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Discovery and Optimization of Pyrrolopyrimidine Derivatives as Selective Disruptors of the Perinucleolar Compartment, a Marker of Tumor Progression toward Metastasis

Authors :
Kevin J. Frankowski
Samarjit Patnaik
Chen Wang
Noel Southall
Dipannita Dutta
Soumitta De
Dandan Li
Christopher Dextras
Yi-Han Lin
Marthe Bryant-Connah
Danielle Davis
Feijun Wang
Leah M. Wachsmuth
Pranav Shah
Jordan Williams
Md Kabir
Edward Zhu
Bolormaa Baljinnyam
Amy Wang
Xin Xu
John Norton
Marc Ferrer
Steve Titus
Anton Simeonov
Wei Zheng
Lesley A. Mathews Griner
Ajit Jadhav
Jeffrey Aubé
Mark J. Henderson
Udo Rudloff
Frank J. Schoenen
Sui Huang
Juan J. Marugan
Source :
J Med Chem
Publication Year :
2022
Publisher :
American Chemical Society (ACS), 2022.

Abstract

The perinucleolar compartment (PNC) is a dynamic subnuclear body found at the periphery of the nucleolus. The PNC is enriched with RNA transcripts and RNA-binding proteins, reflecting different states of genome organization. PNC prevalence positively correlates with cancer progression and metastatic capacity, making it a useful marker for metastatic cancer progression. A high-throughput, high-content assay was developed to identify novel small molecules that selectively reduce PNC prevalence in cancer cells. We identified and further optimized a pyrrolopyrimidine series able to reduce PNC prevalence in PC3M cancer cells at submicromolar concentrations without affecting cell viability. SAR exploration of the structural elements necessary for activity resulted in the discovery of several potent compounds. Analysis of in vitro drug-like properties led to the discovery of the bioavailable analogue, metarrestin, which has shown potent antimetastatic activity with improved survival in rodent models and is currently being evaluated in a first-in-human Phase 1 clinical trial.

Details

ISSN :
15204804 and 00222623
Volume :
65
Database :
OpenAIRE
Journal :
Journal of Medicinal Chemistry
Accession number :
edsair.doi.dedup.....77cb0efba8b4e86b0d112961571f1a63
Full Text :
https://doi.org/10.1021/acs.jmedchem.2c00204