Details
Stereochemistry | ACHIRAL |
Molecular Formula | C22H32O2 |
Molecular Weight | 328.4883 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 4 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)OC\C=C(C)\C=C\C=C(C)/C=C/C1=C(C)CCCC1(C)C
InChI
InChIKey=QGNJRVVDBSJHIZ-AQDFTDIISA-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+
Molecular Formula | C22H32O2 |
Molecular Weight | 328.4883 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 4 |
Optical Activity | NONE |
Zuretinol (QLT091001, 9-cis-retinol) is a retinoid. Retinoids (vitamin A and its analogs) are essential dietary substances that are needed by mammals for reproduction, normal embryogenesis, growth, vision, and maintaining normal cellular differentiation and the integrity of the immune system. Within cells, retinoids regulate gene transcription acting through ligand-dependent transcription factors, the retinoic acid receptors (RARs), and the retinoid X receptors (RXRs). All-trans-retinoic acid binds only to RARs with high affinity, whereas its 9-cis isomer binds with high affinity to both RARs and RXRs. The actions of all-trans- and 9-cis-retinoic acid in regulating cellular responses are distinct and not interchangeable. Zuretinol is a retinal derivative for treatment of visual disorders. It is a synthetic retinoid replacement for 11-cis-retinal. It is an investigational product under development for the treatment of retinal diseases caused by gene mutations that interfere with the availability of 11-cis-retinal. The therapeutic strategy with Zuretinol is to facilitate recovery or restoration of visual function by acting as a replacement for missing 11-cis-retinal and restoring a key biochemical component of the visual (retinoid) cycle. Novelion Therapeutics is currently developing QLT091001 for the treatment of Inherited Retinal Disease caused by retinal pigment epithelium protein 65 (“RPE65”) and lecithin:retinol acyltransferase (“LRAT”) gene mutations, which include Leber Congenital Amaurosis (“LCA”) and Retinitis Pigmentosa (“RP”). QLT091001 has received orphan drug designations for the treatment of LCA (due to inherited mutations in the LRAT and RPE65 genes) and RP (all mutations) by the U.S. Food and Drug Administration (the “FDA”), and for the treatment of LCA and RP (all mutations) by the European Medicines Agency (the “EMA”).
Originator
Approval Year
PubMed
Title | Date | PubMed |
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Identification and characterization of a stereospecific human enzyme that catalyzes 9-cis-retinol oxidation. A possible role in 9-cis-retinoic acid formation. | 1997 May 2 |
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QLT091001, a 9-cis-retinal analog, is well-tolerated by retinas of mice with impaired visual cycles. | 2013 Jan 17 |
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Safety and Proof-of-Concept Study of Oral QLT091001 in Retinitis Pigmentosa Due to Inherited Deficiencies of Retinal Pigment Epithelial 65 Protein (RPE65) or Lecithin:Retinol Acyltransferase (LRAT). | 2015 |
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Outer Segment Thickness Predicts Visual Field Response to QLT091001 in Patients with RPE65 or LRAT Mutations. | 2015 Oct |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25030840
Patients received 7 days of oral Zuretinol (QLT091001) (10-40 mg/m(2) per day).
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/28254816
Pretreatment with 9-cis-RA (20 umol/L) inhibited platelet aggregation
to collagen (1 ug/mL), the GPVI collagen
receptor–specific agonist, CRP-XL (0.25 ug/mL),
and thrombin (0.05 U/mL) compared with vehicle
controls (containing 0.1% dimethyl sulfoxide), with ≈60% and
20% inhibition after stimulation by collagen (and CRP-XL)
and thrombin, respectively.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 01:26:16 GMT 2023
by
admin
on
Sat Dec 16 01:26:16 GMT 2023
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Record UNII |
2K3YP54BYU
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C804
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FDA ORPHAN DRUG |
324410
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FDA ORPHAN DRUG |
320410
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EU-Orphan Drug |
EU/3/11/861
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Code System | Code | Type | Description | ||
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EU/3/11/861(POSITIVE)
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PRIMARY | Treatment of Leber’s congenital amaurosis 13/05/2011 Positive | ||
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29584-22-3
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PRIMARY | |||
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C152967
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PRIMARY | |||
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DB12112
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PRIMARY | |||
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100000178277
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SUB193919
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PRIMARY | |||
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9892
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PRIMARY | |||
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EU/3/11/865(POSITIVE)
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admin on Sat Dec 16 01:26:16 GMT 2023 , Edited by admin on Sat Dec 16 01:26:16 GMT 2023
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PRIMARY | Treatment of retinitis pigmentosa 13/05/2011 Positive | ||
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2K3YP54BYU
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10245972
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Related Record | Type | Details | ||
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METABOLITE ACTIVE -> PRODRUG |
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
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