ライフサイエンスコーパス: nitrophenyl

1 n octanoyl fatty acid, beta-D-glucose, and p-nitrophenyl.

2 4-(2-Chloro-5-nitrophenyl)-1,2,3-thiadiazole undergoes ring opening to

3 4-(2-Chloro-5-nitrophenyl)-1,2,3-thiadiazole undergoes ring-opening to

4 hed GLUT5 inhibitors N-[4-(methylsulfonyl)-2-nitrophenyl]-1,3-benzodioxol-5-amine (MSNBA) and (-)-epi

5 model and identified N-[4-(methylsulfonyl)-2-nitrophenyl]-1,3-benzodioxol-5-amine (MSNBA) as an inhib

6 methyl phosphate (2)] and two RNA models [p-nitrophenyl 2-hydroxypropyl phosphate (3) and phenyl 2-h

7 trophenyl-beta-d-galactopyranoside to give 4-nitrophenyl-2-deoxy-beta-d-galactopyranoside causes (1)

8 ng step for enzyme-catalyzed hydrolysis of 4-nitrophenyl-2-deoxy-beta-d-galactopyranoside from breakd

9 ine compounds: 1-(4-chlorophenylacetyl)-5-(4-nitrophenyl)-3-(thiophen-2-yl)-4,5-dihydro-1 H-pyrazole

10 Two of these analogues, 1-isatin-4-(4'-nitrophenyl)-3-thiosemicarbazone (22, 8.3-fold selective

11 s))), 2,6-bismethoxyphenyl (3H(Phl(OMe))), 4-nitrophenyl (3H(Phl(NO2))), or 4-tert-butylcarboxyphenyl

12 The conjugation of RNase A with 4-nitrophenyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-

13 itors of MGL [N-arachidonoyl maleimide and 4-nitrophenyl 4-(dibenzo[d][1,3]dioxol-5-yl(hydroxy)methyl

14 genously added phosphodiesterase substrate p-nitrophenyl 5'-dTMP (p-Nph-5'-TMP).

15 inhibitors using a colorimetric assay with p-nitrophenyl 5'-thymidine monophosphate (p-Nph-5'-TMP) as

16 2-pyrrolyl (3), 4-dimethylaminophenyl (4), 4-nitrophenyl (5), and carboxyl group (6) as substituents

17 etrazolium salt WST-1 [2-(4-indophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H tetrazolium, monos

18 nhibitors, PD169316 [4-(4-fluorophenyl)-2-(4-nitrophenyl)-5-(4-pyridyl)-1H-imidazole] or SB203580 [4-

19 6-(4-(Diethylamino)-3-nitrophenyl)-5-methyl-4,5-dihydropyridazin-3(2H)-one (DN

20 eld was obtained for the furanosylation of p-nitrophenyl 6-O-acetyl mannopyranoside.

21 It catalyses p-nitrophenyl acetate (pNPA) hydrolysis with an efficiency

22 etyl donors, acetyl coenzyme A (AcCoA) and p-nitrophenyl acetate (PNPA), and four arylamine substrate

23 dentify residues that become acetylated by p-nitrophenyl acetate and determine the relationship betwe

24 rase activity was confirmed in vitro using p-nitrophenyl acetate and O-acetylated PG as substrates.

25 sts with reactions of aryl oxide ions with p-nitrophenyl acetate and with similar acyl transfers whic

26 namely, the pre-steady-state hydrolysis of p-nitrophenyl acetate by the enzyme chymotrypsin, the kine

27 However, p-nitrophenyl acetate creates multiple, stable, acetylated

28 II, including Michaelis-Menten kinetics of 4-nitrophenyl acetate esterase cleavage, liquid chromatogr

29 cetate for 5 min to 2 weeks, or with 10 mm p-nitrophenyl acetate for 48 h to 2 weeks.

30 free human albumin was treated with 0.5 mm p-nitrophenyl acetate for 5 min to 2 weeks, or with 10 mm

31 Esterase activity with p-nitrophenyl acetate has been attributed to turnover at t

32 d position, while catalytic efficiency for p-nitrophenyl acetate hydrolysis can be retained regardles

33 binant PelA hydrolyzed the pseudosubstrate p-nitrophenyl acetate in vitro, and site-specific mutation

34 Treatment with 10 mm p-nitrophenyl acetate resulted in acetylation of 59 lysine

35 NAD(H) increased the rate of hydrolysis of p-nitrophenyl acetate showing that the metal only affects

36 When a more sensitive esterase substrate, p-nitrophenyl acetate was utilized, only 21.4% and 0.6% ca

37 MID1-zinc hydrolyzes 4-nitrophenyl acetate with a rate acceleration of 10(5) an

38 amic acid triads on each helix, hydrolyses p-nitrophenyl acetate with catalytic efficiencies that mat

39 In a CA-II inhibition assay (4-nitrophenyl acetate), the K i for 3 was approximately 30

40 inc-catalyzed carbonic anhydrase activity (p-nitrophenyl acetate, pNPA) is effectively ablated.

