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

William C. Lumma
John W. Clader United States
Stephen W. Kaldor United States
Krishna C. Agrawal United States
Terry A. Lyle United States
Sander G. Mills United States
Elizabeth A. Lunney United States
Joel C. Barrish United States
Paul E. Brennan United Kingdom
John W. Clader United States
William C. Lumma
Citations per year, relative to William C. Lumma William C. Lumma (= 1×) peers John W. Clader

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

20 of 20 papers shown
1.
Tucker, Thomas J., Marc Abrams, Carolyn A. Buser, et al.. (2002). The synthesis and biological evaluation of a series of potent dual inhibitors of farnesyl and geranyl-Geranyl protein transferases. Bioorganic & Medicinal Chemistry Letters. 12(15). 2027–2030. 13 indexed citations
2.
Huber, Hans E., R. Robinson, Deborah D. Nahas, et al.. (2001). Anions Modulate the Potency of Geranylgeranyl-Protein Transferase I Inhibitors. Journal of Biological Chemistry. 276(27). 24457–24465. 16 indexed citations
3.
Lumma, William C., Keith M. Witherup, Thomas J. Tucker, et al.. (1998). 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. 41(7). 1011–1013. 63 indexed citations
4.
Tucker, Thomas J., William C. Lumma, & Joseph Culberson. (1996). [24] Development of nonnucleoside HIV reverse transcriptase inhibitors. Methods in enzymology on CD-ROM/Methods in enzymology. 275. 440–472. 11 indexed citations
5.
Witherup, Keith M., Richard W. Ransom, Amy C. Graham, et al.. (1995). Martinelline and Martinellic Acid, Novel G-Protein Linked Receptor Antagonists from the Tropical Plant Martinella iquitosensis (Bignoniaceae). Journal of the American Chemical Society. 117(25). 6682–6685. 253 indexed citations
6.
Tucker, Thomas J., Terry A. Lyle, Susan F. Britcher, et al.. (1994). 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. 37(15). 2437–2444. 54 indexed citations
7.
Tucker, Thomas J., William C. Lumma, Linda S. Payne, et al.. (1992). 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. 35(14). 2525–2533. 39 indexed citations
8.
Lumma, William C., et al.. (1992). Synthesis, cardiac electrophysiology, and .beta.-blocking activity of novel arylpiperazines with potential as class II/III antiarrhythmic agents. Journal of Medicinal Chemistry. 35(4). 743–750. 16 indexed citations
9.
Rubanyi, Gabor M., Elena Ho, Elinor H. Cantor, William C. Lumma, & L Botelho. (1991). Cytoprotective function of nitric oxide: Inactivation of superoxide radicals produced by human leukocytes. Biochemical and Biophysical Research Communications. 181(3). 1392–1397. 316 indexed citations
10.
Mohan, Raju, et al.. (1991). Synthesis and biological activity of angiotensin II analog containing a Val-His replacement, Val.psi.[CH(CONH2)HN]His. Journal of Medicinal Chemistry. 34(8). 2402–2410. 18 indexed citations
11.
Cade, Christina, et al.. (1990). Lack of biological activity of preproendothelin [110–130] in several endothelin assays. Life Sciences. 47(23). 2097–2103. 4 indexed citations
12.
Lampe, John W., Paul Erhardt, William C. Lumma, et al.. (1990). Cardiotonic agents. 6. Histamine analogs as potential cardiovascular selective H2 agonists. Journal of Medicinal Chemistry. 33(6). 1688–1697. 6 indexed citations
14.
Lampe, John W., et al.. (1989). Heterocyclic analogs of benzamide antiarrhythmic agents. Journal of Medicinal Chemistry. 32(3). 688–693. 3 indexed citations
15.
Lumma, William C., et al.. (1987). 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. 30(12). 2303–2309. 11 indexed citations
16.
Erhardt, Paul, William C. Lumma, Jay R. Wiggins, et al.. (1987). 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. 30(8). 1337–1342. 98 indexed citations
17.
Lumma, William C., David D. Davey, Thomas M. Argentieri, et al.. (1987). Rational design of 4-[(methylsulfonyl)amino]benzamides as class III antiarrhythmic agents. Journal of Medicinal Chemistry. 30(5). 755–758. 33 indexed citations
18.
Lumma, William C., et al.. (1983). Piperazinylimidazo[1,2-a]pyrazines with selective affinity for in vitro .alpha.-adrenergic receptor subtypes. Journal of Medicinal Chemistry. 26(3). 357–363. 40 indexed citations
19.
HOFFMAN, J. M., Charles N. Habecker, Brian T. Phillips, et al.. (1983). Conformational requirements for histamine H2-receptor inhibitors: a structure-activity study of phenylene analogs related to cimetidine and tiotidine. Journal of Medicinal Chemistry. 26(2). 140–144. 9 indexed citations
20.
Baldwin, John J., William C. Lumma, G. F. Lundell, et al.. (1979). Symbiotic approach to drug design: antihypertensive .beta.-adrenergic blocking agents. Journal of Medicinal Chemistry. 22(11). 1284–1290. 17 indexed citations

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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