ライフサイエンスコーパス: 8-hydroxyquinoline

1 synthetic complex formed between Cu(2+) and 8-hydroxyquinoline.

2 transfer between the gold nanoparticles and 8-hydroxyquinoline.

3 n of corrosion of pure aluminum by CeCl3 and 8-hydroxyquinoline.

4 by a colloidal solution of Fe-nanoparticles/8-hydroxyquinoline.

5 antimicrobial tolerance to chloroxylenol and 8-hydroxyquinoline.

6 ved 11.1-14.8 MBq (300-400 micro Ci) (111)In-8-hydroxyquinoline ((111)In-oxine) or (111)In-mercaptopy

7 wn ethers 17-19 by reductive amination using 8-hydroxyquinoline-2-carboxaldehyde.

8 Compounds 11, 13, 14, and 8-hydroxyquinoline (5) underwent selective ionic hydroge

9 exing aluminum ions with the chelating agent 8-hydroxyquinoline-5-sulfonic acid (HQS) to form Al(HQS)

10 the Zn2+ chelators 1,10-O-phenanthroline or 8-hydroxyquinoline-5-sulfonic acid results in dissociati

11 The electrochemiluminescence (ECL) of tris(8-hydroxyquinoline-5-sulfonic acid)aluminum(III) in aque

12 nd zinc when treated with the metal chelator 8-hydroxyquinoline-5-sulfonic acid.

13 ors utilized in the arrays comprise the same 8-hydroxyquinoline (8-HQ) receptor and various conjugate

14 The 8-hydroxyquinolines (8-HQ) clioquinol (CQ) and PBT2 were

15 One group of hit compounds was 8-hydroxyquinolines (8-OHQ), a class of clinically relev

16 Of approximately 30 hits, several were 8-hydroxyquinolines (8-OHQs).

17 chelation-enhanced fluorescence property of 8-hydroxyquinoline (8HQ) following Ca(2+) complexation w

18 commercially available or newly synthetized 8-hydroxyquinoline (8OHQ) derivatives whose toxicity is

19 -carbomethoxy-2,2'-bipyridine 8 or 5-carboxy-8-hydroxyquinoline 9, two 2-oxoglutarate competitive tem

20 The sensor functionalized with 8-hydroxyquinoline allowed sensing through inducing Donn

21 )) on the common organic semiconductor tris-(8-hydroxyquinoline)aluminium in the range +/-500 uT disp

22 magnetoelectroluminescence (MEL) of a tris-(8-hydroxyquinoline)aluminium-based (Alq(3)) OLED within

23 interrogate interfaces formed between tris-(8-hydroxyquinoline) aluminum (Alq(3)) and vapor-deposite

24 ~300% at T = 10 K) has been reached in tris-(8-hydroxyquinoline) aluminum (Alq(3))-based organic spin

25 pal organic electroluminescent molecule tris(8-hydroxyquinoline) aluminum (Alq(3)).

26 d of a thin-film organic semiconductor tris-(8-hydroxyquinoline) aluminum (Alq3) doped with DCM laser

27 Working examples of tris(8-hydroxyquinoline)aluminum(III)-based OLEDs have been f

28 yers) of organic semiconductors, Alq3 (Tris-(8-hydroxyquinoline)aluminum) and DSA-Ph (1,4-di-[4-(N,N-

29 nce from an Alq(3)/TPD heterojunction (tris-(8-hydroxyquinoline)aluminum/N,N'-bis(3-methylphenyl)-N,N

30 fect of the metal on fluorescent emission of 8-hydroxyquinoline and o-phenanthroline at lambda(em) =

31 nary and abortive ternary complex containing 8-hydroxyquinoline, and contrast with previously reporte

32 lecules-ciclopirox olamine (CPX), piroctone, 8-hydroxyquinoline, and deferasirox-were also shown to e

33 X, and we extended this effect to piroctone, 8-hydroxyquinoline, and deferasirox.

34 -(4-(2-hydroxyethyl) piperazin-1-yl (methyl)-8-hydroxyquinoline], and its derivative M30 [5-(N-methyl

35 , nickel, lead and zinc at trace level using 8-hydroxyquinoline as a chelating agent and lanthanum(II

36 Using 8-hydroxyquinoline as a colloidal agent, a new, fast, an

37 ation of copper from biological samples with 8-hydroxyquinoline as a colorimetric indicator affords a

38 ion was made feasible by the use of 5-chloro-8-hydroxyquinoline as a ligand along with NiBr(2) .DME a

39 ilizes tetraethylammonium carbonate as base, 8-hydroxyquinoline as ligand, and H2O as cosolvent.