41 in the first 5 min of reaction with 0.5 mm p-nitrophenyl acetate.

42 acids, yielding the highest activity with p-nitrophenyl acetate.

43 ts esterase activity and ability to cleave p-nitrophenyl acetate.

44 a catalytic efficiency of 12mM s(-1) on para-nitrophenyl-acetate, and on methyl-ferulate, the value w

45 us photocage {bis[(2-pyridyl)methyl]amino}(m-nitrophenyl)acetic acid (DPAdeCage, 2), which uses a m-n

46 ered T cell-dependent Ag, hapten 4-hydroxy-3-nitrophenyl acetyl (NP)-conjugated chicken gamma globuli

47 r OT-II mice were immunized with 4-hydroxy-3-nitrophenyl acetyl (NP)-conjugated keyhole limpet hemocy

48 er immunization with the TI-2 Ag 4-hydroxy-3-nitrophenyl acetyl (NP)-Ficoll.

49 ll high affinity IgG anti-4-hydroxy-5-iodo-3-nitrophenyl acetyl in the second week.

50 tailed humoral responses both in 4-hydroxy-3-nitrophenyl acetyl-Ficoll and in 4-hydroxy-3-nitrophenyl

51 ed whether an immune response to 4-hydroxy-3-nitrophenyl acetyl-keyhole limpet hemocyanin (NP-KLH) an

52 nitrophenyl acetyl-Ficoll and in 4-hydroxy-3-nitrophenyl acetyl-keyhole limpet hemocyanin immunized a

53 receptor through a conjugate of 4-hydroxy-3-nitrophenyl acetyl-PG, T cells in mIgM mice were activat

54 eficient C57BL/6 (B6) mice with (4-hydroxy-3-nitrophenyl) acetyl (NP) hapten and evaluated the bindin

55 yed for antibodies to a hapten, (4-hydroxy-3-nitrophenyl) acetyl (NP), after boosting with OVA-NP.

56 against the T cell-dependent Ag (4-hydroxy-3-nitrophenyl) acetyl-chicken gamma globulin.

57 d in vitro by coculturing 6-day (4-hydroxy-3-nitrophenyl) acetyl-primed but unmutated lambda+ B cells

58 C response after challenge with (4-hydroxy-3-nitrophenyl)acetyl (NP) in C57BL/6 mice.

59 ic T cell-dependent response to (4-hydroxy-3-nitrophenyl)acetyl conjugated to chicken gamma globulin

60 sis following immunization with (4-hydroxy-3-nitrophenyl)acetyl coupled to chicken gamma globulin sho

61 Interestingly, (4-hydroxy-3-nitrophenyl)acetyl-Ficoll (NP-Ficoll), a prototype TI-2

62 ut mice with CpG ODN containing (4-hydroxy-3-nitrophenyl)acetyl-Ficoll led to development of IgG Abs

63 development of IgG Abs against (4-hydroxy-3-nitrophenyl)acetyl.

64 h pneumococcal polysaccharide or 4-hydroxy-3-nitrophenyl-acetyl (NP)-Ficoll, all of which induce robu

65 ponses to PPS vaccination and to 4-hydroxy-3-nitrophenyl-acetyl-Ficoll, a widely studied model TI Ag,

66 e response to a T-dependent Ag ([4-hydroxy-3-nitrophenyl]acetyl hapten) were nearly identical to wild

67 , functionalized by covalent attachment of 4-nitrophenyl-acetylacetonate or coumarin 343 adsorbates,

68 (i))(20) (Ti(17)) functionalized with four p-nitrophenyl acetylacetone (NPA-H) adsorbates, of which t

69 The key nitrophenyl alanine intermediates are prepared enantiose

70 catalytically slower than the WT enzyme on p-nitrophenyl alpha-d-galactopyranoside.

