List of works - Richard L. Apodaca

1-Aryl-2-((6-aryl)pyrimidin-4-yl)amino)ethanols as competitive inhibitors of fatty acid amide hydrolase

scientific article published on 31 January 2014

4-phenoxypiperidines: potent, conformationally restricted, non-imidazole histamine H3 antagonists

scientific article

A convenient synthesis of protected and free homoallylic alcohols: Catalytic use of dibutyltin dichloride in the allylation of aldehydes with allyltributyltin

A new class of diamine-based human histamine H3 receptor antagonists: 4-(aminoalkoxy)benzylamines

scientific article published in August 2003

Acute wake-promoting actions of JNJ-5207852, a novel, diamine-based H3 antagonist

scientific article

Aplysamine-1 and related analogs as histamine H3 receptor antagonists

scientific article

Aryl Piperazinyl Ureas as Inhibitors of Fatty Acid Amide Hydrolase (FAAH) in Rat, Dog, and Primate

scientific article

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

scientific article

Comphrehensive Organic Functional Group Transformations, Volumes 1−7 Edited by Alan R. Katritzky, Otto Meth-Cohn, and Charles W. Rees. Elsevier: Amsterdam. 1996. 7500+ pp. $6846.00. ISBN 0-08-040604-1

article

Corrigendum to acute wake-promoting actions of JNJ-5207852, a novel, diamine-based H3 antagonist.

scientific article

Diamine-based human histamine H3 receptor antagonists: (4-aminobutyn-1-yl)benzylamines

scientific article

Direct Reductive Amination of Aldehydes and Ketones Using Phenylsilane: Catalysis by Dibutyltin Dichloride

scientific article published on 01 May 2001

Heterocyclic replacement of the central phenyl core of diamine-based histamine H3 receptor antagonists

scientific article

Lead identification of acetylcholinesterase inhibitors-histamine H3 receptor antagonists from molecular modeling

scientific article

Mobile apps for chemistry in the world of drug discovery

scientific article published on 06 September 2011

Novel benzamide-based histamine h3 receptor antagonists: the identification of two candidates for clinical development

scientific article published on 13 March 2015

Novel ketooxazole based inhibitors of fatty acid amide hydrolase (FAAH).

scientific article

Potent and selective alpha-ketoheterocycle-based inhibitors of the anandamide and oleamide catabolizing enzyme, fatty acid amide hydrolase

scientific article published on 6 February 2007

Studies in enantioselective catalysis : (1) a new class of chiral C₂-symmetric bisphenols ; (2) Diorganotin

PhD thesis from 1996

Synthesis and resolution of a new chiral C2-symmetric bisphenol: trans-1,2-bis(2-hydroxyphenyl)cyclopentane

The SAR of brain penetration for a series of heteroaryl urea FAAH inhibitors

scientific article

Thiadiazolopiperazinyl ureas as inhibitors of fatty acid amide hydrolase

scientific article published on 25 July 2008

List of works by Richard L. Apodaca

1-Aryl-2-((6-aryl)pyrimidin-4-yl)amino)ethanols as competitive inhibitors of fatty acid amide hydrolase

4-phenoxypiperidines: potent, conformationally restricted, non-imidazole histamine H3 antagonists

A convenient synthesis of protected and free homoallylic alcohols: Catalytic use of dibutyltin dichloride in the allylation of aldehydes with allyltributyltin

A new class of diamine-based human histamine H3 receptor antagonists: 4-(aminoalkoxy)benzylamines

Acute wake-promoting actions of JNJ-5207852, a novel, diamine-based H3 antagonist

Aplysamine-1 and related analogs as histamine H3 receptor antagonists

Aryl Piperazinyl Ureas as Inhibitors of Fatty Acid Amide Hydrolase (FAAH) in Rat, Dog, and Primate

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

Comphrehensive Organic Functional Group Transformations, Volumes 1−7 Edited by Alan R. Katritzky, Otto Meth-Cohn, and Charles W. Rees. Elsevier: Amsterdam. 1996. 7500+ pp. $6846.00. ISBN 0-08-040604-1

Corrigendum to acute wake-promoting actions of JNJ-5207852, a novel, diamine-based H3 antagonist.

Diamine-based human histamine H3 receptor antagonists: (4-aminobutyn-1-yl)benzylamines

Direct Reductive Amination of Aldehydes and Ketones Using Phenylsilane: Catalysis by Dibutyltin Dichloride

Heterocyclic replacement of the central phenyl core of diamine-based histamine H3 receptor antagonists

Lead identification of acetylcholinesterase inhibitors-histamine H3 receptor antagonists from molecular modeling

Mobile apps for chemistry in the world of drug discovery

Novel benzamide-based histamine h3 receptor antagonists: the identification of two candidates for clinical development

Novel ketooxazole based inhibitors of fatty acid amide hydrolase (FAAH).

Potent and selective alpha-ketoheterocycle-based inhibitors of the anandamide and oleamide catabolizing enzyme, fatty acid amide hydrolase

Studies in enantioselective catalysis : (1) a new class of chiral C₂-symmetric bisphenols ; (2) Diorganotin

Synthesis and resolution of a new chiral C2-symmetric bisphenol: trans-1,2-bis(2-hydroxyphenyl)cyclopentane

The SAR of brain penetration for a series of heteroaryl urea FAAH inhibitors

Thiadiazolopiperazinyl ureas as inhibitors of fatty acid amide hydrolase

Trimethylsilylcyanation of aldehydes and ketones catalyzed by diorganotin dichlorides