John D. McCarter

7.1k total citations · 1 hit paper
47 papers, 2.7k citations indexed

About

John D. McCarter is a scholar working on Molecular Biology, Organic Chemistry and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, John D. McCarter has authored 47 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 20 papers in Organic Chemistry and 6 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in John D. McCarter's work include Carbohydrate Chemistry and Synthesis (14 papers), Glycosylation and Glycoproteins Research (8 papers) and PI3K/AKT/mTOR signaling in cancer (6 papers). John D. McCarter is often cited by papers focused on Carbohydrate Chemistry and Synthesis (14 papers), Glycosylation and Glycoproteins Research (8 papers) and PI3K/AKT/mTOR signaling in cancer (6 papers). John D. McCarter collaborates with scholars based in United States, Canada and Switzerland. John D. McCarter's co-authors include George Withers, Stephen G. Withers, Mark Namchuk, Victor J. Cee, M.J. Adam, Trevor Andrews, Adam Becalski, Lloyd Mackenzie, Andrea Vasella and Brian W. Matthews and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and Biochemistry.

In The Last Decade

John D. McCarter

46 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mechanisms of enzymatic glycoside hydrolysis

1994 698 citations John D. McCarter et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
John D. McCarter United States	26	1.8k	1.2k	802	311	258	47	2.7k
Tom D. Heightman United Kingdom	30	3.0k 1.7×	1.7k 1.4×	441 0.5×	215 0.7×	134 0.5×	54	4.0k
Jun Hiratake Japan	33	2.3k 1.3×	967 0.8×	328 0.4×	445 1.4×	311 1.2×	84	3.6k
Ian P. Street Australia	31	1.9k 1.1×	998 0.9×	418 0.5×	103 0.3×	152 0.6×	57	3.0k
Günter Legler Germany	35	2.4k 1.3×	2.2k 1.9×	919 1.1×	177 0.6×	260 1.0×	73	3.4k
Ángeles Canales Spain	30	1.5k 0.8×	733 0.6×	198 0.2×	150 0.5×	117 0.5×	88	2.4k
Katsumi Ajisaka Japan	25	1.1k 0.6×	748 0.6×	611 0.8×	160 0.5×	388 1.5×	93	1.8k
Hiromune Ando Japan	28	2.3k 1.3×	1.9k 1.6×	157 0.2×	72 0.2×	178 0.7×	160	3.2k
Kuniaki Tatsuta Japan	35	2.7k 1.5×	3.8k 3.3×	683 0.9×	78 0.3×	160 0.6×	222	5.4k
C.A. Bingman United States	34	2.4k 1.4×	298 0.3×	206 0.3×	175 0.6×	100 0.4×	126	3.2k
David Y. Gin United States	42	3.0k 1.7×	3.2k 2.7×	408 0.5×	63 0.2×	98 0.4×	85	4.7k

Countries citing papers authored by John D. McCarter

Since Specialization

Citations

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

Fields of papers citing papers by John D. McCarter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John D. McCarter. 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 John D. McCarter. The network helps show where John D. McCarter may publish in the future.

Co-authorship network of co-authors of John D. McCarter

This figure shows the co-authorship network connecting the top 25 collaborators of John D. McCarter. A scholar is included among the top collaborators of John D. McCarter 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 John D. McCarter. John D. McCarter 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

Kopecky, David J., Laurie P. Volak, Michael D. Bartberger, et al.. (2020). Systematic Study of the Glutathione Reactivity of N -Phenylacrylamides: 2. Effects of Acrylamide Substitution. Journal of Medicinal Chemistry. 63(20). 11602–11614. 44 indexed citations

Sahasrabuddhe, Aniruddha, et al.. (2020). Development of a High-Throughput Affinity Mass Spectrometry (AMS) Platform Using Laser Diode Thermal Desorption Ionization Coupled to Mass Spectrometry (LDTD-MS). SLAS DISCOVERY. 26(2). 230–241. 4 indexed citations

Saiki, Anne Y., Kevin Gaida, Karen Rex, et al.. (2019). Abstract 4484: Discovery and in vitro characterization of AMG 510–a potent and selective covalent small-molecule inhibitor of KRAS^G12C. 4484–4484. 1 indexed citations

Xia, Fang, et al.. (2015). Development of a nucleotide sugar purification method using a mixed mode column & mass spectrometry detection. Journal of Pharmaceutical and Biomedical Analysis. 115. 402–409. 7 indexed citations

Campuzano, Iain D. G., et al.. (2015). High-Throughput Mass Spectrometric Analysis of Covalent Protein-Inhibitor Adducts for the Discovery of Irreversible Inhibitors: A Complete Workflow. SLAS DISCOVERY. 21(2). 136–144. 46 indexed citations

