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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
5 of the imidazole antimycotics, clotrimazole, econazole and miconazole, which are potent P450 inhibito
9 of the crystal structures of ligand-free and econazole-bound CYP130 at a resolution of 1.46 and 3.0A(
10 open" conformation as a monomer, whereas the econazole-bound form crystallizes in a "closed" conforma
15 ibitor potency was found to be Lu(3+)>La(3+)=econazole=Gd(3+)>1-[2-(4-methoxyphenyl)-2-[3-(4-methoxyp
16 curves were generated for Lu(3+), Gd(3+) and econazole, giving IC(50)s of 0.09, 1.51 and 1.13 microM,
17 contact lenses were created by encapsulating econazole-impregnated poly(lactic-co-glycolic) acid (PLG
18 t the log Ppw of the neutral form of racemic econazole is 4.83(+/-0.06), for the cationic form (presu
21 50 arachidonic acid metabolism with SKF525A, econazole, or N-methylsulfonyl-6-(2-propargyloxyphenyl)h
22 d effectiveness depending on the mass of the econazole-PLGA film encapsulated in the contact lens.
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