71 for the hydroxide-catalyzed hydrolysis of 4-nitrophenyl alpha-d-mannopyranoside in aqueous media has

72 reagent panel containing ten 4-substituted 4-nitrophenyl alpha-D-sialosides and a second panel of the

73 e chromogenic sulfoquinovosidase substrate 4-nitrophenyl alpha-sulfoquinovoside.

74 ant Gly-46-->Trp/Gly-262-->Trp) with bound p-nitrophenyl-alpha-d-galactopyranoside (alpha-NPG), a hig

75 n neck+CRD bound to the aromatic glycoside p-nitrophenyl-alpha-D-maltoside with nearly a log-fold hig

76 m the reaction of the enzyme with 2-chloro-4-nitrophenyl-alpha-d-maltotrioside (CNPG3) substrate.

77 It was active on p-nitrophenyl-alpha-d-xyloside, isoprimeverose, xyloglucan

78 decreased binding affinity for melibiose or nitrophenyl-alpha-galactoside.

79 ward the small molecule acceptor substrate 4-nitrophenyl-alpha-L-fucopyranoside to judge their effect

80 model haptenated lipid molecule, 4-hydroxy-3-nitrophenyl-alphaGalactosylCeramide (NP-alphaGalCer), to

81 yridinyl)cyclohexyl]methyl]-a-methyl-a-[[-(4-nitrophenyl )amino]carbonyl]amino-1H-indole-3-propanamid

82 eeded melt crystallization of 5-methyl-2-[(2-nitrophenyl)amino]-3-thiophenecarbonitrile (ROY), curren

83 e pharmaceutical intermediate 5-methyl-2-[(2-nitrophenyl)amino]-3-thiophenecarbonitrile (ROY).

84 ptors (BB/BB) PD168368 [(S)-a-methyl-a-[[[(4-nitrophenyl)amino]carbonyl]amino]-N-[[1-(2-pyridinyl) cy

85 hod of using sulfo-succinimidyl-6-(4-azido-2-nitrophenyl-amino) hexanoate (sulfo-SANPAH).

86 s of cardiolipin replaced by 12-(N-4-azido-2-nitrophenyl) aminododecanoic acid.

87 The 4-nitrophenyl analogue 7 was the most potent compound in t

88 yl phenyl, p-hydroxyphenyl, p-cyanophenyl, p-nitrophenyl, and p-formylphenyl groups at the 1-position

89 ary ureas possessing 1-naphthylenyl and/or 4-nitrophenyl are reported.

90 xyphenyl azide, 3-methoxyphenyl azide, and 3-nitrophenyl azide in water and in HEPES buffer were stud

91 with respect to the widely applied 4-amino-3-nitrophenyl azide is discussed.

92 used photoaffinity labeling system 4-amino-3-nitrophenyl azide, 5, has been studied by transient abso

93 analog, 2,5-dichloro-N-methyl-N-(2-methyl-4-nitrophenyl)benzenesulfonamide (FH535-M), was inactive a

94 y than wild-type CALB in the hydrolysis of 4-nitrophenyl benzoate, and tolerating bulky substrates.

95 pH of the enzyme was 2.8 and it hydrolysed o-nitrophenyl beta-d galactopyranoside (ONPG) with a K(m)

96 Study of hydrolysis of 4-nitrophenyl beta-D-apiofuranoside revealed that this rea

97 The substrate 2-fluoro-4-nitrophenyl beta-D-galactopyranoside (OFPNPG) is readily

98 termined to be 40 degrees C and pH 6 using 4-nitrophenyl beta-D-glucuronide as an indicator.

99 p-Nitrophenyl beta-D-ribose 5'-phosphate is a poor substra

100 lucosidase activity of purified enzymes on p-nitrophenyl beta-glucoside and mogroside V.

101 k(cat)/K(M) in reactions with the novel para-nitrophenyl-beta-d-fucopyranoside substrate; 39-fold dec

102 n compared with the colorimetric substrate o-nitrophenyl-beta-d-galactopyranoside (ONPG), the signal-

103 decrease in reactivity with the "native"para-nitrophenyl-beta-d-galactopyranoside substrate) were evo

104 Substitution of the C2-OH group by C2-H at 4-nitrophenyl-beta-d-galactopyranoside to give 4-nitrophen

105 ollow the enzymatic hydrolysis of 2-chloro-4-nitrophenyl-beta-D-galactopyranoside using UV-vis spectr

106 interaction between beta-galactosidase and o-nitrophenyl-beta-d-galactoside, reducing their affinity

107 nd increased K(m) values for the substrate p-nitrophenyl-beta-D-glucopyranoside and reduced sensitivi

108 the removal of the fatty acid and releases p-nitrophenyl-beta-D-glucoside.

