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1 H solely by changes in the fluorescence of 9-aminoacridine.
3 inonapthalene (DAN), p-nitroaniline (NIT), 9-aminoacridine (9-AA), and 2-mercaptobenzothiazole (MBT)
4 SA), 1,5-diaminonaphthelene (1,5-DAN), and 9-aminoacridine (9-AA), for the analysis of lipid, peptide
5 re used to study the dynamic properties of 9-aminoacridine (9AA) and four bis(acridine) complexes wit
8 n the activity of small-molecule inhibitor 9-aminoacridine (9AA), an anticancer drug that targets two
9 the compounds isolated were derivatives of 9-aminoacridine (9AA), including the antimalaria drug quin
10 lationship of seventy 4-aminoquinoline and 9-aminoacridine analogues reveals that increased activity
11 ibit topo II activity as compared with the 9-aminoacridine and 9-(N-butyl)aminoacridine controls (at
12 ibit TOPO-II activity as compared with the 9-aminoacridine and 9-(N-butyl)aminoacridine controls (at
14 analysis of anionic metabolites by MALDI, 9-aminoacridine as the matrix yielded a far superior signa
23 kaged short dsDNA substrates and removes all aminoacridine dye from packaged genomic DNA in vivo.
24 intercalating agents ethidium bromide and 9-aminoacridine enhanced oxopropenylation by severalfold.
27 r the rapid elucidation of 3-(acetylamino)-6-aminoacridine-labeled N-glycans present on MAbs using li
30 ode can be significantly improved by using 9-aminoacridine together with a robust deposition method,
31 hree compounds, chlorhexidine, Lys-05, and 9-aminoacridine, triggered transient Ca(2+) signals linked
32 r, ferricyanide and the DeltapH indicator, 9-aminoacridine, was used to measure simultaneously electr