Lucille A. Cosby

648 total citations
19 papers, 456 citations indexed

About

Lucille A. Cosby is a scholar working on Organic Chemistry, Molecular Biology and Toxicology. According to data from OpenAlex, Lucille A. Cosby has authored 19 papers receiving a total of 456 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 6 papers in Molecular Biology and 6 papers in Toxicology. Recurrent topics in Lucille A. Cosby's work include Synthesis and biological activity (10 papers), Synthesis and Characterization of Heterocyclic Compounds (7 papers) and Bioactive Compounds and Antitumor Agents (5 papers). Lucille A. Cosby is often cited by papers focused on Synthesis and biological activity (10 papers), Synthesis and Characterization of Heterocyclic Compounds (7 papers) and Bioactive Compounds and Antitumor Agents (5 papers). Lucille A. Cosby collaborates with scholars based in United States. Lucille A. Cosby's co-authors include Alan C. Sartorelli, Lin Ai, Charles W. Shansky, Krishnamurthy Shyam, Ronald S. Pardini, Ippolito Antonini, Tai Shun Lin, Brian J. Lillis, Shiping Xu and Liya Zhu and has published in prestigious journals such as The Journal of Physical Chemistry, Journal of Medicinal Chemistry and PubMed.

In The Last Decade

Lucille A. Cosby

18 papers receiving 432 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Lucille A. Cosby United States 13 256 212 145 77 51 19 456
Satoru Nagamura Japan 16 338 1.3× 359 1.7× 97 0.7× 85 1.1× 65 1.3× 23 578
Anne Birmingham United States 8 169 0.7× 317 1.5× 119 0.8× 125 1.6× 68 1.3× 8 579
Rita Fiaschi Italy 17 358 1.4× 189 0.9× 49 0.3× 35 0.5× 105 2.1× 36 601
P. CATSOULACOS Greece 14 366 1.4× 487 2.3× 55 0.4× 80 1.0× 67 1.3× 99 718
John H. Mowat United States 10 161 0.6× 169 0.8× 82 0.6× 20 0.3× 27 0.5× 16 378
William Fulmor United States 12 357 1.4× 314 1.5× 99 0.7× 52 0.7× 34 0.7× 18 641
Alummoottil V. Joshua Canada 12 231 0.9× 183 0.9× 36 0.2× 64 0.8× 66 1.3× 23 402
Joong‐Kwon Choi South Korea 14 313 1.2× 252 1.2× 56 0.4× 24 0.3× 47 0.9× 32 538
G. Pastorini Italy 13 362 1.4× 199 0.9× 86 0.6× 62 0.8× 23 0.5× 42 562
Gregory A. Rener United States 11 336 1.3× 285 1.3× 28 0.2× 41 0.5× 93 1.8× 20 596

Countries citing papers authored by Lucille A. Cosby

Since Specialization
Citations

This map shows the geographic impact of Lucille A. Cosby'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 Lucille A. Cosby with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lucille A. Cosby more than expected).

Fields of papers citing papers by Lucille A. Cosby

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lucille A. Cosby. 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 Lucille A. Cosby. The network helps show where Lucille A. Cosby may publish in the future.