109 as measured using the synthetic substrate, p-nitrophenyl-beta-D-glucoside.

110 uronidase activity that was not induced by 4-nitrophenyl-beta-D-glucuronide.

111 Treatment with heparinase-III and p-nitrophenyl-beta-D-xylopyranoside (PNPX), an inhibitor o

112 alactosidase with the artificial substrate o-nitrophenyl-beta-galactoside.

113 degrees C using the chromogenic substrate o-nitrophenyl-beta-galactoside.

114 (either isolated or prepared in situ from p-nitrophenyl bromoacetate and the corresponding allylic a

115 teroaromatic betaine across a tethered 4-((2-nitrophenyl)but-3-enyl) side chain.

116 sponsible for (2S,3R)-2-amino-3-hydroxy-4-(4-nitrophenyl)butanoate biosynthesis.

117 the interfacial conversion of hydrophobic p-nitrophenyl butyrate into yellow water-soluble p-nitroph

118 Desiccated substrates in liquid (p-nitrophenyl butyrate) or solid (p-nitrophenyl palmitate)

119 Sse hydrolyzes p-nitrophenyl butyrate, and the residue (178)Ser is critic

120 acyl hydrolase activity of patatin towards o-nitrophenyl butyrate, whereas FeCl3-based one exhibited

121 ) catalyzes the hydrolysis reaction of bis(4-nitrophenyl)carbonate (1) but inhibits that of bis(4-nit

122 gh activity towards short- to medium-chain p-nitrophenyl carboxylic esters with optimal activity towa

123 y to challenge with T-cell-dependent antigen nitrophenyl-chicken gamma globulin but not to the T-cell

124 ing trans diastereomer than the related 1-(4-nitrophenyl) cis diastereomer epimerized.

125 schloroepibatidines 5b-g, analogues of 3'-(4-nitrophenyl) compound 5a.

126 mmunization with a hapten-carrier conjugate, nitrophenyl-coupled chicken gamma-globulin (NP-CGG), the

127 Nrf2 activators, the most potent compound, a nitrophenyl derivative of 2-chloro-5-nitro-N-phenyl-benz

128 trochemical reduction of in situ generated 4-nitrophenyl diazonium cations in aqueous acidic solution

129 The "reduced platinum phase" reacts with nitrophenyl diazonium salts, without applying any extern

130 Ca(2+) by UV uncaging of 1-(4,5-dimethoxy-2-nitrophenyl)-EDTA-potentiated TRPA1 currents.

131 The caged calcium probe o-nitrophenyl EGTA and UV uncaging were used to increase c

132 calized photolytic uncaging of Ca(2+) from o-nitrophenyl-EGTA in somatic ER caused an abrupt Ca(2+) i

133 In contrast, photolysis of caged Ca(2+) (o-nitrophenyl-EGTA) in astrocytes led to neuronal depolari

134 ough the use of an activated C-terminal para nitrophenyl ester (1), it is possible to achieve direct

135 0 muM inhibited thymidine 5'-monophosphate p-nitrophenyl ester hydrolysis by NPP1 and NPP3 by >90% an

136 protein, resulted in loss of hydrolysis of p-nitrophenyl ester of caproate.

137 accelerate the transesterification of the p-nitrophenyl ester of N-carboxybenzylphenylalanine by mor

138 ide release from an alpha,beta-unsaturated p-nitrophenyl ester substrate to facilitate catalyst turno

139 type recombinant protein cleaves synthetic p-nitrophenyl ester substrates in vitro.

140 st acylation by the alpha,beta-unsaturated p-nitrophenyl ester, and a recently reported variable-time

141 ) of 400 M(-1) s(-1) for the cleavage of a p-nitrophenyl ester.

