Dequalinium chloride CAS: 522-51-0

26-05-2023

522-51-0 - Physico-chemical Properties

Molecular FormulaC30H40Cl2N4
Molar Mass527.57
Melting Point≥300°C(lit.)
SolubilitySlightly soluble in water and in ethanol (96 per cent).
Appearanceneat
ColorBeige
Merck13,2930
Storage Condition2-8°C
StabilityStable for 2 years as supplied. Solutions in DMSO or distilled water may be stored at -20° for up to 3 months.
UseBroad-spectrum antibacterial drugs for acute pharyngitis, oral Disinfection
In vitro studyDequalinium chloride (DECA) is a cationic lipophilic compound with a structure similar to the dye Rhodamine 123. DECA selectively accumulates and is retained in the mitochondria of tumor cells, where it acts as a mitochondrial poison by blocking mitochondrial enzymes and subsequently disrupts cellular energy production, ultimately leading to cell death. Dequalinium Chloride is a ganglion conduction blocker (EC50=2 μm). Dequalinium is a potent inhibitor of potassium channels in melittin-sensitive hepatocytes and of nicotine response in skeletal muscle. Dequalinium blocks angiotensin II-induced potassium loss with an IC50 of 1.5 μm and inhibits Dequalinium-sensitive posterior hyperpolarization (AHP) in cultured rat sympathetic neurons the component can be rapidly and reversibly inhibited, followed by the generation of a single action potential. Dequalinium Chloride (DECA) is a cationic lipophilic PKC inhibitor. When exposed to UV light, DECA covalently binds and reversibly inhibits PKC α and PKC β.
In vivo studyIn mice bearing bladder MB49 tumors, Dequalinium chloride (2 mg/kg/d, I. p.) showed anticancer activity with a T/C of 210%.

522-51-0 - Reference Information

biological activityDequalinium Chloride is a PKC inhibitor with an IC50 of 7-18 μM, and is also a selective bee toxin peptide sensitive potassium channel blocker with an IC50 of 1.1 μM.
TargetValue
PKC7 μM-18 μM
usebroad-spectrum antibacterial drugs for acute pharyngitis, oral disinfection, etc.


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