James R. McCarthy

4.7k total citations
117 papers, 3.6k citations indexed

About

James R. McCarthy is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, James R. McCarthy has authored 117 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Organic Chemistry, 45 papers in Molecular Biology and 28 papers in Pharmaceutical Science. Recurrent topics in James R. McCarthy's work include Fluorine in Organic Chemistry (27 papers), Stress Responses and Cortisol (16 papers) and Chemical Synthesis and Analysis (16 papers). James R. McCarthy is often cited by papers focused on Fluorine in Organic Chemistry (27 papers), Stress Responses and Cortisol (16 papers) and Chemical Synthesis and Analysis (16 papers). James R. McCarthy collaborates with scholars based in United States, Spain and Canada. James R. McCarthy's co-authors include Donald P. Matthews, Jeffrey P. Whitten, Esa T. Jarvi, Dimitri E. Grigoriadis, Mustapha Haddach, Morris J. Robins, Keith Wilcoxen, David M. Stemerick, M. L. EDWARDS and Charles Q. Huang and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Immunology and Biochemistry.

In The Last Decade

James R. McCarthy

114 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
James R. McCarthy United States	37	2.2k	1.2k	1.1k	363	354	117	3.6k
John Saunders United States	28	1.3k 0.6×	1.3k 1.1×	109 0.1×	125 0.3×	111 0.3×	139	3.1k
Andrew P. Combs United States	25	2.4k 1.1×	1.7k 1.4×	86 0.1×	188 0.5×	96 0.3×	65	3.9k
Tracey Pirali Italy	27	2.8k 1.3×	1.6k 1.4×	753 0.7×	432 1.2×	20 0.1×	67	4.2k
Mark G. Bock United States	29	1.8k 0.8×	1.9k 1.6×	96 0.1×	119 0.3×	46 0.1×	109	3.8k
William H. Okamura United States	38	1.8k 0.8×	1.1k 0.9×	338 0.3×	128 0.4×	46 0.1×	130	4.9k
Leggy A. Arnold United States	32	1.9k 0.9×	1.3k 1.1×	47 0.0×	890 2.5×	54 0.2×	114	3.6k
Joseph M. Ready United States	36	2.7k 1.2×	902 0.8×	143 0.1×	674 1.9×	23 0.1×	101	4.1k
George Just Canada	30	1.9k 0.9×	1.5k 1.2×	149 0.1×	133 0.4×	21 0.1×	205	3.3k
Raphaël Frédérick Belgium	27	703 0.3×	1.2k 1.0×	73 0.1×	62 0.2×	176 0.5×	80	2.5k
Andrew W. Thomas Switzerland	20	3.9k 1.8×	970 0.8×	214 0.2×	498 1.4×	18 0.1×	44	4.9k

Countries citing papers authored by James R. McCarthy

Since Specialization

Citations

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

Fields of papers citing papers by James R. McCarthy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James R. McCarthy. 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 James R. McCarthy. The network helps show where James R. McCarthy may publish in the future.

Co-authorship network of co-authors of James R. McCarthy

This figure shows the co-authorship network connecting the top 25 collaborators of James R. McCarthy. A scholar is included among the top collaborators of James R. McCarthy 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 James R. McCarthy. James R. McCarthy 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

Rojo, I., Howard B. Broughton, David E. Timm, et al.. (2005). Macrocyclic peptidomimetic inhibitors of β-secretase (BACE): First X-ray structure of a macrocyclic peptidomimetic-BACE complex. Bioorganic & Medicinal Chemistry Letters. 16(1). 191–195. 26 indexed citations

Huang, Charles Q., Keith Wilcoxen, Dimitri E. Grigoriadis, James R. McCarthy, & Chen Chen. (2004). Design and synthesis of 3-(2-pyridyl)pyrazolo[1,5-a]pyrimidines as potent CRF1 receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 14(15). 3943–3947. 29 indexed citations

Chen, Chen, Keith Wilcoxen, Charles Q. Huang, et al.. (2004). Optimization of 3-phenylpyrazolo[1,5-a]pyrimidines as potent corticotropin-releasing factor-1 antagonists with adequate lipophilicity and water solubility. Bioorganic & Medicinal Chemistry Letters. 14(14). 3669–3673. 22 indexed citations

Huang, Charles Q., Dimitri E. Grigoriadis, Zhengyu Liu, et al.. (2004). Design, synthesis, and SAR of 2-dialkylamino-4-arylpyrimidines as potent and selective corticotropin-releasing factor 1 (CRF 1 ) receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 14(9). 2083–2086. 8 indexed citations

Webb, Thomas R., et al.. (2004). Synthesis of benzoylpyrimidines as antagonists of the corticotropin-releasing factor-1 receptor. Bioorganic & Medicinal Chemistry Letters. 14(15). 3869–3873. 5 indexed citations