142 Replacing chlorophyll with p-nitrophenyl-ester substrates eliminates the extraction s

143 of nitroalkanes to alpha,beta-unsaturated p-nitrophenyl esters in generally good yield and with exce

144 A series of artificial substrates (p-nitrophenyl esters of various amino acids/aliphatic acid

145 e purified enzymes were investigated using p-nitrophenyl esters with chain lengths from C(2) to C(16)

146 a new chiral amine building block, (S)-1-(2-nitrophenyl)ethanamine (s2ne), which could be readily in

147 Reaction of 1-(2-chloro-5-nitrophenyl)ethanone 1, via Willgerodt-Kindler routes, u

148 precatalysts in the hydrosilylation of 1-(4-nitrophenyl)ethanone confirms that the effect of the ach

149 nimolecular Claisen rearrangement of allyl p-nitrophenyl ether (ApNE) dissolved in naphthalene was st

150 s(methylsulfonyl)-1-(2-chloroethyl)-2-[[1-(4-nitrophenyl)ethoxy]carb onyl]hydrazine (KS119), requires

151 tivated by flash photolysis of the P(3)-1-(2 nitrophenyl) ethyl ester of ATP (NPE-caged ATP), and tim

152 hotolabile caging groups, including the 1-(2-nitrophenyl)ethyl (NPE) group, have been applied to prob

153 we observed that incorporation of N-(S)-1-(4-nitrophenyl)ethylglycine (Nsnp, a p-nitro monomer) at th

154 A new platform based on 4-Fluoro-3-nitrophenyl (FNP) grafted gold disk electrode prepared v

155 inkages and displays minimal activity with p-nitrophenyl fucoside with an acidic pH optimum of 4.6.

156 f 2-chloro-5-((Z)-((E)-5-((5-(4,5-dimethyl-2-nitrophenyl)furan-2-yl)methylene)-4-ox othiazolidin-2-yl

157 e course of enzyme-catalyzed hydrolysis of p-nitrophenyl-galactopyranosides.

158 Michaelis-Menten parameters of 4-nitrophenyl glucopyranoside hydrolysis by sweet almond b

159 ant NDP acceptors and six variant 2-chloro-4-nitrophenyl glycoside donors to produce 30 distinct NDP-

160 creening, using an assay employing unnatural nitrophenyl glycosides as activated donors, resulted in

161 The electronic nature of the nitrophenyl group, the steric and electronic nature of t

162 idyl-amide arms connected by a photoreactive nitrophenyl group.

163 optimized in order to generate monolayer of nitrophenyl groups on the graphene surface without compl

164 ments evidence the presence of ferrocene and nitrophenyl groups on the Pt surface.

165 potential, and conduces to the attachment of nitrophenyl groups onto the surface.

166 The addition of nitrophenyl groups to the surface of few-layer epitaxial

167 antigens', such as chicken egg ovalbumin or nitrophenyl haptens, to study immune responses in model

168 ed saline) using 1 equiv of N-phenethyl-O-(4-nitrophenyl)hydroxylamine and 2 equiv of pyruvic acid in

169 A series of O-(4-nitrophenyl)hydroxylamines were synthesized from their r

170 y two different methods, and the use of 1-(2-nitrophenyl)indole as a radical generator gives an optim

171 2-Nitrophenyl isocyanide is introduced as a convertible is

172 strates, such as S-ethyl-l-cysteine and S-(o-nitrophenyl)-l-cysteine.

173 one exhibited the highest activity towards 4-nitrophenyl laurate.

174 ) were synthesized as bioisosteres of the 4'-nitrophenyl lead compounds 5a and 5g.

175 ed phosphorescence at 77 K are attributed to nitrophenyl-localized lowest energy singlet and triplet

176 man neck+CRD complexed with maltotriose or p-nitrophenyl-maltoside showed stacking of the terminal gl

177 epared by the dispersion polymerization of 4-nitrophenyl methacrylate in the presence of magnetite na

178 of MNPs covered with reactive polymer poly(4-nitrophenyl methacrylate).

179 -2 inhibitor, or NS398 [N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide; 10 mg/kg] a selective CO

180 7943) and the structurally related 2-[[4-[(4-Nitrophenyl)methoxy]phenyl]methyl]-4-thiazoli dinecarbox

181 eory study of the cleavage of a DNA model [p-nitrophenyl methyl phosphate (2)] and two RNA models [p-

182 umarin dyes has been replaced by the cyano(4-nitrophenyl)methylene moiety.

183 Four 4-[[(4-nitrophenyl)methylene]imino]phenols (2a-d) were synthesi

184 b-AP15 [(3E,5E)-3,5-bis[(4-nitrophenyl)methylidene]-1-(prop-2-enoyl)piperidin-4-one

185 so efficiently catalyzes the hydrolysis of 4-nitrophenyl methylphosphonate (4NPMP).

186 le reagents bearing, for example, alkynyl or nitrophenyl moieties, hydrolyze extremely slowly.

187 with secondary amines forming 2-(2-chloro-5-nitrophenyl)-N,N-dialkylthioacetamides.

