Publications by authors named "Matthew Surman"

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Development of clinically viable non-muscle myosin II small molecule inhibitors.
Laszlo Radnai, Erica J Young, Carlos Kikuti, Katalin Toth, Minghai Zhou, Matthew Surman

Cell· August 2025

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Precursor Development and Aerosol-Assisted Chemical Vapour Deposition for BiVO and W-Doped BiVO Photoanodes: A Universal Ligand Approach.
Thom R Harris-Lee, Matthew K Surman, Andrew J Straiton, Frank Marken, Andrew L Johnson

ChemSusChem· February 2025

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Development of Clinically Viable Non-Muscle Myosin II Small Molecule Inhibitors with Broad Therapeutic Potential.
Laszlo Radnai, Erica J Young, Carlos Kikuti, Madalyn Hafenbreidel, Rebecca F Stremel, Matthew Surman

bioRxiv· October 2024

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Optimization of a Novel Mandelamide-Derived Pyrrolopyrimidine Series of PERK Inhibitors.
Michael E Stokes, Matthew D Surman, Veronica Calvo, David Surguladze, An-Hu Li

Pharmaceutics· October 2022

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Discovery of Selective Inhibitors for and Interrogation of Skeletal Myosin II.
Laszlo Radnai, Matthew Surman, Madalyn Hafenbreidel, Erica J Young, Rebecca F Stremel

ACS Chem Biol· November 2021

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Discovery of 2-amino-3-amido-5-aryl-pyridines as highly potent, orally bioavailable, and efficacious PERK kinase inhibitors.
Veronica Calvo, David Surguladze, An-Hu Li, Matthew D Surman, Srikanth Malibhatla

Bioorg Med Chem Lett· July 2021

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Design and Synthesis of Selective Phosphodiesterase 4D (PDE4D) Allosteric Inhibitors for the Treatment of Fragile X Syndrome and Other Brain Disorders.
Mark E Gurney, Richard A Nugent, Xuesheng Mo, Janice A Sindac, Timothy J Hagen, Matthew D Surman

J Med Chem· May 2019

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From preclinical to clinical development: the example of a novel treatment for obesity.
Nicholas A Moore, Bruce J Sargent, Peter R Guzzo, Matthew D Surman

Neurobiol Dis· January 2014

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Synthesis and SAR of 4-aryl-1-(indazol-5-yl)pyridin-2(1H)ones as MCH-1 antagonists for the treatment of obesity.
Mark Hadden, Dustin M Deering, Alan J Henderson, Matthew D Surman, Michele Luche

Bioorg Med Chem Lett· December 2010

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Tetrahydrocarboline analogs as MCH-1 antagonists.
Alan J Henderson, Dustin Deering, James F Grabowski, Mark Hadden, Xiaowu Jiang, Matthew D Surman

Bioorg Med Chem Lett· December 2010

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5-(pyridinon-1-yl)indazoles and 5-(furopyridinon-5-yl)indazoles as MCH-1 antagonists.
Matthew D Surman, Emily E Freeman, James F Grabowski, Mark Hadden, Alan J Henderson

Bioorg Med Chem Lett· December 2010

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Synthesis and SAR of vinca alkaloid analogues.
Matthew E Voss, Jeffery M Ralph, Dejian Xie, David D Manning, Xinchao Chen, Matthew D Surman

Bioorg Med Chem Lett· February 2009

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Stereo- and regioselectivity of Pd(0)/InI-mediated allylic additions to aldehydes and ketones. In situ generation of allylindium(III) intermediates from N-acylnitroso Diels-Alder cycloadducts and 1-amino-4-acetoxycyclopentenes.
Wenlin Lee, Kyung-Hee Kim, Matthew D Surman, Marvin J Miller

J Org Chem· January 2003

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Regio- and stereoselective ring openings of 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene systems with copper catalyst-modified grignard reagents: application to the synthesis of an inhibitor of 5-lipoxygenase.
Matthew D Surman, Mark J Mulvihill, Marvin J Miller

J Org Chem· June 2002

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Novel 1,4-benzodiazepines from acylnitroso-derived hetero-Diels-Alder cycloadducts.
Matthew D Surman, Mark J Mulvihill, Marvin J Miller

Org Lett· January 2002

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