CAS 522-51-0
:Cloruro de dequalinio
Descripción:
Cloruro de dequalinio es un compuesto de amonio cuaternario caracterizado por sus propiedades antimicrobianas de amplio espectro. Aparece como un polvo cristalino blanco a blanco sucio y es soluble en agua, lo que lo hace adecuado para diversas aplicaciones, particularmente en productos farmacéuticos y de cuidado personal. Se conoce que el compuesto es efectivo contra una variedad de bacterias y hongos, lo que lo hace valioso en formulaciones antisépticas y como conservante. Cloruro de dequalinio funciona al interrumpir las membranas celulares microbianas, lo que lleva a la muerte celular. A menudo se utiliza en pastillas para la garganta, enjuagues bucales y antisépticos tópicos. Además, se ha investigado su posible uso en el tratamiento de infecciones y como desinfectante. Aunque generalmente se considera seguro cuando se usa según las indicaciones, puede causar irritación en algunas personas, particularmente en áreas sensibles. Al igual que con cualquier sustancia química, el manejo adecuado y la adherencia a las pautas de seguridad son esenciales para minimizar los riesgos asociados con la exposición.
Fórmula:C30H40N4·2Cl
InChI:InChI=1S/C30H38N4.2ClH/c1-23-21-27(31)25-15-9-11-17-29(25)33(23)19-13-7-5-3-4-6-8-14-20-34-24(2)22-28(32)26-16-10-12-18-30(26)34;;/h9-12,15-18,21-22,31-32H,3-8,13-14,19-20H2,1-2H3;2*1H
Clave InChI:InChIKey=LTNZEXKYNRNOGT-UHFFFAOYSA-N
SMILES:C(CCCCCCCCC[N+]=1C2=C(C(N)=CC1C)C=CC=C2)[N+]=3C4=C(C(N)=CC3C)C=CC=C4.[Cl-]
Sinónimos:- 1,1'-Decane-1,10-Diylbis(4-Amino-2-Methylquinolinium) Dichloride
- 1,1′-Decamethylenebis[4-aminoquinaldinium chloride]
- Badq 10
- Baqd 10
- Decamethylenebis[4-aminoquinaldinium chloride]
- Decamine
- Decamine (pharmaceutical)
- Decatylen
- Dekadin
- Dekamiln
- Dekamin
- Dequacets
- Dequadin
- Dequadin chloride
- Dequafungen
- Dequalinum Chloride
- Dequavagyn
- Dequavet
- Efisol
- Eriosept
- Evazol
- Fluomizin
- Fluomycin N
- Grocreme
- Ivazil
- Labosept
- Ldn 0096422
- NSC 166454
- Optipect
- Oralgol
- Phylletten
- Polycidine
- Quinaldinium, 1,1′-decamethylenebis[4-amino-, dichloride
- Quinolinium, 1,1′-(1,10-decanediyl)bis[4-amino-2-methyl-, chloride (1:2)
- Quinolinium, 1,1′-(1,10-decanediyl)bis[4-amino-2-methyl-, dichloride
- Rumilet
- Sanoral
- Sentril
- Ver más sinónimos
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Encontrado 14 productos.
Dequalinium chloride
CAS:<p>Dequalinium chloride: topical bacteriostat, blocks apamin-sensitive K+ channels, used for wounds, oral infections, potential antifungal, risk of skin ulcers.</p>Fórmula:C30H40Cl2N4Pureza:99.79% - 99.9%Forma y color:SolidPeso molecular:527.591,1'-(Decane-1,10-Diyl)Bis(4-Amino-2-Methylquinolin-1-Ium) Chloride
CAS:1,1'-(Decane-1,10-Diyl)Bis(4-Amino-2-Methylquinolin-1-Ium) ChloridePureza:98%Peso molecular:527.57g/molDequalinium Dichloride
CAS:Fórmula:C30H40N4·2ClForma y color:Off-White SolidPeso molecular:456.68 2*35.45Dequalinium chloride
CAS:Fórmula:C30H40Cl2N4·xH2OPureza:95.0 - 101.0 % (dried basis)Forma y color:White, off-white or light yellow powderPeso molecular:527.57 (anhydrous)Dequalinium chloride
CAS:<p>Dequalinium chloride is a quaternary ammonium compound that has been discovered to be an inhibitor of the cytopathic effects of some syndrome viruses. It is able to inhibit the replication of the virus in various clinical isolates and in cell culture models. Dequalinium chloride also inhibits acetylcholine receptor-mediated endocytosis, which is one of the mechanisms by which cells resist infection. The mechanism by which dequalinium chloride inhibits acetylcholine receptor-mediated endocytosis is not yet known, but it has been suggested that it might be due to its inhibitory activity on mitochondrial uncoupler proteins. This property may make dequalinium chloride an effective treatment against bacterial infections and respiratory diseases such as cystic fibrosis and asthma.</p>Fórmula:C30H40Cl2N4Pureza:Min. 95%Forma y color:PowderPeso molecular:527.57 g/molDequalinium chloride
CAS:<p>Dequalinium chloride is a novel, broad spectrum antimicrobial agent with a mechanism of action that inhibits the mitochondria-dependent respiratory chain. Studies have shown that it inhibits the growth of resistant microorganisms in cell-based experiments and in bacterial infections. Dequalinium chloride also has cytopathic effects on thp-1 cells, which are specific for Mycobacterium tuberculosis. In addition to inhibiting mitochondria-dependent respiration, this compound also increases acetylcholine receptor sensitivity in A549 lung cancer cells. Dequalinium chloride is a quaternary ammonium cation and has been shown to be effective against clinical isolates and inhibitory concentrations of a variety of virus species, including human rhinovirus (HRV) and Coxsackie virus type B4 (CoxB4).</p>Fórmula:C30H40Cl2N4Pureza:Min. 95.0 Area-%Peso molecular:527.57 g/molRef: 3D-W-105841
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