István Káldor

1.3k total citations
21 papers, 482 citations indexed

About

István Káldor is a scholar working on Organic Chemistry, Molecular Biology and Infectious Diseases. According to data from OpenAlex, István Káldor has authored 21 papers receiving a total of 482 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Organic Chemistry, 6 papers in Molecular Biology and 4 papers in Infectious Diseases. Recurrent topics in István Káldor's work include HIV Research and Treatment (4 papers), HIV/AIDS drug development and treatment (4 papers) and Drug Transport and Resistance Mechanisms (2 papers). István Káldor is often cited by papers focused on HIV Research and Treatment (4 papers), HIV/AIDS drug development and treatment (4 papers) and Drug Transport and Resistance Mechanisms (2 papers). István Káldor collaborates with scholars based in United States and China. István Káldor's co-authors include Andrew S. Kende, Kevin Koch, Gilbert Dorey, David N. Deaton, Andrew Spaltenstein, Robert Aslanian, John F. Miller, Eric S. Furfine, Katrina L. Creech and Derek J. Parks and has published in prestigious journals such as Journal of the American Chemical Society, Biochemistry and Journal of Medicinal Chemistry.

In The Last Decade

István Káldor

17 papers receiving 457 citations

Peers

István Káldor
Michael C. Matelich United States
Mary Ann M. Fuhry United States
Alicia Regueiro‐Ren United States
Toomas Mitt United States
Barrie E. Kirk United Kingdom
Monica Donghi Italy
Jorge Gomez‐Galeno United States
Michael Hale United States
Denis R. St. Laurent United States
Tobias Wunberg Germany
Michael C. Matelich United States
István Káldor
Citations per year, relative to István Káldor István Káldor (= 1×) peers Michael C. Matelich

Countries citing papers authored by István Káldor

Since Specialization
Citations

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

Fields of papers citing papers by István Káldor

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by István Káldor. 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 István Káldor. The network helps show where István Káldor may publish in the future.

Co-authorship network of co-authors of István Káldor

This figure shows the co-authorship network connecting the top 25 collaborators of István Káldor. A scholar is included among the top collaborators of István Káldor 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 István Káldor. István Káldor 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.
Becherer, J. David, Eric E. Boros, Tiffany Carpenter, et al.. (2015). Discovery of 4-Amino-8-quinoline Carboxamides as Novel, Submicromolar Inhibitors of NAD-Hydrolyzing Enzyme CD38. Journal of Medicinal Chemistry. 58(17). 7021–7056. 44 indexed citations
2.
Smalley, Terrence L., Sharon Boggs, Justin A. Caravella, et al.. (2014). Novel heterocyclic scaffolds of GW4064 as farnesoid X receptor agonists. Bioorganic & Medicinal Chemistry Letters. 25(2). 280–284. 15 indexed citations
3.
Boros, Eric E. & István Káldor. (2014). Thermal Synthesis of 3‐Bromothieno[3,2‐c]pyridin‐4‐(5H)‐one: A Telescoped Procedure with Tributylamine. Journal of Heterocyclic Chemistry. 52(1). 302–305. 3 indexed citations
4.
Boros, Eric E., István Káldor, & Philip Turnbull. (2011). A scalable Nenitzescu synthesis of 2‐methyl‐4‐(trifluoromethyl)‐1H‐indole‐5‐carbonitrile. Journal of Heterocyclic Chemistry. 48(3). 733–736. 2 indexed citations
5.
Bass, Jonathan Y., Richard D. Caldwell, Justin A. Caravella, et al.. (2008). Conformationally constrained farnesoid X receptor (FXR) agonists: Naphthoic acid-based analogs of GW 4064. Bioorganic & Medicinal Chemistry Letters. 18(15). 4339–4343. 118 indexed citations
6.
7.
Miller, John F., C. Webster Andrews, Eric S. Furfine, et al.. (2006). Ultra-potent P1 modified arylsulfonamide HIV protease inhibitors: The discovery of GW0385. Bioorganic & Medicinal Chemistry Letters. 16(7). 1788–1794. 70 indexed citations
8.
Miller, John F., Eric S. Furfine, Richard Hazen, et al.. (2005). Novel P1 chain-extended HIV protease inhibitors possessing potent anti-HIV activity and remarkable inverse antiviral resistance profiles. Bioorganic & Medicinal Chemistry Letters. 15(15). 3496–3500. 15 indexed citations
9.
Hanlon, Mary H., David Porter, Eric S. Furfine, et al.. (2004). Inhibition of Wild-Type and Mutant Human Immunodeficiency Virus Type 1 Proteases by GW0385 and Other Arylsulfonamides. Biochemistry. 43(45). 14500–14507. 14 indexed citations
10.
Pacofsky, Gregory J., Jeffrey A. Stafford, Richard F. Cox, et al.. (2002). Relating the Structure, Activity, and Physical Properties of Ultrashort-Acting Benzodiazepine Receptor Agonists. Bioorganic & Medicinal Chemistry Letters. 12(21). 3219–3222. 10 indexed citations
11.
Boros, Eric E., István Káldor, Peter J. Brown, & Virgil L. Styles. (2001). A CONVENIENT SYNTHESIS OF THIOFIBRATE ANALOGS FROM ARYL SULFONYL CHLORIDES. Synthetic Communications. 31(4). 505–510. 3 indexed citations
12.
Káldor, István, Paul L. Feldman, Robert A. Mook, et al.. (2001). Stereocontrolled Synthesis ofcis-Dibenzoquinolizine Chlorofumarates:  Curare-Like Agents of Ultrashort Duration. The Journal of Organic Chemistry. 66(10). 3495–3501. 21 indexed citations
13.
Kende, Andrew S., et al.. (1996). SYNTHESIS OF SOME NOVEL FUNCTIONALIZED DOUBLE MICHAEL ACCEPTORS BASED ONbis(VINYLSULFONYL)METHANE (BVSM). Organic Preparations and Procedures International. 28(6). 683–690.
14.
Kende, Andrew S., et al.. (1995). Total Synthesis of the Macrolide Antitumor Antibiotic Lankacidin C. Journal of the American Chemical Society. 117(31). 8258–8270. 71 indexed citations
15.
Kende, Andrew S., Kevin Koch, Gilbert Dorey, István Káldor, & Kun Liu. (1993). Enantioselective total synthesis of lankacidin C. Journal of the American Chemical Society. 115(21). 9842–9843. 33 indexed citations
16.
Kende, Andrew S. & István Káldor. (1989). “Accordion” rearrangements of cyclobutane α-sulfonyl lactones. Tetrahedron Letters. 30(52). 7329–7332. 5 indexed citations
17.
Kende, Andrew S., István Káldor, & Robert Aslanian. (1988). Total synthesis of (.+-.)-punctaporonin B. Journal of the American Chemical Society. 110(18). 6265–6266. 26 indexed citations
18.
Bíró, I, et al.. (1964). Cryoglobulinemia and porphyria hepatica chronica (porphyria cutanea tarda).. PubMed. 44(3). 226–7. 3 indexed citations
19.
Lengyel, Judith A., et al.. (1964). Simultane Infektion durgh Aktinomykose und Blastomykose. Mycopathologia. 24(4). 289–293. 1 indexed citations
20.
Bíró, I, et al.. (1964). [CRYOGLOBULINEMIA ASSOCIATED WITH PORPHYRIA HEPATICA CHRONICA (PORPHYRIA CUTANEA TARDA)].. PubMed. 105. 341–3. 1 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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