Novel Substituted Indazoles as Small Molecule-Based Inhibitors of KRAS Proteins

This patent discloses a series of substituted indazole compounds as novel inhibitors of KRAS, with potential utility as anticancer therapeutics. The invention describes the chemical structures of these substituted indazoles, their pharmaceutical compositions, and methods of use for treating KRAS-driven malignancies. The disclosed compounds are designed to modulate oncogenic KRAS signaling and may offer a new therapeutic strategy for cancers associated with KRAS mutations.

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Publication Details

Journal
ACS Medicinal Chemistry Letters
Published
2026-03-04
DOI
https://doi.org/10.1021/acsmedchemlett.6c00097
Primary Topic
Protein Kinase Regulation and GTPase Signaling
Type
article
Field-Weighted Citation Impact
0.00
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article

Novel Substituted Indazoles as Small Molecule-Based Inhibitors of KRAS Proteins

Steven H. Liang, Jian Rong
ACS Medicinal Chemistry Letters
Protein Kinase Regulation and GTPase Signaling
article

Novel Substituted Indazoles as Small Molecule-Based Inhibitors of KRAS Proteins

Steven H. Liang, Jian Rong
article en

Abstract

This patent discloses a series of substituted indazole compounds as novel inhibitors of KRAS, with potential utility as anticancer therapeutics. The invention describes the chemical structures of these substituted indazoles, their pharmaceutical compositions, and methods of use for treating KRAS-driven malignancies. The disclosed compounds are designed to modulate oncogenic KRAS signaling and may offer a new therapeutic strategy for cancers associated with KRAS mutations.

ACS Medicinal Chemistry Letters
Emory University (US), Union Hospital (CN)
Zero hunger
Openalex Percentile: Top 34%
Protein Kinase Regulation and GTPase Signaling
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