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Gildeuretinol

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Gildeuretinol
Clinical data
Other namesALK-001, KL-49
Identifiers
  • (2E,4E,6E,8E)-7-methyl-3-(trideuteriomethyl)-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraen-1-ol
CAS Number
PubChem CID
UNII
KEGG
ChEMBL
Chemical and physical data
FormulaC20H30D3O
Molar mass292.500 g·mol−1
3D model (JSmol)
  • [2H]C([2H])([2H])/C(=C\CO)/C=C/C=C(\C)/C=C/C1=C(CCCC1(C)C)C
  • InChI=InChI=1S/C20H30O/c1-16(8-6-9-17(2)13-15-21)11-12-19-18(3)10-7-14-20(19,4)5/h6,8-9,11-13,21H,7,10,14-15H2,1-5H3/b9-6+,12-11+,16-8+,17-13+/i2D3
  • Key:FPIPGXGPPPQFEQ-QZNDTXPVSA-N

Gildeuretinol is an investigational new drug being developed by Alkeus Pharmaceuticals for the treatment of retinal diseases, particularly Stargardt disease and geographic atrophy secondary to age-related macular degeneration (AMD). Stargardt disease is caused by a defect in the ABCA4 gene that clears toxic byproducts resulting from the dimerization of vitamin A. Gildeuretinol is a deuterated derivative of Vitamin A that is designed to reduce the dimerization of vitamin A without affecting the visual cycle.[1]

Gildeuretinol has received breakthrough therapy and orphan drug designations from the U.S. Food and Drug Administration.[2]

References

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  1. ^ Zaydon YA, Tsang SH (July 2024). "The ABCs of Stargardt disease: the latest advances in precision medicine". Cell & Bioscience. 14 (1): 98. doi:10.1186/s13578-024-01272-y. PMC 11282698. PMID 39060921.
  2. ^ Fitch J (22 November 2024). "Gildeuretinol for Stargardt disease receives Rare Pediatric Disease, Fast Track Designations". Contemporary Pediatrics.