Diene Substitution Patterns in the Conformation‐Activity Relationships of GEX1A

GEX1A (herboxidiene) is a polyketide natural product that possesses potent biological activities for a number of indications. GEX1A binds the splicing factor 3B subunit 1 (SF3B1), inhibiting the splicing of pre-mRNA. Moreover, we have reported that GEX1A reverses cholesterol accumulation in Niemann-Pick Type C mutant fibroblasts. Several groups have investigated the structure-activity relationships of this polyketide, mostly focusing on the tetrahydropyran core and the distal, oxygenated section of the side chain. Herein, we present the design, synthesis, and conformational studies of a series of analogues to explore substitution on the diene section of GEX1A. We employed computational and high-field NMR studies to describe the analogues' conformational landscape and their relative biological activities to describe their conformational-activity profile. We found that modifications on the diene section brought significant changes to both the molecule's conformation and biological activity.

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Journal
ChemMedChem
Published
2026-05-22
DOI
https://doi.org/10.1002/cmdc.70309
Primary Topic
RNA and protein synthesis mechanisms
Type
article
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article

Diene Substitution Patterns in the Conformation‐Activity Relationships of GEX1A

Taylor R. Quinn, Christian A. Umaña, Duoming Ma, Matthew C. Rhodes et al.
ChemMedChem
RNA and protein synthesis mechanisms
article

Diene Substitution Patterns in the Conformation‐Activity Relationships of GEX1A

Taylor R. Quinn, Christian A. Umaña, Duoming Ma, Matthew C. Rhodes, Jeffrey L. Henry, Richard E. Taylor
article en

Abstract

GEX1A (herboxidiene) is a polyketide natural product that possesses potent biological activities for a number of indications. GEX1A binds the splicing factor 3B subunit 1 (SF3B1), inhibiting the splicing of pre-mRNA. Moreover, we have reported that GEX1A reverses cholesterol accumulation in Niemann-Pick Type C mutant fibroblasts. Several groups have investigated the structure-activity relationships of this polyketide, mostly focusing on the tetrahydropyran core and the distal, oxygenated section of the side chain. Herein, we present the design, synthesis, and conformational studies of a series of analogues to explore substitution on the diene section of GEX1A. We employed computational and high-field NMR studies to describe the analogues' conformational landscape and their relative biological activities to describe their conformational-activity profile. We found that modifications on the diene section brought significant changes to both the molecule's conformation and biological activity.

ChemMedChemVol. 21(10)
University of Notre Dame (US)
Life in Land
Openalex Percentile: Top 8%
RNA and protein synthesis mechanisms
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