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Biology and Biochemistry

D-Index
66
Citations
20183
World Ranking
8512
National Ranking
624

Overview

Ajit Jadhav is a researcher affiliated with Pfizer (Germany) in Germany, focusing primarily on the fields of Biochemistry, Genetics, and Molecular Biology, with significant contributions in Medicine.

Their publication record spans multiple disciplines with an emphasis on Molecular Biology, Cancer Research, Oncology, Immunology, and Radiology, Nuclear Medicine, and Imaging. Jadhav's research addresses topics such as Cancer, Hypoxia, and Metabolism; Cancer-related Gene Regulation; Epigenetics and DNA Methylation; RNA Modifications and Cancer; ATP Synthase and ATPases Research; Mitochondrial Function and Pathology; and Computational Drug Discovery Methods.

Their recent papers include:

  • Dynamic Imaging of LDH Inhibition in Tumors Reveals Rapid In Vivo Metabolic Rewiring and Vulnerability to Combination Therapy, 2020, Cell Reports
  • Pyrazole-Based Lactate Dehydrogenase Inhibitors with Optimized Cell Activity and Pharmacokinetic Properties, 2020, Journal of Medicinal Chemistry
  • NCATS Inxight Drugs: a comprehensive and curated portal for translational research, 2021, Nucleic Acids Research
  • Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors, 2020, Proceedings of the National Academy of Sciences
  • Characterization of Lead Compounds Targeting the Selenoprotein Thioredoxin Glutathione Reductase for Treatment of Schistosomiasis, 2020, ACS Infectious Diseases

Frequent collaborators in Jadhav's research include Anton Simeonov, Ganesha Rai, David J. Maloney, Alexey Zakharov, and Adam Yasgar.

They have published extensively in high-impact venues such as Scientific Reports, UNC Libraries, Cell Reports, Journal of Medicinal Chemistry, and Cancer Research.

Best Publications

  • Sharing and community curation of mass spectrometry data with Global Natural Products Social Molecular Networking

    Mingxun Wang;Jeremy J Carver;Vanessa V Phelan;Laura M Sanchez

  • Quantitative high-throughput screening: a titration-based approach that efficiently identifies biological activities in large chemical libraries.

    James Inglese;Douglas S. Auld;Ajit Jadhav;Ronald L. Johnson

  • Drug-based modulation of endogenous stem cells promotes functional remyelination in vivo.

    Fadi J. Najm;Mayur Madhavan;Anita Zaremba;Elizabeth Shick

  • The NCGC Pharmaceutical Collection: A Comprehensive Resource of Clinically Approved Drugs Enabling Repurposing and Chemical Genomics

    Ruili Huang;Noel Southall;Yuhong Wang;Adam Yasgar

  • High-throughput combinatorial screening identifies drugs that cooperate with ibrutinib to kill activated B-cell–like diffuse large B-cell lymphoma cells

    Lesley A. Mathews Griner;Rajarshi Guha;Paul Shinn;Ryan M. Young

  • Open Source Drug Discovery with the Malaria Box Compound Collection for Neglected Diseases and Beyond.

    Wesley C. Van Voorhis;John H. Adams;Roberto Adelfio;Roberto Adelfio;Vida Ahyong

  • A high-throughput screen for aggregation-based inhibition in a large compound library.

    Brian Y. Feng;Anton Simeonov;Ajit Jadhav;Kerim Babaoglu

  • Unexplored therapeutic opportunities in the human genome.

    Tudor I. Oprea;Cristian G. Bologa;Søren Brunak;Allen Campbell

  • Pharos: Collating protein information to shed light on the druggable genome

    Dac-Trung Nguyen;Stephen L. Mathias;Cristian Bologa;Søren Brunak

  • The NCATS BioPlanet - An Integrated Platform for Exploring the Universe of Cellular Signaling Pathways for Toxicology, Systems Biology, and Chemical Genomics.

    Ruili Huang;Ivan Grishagin;Yuhong Wang;Tongan Zhao

  • Compound cytotoxicity profiling using quantitative high-throughput screening.

    Menghang Xia;Ruili Huang;Kristine L. Witt;Noel Southall

  • A selective USP1–UAF1 inhibitor links deubiquitination to DNA damage responses

    Qin Liang;Thomas S Dexheimer;Ping Zhang;Andrew S Rosenthal

  • Fluorescence Spectroscopic Profiling of Compound Libraries

    Anton Simeonov;Ajit Jadhav;Craig J. Thomas;Yuhong Wang

  • Complementarity between a docking and a high-throughput screen in discovering new cruzain inhibitors.

    Rafaela S. Ferreira;Anton Simeonov;Ajit Jadhav;Oliv Eidam

  • Quantitative Analyses of Aggregation, Autofluorescence, and Reactivity Artifacts in a Screen for Inhibitors of a Thiol Protease

    Ajit Jadhav;Rafaela S. Ferreira;Carleen Klumpp;Bryan T. Mott

  • 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

  • Quantitative high-throughput screening identifies 8-hydroxyquinolines as cell-active histone demethylase inhibitors.

    Oliver N. F. King;Xuan Shirley Li;Masaaki Sakurai;Akane Kawamura

  • Selective and Cell-Active Inhibitors of the USP1/ UAF1 Deubiquitinase Complex Reverse Cisplatin Resistance in Non-small Cell Lung Cancer Cells

    Junjun Chen;Thomas S. Dexheimer;Yongxing Ai;Qin Liang

  • Characterization of chemical libraries for luciferase inhibitory activity.

    Douglas S. Auld;Noel T. Southall;Ajit Jadhav;Ronald L. Johnson

  • 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

Frequent Co-Authors

Anton Simeonov
Anton Simeonov National Institutes of Health
James Inglese
James Inglese National Institutes of Health
Matthew D. Hall
Matthew D. Hall National Institutes of Health
Craig J. Thomas
Craig J. Thomas National Institutes of Health
Rajarshi Guha
Rajarshi Guha Google (United States)
Christopher P. Austin
Christopher P. Austin National Institutes of Health
Theodore R. Holman
Theodore R. Holman University of California, Santa Cruz
Ruili Huang
Ruili Huang National Institutes of Health
Wei Zheng
Wei Zheng National Institutes of Health
David G. Maloney
David G. Maloney Fred Hutchinson Cancer Research Center

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