40 is is the first study providing evidence for 8-hydroxyquinolines as novel inhibitors of the IN-LEDGF/

41 lish this, fullerene was functionalized with 8-hydroxyquinoline at different ligand positions and the

42 n equilibrium of the immobilized ligand, p-((8-hydroxyquinoline)azo)benzenethiol (SHQ).

43 describe the synthesis of novel, red-shifted 8-hydroxyquinoline-based fluorophores and their incorpor

44 gel synthesis is used to develop multiligand 8-hydroxyquinoline binding sites in porous silica struct

45 pair of Q-PNA strands that each contain one 8-hydroxyquinoline, but below the melting temperature, t

46 mouse hearts and were superfused with Fe(3+)/8-hydroxyquinoline complex (5-100 uM).

47 in myocytes superfused with 15 umol/L Fe(3+)/8-hydroxyquinoline complex.

48 odifications at the C5 and C7 carbons of the 8-hydroxyquinoline core improved potency, but reduction

49 this context, revisiting known classes like 8-hydroxyquinolines could be an interesting strategy to

50 st investigated molecular targets concerning 8-hydroxyquinoline derivatives are explored in the final

51 The 8-hydroxyquinoline derivatives nitroxoline and clioquino

52 chemical space around previously identified 8-hydroxyquinoline-derived Mannich bases with robust MDR

53 nthanum(III) as a carrier element, amount of 8-hydroxyquinoline, duration of co-precipitation was exa

54 livery of iron with membrane-permeant Fe(3+)/8-hydroxyquinoline (FeHQ) quenched MFF fluorescence by ~

55 ) interface , we developed a set of modified 8-hydroxyquinoline fragments demonstrating micromolar IC

56 s such as Cu2+, Co2+, Ni2+, and Zn2+ bind to 8-hydroxyquinoline groups covalently attached to the PCC

57 ors using the cocrystal structure of 5-nitro-8-hydroxyquinoline in the cathepsin B active site.

58 tive M30 [5-(N-methyl-N-propargyaminomethyl)-8-hydroxyquinoline] in vivo to test their neuroprotectiv

59 sistent indications that cerium chloride and 8-hydroxyquinoline inhibit corrosion effectively.

60 monitored with the fiber, it was shown that 8-hydroxyquinoline is a more effective inhibitor than ce

61 extended conjugated chromophores attached to 8-hydroxyquinoline is reported.

62 Strategic substitution of 8-hydroxyquinoline ligands and control of the structural

63 solid-phase extraction of the analyte on an 8-hydroxyquinoline microcolumn.

64 studying the 10-hydroxybenzo[h]quinoline and 8-hydroxyquinoline molecules using anion photoelectron s

65 lti-walled carbon nanotubes coated with poly 8-hydroxyquinoline (MWCNTs/Fe(3)O(4)@PHQ) as a novel sor

66 f this class in the perspective of using the 8-hydroxyquinoline nucleus for the search for novel anti

67 eral targets and the privileged structure of 8-hydroxyquinoline nucleus have prompted an increased in

68 We have introduced 8-hydroxyquinoline Q in 10-mer PNA strands with various

69 Herein, we investigated 8-hydroxyquinoline (quinolin-8-ol) as a potential inhibi

70 yrene film containing gold nanoparticles and 8-hydroxyquinoline sandwiched between two metal electrod

71 azatrithia-16-crown-5 ligands containing two 8-hydroxyquinoline sidearms are reported.

72 cations form bisliganded complexes with two 8-hydroxyquinolines that cross-link the hydrogel and cau

73 1% m/v 8-Hydroxyquinoline was used as the modifier to enhance t

74 vorable binding of the "privileged" fragment 8-hydroxyquinoline with HIV-1 integrase (IN) at the IN-l

75 vacuum-deposited thin films of zinc(II) bis(8-hydroxyquinoline) (Znq(2)).