Juan Jose Marugan, Ph.D.
Leader
Division of Preclinical Innovation
Chemistry Technologies
Contact Info
Biography
Juan Jose Marugan, Ph.D., is the leader of the Chemistry Technology program within NCATS' Division of Preclinical Innovation. He joined NIH in 2008 and subsequently joined NCATS. Marugan has extensive experience as a team leader of programs at the lead optimization stage; several leads have been licensed to pharmaceutical companies, and several molecules have advanced toward preclinical development or clinical trials. Marugan’s job responsibilities have included lead discovery and optimization with early absorption, distribution, metabolism and excretion as well as pharmacokinetics profiling; managing internal and external resources; structure-activity relationship optimization; chiral separation; and in vivo studies
Marugan has more than 20 years of experience in drug discovery and development, from classical medicinal chemistry to structure-based drug design, high-throughput screening, enzymatic and cell assays, and in vivo models. His involvement in pharmaceuticals began during his doctoral studies, carried out in in partnership with Pharma Mar S.A., a Spanish pharmaceutical company involved in the development of marine natural products. After holding medicinal chemistry postdoctoral positions at the University of Pittsburgh and Tufts University, Marugan moved to the pharmaceutical sector, holding positions of increasing responsibility from research scientist to head of preclinical drug research.
Marugan earned his doctorate in organic chemistry from the Universidad Complutense de Madrid and his Bachelor of Science in chemistry from the Universidad de Salamanca.
Research Topics
During the course of his scientific life, Marugan has been involved in the investigation of active compounds in numerous therapeutic areas, including antivirals; antibiotics; oncology; and cardiovascular, central nervous system, and rare and neglected diseases. He serves as a co-leader of an interdisciplinary project team with a diverse target portfolio, including:
- Lysosomal storage disorders: Niemann-Pick disease type C, Gaucher disease, Pompe disease, metachromatic leukodystrophy
- Neurodegenerative disorders: Alzheimer’s disease, Huntington’s disease, amyotrophic lateral sclerosis, Parkinson’s disease, spinal muscular atrophy
- Neurodevelopment and mood disorders: autism, neurogenesis and synaptogenesis, schizophrenia
- Cancer: metastasis, immune activation, Eya phosphatase
- G protein–coupled receptor modulators: RXFP1, GPR120, GPR110, GPR32, TSHR, D2R
- Virus: influenza, hepatitis C virus, Venezuelan equine encephalitis virus
Selected Publications
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Chlorcyclizine Inhibits Viral Fusion of Hepatitis C Virus Entry by Directly Targeting HCV Envelope Glycoprotein 1
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Identification of Small Molecule Enhancers of Immunotherapy for Melanoma
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Validation and Characterization of Five Distinct Novel Inhibitors of Human Cytomegalovirus
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Metabolism and pharmacokinetics characterization of metarrestin in multiple species
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Synaptamide activates the adhesion GPCR GPR110 (ADGRF1) through GAIN domain binding