Co-authorship network of co-authors of Lucille A. Cosby

This figure shows the co-authorship network connecting the top 25 collaborators of Lucille A. Cosby. A scholar is included among the top collaborators of Lucille A. Cosby 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 Lucille A. Cosby. Lucille A. Cosby is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Xu, Shiping, et al.. (1989). Synthesis of 2,3-diaziridinyl-1,4-naphthoquinonyl sulfonate derivatives as potential antineoplastic agents. Journal of Medicinal Chemistry. 32(7). 1467–1471. 20 indexed citations
2.
Shyam, Krishnamurthy, et al.. (1987). 1,2-Bis(sulfonyl)hydrazines. 3. Effects of structural modification on antineoplastic activity. Journal of Medicinal Chemistry. 30(11). 2157–2161. 27 indexed citations
3.
Shyam, Krishnamurthy, et al.. (1986). Synthesis and evaluation of 2-substituted 1-methyl-1-(4-tolylsulfonyl)hydrazines as antineoplastic agents. Journal of Medicinal Chemistry. 29(7). 1299–1301. 10 indexed citations
4.
Shyam, Krishnamurthy, et al.. (1986). Synthesis and evaluation of 1-(arylsulfonyl)-2-[(methoxycarbonyl)sulfenyl]-1-methylhydrazines as antineoplastic agents. Journal of Medicinal Chemistry. 29(9). 1777–1779. 7 indexed citations
5.
Lin, Tai Shun, Lin Wang, Ippolito Antonini, et al.. (1986). (o- and p-Nitrobenzyloxycarbonyl)-5-fluorouracil derivatives as potential conjugated bioreductive alkylating agents. Journal of Medicinal Chemistry. 29(1). 84–89. 16 indexed citations
6.
Shyam, Krishnamurthy, Lucille A. Cosby, & Alan C. Sartorelli. (1986). 1,2-Bis(arylsulfonyl)hydrazines. 2. The influence of arenesulfonyl and aralkylsulfonyl substituents on antitumor and alkylating activity. Journal of Medicinal Chemistry. 29(7). 1323–1325. 14 indexed citations
7.
Shyam, Krishnamurthy, Lucille A. Cosby, & Alan C. Sartorelli. (1985). Synthesis and evaluation of N,N'-bis(arylsulfonyl)hydrazines as antineoplastic agents. Journal of Medicinal Chemistry. 28(4). 525–527. 24 indexed citations
8.
Shyam, Krishnamurthy, Lucille A. Cosby, & Alan C. Sartorelli. (1985). Relationship between structure and antineoplastic activity of (arylsulfonyl)hydrazones of 4-pyridinecarboxaldehyde. Journal of Medicinal Chemistry. 28(1). 149–152. 14 indexed citations
9.
LIN, T.‐S., Ippolito Antonini, Lucille A. Cosby, & Alan C. Sartorelli. (1984). ChemInform Abstract: 2,3‐DIMETHYL‐1,4‐NAPHTHOQUINONE DERIVATIVES AS BIOREDUCTIVE ALKYLATING AGENTS WITH CROSSLINKING POTENTIAL. Chemischer Informationsdienst. 15(44). 3 indexed citations
10.
Lin, Tai Shun, Ippolito Antonini, Lucille A. Cosby, & Alan C. Sartorelli. (1984). 2,3-Dimethyl-1,4-naphthoquinone derivatives as bioreductive alkylating agents with crosslinking potential. Journal of Medicinal Chemistry. 27(6). 813–815. 13 indexed citations
11.
Cosby, Lucille A., et al.. (1984). Mechanism of action of arenesulfonylhydrazones of 2-pyridinecarboxaldehyde 1-oxide in L1210 cells.. PubMed. 44(12 Pt 1). 5707–11. 4 indexed citations
12.
Antonini, Ippolito, et al.. (1982). 2- and 6-Methyl-1,4-naphthoquinone derivatives as potential bioreductive alkylating agents. Journal of Medicinal Chemistry. 25(6). 730–735. 30 indexed citations
13.
14.
Cosby, Lucille A., et al.. (1980). Synthesis and antineoplastic activity of phenyl-substituted phenylsulfonylhydrazones of 1-pyridinecarboxaldehyde 1-oxide. Journal of Medicinal Chemistry. 23(6). 631–634. 17 indexed citations
15.
Lemke, Thomas, et al.. (1977). Synthesis of 5,6-dihydro-8(7H)-quinolinone thiosemicarbazones as potential antitumor agents. Journal of Medicinal Chemistry. 20(10). 1351–1354. 18 indexed citations
16.
Cosby, Lucille A., et al.. (1976). Mode of action of the bioreductive alkylating agent, 2,3-bis(chloromethyl)-1,4-naphthoquinone.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 36(11 Pt 1). 4023–31. 12 indexed citations
17.
Cosby, Lucille A. & George L. Humphrey. (1975). Kinetics of malonic acid pyrolysis in alkali halide matrices. The Journal of Physical Chemistry. 79(1). 38–41.
18.
Ai, Lin, Ronald S. Pardini, Lucille A. Cosby, et al.. (1973). Potential bioreductive alkylating agents. 2. Antitumor effect and biochemical studies of naphthoquinone derivatives. Journal of Medicinal Chemistry. 16(11). 1268–1271. 67 indexed citations
19.
Ai, Lin, Lucille A. Cosby, Charles W. Shansky, & Alan C. Sartorelli. (1972). Potential bioreductive alkylating agents. 1. Benzoquinone derivatives. Journal of Medicinal Chemistry. 15(12). 1247–1252. 157 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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