Chlorquinaldol
| |
| Names | |
|---|---|
| Preferred IUPAC name
5,7-Dichloro-2-methylquinolin-8-ol | |
| Other names
Anginazol; Lacoid, Nerisone
| |
| Identifiers | |
3D model (JSmol)
|
|
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.000.718 |
| KEGG | |
PubChemCID
|
|
| UNII | |
CompTox Dashboard(EPA)
|
|
| |
| |
| Properties | |
| C10H7Cl2NO | |
| Molar mass | 228.07 g/mol |
| Pharmacology | |
| D08AH02(WHO)G01AC03(WHO),P01AA04(WHO),R02AA11(WHO) | |
Except where otherwise noted, data are given for materials in theirstandard state(at 25 °C [77 °F], 100 kPa).
| |
Chlorquinaldolis anantimicrobialagent and antiseptic.[1]It is achlorinatedderivative of the popular chelating agent8-hydroxyquinoline.It is applied topically as a cream and internally as alosenge.[2]
It was marketed byGeigyas an intestinal antiseptic andamebicidewith the trade nameSiosteran.[citation needed]
References
[edit]- ^Mett H, Gyr K, Zak O, Vosbeck K (July 1984)."Duodeno-pancreatic secretions enhance bactericidal activity of antimicrobial drugs".Antimicrob. Agents Chemother.26(1): 35–8.doi:10.1128/aac.26.1.35.PMC179912.PMID6236746.
- ^Kutscher, Bernhard (2020). "Dermatologicals ( D ), 4. Antiseptics and Disinfectants ( D 08), Anti‐Acne Preparations ( D 10), and Other Dermatological Preparations ( D 11)".Ullmann's Encyclopedia of Industrial Chemistry.Weinheim: Wiley-VCH. pp. 1–22.doi:10.1002/14356007.w08_w03.ISBN978-3527306732.
 | Thisantiinfectivedrugarticle is astub.You can help Wikipedia byexpanding it. |
 | Thisdrugarticle relating to thegenito-urinary systemis astub.You can help Wikipedia byexpanding it. |