Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H7Cl2NO |
Molecular Weight | 228.075 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=NC2=C(C=C1)C(Cl)=CC(Cl)=C2O
InChI
InChIKey=GPTXWRGISTZRIO-UHFFFAOYSA-N
InChI=1S/C10H7Cl2NO/c1-5-2-3-6-7(11)4-8(12)10(14)9(6)13-5/h2-4,14H,1H3
Molecular Formula | C10H7Cl2NO |
Molecular Weight | 228.075 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionCurator's Comment: Description is created based on several sources, including http://www.sciencedirect.com/science/article/pii/S0022202X15488141 and http://www.ncbi.nlm.nih.gov/pubmed/140848
Curator's Comment: Description is created based on several sources, including http://www.sciencedirect.com/science/article/pii/S0022202X15488141 and http://www.ncbi.nlm.nih.gov/pubmed/140848
Chlorquinaldol is a halogenated hydroxyquinoline with properties similar to those of clioquinol. It is mainly applied topically in infected skin conditions and in vaginal infections. The product is applied for local treatment of cortico-sensitive dermatosis with moderately manifested superinfection, acute and subacute eczema, dermatitis, pyodermia, intertrigo, infected wounds, dermatomycosis, pemphigus in newborn. Chlorquinaldol is also used as antiseptic, fungistat, or deodorant. Chlorquinaldol is not commercially available in the U.S. but is used in other countries principally as an amebicide for nonspecific diarrheas and gynecologic infections. It is known most commonly under the proprietary name of Sterosan. Other trade names include Cynotherax, Gyno-Sterosan, Saprosan, Siogeno, Siosteran, Slosteran and Steroxin.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: Escherichia coli growth Sources: http://www.ncbi.nlm.nih.gov/pubmed/6236746 |
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Target ID: CHEMBL5192 Sources: http://www.ncbi.nlm.nih.gov/pubmed/24387280 |
10.1 µM [IC50] | ||
Target ID: Mycobacterium tuberculosis growth Sources: http://www.ncbi.nlm.nih.gov/pubmed/?term=17178795 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Curative | Chlorquinaldol Approved UseChlorquinaldol is primarily indicated in conditions like skin infections, vaginal infections. Launch Date2007 |
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Curative | Gynosan Vaginal Pessary Approved UseGynosan Vaginal Pessary is used in the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms: skin infections, vaginal infections |
PubMed
Title | Date | PubMed |
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[Treatment of fungal infections of upper respiratory tract and ear]. | 2007 |
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[Gynalgin--one more opportunity in the treatment of bacterial vaginosis]. | 2007 |
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Therapeutic use of topical corticosteroids in the vesiculobullous lesions of incontinentia pigmenti. | 2009 Dec |
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3-[(E)-2-(5,7-Dichloro-8-hydroxy-quinolin-2-yl)vin-yl]-4-hydroxy-phenyl acetate. | 2009 Feb 11 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.sopharma.com/chlorquinaldol-h.php
Applied in a thin layer on affected skin areas 1-3 times daily. Therapy duration is up to 8 days.
Route of Administration:
Topical
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/6236746
Chlorquinaldol displayed enhanced E. coli 205 bactericidal activity in human duodeno-pancreatic secretions with MIC 0.5ug/ml
Substance Class |
Chemical
Created
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Record UNII |
D6VHC87LLS
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Record Status |
Validated (UNII)
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WHO-ATC |
D08AH02
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P01AA04
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NCI_THESAURUS |
C28394
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N0000185508
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G01AC03
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QD08AH02
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C77042
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N0000175629
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N0000184306
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CHLORQUINALDOL
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Related Record | Type | Details | ||
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