ライフサイエンスコーパス: aminoacridine

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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 re used to study the dynamic properties of 9-aminoacridine (9AA) and four bis(acridine) complexes wit

5 The small molecule 9-aminoacridine (9AA) and its derivative, the antimalaria

6 The 9-aminoacridine (9AA) derivative quinacrine (QC) has a lon

7 n the activity of small-molecule inhibitor 9-aminoacridine (9AA), an anticancer drug that targets two

8 the compounds isolated were derivatives of 9-aminoacridine (9AA), including the antimalaria drug quin

9 lationship of seventy 4-aminoquinoline and 9-aminoacridine analogues reveals that increased activity

10 ibit topo II activity as compared with the 9-aminoacridine and 9-(N-butyl)aminoacridine controls (at

11 ibit TOPO-II activity as compared with the 9-aminoacridine and 9-(N-butyl)aminoacridine controls (at

12 kanamycin A, and tobramycin conjugates of 9-aminoacridine are presented.

13 analysis of anionic metabolites by MALDI, 9-aminoacridine as the matrix yielded a far superior signa

14 30-fold increase in S/N was achieved using 9-aminoacridine as the matrix.

15 The 9-aminoacridine chromophore is an important building block

16 We have identified a series of 9-aminoacridine compounds that demonstrate allosteric modu

17 For 13 aminoquinoline and aminoacridine compounds, relative drug resistance was ne

18 A 9-aminoacridine conjugate of a silyl-protected bis(acetoxy

19 ared with the 9-aminoacridine and 9-(N-butyl)aminoacridine controls (at 10 microM).

20 ared with the 9-aminoacridine and 9-(N-butyl)aminoacridine controls (at 5 microM).

21 An aminoacridine derivative (AD2) was identified that binds

22 kaged short dsDNA substrates and removes all aminoacridine dye from packaged genomic DNA in vivo.

23 intercalating agents ethidium bromide and 9-aminoacridine enhanced oxopropenylation by severalfold.

24 The 9-aminoacridines increase the rate of [(3)H]prazosin disso

25 A series of substituted 9-aminoacridines is evaluated for antiproliferative activi

26 r the rapid elucidation of 3-(acetylamino)-6-aminoacridine-labeled N-glycans present on MAbs using li

27 Conjugation of two 9-aminoacridine pharmacophores, using linkers of varying l

28 ode can be significantly improved by using 9-aminoacridine together with a robust deposition method,

29 r, ferricyanide and the DeltapH indicator, 9-aminoacridine, was used to measure simultaneously electr

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