The Discovery of GS-1291269: A Neutral Ketohexokinase (KHK) Inhibitor with an Unusual Thietane Amine Functional Group

Ketohexokinase (KHK) is the primary enzyme involved in fructose metabolism, converting fructose to fructose-1-phosphate (F1P). KHK is implicated in diseases, including metabolic-dysfunction-associated steatotic liver disease (MASLD) and diabetic kidney disease (DKD), among others. Herein, we describe the discovery of GS-1291269, a potent, neutral KHK inhibitor. GS-1291269 has pharmacokinetic parameters in preclinical species that support once-daily dosing in humans. The high potency and favorable PK profile of GS-1291269 can be attributed to the uncommon dioxo-thietane amine functional group, which avoids potential PK liabilities associated with acidic or basic molecules yet provides a hydrogen bond donor that is critical for potency. Furthermore, GS-1291269 demonstrated liver and kidney fructose-1-phosphate (F1P) reduction in a fructose challenge model in rats.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-12-23
DOI
https://doi.org/10.1021/acs.jmedchem.5c02896
Citations
1
Primary Topic
Diet, Metabolism, and Disease
Type
article
Field-Weighted Citation Impact
1.29
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article

The Discovery of GS-1291269: A Neutral Ketohexokinase (KHK) Inhibitor with an Unusual Thietane Amine Functional Group

Petr Jansa, Joshua A. Kaplan, Ryan Ferrao, Jennifer R. Lo et al.
1 citations
Journal of Medicinal Chemistry
Diet, Metabolism, and Disease
1.29
article

The Discovery of GS-1291269: A Neutral Ketohexokinase (KHK) Inhibitor with an Unusual Thietane Amine Functional Group

Petr Jansa, Joshua A. Kaplan, Ryan Ferrao, Jennifer R. Lo, NATALIE SRODA, Shawn S. Badal, Maile Velasquez, J. Logan Bachman, Brian Stafford, Jennifer Loyer-Drew, Tina L. Mistry, Zachary A. Kasun, Kirk L. Stevens, Jia Hao, Megan E. Neubig, Christopher T. Clark, Nathaniel H. Stanley, Daniel H. Byun, Judy Mwangi, Xiaomin Liang
article en
1 citations

Abstract

Ketohexokinase (KHK) is the primary enzyme involved in fructose metabolism, converting fructose to fructose-1-phosphate (F1P). KHK is implicated in diseases, including metabolic-dysfunction-associated steatotic liver disease (MASLD) and diabetic kidney disease (DKD), among others. Herein, we describe the discovery of GS-1291269, a potent, neutral KHK inhibitor. GS-1291269 has pharmacokinetic parameters in preclinical species that support once-daily dosing in humans. The high potency and favorable PK profile of GS-1291269 can be attributed to the uncommon dioxo-thietane amine functional group, which avoids potential PK liabilities associated with acidic or basic molecules yet provides a hydrogen bond donor that is critical for potency. Furthermore, GS-1291269 demonstrated liver and kidney fructose-1-phosphate (F1P) reduction in a fructose challenge model in rats.

Journal of Medicinal ChemistryVol. 69(1)
Gilead Sciences (United States) (US)
Openalex Percentile: Top 13%
Diet, Metabolism, and Disease
1.29
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The Discovery of GS-1291269: A Neutral Ketohexokinase (KHK) Inhibitor with an Unusual Thietane Amine Functional Group — Petr Jansa, Joshua A. Kaplan, et al. · Journal of Medicinal Chemistry (2025) | TGRS Research Map | TGRS