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1 by okadaic acid, a phosphatase inhibitor, or econazole.
2 nantioselective syntheses of enantiopure (S)-econazole and (R)-mirabegron a late-stage intermediate.
3  with virtually the same binding affinity as econazole and clotrimazole and ketoconazole with somewha
4                                   Binding of econazole and clotrimazole exhibits positive cooperativi
5 of the imidazole antimycotics, clotrimazole, econazole and miconazole, which are potent P450 inhibito
6 se data, two pairs of positives, sulconazole/econazole and pararosaniline/cetylpyridinium, predicted
7                 In this study, we identified econazole and sulconazole, two small molecules that disr
8 uman TRPV6 inhibition by the antifungal drug econazole and the universal ion channel blocker rutheniu
9 d by extracellular application of genistein, econazole, and SKF 96365.
10                  Three of these, miconazole, econazole, and sulconazole, were promiscuous but the oth
11        The Ca2+ channel blockers, nickel and econazole, and the K+ channel blockers, tetraethylammoni
12             Structurally related miconazole, econazole, and tioconazole bound with submicromolar diss
13                                              Econazole binds to an allosteric site at the channel's p
14 of the crystal structures of ligand-free and econazole-bound CYP130 at a resolution of 1.46 and 3.0A(
15 open" conformation as a monomer, whereas the econazole-bound form crystallizes in a "closed" conforma
16                         The four imidazoles (econazole, clotrimazole, miconazole, and ketoconazole) w
17 zole slows photoresponse kinetics, whereas S-econazole decreased the sensitivity of rods without effe
18  azole antifungals, such as ketoconazole and econazole, did not alter glycan processing.
19                                           An econazole-eluting contact lens could be used as a treatm
20                                              Econazole-eluting contact lenses provided extended antif
21 ibitor potency was found to be Lu(3+)>La(3+)=econazole=Gd(3+)>1-[2-(4-methoxyphenyl)-2-[3-(4-methoxyp
22 curves were generated for Lu(3+), Gd(3+) and econazole, giving IC(50)s of 0.09, 1.51 and 1.13 microM,
23 contact lenses were created by encapsulating econazole-impregnated poly(lactic-co-glycolic) acid (PLG
24 t the log Ppw of the neutral form of racemic econazole is 4.83(+/-0.06), for the cationic form (presu
25 e and sulconazole have intermediate activity econazole is least effective.
26                                Clotrimazole, econazole, miconazole and CN- also significantly inhibit
27 escence in vitro, we found that binding of R-econazole modulates the formation of Meta III and quench
28 50 arachidonic acid metabolism with SKF525A, econazole, or N-methylsulfonyl-6-(2-propargyloxyphenyl)h
29 d effectiveness depending on the mass of the econazole-PLGA film encapsulated in the contact lens.
30 siological ex vivo recording revealed that R-econazole slows photoresponse kinetics, whereas S-econaz
31                                   Binding of econazole to CYP130 involves a conformational change and