ライフサイエンスコーパス: nitroaromatic

1 sly for the rapid detection of TNT and other nitroaromatics.

2 ave been designed for selective detection of nitroaromatics.

3 velength shifts in real time, in response to nitroaromatic adsorption, results in the first single-na

4 ted unique fingerprints for each of the nine nitroaromatic analytes tested, including unique response

5 y the sensing mechanisms's ability to detect nitroaromatic analytes, the fluorescent-labeled MIP part

6 The simultaneous measurement of nitroaromatic and ionic explosives is used for demonstra

7 as a postcolumn reagent for the detection of nitroaromatic and nitramine explosive compounds.

8 f a microchip, enabled the separation of six nitroaromatic and nitramine explosives and their degrada

9 xplosive molecules including nitrate esters, nitroaromatics and cyclic triazine compounds.

10 We envisage applications to detecting other nitroaromatics and security-related gas targets, and hig

11 te hypothesis for the mechanism of action of nitroaromatic anti-TB agents, in that the cysteine thiol

12 nown nitrovasodilators, but also occurs with nitroaromatic antimicrobials.

13 Nitroaromatics are among the most important and commonly

14 As contaminant nitroaromatics are transported up the roots and stem int

15 lly act as luminescent reporters of volatile nitroaromatics at sub-parts per million levels.

16 at black carbon-mediated reduction of sorbed nitroaromatics by sulfides involves electron transfer di

17 ally used for photolysis of many widely used nitroaromatic caged compounds (e.g., 4-carboxymethoxy-5,

18 Since many nitroaromatic caged compounds are two-photon active at 7

19 Monooxygenation is an important route of nitroaromatic compound (NAC) biodegradation and it is wi

20 rrays to monitor fluorescence changes during nitroaromatic compound (NAC) vapor exposure.

21 exposure of the modified QCM surface to the nitroaromatic compound 2,4-dinitrotoluene (DNT) in solut

22 at the modified electrode, depending on the nitroaromatic compound present.

23 ent arrays permit the detection of low-level nitroaromatic compound vapors because of sensor-to-senso

24 mparisons of measurements taken with related nitroaromatic compounds (1,3,5 trinitrobenzene, 1,3 dini

25 observed during the event were attributed to nitroaromatic compounds (NAC), comprising 28 elemental f

26 c analysis of stable C, N, and H isotopes in nitroaromatic compounds (NACs) and characterized biodegr

27 Nitroaromatic compounds (NACs) are ubiquitous environmen

28 The evaluation of new energetic nitroaromatic compounds (NACs) for use in green munition

29 are fruitfully employed for rapid sensing of nitroaromatic compounds (NACs) where picric acid (PA, as

30 his receptor (and other related pyrenes) and nitroaromatic compounds (NACs), in both solution and in

31 such as the alkaline hydrolysis of energetic nitroaromatic compounds (NACs).

32 ically investigated the dioxygenation of two nitroaromatic compounds (nitrobenzene and 2-nitrotoluene

33 le aromatic compounds, including an array of nitroaromatic compounds (nitrobenzene, 2-, 3-, and 4-nit

34 etry (PM) determination of several explosive nitroaromatic compounds (NTs) including 2,4,6-trinitroph

35 use toward the electrochemical detection of nitroaromatic compounds 2,4,6-trinitrotoluene (TNT), 2,4

36 articles was investigated by using different nitroaromatic compounds [m-nitroaniline and p-nitroanili

37 Biodegradation pathways of synthetic nitroaromatic compounds and anilines are well documented

38 roup of enzymes that reduce a broad range of nitroaromatic compounds and has potential uses in chemot

39 zes the reduction of the nitrogroup (NO2) in nitroaromatic compounds and the flavohemoglobin HmpA, wh

40 As previously observed for nitroaromatic compounds and uranium, magnetite stoichiom

41 The nitroaromatic compounds appear to be the actual effector

42 Nitroaromatic compounds are groundwater pollutants that

43 nitrotoluene degradation genes not only when nitroaromatic compounds are present, but also in the pre

44 tuted aromatic carbons of BTZ043 and related nitroaromatic compounds are the most electron-deficient

45 ntaminants, such as chromium or arsenic, and nitroaromatic compounds functioning both as sorbent and

46 Direct detection of several nitroaromatic compounds in a complex mixture without pri

47 The determination of nitroaromatic compounds in aqueous solution was investig

48 method was also used to separate and detect nitroaromatic compounds in extracts from spiked soil sam

