Michael Schultz

Michael Schultz

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Co-Founder and Chief Science Officer Viewpoint Molecular Targeting, DBA Perspective Therapeutics
Coralville, Iowa, United States

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  • Perspective Therapeutics
    Co-Founder and Chief Science Officer Viewpoint Molecular Targeting, DBA Perspective Therapeutics
    Perspective Therapeutics
    Jan 2023 - Current (3 years 4 months)
    Perspective Therapeutics is a clinical stage radiopharmaceutical company developing the next generation of alpha particle therapeutics for cancer.
  • Viewpoint Molecular Targeting Inc
    Chief Science Officer
    Viewpoint Molecular Targeting Inc
    Aug 2013 - Current (12 years 9 months)
    Founder and Chief Science Officer of a pharmaceutical company specializing in radiopharmaceutical therapies for cancer. Successful in securing over $35M in NIH/NCI SBIR/STTR funding and capital investment to move lead products into the clinical stage of development.
  • University of Iowa
    Associate Professor
    University of Iowa
    Aug 2006 - Current (19 years 9 months)
    Associate Professor of Radiology, with appointments in Pediatrics, Radiation Oncology, Chemistry, Human Toxicology, and the Free Radical and Radiation Biology Program.
Education verified_user 0% verified
  • Florida State University
    Doctor of Philosophy - PhD, Oceanography, Chemical and Physical
    Florida State University
Publications verified_user 0% verified
  • F
    N-alkyl triphenylvinylpyridinium conjugated dihydroartemisinin perturbs mitochondrial functions resulting in enhanced ca
    Free Radical Biology and Medicine
    Feb 2021
    Dihydroartemisinin (DHA) is an FDA-approved antimalarial drug that has been repurposed for cancer therapy because of its preferential antiproliferative effects on cancer versus normal cells. Mitochondria represent an attractive target for cancer therapy based on their regulatory role in proliferation and cell death. This study investigates whether DHA conjugated to innately fluorescent N-alkyl triphenylvinylpyridinium (TPVP) perturbs mitochondrial functions resulting in a differential toxicity of cancer versus normal cells. TPVP-DHA treatments resulted in a dose-dependent toxicity of human melanoma and pancreatic cancer cells, whereas normal human fibroblasts were resistant to this treatment. TPVP-DHA treatments resulted in a G1-delay of th
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