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1 d varying from 2.0 for glucose to 1.29 for 4-nitrocatechol.
2 3-methyl-5-nitrocatechol (3M5NC), 3-methyl-4-nitrocatechol (3M4NC), and a negligible amount of 3-meth
3 ations predicted the formation of 3-methyl-5-nitrocatechol (3M5NC), 3-methyl-4-nitrocatechol (3M4NC),
4 M4NC), and a negligible amount of 3-methyl-6-nitrocatechol (3M6NC).
5 haracterize the RH-dependent properties of 4-nitrocatechol (4-NC) and its mixtures with ammonium sulf
6 dihydroxybenzoic acid (PCA), the inhibitor 4-nitrocatechol (4-NC), or cyanide (CN(-)) have been solve
7 ly resemble those of nebulized crystalline 4-nitrocatechol (4-NC), suggesting the presence of crystal
8 s whereas 3-methyl-4-nitrophenol, 3-methyl-4-nitrocatechol, 4-nitrophenol, 3-nitrophenol, and 4-chlor
9 work was to characterize the photolysis of 4-nitrocatechol (4NC) and 2,4-dinitrophenol (24DNP) in sem
10 ectable by using the alternative substrate 4-nitrocatechol (4NC) and mutation of the active site His2
11 ng cleavage of the electron-poor substrate 4-nitrocatechol (4NC) by Co(II)-homoprotocatechuate 2,3-di
12 ing reaction of the chromophoric substrate 4-nitrocatechol (4NC) is shown to proceed with rate consta
13 red by utilizing the alternative substrate 4-nitrocatechol (4NC), which is also cleaved in the proxim
14 huate (HPCA) and the alternative substrate 4-nitrocatechol (4NC).
15 ative, iron(II) soybean lipoxygenase 3 and 4-nitrocatechol, a known inhibitor of the enzyme, has been
16 pe NDO, and that produced 3-amino-4-methyl-5-nitrocatechol and 2-amino-4,6-dinitrobenzyl alcohol from
17                  Purified ARSK turned over p-nitrocatechol and p-nitrophenyl sulfate.
18 edict more than one stable complex between 4-nitrocatechol and the central cavity of lipoxygenase 3,
19                                    MNC and 4-nitrocatechol are good substrates whereas 3-methyl-4-nit
20 strates, including homoprotocatechuate and p-nitrocatechol, are nonessential activators of the catala
21 The work detects the ultrafast generation of nitrocatechol (aromatic) compounds, which are major cons
22  diols investigated, including cyclic diols, nitrocatechol, biologically relevant compounds, and poly
23 III)-O2(-) pair found for the O2 adduct of 4-nitrocatechol-bound homoprotocatechuate 2,3-dioxygenase.
24 mandelate, or the tight-binding inhibitor, p-nitrocatechol, but not in the complexes with weaker bind
25 rophenol C6H5NO3, methylnitrophenol C7H7NO3, nitrocatechol C6H5NO4, methylnitrocatechol C7H7NO4, and
26                         A new library of non-nitrocatechol compounds (HetCAMs) was developed and thei
27                                          New nitrocatechol COMT inhibitors based on naturally occurri
28                                          All nitrocatechol derivatives displayed potent inhibition of
29 ive, simple assay for the determination of 4-nitrocatechol formed during the P450-dependent hydroxyla
30 eated variant F350T that produced 3-methyl-4-nitrocatechol from 2,6-dinitrotoluene (26DNT), that rele
31  modes of distinct chemical composition with nitrocatechol from NO(3) oxidation preferentially conden
32         Second, we identify a new pathway of nitrocatechol hydroxylation, which proceeds simply by ox
33 oxygenase was soaked in the slow substrate 4-nitrocatechol in a low O2 atmosphere.
34 on makes it possible to detect 0.5 pmol of 4-nitrocatechol injected, 30 times less than previously re
35                                            p-Nitrocatechol is shown to bind differently to 2,3-HPCD t
36  initial oxidation of DNT to form 4-methyl-5-nitrocatechol (MNC) and nitrite.
37                                   4-Methyl-5-nitrocatechol (MNC) is an intermediate in the degradatio
38       Two mechanisms are proposed to produce nitrocatechols, one (equivalent to H atom abstraction) f
39                                   However, 4-nitrocatechol oxidation was completely quenched in the p
40  heterogeneous nucleation to an independent, nitrocatechol-rich aerosol phase.
41 eractions with COMT were established via the nitrocatechol ring, allowing derivatization of the side
42  substrate mimicking competitive inhibitor p-nitrocatechol sulfate (PNC) is used as a probe of the ac
43 Using a specific colorimetric substrate para-nitrocatechol sulfate (pNCS), detectable ASA residual ac
44  a specific YopH small molecule inhibitor, p-nitrocatechol sulfate (pNCS), which exhibits a Ki value
45                       Using the docking of p-nitrocatechol sulfate to Yersinia protein tyrosine phosp
46          In addition, the sulfate group of p-nitrocatechol sulfate was found to be important both in
47 n the interfacial production of chromophoric nitrocatechols that modify the absorption properties of
48             Oxidation of 4-nitrophenol and 4-nitrocatechol was observed for both derivatives.
49 ge from 4 to 8 showed that the production of nitrocatechols was favored under the most acidic conditi
50 esides carboxylic acids, 4-nitrophenol and 4-nitrocatechol were identified as further complexing agen