188 Following this, nitrophenyl (NP) diazonium is reduced to graft a second

189 ich feature a high frequency of B cells with nitrophenyl (NP)-binding specificity, respond to NP-hapt

190 Ags that are either T-dependent (4-hydroxy-3-nitrophenyl [NP]-OVA) or T-independent (NP-Ficoll), we a

191 ne (deca-1,9-diene), 1,2-dichlorobenzene, or nitrophenyl octyl ether (1-(2-nitrophenoxy)octane) was s

192 itions in a standard EME system comprising 2-nitrophenyl octyl ether (NPOE) as SLM and 10 mM HCl as s

193 izers [bis(2-ethylhexyl)sebacate (DOS) and 2-nitrophenyl octyl ether (NPOE)] were investigated.

194 Using 2-nitrophenyl octyl ether as the supported liquid membrane

195 d on poly(vinyl chloride) plasticized with o-nitrophenyl octyl ether in a 1:2 mass ratio may be used

196 microm-thick PVC membrane plasticized with 2-nitrophenyl octyl ether was supported on a gold electrod

197 : adsorptive accumulation time, 40 s; SLM, 2-nitrophenyl octyl ether+10% tris-(2-ethylhexyl) phosphat

198 (vinyl chloride) membrane plasticized with 2-nitrophenyl octyl ether.

199 n to previously reported analogues utilizing nitrophenyl or benzonitrile acceptor groups, the weaker

200 f 0.30mM and 2.16s(-1), respectively, when p-nitrophenyl palmitate (p-NPP) was used as the substrate.

201 The stability is confirmed by lipase p-nitrophenyl palmitate (PNP) assay.

202 liquid (p-nitrophenyl butyrate) or solid (p-nitrophenyl palmitate) form can be mixed or solubilized,

203 enyl)phenoxyl radical, 2,6-di-(t)butyl-4-(4'-nitrophenyl) phenoxyl radical ((t)Bu2NPArO(*)) is descri

204 paration and full characterization of the 4-(nitrophenyl)phenoxyl radical, 2,6-di-(t)butyl-4-(4'-nitr

205 midopropyl-4,4'-diaminodiphenylmethane and 2-nitrophenyl phenyl ether 68% (w/w) as plasticizer casted

206 en Au(I) acetylides PPh(3)Au-C=CR, where R = nitrophenyl (PhNO(2)), phenyl (Ph), thiophene (Th), bith

207 In the cleavage of the DNA model bis(4-nitrophenyl)phospate (BNPP), experimental kinetic data h

208 With the substrate 4-nitrophenyl phosphate (4NPP), the reaction exhibits a be

209 und that their in vitro sensitivity to bis-p-nitrophenyl phosphate (BNPP), however, was not shared by

210 e chemical warfare agent simulant dimethyl-4-nitrophenyl phosphate (DMNP) compared to UiO-66-NH(2) ,

211 catalyzes the cleavage of 2-hydroxypropyl p-nitrophenyl phosphate (HPNP) and a number of diribonucle

212 f catalysis of cleavage of 2-hydroxypropyl-4-nitrophenyl phosphate (HpPNP) and uridine-3'-4-nitrophen

213 eavage of the RNA analogue 2-hydroxypropyl-4-nitrophenyl phosphate (HpPNP) at 25 degrees C (I = 0.10

214 The cyclization of 2-(hydroxypropyl)-4-nitrophenyl phosphate (HpPNP) catalyzed by the dinuclear

215 The enthalpy of transfer of p-nitrophenyl phosphate (pNPP) and p-nitrophenyl phosphoro

216 en atoms in the AP-catalyzed hydrolysis of p-nitrophenyl phosphate (pNPP) and p-nitrophenylsulfate (p

217 ent seen in parallel FCS experiments using p-nitrophenyl phosphate (pNPP) as substrate.

218 rase activity at 65 degrees C with ATP and p-nitrophenyl phosphate (pNPP) as substrates.

219 ALP-catalyzed hydrolysis of p-nitrophenyl phosphate (pNPP) leads to the formation of p

220 P2A showed identical kinetics using either p-nitrophenyl phosphate (pNPP) or 32P-myelin basic protein

221 trophenyl phosphate (HpPNP) and uridine-3'-4-nitrophenyl phosphate (UpPNP).

