Duane E. DeMong - Concepedia

Author

Duane E. DeMong

Colorado State University ORCID

Also Known As

Duane DeMong, Duane E DeMong, Duane E. DeMong, Duane E. Demong*

Publications

Citations

H-Index

Concepts

All Affiliations

Colorado State University Merck & Co., Inc., Rahway, NJ, USA (United States)Johnson & Johnson (United States)United States Military Academy

About

Duane E. DeMong is an author at Colorado State University specializing in drug discovery, pharmacology, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	217
2	Natural Sciences	5	5	139
3	Biochemistry	5	5	133
4	Engineering	2	2	65
5	Biomolecular Engineering	2	2	65

Duane E. DeMong

Publications

978

Citations

H-Index

Page 1

	Year	Citations
MLi-2, a Potent, Selective, and Centrally Active Compound for Exploring the Therapeutic Potential and Safety of LRRK2 Kinase Inhibition Matthew Fell, Christian Mirescu, Kallol Basu, Journal of Pharmacology and Experimental Therapeutics	2015	326
A Novel Carbohydrate-Glycosphingolipid Interaction between a β-(1–3)-Glucan Immunomodulator, PGG-glucan, and Lactosylceramide of Human Leukocytes Janet W. Zimmerman, Johanna Lindermuth, Pamela A. Fish, Journal of Biological Chemistry	1998	221
Discovery of a 3-(4-Pyrimidinyl) Indazole (MLi-2), an Orally Available and Selective Leucine-Rich Repeat Kinase 2 (LRRK2) Inhibitor that Reduces Brain Kinase Activity Jack D. Scott, Duane E. DeMong, Thomas J. Greshock, Journal of Medicinal Chemistry Drug TargetPharmacotherapyMedicinal ChemistryBrain Kinase ActivityLrrk2 Inhibitors	2017	140
Asymmetric Synthesis of (2<i>S</i>,3<i>R</i>)-Capreomycidine and the Total Synthesis of Capreomycin IB Duane E. DeMong, Robert M. Williams Journal of the American Chemical Society	2003	71
A chemoenzymatic strategy for site-selective functionalization of native peptides and proteins Anna Fryszkowska, Chihui An, Oscar Alvizo, Science EngineeringBiochemistryProtein FoldingHigh Site SelectivityPenicillin G	2022	53
The asymmetric synthesis of (2 S ,3 R )-capreomycidine Duane E. DeMong, Robert M. Williams Tetrahedron Letters Bioorganic ChemistryBiochemistryNatural SciencesAsymmetric SynthesisStereoselective Synthesis	2001	33
Synthesis, Structure−Activity Relationship and in Vivo Antiinflammatory Efficacy of Substituted Dipiperidines as CCR2 Antagonists Mingde Xia, Cuifen Hou, Duane E. DeMong, Journal of Medicinal Chemistry Pharmaceutical SciencePharmacotherapyChemistryChemical BiologyPharmaceutical Chemistry	2007	25
Discovery and Optimization of Potent, Selective, and Brain-Penetrant 1-Heteroaryl-1 <i>H</i> -Indazole LRRK2 Kinase Inhibitors for the Treatment of Parkinson’s Disease David A. Candito, Vladimir Simov, Anmol Gulati, Journal of Medicinal Chemistry	2022	19
Synthesis and structure–activity relationship of 7-azaindole piperidine derivatives as CCR2 antagonists Mingde Xia, Cuifen Hou, Duane E. DeMong, Bioorganic & Medicinal Chemistry Letters Structure–activity RelationshipMolecular PharmacologyMedicinal ChemistryDerivativesMedicine	2008	16
An efficient asymmetric synthesis of (2S,3S)- and (2R,3R)-β-hydroxyornithine Duane E. DeMong, Robert M. Williams Tetrahedron Letters Organic ChemistryChemistryEfficient Asymmetric SynthesisNatural Product SynthesisAsymmetric Catalysis	2001	16

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