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1 ferent planar drugs, ethidium, propidium and dequalinium.
2 inach chloroplasts is slightly stimulated by dequalinium.
3 bunit when CF1 is photoinactivated with [14C]dequalinium.
4 lphosphonium (TPP+), ethidium, propidium and dequalinium.
5 y reported ELUMO correlation for a series of dequalinium analogues to include all the compounds of bo
6  contrast to previously reported results for dequalinium analogues, there is no correlation of activi
7  activity to previously reported results for dequalinium analogues, there is no correlation of activi
8           The SK/IK channel-blockers apamin, dequalinium, and charybdotoxin caused increases in avera
9 ctivated K+ channel blockers (23) related to dequalinium are described.
10  activity can be reconciled by assuming that dequalinium binds to two sites in CF1, a stimulatory sit
11  Food and Drug Administration (FDA)-approved dequalinium chloride (DECA), could restore proper peroxi
12 and European Medicines Agency-approved drug, dequalinium chloride (DEQ), that inhibits activation of
13 SD] age, 36.7 [9.0] years) were treated with dequalinium chloride (n = 72) or metronidazole (n = 75).
14 te difference in clinical cure rates between dequalinium chloride and metronidazole 7 to 11 days afte
15                                              Dequalinium chloride had a similarly high cure rate but
16   Patients were randomized to treatment with dequalinium chloride vaginal tablets (10 mg once daily f
17 lation, cure rates were 54 of 58 (93.1%) for dequalinium chloride vs 48 of 53 (90.6%) for metronidazo
18 e rates at visit 1 were 64 of 69 (92.8%) for dequalinium chloride vs 69 of 74 (93.2%) for metronidazo
19 r efficacy to metronidazole and clindamycin, dequalinium chloride warrants consideration as first-lin
20   This randomized clinical trial showed that dequalinium chloride was not inferior to metronidazole f
21                          The tolerability of dequalinium chloride was rated as very good by 30 of 50
22 l population confirmed the noninferiority of dequalinium chloride.
23           Analogues of a bipartite compound, dequalinium (DECA) (quinolinium, 1,1'-(1,10-decanediyl)b
24                                              Dequalinium (DECA) is a potent antitumor agent and inhib
25                     In the presence of LDAO, dequalinium does not stimulate the heat-activated Mg2+-A
26 ration-response relationships for apamin and dequalinium had IC(50) values of 0.5 nm and 1.8 microm,
27 cationic drug complex (that of QacR bound to dequalinium) has been determined, and how other longer o
28                                   Similar to dequalinium, hexamidine spans the multidrug-binding pock
29 illus PS3, which are reversibly inhibited by dequalinium in the absence of irradiation, the Mg2+-ATPa
30                                  Conversely, dequalinium is a partial inhibitor (maximal inhibition i
31 ty that it activates, the combined effect of dequalinium is modest stimulation.
32 ylenebis-4-aminoquinaldinium diiodide (DECA; dequalinium) is an anti-tumor agent and protein kinase C
33 bcomplex of CF1 in the presence of 12 microM dequalinium led to rapid photoinactivation.
34                                         That dequalinium slightly stimulates Mg2+-ATPase activity alt
35 alpha3beta3gamma subcomplex of CF1 with [14C]dequalinium, tryptic and peptic digests of the isolated,
36 nhibitor of the generalized stress response, dequalinium, which also indirectly inhibits the SOS resp