18-Crown-6-ether


CAS No. : 17455-13-9

(Synonyms: 18C6; 1,4,7,10,13,16-Hexaoxacyclooctadecane)

17455-13-9
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Cat. No. : HY-D0180
M.Wt: 264.32
Formula: C12H24O6
Purity: >98 %
Solubility: DMSO : ≥ 100 mg/mL
Introduction of 17455-13-9 :

18-Crown-6-ether is a type of crown ether compound and a specific structure dissociating agent. 18-Crown-6-ether can compete with K+ for binding to G-quadruplexes, disrupting their stable structure to regulate the functions of related systems. 18-Crown-6-ether combines with K+ and other metal ions to achieve precise ion transmembrane transport. 18-Crown-6-ether can act as an "susceptibility substrate" for the multi-drug efflux pump EmrE (a bacterial multidrug resistance transporter), ultimately inhibiting bacterial growth. 18-Crown-6-ether can be used in microcapsule controlled release and the research on developing antibacterial enhancers[1][2][3]. In Vitro:18-Crown-6-ether exhibits selectivity towards K⁺. The 18-crown-6-K⁺ complex has a higher transmembrane permeation rate than the Na⁺ complex, mainly due to the higher geometric matching degree between the ionic radius of K⁺ and the molecular cavity of the compound[2].
18-Crown-6-ether allosteric modulates EmrE, converting it from a normal anti-pump to a proton channel, triggering uncoupled proton leakage, thereby dissipating the proton motive force (PMF) of the bacteria and ultimately inhibiting their growth[2].

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