Tze‐Ming Chan

435 total citations
19 papers, 330 citations indexed

About

Tze‐Ming Chan is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Tze‐Ming Chan has authored 19 papers receiving a total of 330 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Organic Chemistry and 6 papers in Pharmacology. Recurrent topics in Tze‐Ming Chan's work include Microbial Natural Products and Biosynthesis (6 papers), Carbohydrate Chemistry and Synthesis (5 papers) and Hepatitis C virus research (4 papers). Tze‐Ming Chan is often cited by papers focused on Microbial Natural Products and Biosynthesis (6 papers), Carbohydrate Chemistry and Synthesis (5 papers) and Hepatitis C virus research (4 papers). Tze‐Ming Chan collaborates with scholars based in United States, United Kingdom and Switzerland. Tze‐Ming Chan's co-authors include Mahesh Patel, Vincent P. Gullo, Vinod R. Hegde, Ronald Mierzwa, Min Chu, Todd A. Black, Wenjun Zhao, Andrew T. McPhail, Mohindar S. Puar and Imbi Truumees and has published in prestigious journals such as Angewandte Chemie International Edition, The Journal of Organic Chemistry and Tetrahedron Letters.

In The Last Decade

Tze‐Ming Chan

19 papers receiving 310 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tze‐Ming Chan United States 11 131 104 83 49 38 19 330
Hyung‐Jung Pyun United States 15 259 2.0× 108 1.0× 88 1.1× 22 0.4× 66 1.7× 23 492
Jian‐Guo Song China 9 140 1.1× 52 0.5× 47 0.6× 90 1.8× 17 0.4× 34 281
Nigel J. Coates United States 9 253 1.9× 82 0.8× 147 1.8× 44 0.9× 14 0.4× 10 371
Imbi Truumees United States 15 152 1.2× 212 2.0× 295 3.6× 47 1.0× 19 0.5× 22 488
Iou‐Jiun Kang Taiwan 11 111 0.8× 296 2.8× 19 0.2× 52 1.1× 23 0.6× 35 489
Yung Chang Belgium 4 83 0.6× 369 3.5× 109 1.3× 24 0.5× 22 0.6× 4 461
Ken‐ichi Suzumura Japan 12 241 1.8× 111 1.1× 149 1.8× 14 0.3× 11 0.3× 20 425
Emil Yu. Yamansarov Russia 12 284 2.2× 99 1.0× 25 0.3× 36 0.7× 12 0.3× 26 375
Nana Du China 12 204 1.6× 115 1.1× 90 1.1× 40 0.8× 73 1.9× 22 457
Matthew M. Ravn United States 11 377 2.9× 85 0.8× 166 2.0× 13 0.3× 8 0.2× 12 462

Countries citing papers authored by Tze‐Ming Chan

Since Specialization
Citations

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

Fields of papers citing papers by Tze‐Ming Chan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tze‐Ming Chan. 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 Tze‐Ming Chan. The network helps show where Tze‐Ming Chan may publish in the future.

