William C. Lumma

3.2k total citations
62 papers, 2.3k citations indexed

About

William C. Lumma is a scholar working on Organic Chemistry, Molecular Biology and Infectious Diseases. According to data from OpenAlex, William C. Lumma has authored 62 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Organic Chemistry, 26 papers in Molecular Biology and 7 papers in Infectious Diseases. Recurrent topics in William C. Lumma's work include Synthesis and Biological Evaluation (13 papers), Synthesis and Reactions of Organic Compounds (11 papers) and Chemical Synthesis and Analysis (9 papers). William C. Lumma is often cited by papers focused on Synthesis and Biological Evaluation (13 papers), Synthesis and Reactions of Organic Compounds (11 papers) and Chemical Synthesis and Analysis (9 papers). William C. Lumma collaborates with scholars based in United States and Japan. William C. Lumma's co-authors include Elinor H. Cantor, Paul Anderson, Gabor M. Rubanyi, L Botelho, Elena Ho, Susan F. Britcher, Joel R. Huff, Steven D. Young, Terry A. Lyle and Linda S. Payne and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and The Journal of Physical Chemistry.

In The Last Decade

William C. Lumma

60 papers receiving 2.2k citations

Peers

Countries citing papers authored by William C. Lumma

Since Specialization

Citations

This map shows the geographic impact of William C. Lumma's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by William C. Lumma with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites William C. Lumma more than expected).

Fields of papers citing papers by William C. Lumma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by William C. Lumma. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by William C. Lumma. The network helps show where William C. Lumma may publish in the future.

Co-authorship network of co-authors of William C. Lumma

This figure shows the co-authorship network connecting the top 25 collaborators of William C. Lumma. A scholar is included among the top collaborators of William C. Lumma based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with William C. Lumma. William C. Lumma is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Title	Journal	Authors	Indexed citations
1	The synthesis and biological evaluation of a series of potent dual inhibitors of farnesyl and geranyl-Geranyl protein transferases	Bioorganic & Medicinal Chemistry Letters	Thomas J. Tucker, Marc Abrams et al.	13
2	Anions Modulate the Potency of Geranylgeranyl-Protein Transferase I Inhibitors	Journal of Biological Chemistry	Hans E. Huber, R. Robinson et al.	16
3	Design of Novel, Potent, Noncovalent Inhibitors of Thrombin with Nonbasic P-1 Substructures: Rapid Structure−Activity Studies by Solid-Phase Synthesis	Journal of Medicinal Chemistry	William C. Lumma, Keith M. Witherup et al.	63
4	[24] Development of nonnucleoside HIV reverse transcriptase inhibitors	Methods in enzymology on CD-ROM/Methods in enzymology	Thomas J. Tucker, William C. Lumma et al.	11
5	Martinelline and Martinellic Acid, Novel G-Protein Linked Receptor Antagonists from the Tropical Plant Martinella iquitosensis (Bignoniaceae)	Journal of the American Chemical Society	Keith M. Witherup, Richard W. Ransom et al.	253
6	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	Journal of Medicinal Chemistry	Thomas J. Tucker, Terry A. Lyle et al.	54
7	A series of potent HIV-1 protease inhibitors containing a hydroxyethyl secondary amine transition state isostere: synthesis, enzyme inhibition, and antiviral activity	Journal of Medicinal Chemistry	Thomas J. Tucker, William C. Lumma et al.	39
8	Synthesis, cardiac electrophysiology, and .beta.-blocking activity of novel arylpiperazines with potential as class II/III antiarrhythmic agents	Journal of Medicinal Chemistry	William C. Lumma, Robert Gomez et al.	16
9	Cytoprotective function of nitric oxide: Inactivation of superoxide radicals produced by human leukocytes	Biochemical and Biophysical Research Communications	Gabor M. Rubanyi, Elena Ho et al.	316
10	Synthesis and biological activity of angiotensin II analog containing a Val-His replacement, Val.psi.[CH(CONH2)HN]His	Journal of Medicinal Chemistry	Raju Mohan, Ron Bihovsky et al.	18
11	Lack of biological activity of preproendothelin [110–130] in several endothelin assays	Life Sciences	Christina Cade, William C. Lumma et al.	4
12	Cardiotonic agents. 6. Histamine analogs as potential cardiovascular selective H2 agonists	Journal of Medicinal Chemistry	John W. Lampe, Paul Erhardt et al.	6
13	Synthesis and pharmacological studies of N-[4-[2-hydroxy-3-[[2-[4-(1H-imidazol-1-yl)phenoxy]ethyl]amino]propoxy]phenyl]methanesulfonamide, a novel antiarrhythmic agent with class II and class III activities	Journal of Medicinal Chemistry	William C. Lumma, Klaus Nickisch et al.	10
14	Heterocyclic analogs of benzamide antiarrhythmic agents	Journal of Medicinal Chemistry	John W. Lampe, William C. Lumma et al.	3
15	Synthesis and antiarrhythmic activity of novel 3-alkyl-1-[.omega.-[4-[(alkylsulfonyl)amino]phenyl]-.omega.-hydroxyalkyl]-1H-imidazolium salts and related compounds. 2	Journal of Medicinal Chemistry	William C. Lumma, Thomas M. Argentieri et al.	11
16	Cardiotonic agents. 1. Novel 8-aryl substituted imidazo[1,2-a]- and -[1,5-a]pyridines and imidazo[1,5-a]pyridinones as potential positive inotropic agents	Journal of Medicinal Chemistry	Paul Erhardt, William C. Lumma et al.	98
17	Rational design of 4-[(methylsulfonyl)amino]benzamides as class III antiarrhythmic agents	Journal of Medicinal Chemistry	William C. Lumma, David D. Davey et al.	33
18	Piperazinylimidazo[1,2-a]pyrazines with selective affinity for in vitro .alpha.-adrenergic receptor subtypes	Journal of Medicinal Chemistry	William C. Lumma, William C. Randall et al.	40
19	Conformational requirements for histamine H2-receptor inhibitors: a structure-activity study of phenylene analogs related to cimetidine and tiotidine	Journal of Medicinal Chemistry	J. M. HOFFMAN, Charles N. Habecker et al.	9
20	Symbiotic approach to drug design: antihypertensive .beta.-adrenergic blocking agents	Journal of Medicinal Chemistry	John J. Baldwin, William C. Lumma et al.	17

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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