49 riminate between the presence and absence of nitroaromatic compounds in high background vapor mixture

50 cate that the system is capable of detecting nitroaromatic compounds in solution with high sensitivit

51 hemical studies on BTZ043 and the additional nitroaromatic compounds synthesized by us and others con

52 ures dominated the screening hits, including nitroaromatic compounds that induce substrate-like shift

53 f the PEA catabolic pathway is to metabolize nitroaromatic compounds that may accumulate in cells exp

54 nvestigated the dioxygenation of a series of nitroaromatic compounds to the corresponding catechols b

55 JS42 and JS765, allowing for recognition of nitroaromatic compounds while retaining the ability to r

56 The results show that all the nitroaromatic compounds, 2-nitroaniline, 3-nitroaniline,

57 of secondary metabolites, the degradation of nitroaromatic compounds, activation of nitroimidazofuran

58 Nitroaromatic compounds, including 1,3-benzothiazin-4-on

59 eractions with electron-deficient molecules (nitroaromatic compounds, NACs), displaying superior dete

60 e reductive transformation of chlorinated or nitroaromatic compounds, no work exists examining the in

61 cubation in a solution with different single nitroaromatic compounds, reduction peaks in the range fr

62 sensitive chemosensors for the detection of nitroaromatic compounds, such as 2,4,6-trinitrotoluene (

63 227 and 232 were key for the recognition of nitroaromatic compounds, while the amino acid at positio

64 sensitive toward the detection of all three nitroaromatic compounds.

65 tection of 2,4,6-trinitrotoluene and related nitroaromatic compounds.

66 . strain U2 has not been reported to oxidize nitroaromatic compounds.

67 diation strategies directed at TNT and other nitroaromatic compounds.

68 lly reduced by the presence of TNT and other nitroaromatic compounds.

69 fides over a 3-day time scale was limited to nitroaromatic compounds.

70 chosen to reassess the therapeutic value of nitroaromatic compounds.

71 anti-TB agents inspired from BTZs and other nitroaromatic compounds.

72 somers in a solution containing a mixture of nitroaromatic compounds.

73 novel quinolones were explored to recognize nitroaromatic compounds.

74 eactions in the alkaline hydrolysis of three nitroaromatic compounds: 2,4,6-trinitrotoluene (TNT), 2,

75 Our study illustrates that dioxygenation of nitroaromatic contaminants exhibits a large C isotope fr

76 This molecule comprises a nitroaromatic core that can be selectively reduced ("unc

77 n additional exciton quenching-based optical nitroaromatic detection method, illustrate that function

78 al when bound to one of the newly identified nitroaromatic drugs.

79 lar triads composed of ferrocene, C(60), and nitroaromatic entities are reported.

80 te (SDS), is used for separating the neutral nitroaromatic explosive and nerve agent compounds, an op

81 The thermal decomposition of a model nitroaromatic explosive, 2,4,6-trinitrotoluene (TNT), is

82 asurement of 2,4,6-Trinitrotoluen (TNT) as a nitroaromatic explosive.

83 Individual nitroaromatic explosives (such as 2,4,6-trinitrotoluene)

84 ctive sensor for the direct determination of nitroaromatic explosives and byproducts is shown based o

85 ing was synthesized for the determination of nitroaromatic explosives and explosive taggants at trace

86 er the same testing conditions, other common nitroaromatic explosives and oxidizing reagents did not

87 In addition, nitroaromatic explosives are found to have unique intera

88 n energy in condensed phase decomposition of nitroaromatic explosives has been an unresolved issue fo

89 Assessing the fate of nitroaromatic explosives in the subsurface is challengin

90 Additional selectivity of amine-substituted nitroaromatic explosives is achieved by using a photoche

91 n developed and deployed for the analysis of nitroaromatic explosives on surfaces in open air, offeri

92 eloped coating for the selective sampling of nitroaromatic explosives were proved achieving LOD value

93 dly enhanced performance in the detection of nitroaromatic explosives, most probably as a result of t

94 aks for several groups of important anaytes (nitroaromatic explosives, organophosphate nerve agents,

95 r TNT) than Ru=APy in the detection of these nitroaromatic explosives, which was ascribed to the exte

96 hat enables degradation of nitrate ester and nitroaromatic explosives.

