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Discovery of Aminopiperidine Indoles That Activate the Guanine Nucleotide Exchange Factor SOS1 and Modulate RAS Signaling. | LitMetric

AI Article Synopsis

  • Deregulated RAS activity, often due to mutations, is involved in around 30% of human cancers, but effective treatments for RAS-driven tumors are currently lacking.
  • A promising strategy involves targeting proteins interacting with RAS, like the guanine nucleotide exchange factor (GEF) SOS1, to modulate RAS activity.
  • Research on an indole series of compounds showed that some can effectively activate the nucleotide exchange process and alter signaling in cancer cells, leading to decreased levels of active RAS-GTP and signaling changes in the MAPK-ERK pathway.

Article Abstract

Deregulated RAS activity, often the result of mutation, is implicated in approximately 30% of all human cancers. Despite this statistic, no clinically successful treatment for RAS-driven tumors has yet been developed. One approach for modulating RAS activity is to target and affect the activity of proteins that interact with RAS, such as the guanine nucleotide exchange factor (GEF) son of sevenless homologue 1 (SOS1). Here, we report on structure-activity relationships (SAR) in an indole series of compounds. Using structure-based design, we systematically explored substitution patterns on the indole nucleus, the pendant amino acid moiety, and the linker unit that connects these two fragments. Best-in-class compounds activate the nucleotide exchange process at submicromolar concentrations in vitro, increase levels of active RAS-GTP in HeLa cells, and elicit signaling changes in the mitogen-activated protein kinase-extracellular regulated kinase (MAPK-ERK) pathway, resulting in a decrease in pERK1/2 protein levels at higher compound concentrations.

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Source
http://dx.doi.org/10.1021/acs.jmedchem.8b00360DOI Listing

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