222 osphorothioate, and the triesters, diethyl p-nitrophenyl phosphate and diethyl p-nitrophenyl phosphor

223 rs measured herein for the diesters, ethyl p-nitrophenyl phosphate and ethyl p-nitrophenyl phosphorot

224 he hydrolysis reactions of the monoesters, p-nitrophenyl phosphate and p-nitrophenyl phosphorothioate

225 Mn(2+)-dependent phosphatase activity with p-nitrophenyl phosphate as a substrate, showing that this

226 says with a low molecular weight substrate p-nitrophenyl phosphate as well as phosphocasein and apopt

227 the standard method based on colorimetric p-nitrophenyl phosphate assay.

228 measured for the reaction of the monoester p-nitrophenyl phosphate by Ce(IV) bis-Tris propane (1.0014

229 tors agree well with values determined for p-nitrophenyl phosphate cleavage.

230 correlate with their binding constants to 4-nitrophenyl phosphate dianion (K(NPP)) used as a minimal

231 2), O,O-diethyl phosphate (3), and O-ethyl 4-nitrophenyl phosphate diester (4).

232 This preferred mechanism for p-nitrophenyl phosphate hydrolysis is difficult to find co

233 hibit recombinant human PTP1B using either p-nitrophenyl phosphate or the tyrosine-phosphorylated ins

234 of the RNA model substrate 2-hydroxypropyl 4-nitrophenyl phosphate promoted by Mg(2+) and Ca(2+), the

235 The calculated kinetic isotope effects for p-nitrophenyl phosphate provide a means to discriminate be

236 We report that CthPnkp also converts bis-p-nitrophenyl phosphate to p-nitrophenol and inorganic pho

237 selectivity of the reaction of O,O-diethyl 4-nitrophenyl phosphate triester (Paraxon, 1) with piperid

238 , ethyl, phenethyl, propargyl, phenyl, and p-nitrophenyl phosphate using [(16)O(18)O] labeled species

239 ) and a k(cat)/K(M) of 630 M(-1) s(-1) and 4-nitrophenyl phosphate with a rate acceleration of 10(4)

240 does not hydrolyze ATP, pyrophosphate, or p-nitrophenyl phosphate, although it hydrolyzes guanosine

241 n of a chemical warfare simulant (dimethyl-4-nitrophenyl phosphate, DMNP) compared to MOFs that are n

242 ive theoretical study of the hydrolysis of p-nitrophenyl phosphate, methyl phosphate and p-nitropheny

243 For the diester, ethyl p-nitrophenyl phosphate, the nonbridge 18O effect for the

244 of the RNA model compound 2-hydroxypropyl p-nitrophenyl phosphate.

245 han a conventional colorimetric assay with p-nitrophenyl phosphate.

246 hout adversely affecting hydrolysis of bis-p-nitrophenyl phosphate.

247 da-Pase, which catalyzes hydrolysis of bis-p-nitrophenyl phosphate.

248 required for Ni2+-dependent hydrolysis of p-nitrophenyl phosphate.

249 the cleavage of the DNA model compound bis(p-nitrophenyl) phosphate (BNPP) in 80% DMSO solution at pH

250 cific carboxylesterase (CES) inhibitor bis(4-nitrophenyl) phosphate and partly with the CES2-specific

251 ion a series of o-(2'-imidazolyl)naphthyl (4-nitrophenyl) phosphate isomers were examined to provide

252 ined, and the best substrate found was bis(p-nitrophenyl) phosphate with a kcat/Km value of 6.7 x 10(

253 se of silane and a catalytic amount of bis(4-nitrophenyl)phosphate.

254 both enzymes were able to dephosphorylate p-nitrophenyl-phosphate and phosphotyrosine-containing sub

255 f Ags including ssDNA, actin, ubiquitin, and nitrophenyl phosphocholine.

256 erminal SnapTag domain react with an ethyl p-nitrophenyl phosphonate (pNPP) or a chloro-pyrimidine (C

257 enzyme cutinase and its suicide substrate p-nitrophenyl phosphonate to covalently attach a variety o

258 p-nitrophenyl phosphonate-conjugated fluorochromes, includ

259 sfer of p-nitrophenyl phosphate (pNPP) and p-nitrophenyl phosphorothioate (pNPPT), from water to 0.6

260 s, ethyl p-nitrophenyl phosphate and ethyl p-nitrophenyl phosphorothioate, and the triesters, diethyl

261 he monoesters, p-nitrophenyl phosphate and p-nitrophenyl phosphorothioate, were compared to the activ

262 iethyl p-nitrophenyl phosphate and diethyl p-nitrophenyl phosphorothioate.

