Catherine M. Wiscount

Author

United States Military Academy

Also Known As

C. M. WISCOUNT, C. M. Wiscount, Catherine M. Wiscount

Publications

326

Citations

H-Index

Concepts

All Affiliations

United States Military Academy Merck & Co., Inc., Rahway, NJ, USA (United States)

About

Catherine M. Wiscount is an author at United States Military Academy specializing in drug discovery, medicinal chemistry, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	206
2	Natural Sciences	4	4	109
3	Biochemistry	3	3	89
4	Chemical Biology	2	2	61
5	Molecular Biology	2	2	48

Catherine M. Wiscount

Publications

319

Citations

H-Index

Page 1

	Year	Citations
Benzocycloalkyl amines as novel C-termini for HIV protease inhibitors Terry A. Lyle, Catherine M. Wiscount, James P. Guare, Journal of Medicinal Chemistry Hiv Protease InhibitorsAltmetric Attention ScorePharmacotherapyAntiviral DrugPharmaceutical Chemistry	1991	97
Synthesis of a Series of 4-(Arylethynyl)-6-chloro-4-cyclopropyl-3,4-dihydroquinazolin-2(1H)-ones as Novel Non-nucleoside HIV-1 Reverse Transcriptase Inhibitors Thomas J. Tucker, Terry A. Lyle, Catherine M. Wiscount, Journal of Medicinal Chemistry	1994	70
Design and Synthesis of Piperazine Sulfonamide Cores Leading to Highly Potent HIV-1 Protease Inhibitors Christopher J. Bungard, Peter Williams, Jürgen Schulz, ACS Medicinal Chemistry Letters	2017	43
Discovery of potent, selective 4-fluoroproline-based thrombin inhibitors with improved metabolic stability Donnette D. Staas, Kelly L. Savage, Vanessa Sherman, Bioorganic & Medicinal Chemistry Chemical BiologyThrombosisMedicinal ChemistryBiochemistryMedicine	2006	37
Discovery of MK-8718, an HIV Protease Inhibitor Containing a Novel Morpholine Aspartate Binding Group Christopher J. Bungard, Peter Williams, Jeanine Ballard, ACS Medicinal Chemistry Letters Crystal StructureMedicinal ChemistryBiochemistryHiv ProteaseNatural Sciences	2016	28
<i>N</i>-Arylalkyl Pseudopeptide Inhibitors of Farnesyltransferase S. J. DESOLMS, Elizabeth A. Giuliani, Samuel Graham, Journal of Medicinal Chemistry Inhibitory ActivityMedicinal ChemistryBiochemistryNatural SciencesMedicine	1998	24
10-Hydroxy-7,8-dihydropyrazino[1′,2′:1,5]pyrrolo[2,3-d]pyridazine-1,9(2H,6H)-diones: Potent, orally bioavailable HIV-1 integrase strand-transfer inhibitors with activity against integrase mutants Catherine M. Wiscount, Peter Williams, Lekhanh O. Tran, Bioorganic & Medicinal Chemistry Letters Medicinal ChemistryIntegrase MutantsMedicineNatural SciencesAntiviral Drug Development	2008	20

Page 1