Michal P. Glogowski

ORCID: 0000-0003-2508-811X
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About
Contact & Profiles
Research Areas
  • Renal and related cancers
  • CRISPR and Genetic Engineering
  • Animal Genetics and Reproduction
  • DNA Repair Mechanisms
  • RNA modifications and cancer
  • Cancer-related gene regulation
  • Digestive system and related health
  • Asymmetric Synthesis and Catalysis
  • Radical Photochemical Reactions
  • Coordination Chemistry and Organometallics
  • Fluorine in Organic Chemistry
  • Biochemical and Molecular Research
  • Genomics and Chromatin Dynamics
  • Endoplasmic Reticulum Stress and Disease
  • Sulfur-Based Synthesis Techniques
  • Catalytic C–H Functionalization Methods

South College
2021-2024

Providence College
2024

GlaxoSmithKline (United States)
2021

Microsatellite-unstable (MSI) cancers require WRN helicase to resolve replication stress due expanded DNA (TA)n dinucleotide repeats. is a promising synthetic lethal target for MSI tumors, and inhibitors are in development. In this study, we used CRISPR-Cas9 base editing map residues critical cells, validating the domain as primary drug target. Fragment-based screening led development of potent highly selective covalent inhibitors. These compounds selectively suppressed model growth vitro...

10.1158/2159-8290.cd-24-0052 article EN Cancer Discovery 2024-04-06

The discussion herein describes a metallaphotoredox reaction that allows for efficient exploration of benzyl structure–activity relationships in medicinal chemistry. use HTE (high-throughput experimentation) and ChemBeads rapid optimization. formation di(hetero)arylmethanes via cross-electrophile coupling between aryl bromides provides access to diverse chemical space. breadth the substrate scope will be discussed, along with utilization batch photochemistry preparation this...

10.1021/acs.orglett.4c00577 article EN Organic Letters 2024-03-18

<div>Abstract<p>Microsatellite-unstable (MSI) cancers require WRN helicase to resolve replication stress due expanded DNA (TA)<sub>n</sub> dinucleotide repeats. is a promising synthetic lethal target for MSI tumors, and inhibitors are in development. In this study, we used CRISPR–Cas9 base editing map residues critical cells, validating the domain as primary drug target. Fragment-based screening led development of potent highly selective covalent inhibitors. These...

10.1158/2159-8290.c.7384699 preprint EN 2024-08-02

<div>Abstract<p>Microsatellite-unstable (MSI) cancers require WRN helicase to resolve replication stress due expanded DNA (TA)<sub>n</sub> dinucleotide repeats. is a promising synthetic lethal target for MSI tumors, and inhibitors are in development. In this study, we used CRISPR–Cas9 base editing map residues critical cells, validating the domain as primary drug target. Fragment-based screening led development of potent highly selective covalent inhibitors. These...

10.1158/2159-8290.c.7384699.v1 preprint EN 2024-08-02

A two-step metal–halogen exchange and diastereoselective copper-mediated Michael addition onto a complex α,β-unsaturated system has been developed applied toward the synthesis of bisaryl Nrf2 activators. Optimization using (n-Bu)3MgLi allowed for preparation custom aryl-functionalized magnesiate reagents at noncryogenic temperatures. Following transmetalation, these were used in highly reactions.

10.1021/acs.joc.0c02639 article EN The Journal of Organic Chemistry 2021-02-08
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