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D-Index & Metrics

Biology and Biochemistry

D-Index
64
Citations
17190
World Ranking
9544
National Ranking
4212

Overview

Stephen V. Frye is affiliated with the University of North Carolina at Chapel Hill in the United States. Their research spans multiple disciplines, primarily in Biochemistry, Genetics, and Molecular Biology, with a significant portion of work also connected to Medicine.

Their main fields of study include:

  • Biochemistry, Genetics and Molecular Biology
  • Medicine

Within these broad areas, Frye's research focuses on specific subfields such as Molecular Biology, Immunology, Organic Chemistry, Computational Theory and Mathematics, and Oncology.

  • Molecular Biology
  • Immunology
  • Organic Chemistry
  • Computational Theory and Mathematics
  • Oncology

The scientist's work addresses various research topics, including:

  • Phagocytosis and Immune Regulation
  • Epigenetics and DNA Methylation
  • Cancer-related gene regulation
  • Computational Drug Discovery Methods
  • Genomics and Chromatin Dynamics
  • Cell death mechanisms and regulation
  • Protein Degradation and Inhibitors

Frye has published in multiple frequent venues where their research output is notably present. These venues include:

  • UNC Libraries
  • OPAL (Open@LaTrobe) (La Trobe University)
  • Cancer Research
  • Journal of Medicinal Chemistry
  • bioRxiv (Cold Spring Harbor Laboratory)

Collaborative efforts form a significant part of Frye's work, with frequent co-authors being:

  • Xiaodong Wang
  • Dmitri Kireev
  • H. Shelton Earp
  • Lindsey I. James
  • Deborah DeRyckere

The scientist's recent notable papers, indicating ongoing research trends and areas of emphasis, include:

  • Target 2035 - update on the quest for a probe for every protein, 2021, RSC Medicinal Chemistry
  • PROTAC Linkerology Leads to an Optimized Bivalent Chemical Degrader of Polycomb Repressive Complex 2 (PRC2) Components, 2023, ACS Chemical Biology
  • MERTK activation drives osimertinib resistance in EGFR-mutant non-small cell lung cancer, 2022, Journal of Clinical Investigation
  • MerTK inhibition decreases immune suppressive glioblastoma-associated macrophages and neoangiogenesis in glioblastoma microenvironment, 2020, Neuro-Oncology Advances
  • Discovery and Optimization of 2H-1λ2-Pyridin-2-one Inhibitors of Mutant Isocitrate Dehydrogenase 1 for the Treatment of Cancer, 2021, Journal of Medicinal Chemistry

Best Publications

  • Oncometabolite 2-Hydroxyglutarate Is a Competitive Inhibitor of α-Ketoglutarate-Dependent Dioxygenases

    Wei Xu;Hui Yang;Ying Liu;Ying Yang

  • The promise and peril of chemical probes.

    Cheryl H. Arrowsmith;James E. Audia;Christopher Austin;Jonathan Baell

  • Dynamic Reprogramming of the Kinome in Response to Targeted MEK Inhibition in Triple-Negative Breast Cancer

    James S. Duncan;Martin C. Whittle;Kazuhiro Nakamura;Amy N. Abell

  • A chemical probe selectively inhibits G9a and GLP methyltransferase activity in cells

    Masoud Vedadi;Dalia Barsyte-Lovejoy;Feng Liu;Sylvie Rival-Gervier

  • An orally bioavailable chemical probe of the Lysine Methyltransferases EZH2 and EZH1.

    Kyle D. Konze;Anqi Ma;Fengling Li;Dalia Barsyte-Lovejoy

  • Too many roads not taken

    Aled M Edwards;Ruth Isserlin;Gary D Bader;Stephen V Frye

  • The art of the chemical probe

    Stephen V Frye

  • Discovery of β-Arrestin–Biased Dopamine D2 Ligands for Probing Signal Transduction Pathways Essential for Antipsychotic Efficacy

    John A. Allen;Julianne M. Yost;Vincent Setola;Xin Chen

  • The human genome and drug discovery after a decade. Roads (still) not taken

    Ruth Isserlin;Gary D. Bader;Aled Edwards;Stephen Frye

  • Oxindole-based inhibitors of cyclin-dependent kinase 2 (CDK2): design, synthesis, enzymatic activities, and X-ray crystallographic analysis.

    H.N. Bramson;J. Corona;S.T. Davis;S.H. Dickerson

  • The discovery of potent cRaf1 kinase inhibitors

    Karen Lackey;Michael Cory;Ronda Davis;Stephen V. Frye

  • Discovery of an in vivo chemical probe of the lysine methyltransferases G9a and GLP.

    Feng Liu;Dalia Barsyte-Lovejoy;Fengling Li;Yan Xiong

  • Structure and Inhibition of Microbiome β-Glucuronidases Essential to the Alleviation of Cancer Drug Toxicity

    Bret D. Wallace;Adam B. Roberts;Rebecca M. Pollet;James D. Ingle

  • Discovery of a 2,4-diamino-7-aminoalkoxyquinazoline as a potent and selective inhibitor of histone lysine methyltransferase G9a.

    Feng Liu;Xin Chen;Abdellah Allali-Hassani;Amy M. Quinn

  • Prevention of chemotherapy-induced alopecia in rats by CDK inhibitors.

    Stephen T. Davis;Bill G. Benson;H. Neal Bramson;Dennis E. Chapman

  • Selective inhibition of EZH2 and EZH1 enzymatic activity by a small molecule suppresses MLL-rearranged leukemia

    Bowen Xu;Doan M. On;Anqi Ma;Trevor Parton

  • Protein lysine methyltransferase g9a inhibitors: Design, synthesis, and structure activity relationships of 2,4-diamino-7-aminoalkoxy-quinazolines.

    Feng Liu;Xin Chen;Abdellah Allali-Hassani;Amy M. Quinn

  • Chelates as intermediates in nucleophilic additions to alkoxy ketones according to Cram's rule (cyclic model)

    Xiangning Chen;Edwin R. Hortelano;Ernest L. Eliel;Stephen V. Frye

  • Unique Preclinical Characteristics of GG745, A Potent Dual Inhibitor of 5AR

    H N Bramson;D Hermann;K W Batchelor;F W Lee

  • Discovery of a chemical probe for the L3MBTL3 methyllysine reader domain

    Lindsey I. James;Dalia Barsyte-Lovejoy;Nan Zhong;Liubov Krichevsky

Frequent Co-Authors

H. Shelton Earp
H. Shelton Earp University of North Carolina at Chapel Hill
Jian Jin
Jian Jin Icahn School of Medicine at Mount Sinai
Cheryl H. Arrowsmith
Cheryl H. Arrowsmith Structural Genomics Consortium
Peter Brown
Peter Brown University of Oxford
Masoud Vedadi
Masoud Vedadi Structural Genomics Consortium
Bryan L. Roth
Bryan L. Roth University of North Carolina at Chapel Hill
Mark T. Bedford
Mark T. Bedford The University of Texas MD Anderson Cancer Center
Aled M. Edwards
Aled M. Edwards Structural Genomics Consortium
Stefan Knapp
Stefan Knapp Goethe University Frankfurt
Timothy M. Willson
Timothy M. Willson University of North Carolina at Chapel Hill

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