Sungsook Lee

673 total citations
30 papers, 566 citations indexed

About

Sungsook Lee is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Sungsook Lee has authored 30 papers receiving a total of 566 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 8 papers in Organic Chemistry and 8 papers in Pharmacology. Recurrent topics in Sungsook Lee's work include Microbial Natural Products and Biosynthesis (8 papers), Metabolism and Genetic Disorders (3 papers) and PARP inhibition in cancer therapy (3 papers). Sungsook Lee is often cited by papers focused on Microbial Natural Products and Biosynthesis (8 papers), Metabolism and Genetic Disorders (3 papers) and PARP inhibition in cancer therapy (3 papers). Sungsook Lee collaborates with scholars based in United States, South Korea and Germany. Sungsook Lee's co-authors include Heinz G. Floss, Taifo Mahmud, Erin Egelkrout, Ingo Tornus, Wolfgang Piepersberg, Juergen Distler, Ansgar Stratmann, Nam Song Choi, Soon Kil Ahn and Bernd Sauerbrei and has published in prestigious journals such as Journal of the American Chemical Society, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Sungsook Lee

28 papers receiving 539 citations

Peers

Sungsook Lee
Comparison fields: 5 of 82
  • Molecular Biology 250
  • Organic Chemistry 232
  • Pharmacology 210
  • Biotechnology 136
  • Plant Science 44
Nidhi Tibrewal United States
Ramesh Dasari India
David L. Burgoyne Canada
Jielu Zhao China
Kento Koketsu Japan
Lanlan Lou China
Felix Ungeheuer Germany
D. G. GRAVALOS Spain
Milton J. Zmijewski United States
Halina Pietraszkiewicz United States
Nidhi Tibrewal United States View profile →
Citations per field, relative to Sungsook Lee
Sungsook Lee · 1×
Citations per year, relative to Sungsook Lee
Sungsook Lee · 1×

Countries citing papers authored by Sungsook Lee

Since Specialization
Citations

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

Fields of papers citing papers by Sungsook Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sungsook Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Sungsook Lee. A scholar is included among the top collaborators of Sungsook Lee 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 Sungsook Lee. Sungsook Lee 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
# Title Journal Authors Indexed citations
1 Quantification of venadaparib, a novel PARP inhibitor, in the rat and dog plasma using liquid chromatography/tandem mass spectrometry Journal of Analytical Science & Technology Jung Woo Lee, Sungsook Lee et al. 0
2 Abstract A106: Development of IDX-1197, a novel, selective, and highly potent PARP inhibitor Molecular Cancer Therapeutics Do‐Hee Kim, Yoon Suk Lee et al. 4
3 (S)-Tetrahydroisoquinoline Alkaloid Inhibits LPS-Induced Arachidonic Acid Release through Downregulation of cPLA2 Expression Molecules and Cells Jong Min Choi, Young Hwa Choi et al. 3
4 Cardiovascular Disease Management among Workers in Small-Sized Enterprise Using Community-Based Approach Occupational Health Nursing Hye‐Sun Jung, Jong Eun Lee et al. 5
5 Discovery of a potent tubulin polymerization inhibitor: Synthesis and evaluation of water-soluble prodrugs of benzophenone analog Bioorganic & Medicinal Chemistry Letters Suyeal Bae, Hojin Choi et al. 27
6 Abstract 4425: Oral efficacy and preclinical ADME evaluation of CKD-516, a novel tubulin polymerization inhibitor Cancer Research Soo Jin Kim, Se‐Mi Kim et al. 1
7 Identification of CKD-516: A Potent Tubulin Polymerization Inhibitor with Marked Antitumor Activity against Murine and Human Solid Tumors Journal of Medicinal Chemistry Soo Jin Kim, Hojin Choi et al. 86
8 Synthesis of novel diaryl ethers and their evaluation as antimitotic agents Bioorganic & Medicinal Chemistry Letters Jae‐Hwan Kwak, Heesoon Lee et al. 18
9 The biosynthesis of acarbose and validamycin The Chemical Record Taifo Mahmud, Sungsook Lee et al. 31
10 Biosynthesis of the Validamycins:  Identification of Intermediates in the Biosynthesis of Validamycin A by Streptomyces hygroscopicus var. limoneus Journal of the American Chemical Society Taifo Mahmud, Ingo Tornus et al. 50
11 The AcbC Protein from Actinoplanes Species Is a C7-cyclitol Synthase Related to 3-Dehydroquinate Synthases and Is Involved in the Biosynthesis of the α-Glucosidase Inhibitor Acarbose Journal of Biological Chemistry Ansgar Stratmann, Taifo Mahmud et al. 69
12 Highly Stereoselective Synthesis of a Chiral Methyl Group by a Facially Controlled Sigmatropic [1,5]-Hydrogen Shift Journal of the American Chemical Society Christoph M. Dehnhardt, Matthew McDonald et al. 14
13 Biosynthetic Studies on the α-Glucosidase Inhibitor Acarbose in Actinoplanes sp.:  2-epi-5-epi-Valiolone Is the Direct Precursor of the Valienamine Moiety Journal of the American Chemical Society Taifo Mahmud, Ingo Tornus et al. 60
14 Biosynthetic Studies on the .ALPHA.-Glucosidase Inhibitor Acarbose in Actinoplanes sp.: Glutamate is the Primary Source of the Nitrogen in Acarbose. The Journal of Antibiotics Sungsook Lee, Erin Egelkrout 24
15 Steric Course of the Methyl Transfer from AdoMet to S-Farnesyl-3-thiopropionate by G-Protein Methyltransferase The Journal of Organic Chemistry Sungsook Lee, Heinz G. Floss et al. 2
16 Biosynthetic Studies on the .ALPHA.-Glucosidase Inbibitor Acarbose in Actinoplanes sp.: Source of the Maltose Unit. The Journal of Antibiotics Sungsook Lee, Bernd Sauerbrei et al. 31
17 Synthesis of [6″-3H]-, (6″-2H)- and (2-2H)-maltotriose Carbohydrate Research Bernd Sauerbrei, Jutta Niggemann et al. 3
18 Stereochemistry of methly transfer catalyzed by tRNA (m5U54)-methyltransferase—evidence for a single displacement mechanism Nucleic Acids Research James T. Kealey, Sungsook Lee et al. 12
19 Stereochemistry of reduction of methylenetetrahydrofolate to methyltetrahydrofolate catalyzed by pig liver methylenetetrahydrofolate reductase Journal of the American Chemical Society Maria A. Vanoni, Sungsook Lee et al. 15
20 Biosynthesis of 7,8-didemethyl-8-hydroxy-5-deazariboflavin, the chromophoric moiety of coenzyme F420 Journal of the American Chemical Society Adelbert Bacher, Paul J. Keller et al. 13

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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