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1      By masking fasudil's active site with a bioreductive 4-nitrobenzyl group, we synthesized a prodr
2 d and evaluated for their ability to undergo bioreductive activation by reductase enzymes under oxyge
3 s of agents that contain nitro groups, their bioreductive activation mechanisms, their toxicities, an
4 odrug of the nitroimidazole class, requiring bioreductive activation of an aromatic nitro group to ex
5  might interact with enzymes involved in the bioreductive activation of this drug.
6 (P)H:quinone oxidoreductase (DT-diaphorase), bioreductive activation to DNA-damaging species, and sel
7           DNA alkylation by AFs, mediated by bioreductive activation, is believed to contribute to cy
8 nyl)-1-(2-chloroethyl)hydrazine (90CE) after bioreductive activation.
9 eactive mitosene intermediate generated upon bioreductive activation.
10  prodrugs of phosphoramide mustard requiring bioreductive activation.
11  hypoxic tumor cells, following one-electron bioreductive activation.
12                      Tirapazamine (TPZ) is a bioreductive agent that forms a toxic-free radical in hy
13 33, WIN 59075) is a benzotriazine-di-N-oxide bioreductive agent that is selectively activated to a re
14 (Sanofi Synthelabo Research, Malvern, PA), a bioreductive agent, in glioblastoma multiforme (GBM) pat
15 trials were run at our institution using the bioreductive alkylating agent mitomycin as an adjunct to
16                                          The bioreductive alkylating agent mitomycin is a safe and ef
17 cal data are presented supporting a proposed bioreductive alkylation mechanism of action.
18 d to an exemplar compound, CH-01, which is a bioreductive Chk1 inhibitor.
19 is compound might undergo hypoxia-selective, bioreductive conversion to the fluorescent product, 6-am
20 , mitomycin C (1) itself is the prototypical bioreductive DNA cross-linking agent.
21 y cellular reductases via a process known as bioreductive drug activation.
22 th an intelligent in silico model to measure bioreductive drug availability inside tumour tissue thro
23    Tirapazamine (TPZ) is a hypoxia-selective bioreductive drug currently in Phases II and III clinica
24                      Tirapazamine (TPZ) is a bioreductive drug that exhibits greatly enhanced cytotox
25 ascular tumours, including the infusion of a bioreductive drug to study the effects of protein bindin
26 amine (TPZ) is the lead member of a class of bioreductive drugs currently in phase II and III clinica
27         To target this resistant population, bioreductive drugs that are preferentially toxic to tumo
28 efit of incorporating TPZ, and perhaps other bioreductive drugs, into a P450/P450 reductase-based gen
29                             The two-electron bioreductive enzyme DT-diaphorase catalyzes the metaboli
30  that Trx provides reducing equivalents to a bioreductive enzyme for redox cycling of daunomycin.
31 he subcellular localization of overexpressed bioreductive enzyme NAD(P)H:quinone oxidoreductase 1 (NQ
32                       To gain information on bioreductive enzymes involved in the activation of KS119
33 nts by measuring the expression of canonical bioreductive enzymes such as cytochrome P450 oxidoreduct
34 tibiotic mitomycin C is activated by several bioreductive enzymes, including DT-diaphorase.
35 validation of a range of indolequinone-based bioreductive fluorescent probes.
36                                       As the bioreductive group is attached to the VHL or cereblon li
37         We outline methods for attaching the bioreductive group to a range of functionalities, and we
38  HAP-TACs, we have attached an indolequinone bioreductive group to an essential functional group of e
39                                              Bioreductive in situ treatment of U-contaminated groundw
40 r investigation of the complexes suggested a bioreductive mechanism causing intracellular release of
41 D(P)H:quinone oxidoreductase 1 (NQO1) in the bioreductive metabolism of 17-(allylamino)-demethoxygeld
42                                              Bioreductive metabolism of nitroaryl compounds represent
43 these diflavin oxidoreductases also enhanced bioreductive metabolism of PR-104A in an anoxia-specific
44           The mono-N-oxide (3) stemming from bioreductive metabolism of tirapazamine converts the C1'
45 10 years of study, the products arising from bioreductive metabolism of tirapazamine have not been co
46                                              Bioreductive metabolism studies of selected model sulfox
47 eduction and, therefore, is found as a major bioreductive metabolite under all conditions.
48 eviously reported racemic mixtures of chiral bioreductive phosphoramidate prodrugs.
49  of systemic ROCK inhibition, we developed a bioreductive prodrug of a ROCK inhibitor, fasudil, that
50 d 24-fold selectivity as a hypoxia-selective bioreductive prodrug, with an IC50 value of 2 microM aga
51 easing biological relevance, to validate the bioreductive prodrug.
52 e dissociation of vehicles and activation of bioreductive prodrugs simultaneously.
53 ompound delivery to hypoxic regions by using bioreductive prodrugs.
54 hyl-2-nitro-1H-imidazole-based precursors of bioreductive prodrugs.
55                                Without AQDS, bioreductive solubilization was slower ( approximately 2
56                                     A facile bioreductive synthesis is described for Au nanoparticles