Philip L. Nyce - Concepedia

Author

Philip L. Nyce

Union Institute & University

Also Known As

P. L. NYCE, P. L. Nyce, P. NYCE, P. Nyce, P.L. Nyce, Philip L. Nyce

Publications

214

Citations

H-Index

Concepts

All Affiliations

Union Institute & University

About

Philip L. Nyce is an author at Union Institute & University specializing in pharmacology, biochemistry, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	6	6	170
2	Medicine	5	5	160
3	Natural Sciences	5	5	158
4	Chemical Biology	1	1	29
5	Chemistry	1	1	10

Philip L. Nyce

Publications

197

Citations

H-Index

Page 1

	Year	Citations
3-(2-Carboxyindol-3-yl)propionic acid-based antagonists of the NMDA (N-methyl-D-aspartic acid) receptor associated glycine binding site Francesco G. Salituro, Boyd L. Harrison, Bruce M. Baron, Journal of Medicinal Chemistry Medicinal ChemistryIndole RingBiochemistryFunctional SelectivityMedicine	1992	74
Syntheses of -2-fluoromethy--tyrosine and -2-difluoromethyl--tyrosine as potential inhibitors of tyrosine hydroxylase Ian A. McDonald, Philip L. Nyce, Michel J. Jung, Tetrahedron Letters Medicinal ChemistryBioorganic ChemistryTyrosine HydroxylaseBiochemistryNatural Sciences	1991	29
CoMFA, Synthesis, and Pharmacological Evaluation of (<i>E</i>)-3-(2-Carboxy-2-arylvinyl)-4,6-dichloro-1<i>H</i>-indole-2-carboxylic Acids: 3-[2-(3-Aminophenyl)-2-carboxyvinyl]-4,6-dichloro-1<i>H</i>-indole-2-carboxylic Acid, a Potent Selective Glycine-Site NMDA Receptor Antagonist Bruce M. Baron, Robert J. Cregge, Robert A. Farr, Journal of Medicinal Chemistry Peptide SciencePharmacotherapyPharmaceutical ChemistrySelective AntagonistMolecular Pharmacology	2005	28
Synthesis of 3( )-phosphonoacetyl-2( )-piperidinecarboxylic acid, a conformationally-restricted glutamate antagonist Jeffrey P. Whitten, Rowena V. Cube, Philip L. Nyce, Bioorganic & Medicinal Chemistry Letters	1991	27
An Efficient Syntesis of 1,8-Naphthyridin-2(1<i>H</i>)-ones: Synthesis of Leukotriene Inhibitor SCH 37224 Philip L. Nyce, D. GALA, Martin Steinman Synthesis New Reaction ProcedureMedicinal ChemistryPharmaceutical ChemistryHeterocyclicBiochemistry	1991	17
Inhibition of steroid 5α-reductase by “inverted”, competitive inhibitors Ian A. McDonald, Philip L. Nyce, Cynthia A. Gates, Bioorganic & Medicinal Chemistry Letters Molecular PharmacologyBiochemistryMedicineCompetitive InhibitorsPharmacotherapy	1994	12
Synthesis of Azetidinones from L-Threonine: Formation of Unusually Stable Bicyclic Hemiketals and<i>cis</i>-Azetidinones Max Kugelman, D. GALA, Robert S. Jaret, Synlett X-ray CrystallographyBicyclic HemiketalHeterocyclicBiochemistryNatural Sciences	1990	10

Page 1