Richard L. Apodaca - Concepedia

Author

Richard L. Apodaca

Johnson & Johnson (United States)ORCID

Also Known As

Apodaca, R., R Apodaca, R. APODACA, R. Apodaca, Rich Apodaca, Richard Apodaca, Richard L. Apodaca

1.6K

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

Johnson & Johnson (United States)Janssen (United States)The University of Texas at Austin

About

Richard L. Apodaca is an author at Johnson & Johnson (United States) specializing in drug discovery, medicine, and pharmacology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	14	716
2	Biochemistry	12	12	676
3	Natural Sciences	6	6	252
4	Engineering	2	2	175
5	Allergy	1	1	27

Richard L. Apodaca

Publications

Citations

H-Index

Page 1

	Year	Citations
Direct Reductive Amination of Aldehydes and Ketones Using Phenylsilane: Catalysis by Dibutyltin Dichloride Richard L. Apodaca, Wei Xiao Organic Letters EngineeringKetones Using PhenylsilaneOrganic ChemistryDirect Reductive AminationCatalysis	2001	162
Acute wake‐promoting actions of JNJ‐5207852, a novel, diamine‐based H<sub>3</sub> antagonist Ann Barbier, Craig W. Berridge, Christine Dugovic, British Journal of Pharmacology Molecular PharmacologyMolecular PhysiologyPharmacological StudyBiochemistryH3 Receptor Antagonist	2004	141
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
Thiadiazolopiperazinyl ureas as inhibitors of fatty acid amide hydrolase John M. Keith, Richard L. Apodaca, Wei Xiao, Bioorganic & Medicinal Chemistry Letters BiochemistryMedicineDrug DevelopmentPharmacologyInhibitory Activity	2008	91
Biochemical and Biological Properties of 4-(3-phenyl-[1,2,4] thiadiazol-5-yl)-piperazine-1-carboxylic acid phenylamide, a Mechanism-Based Inhibitor of Fatty Acid Amide Hydrolase Mark J. Karbarz, Lin Luo, Leon Chang, Anesthesia & Analgesia Lipid SynthesisBiochemistrySelective Faah InhibitorMedicine-Piperazine-1-carboxylic Acid Phenylamide	2008	74
Potent and Selective α-Ketoheterocycle-Based Inhibitors of the Anandamide and Oleamide Catabolizing Enzyme, Fatty Acid Amide Hydrolase F. Anthony Romero, Wu Du, Inkyu Hwang, Journal of Medicinal Chemistry	2007	74
4-Phenoxypiperidines: Potent, Conformationally Restricted, Non-Imidazole Histamine H<sub>3</sub> Antagonists Curt A. Dvorak, Richard L. Apodaca, Ann Barbier, Journal of Medicinal Chemistry Molecular PharmacologyMedicinal ChemistryBiochemistryFunctional SelectivityMedicine	2005	64
Lead identification of acetylcholinesterase inhibitors–histamine H3 receptor antagonists from molecular modeling Scott D. Bembenek, John M. Keith, Michael A. Letavic, Bioorganic & Medicinal Chemistry Molecular PharmacologyDrug TargetBiochemistryMedicineRational Drug Design	2007	56
Trimethylsilylcyanation of aldehydes and ketones catalyzed by diorganotin dichlorides James K. Whitesell, Richard L. Apodaca Tetrahedron Letters Asymmetric CatalysisDiorganotin DichloridesEnantioselective SynthesisChemistry	1996	53
Aryl Piperazinyl Ureas as Inhibitors of Fatty Acid Amide Hydrolase (FAAH) in Rat, Dog, and Primate John M. Keith, Richard L. Apodaca, Mark S. Tichenor, ACS Medicinal Chemistry Letters BiochemistryOmega-3 Fatty AcidMedicinePhysiologyFatty Acid Ethanolamides	2012	41

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