ライフサイエンスコーパス: 4-nitrophenol

1 high catalytic activity towards reduction of 4-nitrophenol.

2 een demonstrated with catalytic reduction of 4-nitrophenol.

3 gh catalytic activities for the reduction of 4-nitrophenol.

4 ensitivity to the inhibition by 2,6-dichloro-4-nitrophenol.

5 Pd(atz,ur) complex at 457nm by the 2-chloro-4-nitrophenol (2-CNP) which produced from the reaction o

6 The separation of 4-nitrophenol, 2,4-dinitrophenol, 2-methyl-4-nitrophenol

7 ducts: 2-methoxy-5-nitrophenol (2), 2-chloro-4-nitrophenol (3), and 3-chloro-4-methoxyphenol (4), in

8 atechol are good substrates whereas 3-methyl-4-nitrophenol, 3-methyl-4-nitrocatechol, 4-nitrophenol,

9 f 4-nitrophenol, 2,4-dinitrophenol, 2-methyl-4-nitrophenol, 3-methyl-4-nitrophenol, and 2-nitrophenol

10 hyl-4-nitrophenol, 3-methyl-4-nitrocatechol, 4-nitrophenol, 3-nitrophenol, and 4-chlorocatechol were

11 trophenol (3M2NP), (22.8 +/- 1.8) % 3-methyl-4-nitrophenol (3M4NP), (23.5 +/- 1.8) % 5-methyl-2-nitro

12 ZVI was investigated during the reduction of 4-nitrophenol (4-NP) in unbuffered pH systems.

13 ibrous web showed the enhancive reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) within 45 s

14 In addition, both enzymes were active toward 4-nitrophenol, a preferred substrate for CYP2E1.

15 enoxy)propionic acid, 3-phenoxybenozic acid, 4-nitrophenol, alachlor, atrazine, azoxystrobin, chlorpy

16 d to bind neutral guests, such as phenol and 4-nitrophenol, albeit weakly.

17 c acid methyl thioester, and the more acidic 4-nitrophenol and 2-chloro-4-nitrophenol which mimic ele

18 ion rates of nitrite and HONO (most notably, 4-nitrophenol and 2-methyl-4-nitrophenol) could signific

19 Oxidation of 4-nitrophenol and 4-nitrocatechol was observed for both

20 clohexylimidazole), toward different proton (4-nitrophenol and [DMF.H(+)](CF3SO3(-))) (DMF = dimethyl

21 Rates of 4-nitrophenol and formaldehyde production from the O-dem

22 viscous films (10(-5)-10(-4) in the case of 4-nitrophenol) and overall reaction yields up to 0.3 in

23 itrophenol, 2-methyl-4-nitrophenol, 3-methyl-4-nitrophenol, and 2-nitrophenol (these are the dominant

24 ol (PFP), hexafluoroisopropyl alcohol (HFP), 4-nitrophenol, and N-hydroxyphthalimide.

25 polar compounds, phenol, 4-chlorophenol and 4-nitrophenol are extracted under headspace SPME conditi

26 ax values for 4-methyl-7-hydroxycoumarin and 4-nitrophenol between on-line and off-line glucuronidati

27 on of estradiol, estrone, 4-aminophenol, and 4-nitrophenol by 103, 187, 162, and 92%, respectively (a

28 EPC [(2S,3S)-trans-3-phenyl-2-oxiranylmethyl 4-nitrophenol carbonate], suggesting that Cif may be red

29 NO (most notably, 4-nitrophenol and 2-methyl-4-nitrophenol) could significantly contribute to the occ

30 ors pentachlorophenol (PCP) and 2,6-dichloro-4-nitrophenol (DCNP) were used to modulate DNA adduct an

31 -containing polymers extracted up to >99% of 4-nitrophenol from aqueous solution, and the solvent-ext

32 ion of 5-nitro-benzisoxazole forming 2-cyano-4-nitrophenol has long served as a design platform of en

33 2,6-Dichloro-4-nitrophenol inhibits phenolsulfotransferases, but not

34 to be catalytically active for conversion of 4-nitrophenol into 4-aminophenol, providing an example o

35 pH optimum for the standard assay substrate 4-nitrophenol is at pH 5.5; upon oxidation, the optimum

36 d lipophilicity of 2-nitrophenol over 3- and 4-nitrophenol is the lack of hydrogen bond acidity of 2-

37 d 4-6 ppm upfield from the aglycone 2-fluoro-4-nitrophenol (OFPNP).

38 ailed to catalyze the sulfate conjugation of 4-nitrophenol or 17beta-estradiol, prototypic substrates

39 demonstrated in a recyclable manner by using 4-nitrophenol reduction as a probe reaction.

40 ssibility of Au25 (SG)18 is evaluated by the 4-nitrophenol reduction reaction.

41 palladium- or silver-nanoparticle-catalyzed 4-nitrophenol reduction, and 3) gold-nanoparticle-cataly

42 The lampricides 3-trifluoromethyl-4-nitrophenol (TFM) and 2',5-dichloro-4'-nitrosalicylani

43 s further used to quantify 3-trifluoromethyl-4-nitrophenol (TFM) reductive metabolism.

44 The lampricide, 3-trifluoromethyl-4-nitrophenol (TFM), is a primary component to sea lampr

45 rome P450s CYP3A1 and CYP2B1/2, testosterone/4-nitrophenol uridine diphosphate glucuronosyltransferas

46 time, the investigation of both pyridine and 4-nitrophenol vapor adsorption isotherms at very low con

47 (within 1 s of exposure) and ultrasensitive 4-nitrophenol vapor detection (at a sub-ppb level) were

48 Only when 4-nitrophenol was biodegraded by Pseudomonas sp. 1A did

49 onidation of 4-methyl-7-hydroxy coumarin and 4-nitrophenol were determined using the CE method and by

50 d the more acidic 4-nitrophenol and 2-chloro-4-nitrophenol which mimic electronically excited cofacto

51 s evaluated with respect to the reduction of 4-nitrophenol with NaBH4.