Huang, Charles Q., Keith Wilcoxen, James R. McCarthy, et al.. (2003). Synthesis and SAR of 8-Arylquinolines as potent corticotropin-Releasing factor1 (CRF1) receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 13(19). 3375–3379. 20 indexed citations

Wilcoxen, Keith, Charles Q. Huang, James R. McCarthy, Dimitri E. Grigoriadis, & Chen Chen. (2003). Synthesis of 3-phenylpyrazolo[4,3-b]pyridines via a convenient synthesis of 4-amino-3-arylpyrazoles and SAR of corticotropin-Releasing factor receptor type-1 antagonists. Bioorganic & Medicinal Chemistry Letters. 13(19). 3367–3370. 11 indexed citations

Huang, Charles Q., et al.. (2003). Synthesis of 1-methyl-3-phenylpyrazolo[4,3-b]pyridines via a methylation of 4-phthalimino-3-phenylpyrazoles and optimization toward highly potent corticotropin-releasing factor type-1 antagonists. Bioorganic & Medicinal Chemistry Letters. 13(19). 3371–3374. 3 indexed citations

Zhu, Yunfei, Keith Wilcoxen, Timothy D. Gross, et al.. (2003). 6,7-Dihydroxyisoquinoline-3-carboxylic acids are potent inhibitors on the binding of insulin-Like growth factor (IGF) to IGF-binding proteins: optimization of the 1-position benzoyl side chain. Bioorganic & Medicinal Chemistry Letters. 13(11). 1927–1930. 9 indexed citations

10.

Zorrilla, Eric P., Gery Schulteis, Alwin Klaassen, et al.. (2002). Urocortin shares the memory modulating effects of corticotropin-releasing factor (CRF): mediation by CRF1 receptors. Brain Research. 952(2). 200–210. 40 indexed citations

11.

Chen, Chen, Raymond Dagnino, Charles Q. Huang, James R. McCarthy, & Dimitri E. Grigoriadis. (2001). 1-Alkyl-3-amino-5-aryl-1H-[1,2,4]triazoles: novel synthesis via cyclization of N-Acyl-S-methylisothioureas with alkylhydrazines and their potent corticotropin-Releasing factor-1 (CRF1) receptor antagonist activities. Bioorganic & Medicinal Chemistry Letters. 11(24). 3165–3168. 39 indexed citations

12.

McCarthy, James R., et al.. (1998). Terminal Fluoroolefins. The Synthesis of Novel Carboacyclic Nucleosides. Nucleosides and Nucleotides. 17(6). 1099–1113. 4 indexed citations

13.

Donk, Wilfred A. van der, Guixue Yu, Domingos J. Silva, et al.. (1996). Inactivation of Ribonucleotide Reductase by (E)-2‘-Fluoromethylene-2‘-deoxycytidine 5‘-Diphosphate: A Paradigm for Nucleotide Mechanism-Based Inhibitors. Biochemistry. 35(25). 8381–8391. 59 indexed citations

14.

Frondorf, Kathleen, et al.. (1993). Selective inhibition of T cell activation by an inhibitor of S-adenosyl-L-homocysteine hydrolase. The Journal of Immunology. 150(8). 3264–3273. 39 indexed citations

15.

Matthews, Donald P., et al.. (1993). A new method for the electrophilic fluorination of vinyl stannanes.. Tetrahedron Letters. 34(19). 3057–3060. 58 indexed citations

16.

Prakash, Nellikunja J., Gregory F. Davis, Esa T. Jarvi, et al.. (1992). Antiretroviral activity of mechanism-based irreversible inhibitors of S-Adenosylhomocysteine hydrolase. Life Sciences. 50(19). 1425–1435. 8 indexed citations

17.

Wannamaker, M. Woods, et al.. (1992). N-(1-Oxododecyl)-4.alpha.,10-dimethyl-8-aza-trans-decal-3.beta.-ol: a potent competitive inhibitor of 2,3-oxidosqualene cyclase. Journal of Medicinal Chemistry. 35(19). 3581–3583. 19 indexed citations

18.

McCarthy, James R., Donald P. Matthews, Robert J. Broersma, et al.. (1990). 1-(Thienylalkyl)imidazole-2(3H)-thiones as potent competitive inhibitors of dopamine .beta.-hydroxylase. Journal of Medicinal Chemistry. 33(7). 1866–1873. 6 indexed citations

19.

Mehdi, Shujaath, Esa T. Jarvi, Jack R. Koehl, James R. McCarthy, & Philippe Bey. (1990). The Mechanism of Inhibition of S-Adenosyl-L-Homocysteine Hydrolase by Fluorine-Containing Adenosine Analogs. Journal of enzyme inhibition. 4(1). 1–13. 18 indexed citations

20.

McCarthy, James R., et al.. (1970). 1,3-Bromine migration. Deamination of 3-bromo-2,2-bis(bromomethyl)propylamine. Journal of the American Chemical Society. 92(21). 6376–6378. 4 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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