 1 Interferons by Plasmacytoid Dendritic Cells

2012 · Eduardo Pauls, Natalia Shpiro, et al. · Journal of Biological Chemistry · 43

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A Practical Synthesis of Pyrene-4,5-dione

1998 · Erick R. R. Young, Raymond L. Funk · The Journal of Organic Chemistry · 30

Vinyl and Alkynyl Pyrimidines as Michael Acceptors: An Approach to a Cylindrospermopsin Substructure

2000 · Jane F. Djung, David J. Hart, et al. · The Journal of Organic Chemistry · 29

Substituted 2H-isoquinolin-1-ones as potent Rho-kinase inhibitors: Part 2, optimization for blood pressure reduction in spontaneously hypertensive rats

2010 · John D. Ginn, Todd Bosanac, et al. · Bioorganic & Medicinal Chemistry Letters · 23

BI 5700, a Selective Chemical Inhibitor of I B Kinase 2, Specifically Suppresses Epithelial-Mesenchymal Transition and Metastasis in Mouse Models of Tumor Progression

2010 · M. A. Huber, H. J. Maier, et al. · Genes & Cancer · 20

Substituted 2H-isoquinolin-1-one as potent Rho-Kinase inhibitors. Part 1: Hit-to-lead account

2010 · Frank Wu, Frank H. Büttner, et al. · Bioorganic & Medicinal Chemistry Letters · 19

Hit to Lead Account of the Discovery of Bisbenzamide and Related Ureidobenzamide Inhibitors of Rho Kinase

2009 · Tina Morwick, Frank H. Büttner, et al. · Journal of Medicinal Chemistry · 16

Identification of a novel class of succinyl-nitrile-based Cathepsin S inhibitors

2007 · Younes Bekkali, David S. Thomson, et al. · Bioorganic & Medicinal Chemistry Letters · 12

Exploration of cathepsin S inhibitors characterized by a triazole P1–P2 amide replacement

2012 · Neil Moss, Zhaoming Xiong, et al. · Bioorganic & Medicinal Chemistry Letters · 11

IKKβ as a Therapeutic Intervention Point for Diseases Related to Inflammation

2012 · ERICK R. R. YOUNG · Royal Society of Chemistry eBooks · 8

Cathepsin S complexed with Compound 15

2007 · Y.D. Ward, M.J. Emmanuel, et al. · Worldwide Protein Data Bank

ChemInform Abstract: Vinyl and Alkynyl Pyrimidines as Michael Acceptors: An Approach to a Cylindrospermopsin Substructure.

2000 · Jane F. Djung, David J. Hart, et al. · ChemInform

ChemInform Abstract: A Practical Synthesis of Pyrene‐4,5‐dione.

1999 · Erick R. R. Young, Raymond L. Funk · ChemInform

縮合タンニンの合成 Xix (+)-カテキン及び(+)-メスキトールのフェノール酸化的カップリング反応ビス-(+)-カテキンの立体配座

1987 · D A Young, Erick R. R. Young, et al. · Journal of the Chemical Society Perkin Transactions 1

Works count: 19

Citation count: 806

H-index: 12

I10-index: 14