Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C22H32O2 |
| Molecular Weight | 331.5068 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 4 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[2H]C([2H])([2H])C(=C/COC(C)=O)\C=C\C=C(C)\C=C\C1=C(C)CCCC1(C)C
InChI
InChIKey=QGNJRVVDBSJHIZ-QJZZLBIKSA-N
InChI=1S/C22H32O2/c1-17(9-7-10-18(2)14-16-24-20(4)23)12-13-21-19(3)11-8-15-22(21,5)6/h7,9-10,12-14H,8,11,15-16H2,1-6H3/b10-7+,13-12+,17-9+,18-14+/i2D3
| Molecular Formula | C22H32O2 |
| Molecular Weight | 331.5068 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 4 |
| Optical Activity | NONE |
Alkeus Pharma's lead compound, ALK-001, is an oral compound with a well-understood mechanism of action. ALK-001 was specifically designed to prevent the formation of these toxic vitamin A dimers in the eye. ALK-001 is a chemically-modified vitamin A, in which 3 hydrogen atoms have been replaced by 3 deuterium atoms at carbon number 20. Replacing the retina's vitamin A with ALK-001 slows the formation of toxic vitamin A dimers. ALK-001 is in phase II clinical trials for the treatment of Stargardt's disease. The compound was co-developed by Alkeus Pharmaceuticals and Columbia University.
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Novel therapeutics for Stargardt disease. | 2017-06 |
|
| Can Vitamin A be Improved to Prevent Blindness due to Age-Related Macular Degeneration, Stargardt Disease and Other Retinal Dystrophies? | 2016 |
|
| Rescue of the Stargardt phenotype in Abca4 knockout mice through inhibition of vitamin A dimerization. | 2015-07-07 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26106163
Curator's Comment: Human phase II clinical trial (Stargardt Disease):
Daily, oral administration of ALK-001 for 24 months
https://clinicaltrials.gov/ct2/show/NCT02402660
Mice: C20-D3-retinyl acetate (ALK-001) was blended with olive oil, and added to a grain-based diet at
15,000 IU/kg diet otherwise deficient in vitamin A.
Route of Administration:
Oral
| Substance Class |
Chemical
Created
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admin
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Tue Apr 01 17:00:13 GMT 2025
by
admin
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Tue Apr 01 17:00:13 GMT 2025
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| Record UNII |
JN7W3M3OI7
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| Record Status |
Validated (UNII)
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FDA ORPHAN DRUG |
317210
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