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1 H solely by changes in the fluorescence of 9-aminoacridine.
2 nticancer agent N-[2-(dimethylamino)ethyl]-9-aminoacridine-4-carboxamide (AAC) are investigated.
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
6                         The small molecule 9-aminoacridine (9AA) and its derivative, the antimalaria
7                                        The 9-aminoacridine (9AA) derivative quinacrine (QC) has a lon
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
13  kanamycin A, and tobramycin conjugates of 9-aminoacridine are presented.
14  analysis of anionic metabolites by MALDI, 9-aminoacridine as the matrix yielded a far superior signa
15 30-fold increase in S/N was achieved using 9-aminoacridine as the matrix.
16                                        The 9-aminoacridine chromophore is an important building block
17             We have identified a series of 9-aminoacridine compounds that demonstrate allosteric modu
18                    For 13 aminoquinoline and aminoacridine compounds, relative drug resistance was ne
19                                          A 9-aminoacridine conjugate of a silyl-protected bis(acetoxy
20 ared with the 9-aminoacridine and 9-(N-butyl)aminoacridine controls (at 10 microM).
21 ared with the 9-aminoacridine and 9-(N-butyl)aminoacridine controls (at 5 microM).
22                                           An aminoacridine derivative (AD2) was identified that binds
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.
25                                        The 9-aminoacridines increase the rate of [(3)H]prazosin disso
26                    A series of substituted 9-aminoacridines is evaluated for antiproliferative activi
27 r the rapid elucidation of 3-(acetylamino)-6-aminoacridine-labeled N-glycans present on MAbs using li
28                         Conjugation of two 9-aminoacridine pharmacophores, using linkers of varying l
29                   The design is based on a 9-aminoacridine scaffold with various acceptor groups at C
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