263 th excess readily available 3-carbomethoxy-2-nitrophenyl pinacol boronate afforded the hindered highl

264 with different specificities for either para-nitrophenyl (pNP)-linked substrates or substituted xyloo

265 -dichlorophenyl)-thiazol-2-ylhydrazono)-3-(2-nitrophenyl)]propionic acid), an inhibitor of eFI4E-eIF4

266 oxamide, (NO2)L = N,N'-bis(2,6-diisopropyl-4-nitrophenyl)pyridine-2,6-dicarboxamide), are reported wh

267 o]phenyl}pyrrolocytosine (DABCYLpC) and 6-(p-nitrophenyl)pyrrolocytosine (p-NO2-PhpC) nucleobase anal

268 toredox catalyst Ru(bpy)3(PF6)2 to produce p-nitrophenyl radicals that graft onto gold substrates.

269 Interestingly, p-nitrophenyl riboside 5'-phosphate bound to OPRTs with Kd

270 e showed stacking of the terminal glucose or nitrophenyl ring with the aromatic ring of Phe-335.

271 rea-functionalized arms are decorated with p-nitrophenyl rings, behaves as a highly selective chromog

272 orimetric assay based on the hydrolysis of 4-nitrophenyl silyl ethers.

273 Mice with transgenic nitrophenyl-specific B cells unable to secrete immunoglo

274 ransgenic mice with nitrophenyl to stimulate nitrophenyl-specific lambda(+) germinal center B cells a

275 The host molecule bearing 4-nitrophenyl substituents on the bisurea binding pocket s

276 pid, sensitive and selective monitoring of p-nitrophenyl substituted organophosphate pesticides (OPs)

277 n the basis of activation of SULT1A1 by para-nitrophenyl sulfate (pNPS), an ordered bypass mechanism

278 For p-nitrophenyl sulfate hydrolysis there is only one viable

279 ase-catalyzed sulfuryl (SO3) transfer from p-nitrophenyl sulfate to the 5'-phosphoryl group of 3'-pho

280 (15(V/K) refers to the nitro group in p-nitrophenyl sulfate).

281 itrophenyl phosphate, methyl phosphate and p-nitrophenyl sulfate, all of which have served as key mod

282 ified ARSK turned over p-nitrocatechol and p-nitrophenyl sulfate.

283 e to the simultaneous precipitation of the o-nitrophenyl sulfenic acid byproduct.

284 O-Nitrophenyl,sulfenyl-adrenocorticotropin, which produces

285 o-Nitrophenyl sulfoxides were found to be efficient synthe

286 in late gestation with 3,4-dimethoxy-N-[4-(3-nitrophenyl)thiazol-2-yl]-benzene-sulphonamide (Ro61-804

287 test was 3beta-(4-methylphenyl-2 beta-[5-(3-nitrophenyl)thiazol-2-yl]tropane (4p).

288 The thienopyrimidinone 5,6-dimethyl-2-(4-nitrophenyl)thieno[2,3-d]pyrimidin-4(3H)-one (DNTP) occu

289 ilic cyclization to afford 4-methylene-3-[(4-nitrophenyl)thio]-1-pyrrolines in good to high yields.

290 efficient method for the synthesis of 3-[(4-nitrophenyl)thio]-substituted 4-methylene-1-pyrrolines i

291 ty of the rearrangement of N,N-dimethyl O-(p-nitrophenyl)thiocarbamate 1a in N,N-dimethylacetamide so

292 nyl)carbonate (1) but inhibits that of bis(4-nitrophenyl)thiocarbonate (2).

293 the RP-enantiomer of O-methyl O-cyclohexyl p-nitrophenyl thiophosphate with net inversion of configur

294 h FS-3 and the phosphodiesterase substrate p-nitrophenyl thymidine 5'-monophosphate.

295 ason, we have designed a novel assay using p-nitrophenyl-thymidine-5'-phosphate (T5PNP) as a substrat

296 immunized B1-8 H chain transgenic mice with nitrophenyl to stimulate nitrophenyl-specific lambda(+)

297 t wild type secretes activity against both p-nitrophenyl triacetyl chitotriose and glycol chitin.

298 our different crystalline forms of 1,3-bis(m-nitrophenyl) urea (MNPU), a classic molecular crystal sy

299 A bis-(p-nitrophenyl)ureidodecalin shows especially promising act

300 The apparent K(m) value was 0.55 mM, using p-nitrophenyl xylopyranoside as substrate, and the catalyt