97 aryl chlorides, triflates, and nonaflates to nitroaromatics has been developed.

98 nes and aminoazo dyes, three mycotoxins, two nitroaromatic hydrocarbons, N-nitrosodimethylamine, viny

99 nsitive for the detection of trace amount of nitroaromatics in solution, solid, and contact mode.

100 8 and 9 also showed enhanced sensitivity for nitroaromatics in the solid state, and their enhanced se

101 mers, the different binding strengths of the nitroaromatic isomer guests to the beta-CD host, and exc

102 fferent reduction potentials for the various nitroaromatic isomers, the different binding strengths o

103 Structural data also reveal that nitroaromatic ligands "moonlight" as substrates by displ

104 an be quenched by numerous agents, including nitroaromatics like TNT and nitramines like RDX, it is d

105 etecting aqueous 2,4-dinitrotoluene (DNT), a nitroaromatic molecule very similar to TNT, as well as T

106 on, orientation, and SERS detection limit of nitroaromatic molecules in aqueous solutions.

107 Detection of nitroaromatic molecules, such as nitrobenzene (NB), 2,4-

108 ectroscopy of the peptoids revealed that the nitroaromatic monomer has a significant effect on peptoi

109 and characterization of peptoids containing nitroaromatic monomer units.

110 ant substances in aqueous solution including nitroaromatics, neurotransmitters, amino acids, and nucl

111 igated for the direct determination of trace nitroaromatics, nitrate esters, and nitramine explosives

112 e, fast, and facile quantitative methods for nitroaromatic OP compounds.

113 finity of zirconia for the phosphoric group, nitroaromatic OPs strongly bind to the ZrO(2) nanopartic

114 d to electrochemically sense the presence of nitroaromatics owing to the selective ability of nitroar

115 We have designed a nitroaromatic photochemical protecting group that absorb

116 trimers making face-to-face contact with the nitroaromatic portion of the electron acceptor.

117 The reaction for a series of substituted nitroaromatics proceeded by reduction, as indicated by f

118 Nitroaromatic prodrugs are used to treat a range of micr

119 EPT) applications as a activating enzyme for nitroaromatic prodrugs of the dinitrobenzamide class.

120 Nitroaromatics quench the fluorescence of Zn(salicylaldi

121 catalyze the oxygen-insensitive reduction of nitroaromatics, quinones, and riboflavin derivatives.

122 sually respond to a class of analytes (e.g., nitroaromatics), rather than a single specific target.

123 olitin family, not previously identified for nitroaromatic recognition, allows near-infrared fluoresc

124 ombination of two physical properties of the nitroaromatics: redox potential and log P.

125 agents were placed in separate compartments, nitroaromatic reduction only occurred when sulfides were

126 opropane carboxylic acids substituted with p-nitroaromatic rings.

127 The array was able to discriminate unknown nitroaromatic samples in solution.

128 Additional experiments revealed that nitroaromatic side chains can influence peptoid nonamer

129 In response to the binding of specific nitroaromatic species, such peptide-nanotube complexes f

130 based on the oxygen-dependent reduction of a nitroaromatic spiroadamantane 1,2-dioxetane scaffold.

131 rofurazone as substrate, leading to reversed nitroaromatic substrate selectivity for the double and t

132 on to the reaction rate varies for different nitroaromatic substrates of NBDO and 2NTDO.

133 lide from a variety of electrophilic aza- or nitroaromatic substrates to form O(2)-arylated derivativ

134 rotein that reduces a variety of quinone and nitroaromatic substrates.

135 rotein that reduces a variety of quinone and nitroaromatic substrates.

136 ction limit of 39 or 48 ppb along with other nitroaromatics such as p-nitrotoluene and p-nitrophenol.

137 Sensitivities of the clones to 11 HAP (six nitroaromatics, three benzotriazine N-oxides, and two qu

138 their ability to detect nitramine (RDX) and nitroaromatic (TNT) explosives.

139 oaromatics owing to the selective ability of nitroaromatics to decouple the inhibition of pyruvate me

140 cae (NR) catalyzes two-electron reduction of nitroaromatics to the corresponding nitroso compounds an

141 ases have rarely supported full reduction of nitroaromatics to their amine products, and more typical

142 ed to the peptide Bombolitin II to recognize nitroaromatics via infrared fluorescent emission, and po

143 ) sensor array that accurately discriminated nitroaromatics, which are mimics of plastic explosives.