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1 antimicrobial tolerance to chloroxylenol and 8-hydroxyquinoline.
2 synthetic complex formed between Cu(2+) and 8-hydroxyquinoline.
3 transfer between the gold nanoparticles and 8-hydroxyquinoline.
4 n of corrosion of pure aluminum by CeCl3 and 8-hydroxyquinoline.
5 ved 11.1-14.8 MBq (300-400 micro Ci) (111)In-8-hydroxyquinoline ((111)In-oxine) or (111)In-mercaptopy
8 exing aluminum ions with the chelating agent 8-hydroxyquinoline-5-sulfonic acid (HQS) to form Al(HQS)
9 the Zn2+ chelators 1,10-O-phenanthroline or 8-hydroxyquinoline-5-sulfonic acid results in dissociati
10 The electrochemiluminescence (ECL) of tris(8-hydroxyquinoline-5-sulfonic acid)aluminum(III) in aque
12 ors utilized in the arrays comprise the same 8-hydroxyquinoline (8-HQ) receptor and various conjugate
16 chelation-enhanced fluorescence property of 8-hydroxyquinoline (8HQ) following Ca(2+) complexation w
17 -carbomethoxy-2,2'-bipyridine 8 or 5-carboxy-8-hydroxyquinoline 9, two 2-oxoglutarate competitive tem
19 interrogate interfaces formed between tris-(8-hydroxyquinoline) aluminum (Alq(3)) and vapor-deposite
21 d of a thin-film organic semiconductor tris-(8-hydroxyquinoline) aluminum (Alq3) doped with DCM laser
23 nce from an Alq(3)/TPD heterojunction (tris-(8-hydroxyquinoline)aluminum/N,N'-bis(3-methylphenyl)-N,N
24 nary and abortive ternary complex containing 8-hydroxyquinoline, and contrast with previously reporte
25 lecules-ciclopirox olamine (CPX), piroctone, 8-hydroxyquinoline, and deferasirox-were also shown to e
27 -(4-(2-hydroxyethyl) piperazin-1-yl (methyl)-8-hydroxyquinoline], and its derivative M30 [5-(N-methyl
28 , nickel, lead and zinc at trace level using 8-hydroxyquinoline as a chelating agent and lanthanum(II
29 ation of copper from biological samples with 8-hydroxyquinoline as a colorimetric indicator affords a
31 is is the first study providing evidence for 8-hydroxyquinolines as novel inhibitors of the IN-LEDGF/
32 lish this, fullerene was functionalized with 8-hydroxyquinoline at different ligand positions and the
34 describe the synthesis of novel, red-shifted 8-hydroxyquinoline-based fluorophores and their incorpor
35 gel synthesis is used to develop multiligand 8-hydroxyquinoline binding sites in porous silica struct
36 pair of Q-PNA strands that each contain one 8-hydroxyquinoline, but below the melting temperature, t
37 odifications at the C5 and C7 carbons of the 8-hydroxyquinoline core improved potency, but reduction
38 nthanum(III) as a carrier element, amount of 8-hydroxyquinoline, duration of co-precipitation was exa
39 ) interface , we developed a set of modified 8-hydroxyquinoline fragments demonstrating micromolar IC
40 s such as Cu2+, Co2+, Ni2+, and Zn2+ bind to 8-hydroxyquinoline groups covalently attached to the PCC
42 tive M30 [5-(N-methyl-N-propargyaminomethyl)-8-hydroxyquinoline] in vivo to test their neuroprotectiv
44 monitored with the fiber, it was shown that 8-hydroxyquinoline is a more effective inhibitor than ce
50 yrene film containing gold nanoparticles and 8-hydroxyquinoline sandwiched between two metal electrod
52 cations form bisliganded complexes with two 8-hydroxyquinolines that cross-link the hydrogel and cau
54 vorable binding of the "privileged" fragment 8-hydroxyquinoline with HIV-1 integrase (IN) at the IN-l
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