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Details

Stereochemistry ACHIRAL
Molecular Formula C20H30O
Molecular Weight 286.4516
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 4
Charge 0

SHOW SMILES / InChI
Structure of ZURETINOL

SMILES

CC(=C/CO)\C=C\C=C(C)/C=C/C1=C(C)CCCC1(C)C

InChI

InChIKey=FPIPGXGPPPQFEQ-MKOSUFFBSA-N
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+

HIDE SMILES / InChI

Molecular Formula C20H30O
Molecular Weight 286.4516
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”).

Approval Year

PubMed

PubMed

TitleDatePubMed
QLT091001, a 9-cis-retinal analog, is well-tolerated by retinas of mice with impaired visual cycles.
2013 Jan 17
Outer Segment Thickness Predicts Visual Field Response to QLT091001 in Patients with RPE65 or LRAT Mutations.
2015 Oct
Patents

Patents

Sample Use Guides

Patients received 7 days of oral Zuretinol (QLT091001) (10-40 mg/m(2) per day).
Route of Administration: Oral
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 Sat Dec 16 07:05:10 GMT 2023
Edited
by admin
on Sat Dec 16 07:05:10 GMT 2023
Record UNII
035JKP3HXH
Record Status Validated (UNII)
Record Version
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Name Type Language
ZURETINOL
WHO-DD  
Common Name English
9-CIS-RETINOL
Common Name English
9-CIS-VITAMIN A ALCOHOL
Common Name English
Zuretinol [WHO-DD]
Common Name English
RETINOL, 9-CIS-
Common Name English
Code System Code Type Description
FDA UNII
035JKP3HXH
Created by admin on Sat Dec 16 07:05:10 GMT 2023 , Edited by admin on Sat Dec 16 07:05:10 GMT 2023
PRIMARY
CAS
22737-97-9
Created by admin on Sat Dec 16 07:05:10 GMT 2023 , Edited by admin on Sat Dec 16 07:05:10 GMT 2023
PRIMARY
PUBCHEM
9947823
Created by admin on Sat Dec 16 07:05:10 GMT 2023 , Edited by admin on Sat Dec 16 07:05:10 GMT 2023
PRIMARY
CHEBI
78272
Created by admin on Sat Dec 16 07:05:10 GMT 2023 , Edited by admin on Sat Dec 16 07:05:10 GMT 2023
PRIMARY
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