Megan Murphy - Concepedia

Author

Megan Murphy

AstraZeneca (United States)

Also Known As

Megan M Murphy, Megan Murphy

Publications

355

Citations

H-Index

Concepts

All Affiliations

AstraZeneca (United States)Wilmington University W.E. Upjohn Institute for Employment Research AstraZeneca (Singapore)

About

Megan Murphy is an author at AstraZeneca (United States) specializing in pharmacology, drug discovery, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	112
2	Engineering	2	2	76
3	Biochemistry	2	2	68
4	Health Sciences	1	1	15
5	Biomolecular Engineering	1	1	31

Megan Murphy

Publications

349

Citations

H-Index

Page 1

	Year	Citations
Pyrazoline bisphosphonate esters as novel antiinflammatory and antiarthritic agents Richard A. Nugent, Megan Murphy, Stephen T. Schlachter, Journal of Medicinal Chemistry	1993	116
Studies on the Synthesis of Aureolic Acid Antibiotics: Acyloin Glycosidation Studies William Roush, Karin Briner, Brenda S. Kesler, The Journal of Organic Chemistry Acyloin Glycosidation StudiesPharmaceutical ScienceBiosynthesisAntimicrobial Drug DiscoveryGlycosylation	1996	53
The synthesis of indolizines: the reaction of .alpha.-halo pyridinium salts with .beta.-dicarbonyl species Richard A. Nugent, Megan Murphy The Journal of Organic Chemistry HalogenationChemical EngineeringDerivative (Chemistry)Engineering.Beta.-dicarbonyl Species	1987	45
The discovery of non-basic atrial natriuretic peptide clearance receptor antagonists. part 1 Chris A. Veale, Vernon Alford, David Aharony, Bioorganic & Medicinal Chemistry Letters Molecular PharmacologyPart 1Cardiovascular DiseaseMedicinePhysiology	2000	44
An improved synthesis of naphthoate precursors to olivin William Roush, Megan Murphy The Journal of Organic Chemistry AltmetricsEngineeringImproved SynthesisInformationDatabases	1992	31
Carbonyl-Containing Bisphosphonate Esters as Novel Antiinflammatory and Antiarthritic Agents Richard A. Nugent, Stephen T. Schlachter, Megan Murphy, Journal of Medicinal Chemistry	1994	25
Synthesis of 7-chloro-2,3-dihydro-2-[1-(pyridinyl)alkyl]-pyridazino[4,5-b]quinoline-1,4,10(5H)-triones as NMDA glycine-site antagonists Dean G. Brown, Rebecca A. Urbanek, Thomas M. Bare, Bioorganic & Medicinal Chemistry Letters	2003	20
Pyridazinoquinolinetriones as NMDA Glycine-Site Antagonists with Oral Antinociceptive Activity in a Model of Neuropathic Pain Thomas M. Bare, Dean G. Brown, Carey L. Horchler, Journal of Medicinal Chemistry Pain TherapyOral BioavailabilityPain MedicineNeuropathic PainMolecular Pain	2007	15

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