Discovery, synthesis and biological evaluation of a series of N-(phenylcarbamothioyl)-2-napthamides as inhibitors of Claudin-1

Viktoriya Mashinson; Thomas M Webster; Anish K Vadukoot; Kirsten T Tolentino; Princess Simeon; Iram Fatima; Punita Dhawan; Corey R Hopkins

doi:10.1016/j.bmc.2023.117416

Discovery, synthesis and biological evaluation of a series of N-(phenylcarbamothioyl)-2-napthamides as inhibitors of Claudin-1

Bioorg Med Chem. 2023 Sep 7:92:117416. doi: 10.1016/j.bmc.2023.117416. Epub 2023 Jul 26.

Authors

Viktoriya Mashinson¹, Thomas M Webster¹, Anish K Vadukoot¹, Kirsten T Tolentino¹, Princess Simeon¹, Iram Fatima², Punita Dhawan³, Corey R Hopkins⁴

Affiliations

¹ Department of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, NE 68198-6125, USA.
² Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, NE 68198, USA.
³ Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, NE 68198, USA; VA Nebraska-Western Iowa Health Care System, Omaha, NE, USA; Buffet Cancer Center, University of Nebraska Medical Center, Omaha, NE, USA.
⁴ Department of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, NE 68198-6125, USA. Electronic address: corey.hopkins@unmc.edu.

PMID: 37541070
PMCID: PMC10530161 (available on 2024-09-07)
DOI: 10.1016/j.bmc.2023.117416

Abstract

Colorectal cancer (CRC) remains a leading cause of cancer-related deaths worldwide, despite advancements in diagnosis. The main reason for this is that many newly diagnosed CRC patients will suffer from metastasis to other organs. Thus, the development of new therapies is of critical importance. Claudin-1 protein is a component of tight junctions in epithelial cells, including those found in the lining of the colon. It plays a critical role in the formation and maintenance of tight junctions, which are essential for regulating the passage of molecules between cells. In CRC, claudin-1 is often overexpressed, leading to an increase in cell adhesion, which can contribute to the development and progression of the disease. Studies show that high levels of claudin-1 are associated with poor prognosis in CRC patients and targeting claudin-1 may have therapeutic potential for the treatment of CRC. Previously, we have identified a small molecule that inhibits claudin-1 dependent CRC progression. Reported herein are our lead optimization efforts around this scaffold to identify the key SAR components and the discovery of a key new compound that exhibits enhanced potency in SW620 cells.

Keywords: Claudin-1; Colorectal cancer; In vitro PK; In vivo PK; Structure–activity relationship; Thiourea.

Publication types

Research Support, N.I.H., Extramural

MeSH terms

Claudin-1
Colorectal Neoplasms* / pathology
Epithelial Cells / metabolism
Humans

Substances

Claudin-1

Grants and funding

R01 CA250383/CA/NCI NIH HHS/United States