Curt A. Dvorak - Concepedia

Author

Curt A. Dvorak

Johnson & Johnson (United States)ORCID

Also Known As

C. A. DVORAK, Curt A Dvorak, Curt A. Dvorak, Curt Dvorak, Curt A. Dvorak, Dvorak, Curt A.

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Johnson & Johnson (United States)Janssen (United States)Colorado State University Janssen (Belgium)

About

Curt A. Dvorak is an author at Johnson & Johnson (United States) specializing in pharmacology, medicine, and drug discovery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	16	925
2	Natural Sciences	9	9	626
3	Engineering	4	4	118
4	Health Sciences	2	2	67
5	Allergy	2	2	135

Curt A. Dvorak

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
Blockade of Orexin-1 Receptors Attenuates Orexin-2 Receptor Antagonism-Induced Sleep Promotion in the Rat Christine Dugovic, Jonathan Shelton, Leah Aluisio, Journal of Pharmacology and Experimental Therapeutics	2009	228
The First Potent and Selective Non-Imidazole Human Histamine H<sub>4</sub>Receptor Antagonists Jill A. Jablonowski, Cheryl A. Grice, Wenying Chai, Journal of Medicinal Chemistry Pharmaceutical ScienceDrug TargetPotential LeadPharmacotherapyChemical Biology	2003	195
The Synthesis of Streptogramin Antibiotics: (−)‐Griseoviridin and Its C‐8 Epimer Curt A. Dvorak, William D. Schmitz, Daniel J. Poon, Angewandte Chemie International Edition	2000	134
A New Class of Diamine-Based Human Histamine H<sub>3</sub> Receptor Antagonists: 4-(Aminoalkoxy)benzylamines Richard L. Apodaca, Curt A. Dvorak, Wei Xiao, Journal of Medicinal Chemistry Molecular PharmacologyMedicinal ChemistryPotent Human HBiochemistryFunctional Selectivity	2003	118
Preparation and Biological Evaluation of Indole, Benzimidazole, and Thienopyrrole Piperazine Carboxamides: Potent Human Histamine H<sub>4</sub>Antagonists Jennifer D. Venable, Hui Cai, Wenying Chai, Journal of Medicinal Chemistry Pharmaceutical SciencePharmacotherapyChemical BiologyPharmaceutical ChemistryMedicinal Chemistry	2005	107
Translational Evaluation of JNJ-18038683, a 5-Hydroxytryptamine Type 7 Receptor Antagonist, on Rapid Eye Movement Sleep and in Major Depressive Disorder Pascal Bonaventure, Christine Dugovic, Michelle Kramer, Journal of Pharmacology and Experimental Therapeutics	2012	83
Novel substituted 4-phenyl-[1,3]dioxanes: potent and selective orexin receptor 2 (OX2R) antagonists Laura C. McAtee, Steven W. Sutton, Dale A. Rudolph, Bioorganic & Medicinal Chemistry Letters Molecular PharmacologyBiochemistryFunctional SelectivityMedicineMechanism Of Action	2004	78
A Dipolar Cycloaddition Reaction To Access 6-Methyl-4,5,6,7-tetrahydro-1<i>H</i>-[1,2,3]triazolo[4,5-<i>c</i>]pyridines Enables the Discovery Synthesis and Preclinical Profiling of a P2X7 Antagonist Clinical Candidate Christa C. Chrovian, Akinola Soyode-Johnson, Alexander A. Peterson, Journal of Medicinal Chemistry	2017	73
GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids l-Tryptophan and l-Phenylalanine Changlu Liu, Pascal Bonaventure, Grace Lee, Molecular Pharmacology	2015	72
Catalysis of benzoin condensation by conformationally-restricted chiral bicyclic thiazolium salts Curt A. Dvorak, Viresh H. Rawal Tetrahedron Letters Chemical EngineeringEngineeringHeterocyclicOrganic ChemistryBenzoin Condensation	1998	70

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