Stec, Markian M., Kristin L. Andrews, Yunxin Bo, et al.. (2015). The imidazo[1,2-a]pyridine ring system as a scaffold for potent dual phosphoinositide-3-kinase (PI3K)/mammalian target of rapamycin (mTOR) inhibitors. Bioorganic & Medicinal Chemistry Letters. 25(19). 4136–4142. 18 indexed citations

Bui, Minna, Xiaolin Hao, Youngsook Shin, et al.. (2015). Synthesis and SAR study of potent and selective PI3Kδ inhibitors. Bioorganic & Medicinal Chemistry Letters. 25(5). 1104–1109. 18 indexed citations

Lanman, Brian A., Anthony B. Reed, Victor J. Cee, et al.. (2014). Phosphoinositide-3-kinase inhibitors: Evaluation of substituted alcohols as replacements for the piperazine sulfonamide portion of AMG 511. Bioorganic & Medicinal Chemistry Letters. 24(24). 5630–5634. 3 indexed citations

Du, Zhimei, John D. McCarter, Dina Fomina‐Yadlin, et al.. (2014). Use of a small molecule cell cycle inhibitor to control cell growth and improve specific productivity and product quality of recombinant proteins in CHO cell cultures. Biotechnology and Bioengineering. 112(1). 141–155. 92 indexed citations

10.

Zhang, Qingchun, Matthew R. Schenauer, John D. McCarter, & Gregory C. Flynn. (2013). IgG1 Thioether Bond Formation in Vivo. Journal of Biological Chemistry. 288(23). 16371–16382. 34 indexed citations

11.

Zhang, Yihong, Robert J. Kurzeja, James Zondlo, et al.. (2011). Abstract 253: Identification of STK33 kinase inhibitors for the validation of a synthetic lethal relationship between STK33 and mutant KRAS. Cancer Research. 71(8_Supplement). 253–253. 1 indexed citations

12.

Liu, Yichin, et al.. (2008). High-throughput assays for sirtuin enzymes: A microfluidic mobility shift assay and a bioluminescence assay. Analytical Biochemistry. 378(1). 53–59. 44 indexed citations

13.

Liu, Yichin, Leeanne Zalameda, Ki Won Kim, Minghan Wang, & John D. McCarter. (2007). Discovery of Acetyl-Coenzyme A Carboxylase 2 Inhibitors: Comparison of a Fluorescence Intensity-Based Phosphate Assay and a Fluorescence Polarization-Based ADP Assay for High-Throughput Screening. Assay and Drug Development Technologies. 5(2). 225–236. 15 indexed citations

14.

Hale, Clarence, et al.. (2006). A High-Throughput Microfluidic Assay for SH2 Domain-Containing Inositol 5-Phosphatase 2. Assay and Drug Development Technologies. 4(2). 175–183. 11 indexed citations

15.

Setti, Eduardo L., et al.. (2003). 3,4-Disubstituted azetidinones as selective inhibitors of the cysteine protease cathepsin K. Exploring P2 elements for selectivity. Bioorganic & Medicinal Chemistry Letters. 13(12). 2051–2053. 46 indexed citations

16.

McCarter, John D., David L. Burgoyne, Shichang Miao, et al.. (1997). Identification of Glu-268 as the Catalytic Nucleophile of Human Lysosomal β-Galactosidase Precursor by Mass Spectrometry. Journal of Biological Chemistry. 272(1). 396–400. 32 indexed citations

17.

McCarter, John D. & Stephen G. Withers. (1996). Unequivocal Identification of Asp-214 as the Catalytic Nucleophile of Saccharomyces cerevisiae α-Glucosidase Using 5-Fluoro Glycosyl Fluorides. Journal of Biological Chemistry. 271(12). 6889–6894. 115 indexed citations

18.

McCarter, John D., Michael J. Adam, & Stephen G. Withers. (1995). Syntheses, radiolabelling, and kinetic evaluation of 2-deoxy-2-fluoro-2-iodo-d-hexoses for medical imaging. Carbohydrate Research. 266(2). 273–277. 13 indexed citations

19.

McCarter, John D., et al.. (1993). Syntheses of 2-deoxy-2-fluoro mono- and oligo-saccharide glycosides from glycals and evaluation as glycosidase inhibitors. Carbohydrate Research. 249(1). 77–90. 48 indexed citations

20.

McCarter, John D., M.J. Adam, & Stephen G. Withers. (1992). Binding energy and catalysis. Fluorinated and deoxygenated glycosides as mechanistic probes of Escherichia coli (lacZ) β-galactosidase. Biochemical Journal. 286(3). 721–727. 106 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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