Chafiq Hamdouchi - Concepedia

Author

Chafiq Hamdouchi

Eli Lilly (United States)ORCID

Also Known As

C. HAMDOUCHI, C. Hamdouchi, Chafiq Hamdouchi

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

Eli Lilly (United States)Eli Lilly (Spain)Universidad Autónoma de Madrid Jubilant Life Sciences (India)École Pratique des Hautes Études

About

Chafiq Hamdouchi is an author at Eli Lilly (United States) specializing in organic chemistry, chemistry, and pharmacology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	10	11	263
2	Natural Sciences	10	11	344
3	Medicine	9	9	584
4	Health Sciences	1	1	21
5	Social Sciences	1	1	242

Chafiq Hamdouchi

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
2-Amino-3-substituted-6-[(<i>E</i>)-1-phenyl-2-(<i>N</i>-methylcarbamoyl)vinyl]imidazo[1,2-<i>a</i>]pyridines as a Novel Class of Inhibitors of Human Rhinovirus: Stereospecific Synthesis and Antiviral Activity Chafiq Hamdouchi, Jesús de Blas, Mirian del Prado, Journal of Medicinal Chemistry	1998	276
3-(4-Chloro-2-Morpholin-4-yl-Thiazol-5-yl)-8-(1-Ethylpropyl)-2,6-Dimethyl-Imidazo[1,2-<i>b</i>]Pyridazine: A Novel Brain-Penetrant, Orally Available Corticotropin-Releasing Factor Receptor 1 Antagonist with Efficacy in Animal Models of Alcoholism Donald R. Gehlert, Andrea Cippitelli, Annika Thorsell, Journal of Neuroscience PsychopharmacologyPharmacotherapyExperimental PharmacologySocial SciencesMolecular Pharmacology	2007	242
Delayed Functional Expression of Neuronal Chemokine Receptors Following Focal Nerve Demyelination in the Rat: A Mechanism for the Development of Chronic Sensitization of Peripheral Nociceptors Sonia K. Bhangoo, Dongjun Ren, Richard J. Miller, Molecular Pain	2007	173
Structure-based design of a new class of highly selective aminoimidazo[1,2-a]pyridine-based inhibitors of cyclin dependent kinases Chafiq Hamdouchi, Boyu Zhong, J. S. MENDOZA, Bioorganic & Medicinal Chemistry Letters Combinatorial ChemistryMedicinal ChemistryDrug TargetBiochemistryDrug Design	2005	90
Structural basis for GPR40 allosteric agonism and incretin stimulation Joseph D. Ho, Betty Chau, Logan Rodgers, Nature Communications	2018	85
On the reaction of chiral sulfinimines with sulfur ylides: a novel route to the asymmetric aziridination JoséL. García Ruano, Inmaculada Fernández, Chafiq Hamdouchi Tetrahedron Letters Sulfur YlidesCross-coupling ReactionEngineeringChiral SulfiniminesOrganic Chemistry	1995	66
A new approach to the synthesis of 2-aminoimidazo[1,2-a]pyridine derivatives through microwave-assisted N-alkylation of 2-halopyridines Juan A. Vega, Juan J. Vaquero, Julio Álvarez‐Buílla, Tetrahedron Microwave-assisted N-alkylationNew ApproachOrganic ChemistryChemistryHalogenation	1999	60
The Discovery, Preclinical, and Early Clinical Development of Potent and Selective GPR40 Agonists for the Treatment of Type 2 Diabetes Mellitus (LY2881835, LY2922083, and LY2922470) Chafiq Hamdouchi, Steven D. Kahl, Anjana Patel Lewis, Journal of Medicinal Chemistry PharmacotherapyInsulin SignalingTranslational PharmacologyMetabolic SyndromeMolecular Pharmacology	2016	58
Chemoselective Arylsulfenylation of 2-Aminoimidazol[1,2-a]pyridines by Phenyliodine(III) Bis(trifluoroacetate) (PIFA) Chafiq Hamdouchi Synthesis Organic ChemistrySynthetic ChemistryChemistryChemoselective Arylsulfenylation	1998	45
Surface nature of Grignard reagent formation. Chiral 1-methylspiro[2.5]octylmagnesium bromide Chafiq Hamdouchi, Marek Topolski, Virgil L. Goedken, The Journal of Organic Chemistry Grignard Reagent FormationAltmetric Attention ScoreOrganic ChemistrySocial Media PresenceStereoselective Synthesis	1993	45

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