Co-authorship network of co-authors of Tze‐Ming Chan

This figure shows the co-authorship network connecting the top 25 collaborators of Tze‐Ming Chan. A scholar is included among the top collaborators of Tze‐Ming Chan 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 Tze‐Ming Chan. Tze‐Ming Chan 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.
Senior, Mary M., Tze‐Ming Chan, Guoqing Li, Ying Huang, & Andrew W. Stamford. (2007). Unambiguous structural characterization of hydantoin reaction products using 2D HMBC NMR spectroscopy. Magnetic Resonance in Chemistry. 45(3). 240–244. 3 indexed citations
2.
3.
Chen, Kevin X., F. George Njoroge, Bancha Vibulbhan, et al.. (2005). Proline‐Based Macrocyclic Inhibitors of the Hepatitis C Virus: Stereoselective Synthesis and Biological Activity. Angewandte Chemie International Edition. 44(43). 7024–7028. 10 indexed citations
4.
Hegde, Vinod R., et al.. (2005). A new antitumor compound from the plant Oryctanthus sp. as a VEGF receptor binding inhibitor. Bioorganic & Medicinal Chemistry Letters. 15(22). 4907–4909. 11 indexed citations
5.
Chen, Kevin X., F. George Njoroge, Bancha Vibulbhan, et al.. (2005). Proline‐Based Macrocyclic Inhibitors of the Hepatitis C Virus: Stereoselective Synthesis and Biological Activity. Angewandte Chemie. 117(43). 7186–7190. 1 indexed citations
6.
Hegde, Vinod R., Mahesh Patel, Todd A. Black, et al.. (2004). Two new bacterial DNA primase inhibitors from the plant Polygonum cuspidatum. Bioorganic & Medicinal Chemistry Letters. 14(9). 2275–2277. 46 indexed citations
7.
Buevich, Alexei V., et al.. (2004). Structure determination and conformation analysis of symmetrical dimers. Magnetic Resonance in Chemistry. 43(3). 187–199. 9 indexed citations
8.
Hegde, Vinod R., Mahesh Patel, Todd A. Black, et al.. (2004). Two New Bacterial DNA Primase Inhibitors from the Plant Polygonum cuspidatum.. ChemInform. 35(36). 5 indexed citations
9.
Hegde, Vinod R., Mohindar S. Puar, Mahesh Patel, et al.. (2003). Condensed aromatic peptide family of microbial metabolites, inhibitors of CD28–CD80 interactions. Bioorganic & Medicinal Chemistry Letters. 13(3). 573–575. 10 indexed citations
10.
Chu, Min, Ronald Mierzwa, Shu‐Wei Yang, et al.. (2003). Structure elucidation of Sch 538415, a novel acyl carrier protein synthase inhibitor from a microorganism. Bioorganic & Medicinal Chemistry Letters. 13(21). 3827–3829. 19 indexed citations
11.
Hegde, Vinod R., Mahesh Patel, Pradip R. Das, et al.. (2003). Two antiviral compounds from the plant Stylogne cauliflora as inhibitors of HCV NS3 protease. Bioorganic & Medicinal Chemistry Letters. 13(17). 2925–2928. 29 indexed citations
12.
Hegde, Vinod R., Mahesh Patel, Pradip R. Das, et al.. (2003). Two Antiviral Compounds from the Plant Stylogne cauliflora as Inhibitors of HCV NS3 Protease. ChemInform. 34(48). 1 indexed citations
13.
Chu, Min, Ronald Mierzwa, Ling He, et al.. (2003). Isolation and Structure Elucidation of Sch 642305, a Novel Bacterial DNA Primase Inhibitor Produced by Penicillium verrucosum. Journal of Natural Products. 66(12). 1527–1530. 45 indexed citations
14.
Chen, Kevin X., F. George Njoroge, Bancha Vibulbhan, et al.. (2002). Syntheses of Novel 4-tert-Alkyl Ether Proline-Based 16- and 17-Membered Macrocyclic Compounds. The Journal of Organic Chemistry. 67(8). 2730–2733. 9 indexed citations
15.
Kaminski, James J., et al.. (1999). Conformational considerations in the design of dual antagonists of platelet-activating factor (PAF) and histamine. Bioorganic & Medicinal Chemistry. 7(7). 1413–1423. 12 indexed citations
16.
17.
Wang, Yongfeng, Malcolm F. G. Stevens, Tze‐Ming Chan, et al.. (1997). Antitumor Imidazotetrazines. 35. New Synthetic Routes to the Antitumor Drug Temozolomide. The Journal of Organic Chemistry. 62(21). 7288–7294. 21 indexed citations
18.
Chu, Min, Ronald Mierzwa, Imbi Truumees, et al.. (1996). Structure of Sch 68631: A new hepatitis C virus proteinase inhibitor from Streptomyces sp.. Tetrahedron Letters. 37(40). 7229–7232. 29 indexed citations
19.
Chu, Min, Ronald Mierzwa, Imbi Truumees, et al.. (1993). Two novel diketopiperazines isolated from the fungus Tolypocladium sp.. Tetrahedron Letters. 34(47). 7537–7540. 39 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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