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 ounds was accomplished via rac-5-(2-fluoro-5-nitrophenyl)-2-methyl-2-azabicyclo[3.3.1]nonan-9beta-ol

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

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

10 4-nitrophenyl-beta-d-galactopyranoside and 4-nitrophenyl-2-deoxy-beta-d-galactopyranoside.

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

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

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

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

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

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

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

18 2-pyrrolyl (3), 4-dimethylaminophenyl (4), 4-nitrophenyl (5), and carboxyl group (6) as substituents

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

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

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

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

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

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

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

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

27 unds toward three mammalian CEs when using o-nitrophenyl acetate as a substrate.

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

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

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

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

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

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

34 enzyme kinetics, the standard reaction of p-nitrophenyl acetate hydrolysis by chymotrypsin was analy

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

55 rs and production of anti-4-hydroxy-5-iodo-3-nitrophenyl acetyl.

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

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

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

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

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

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

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

63 naive lambda(+) B cells, FDCs, (4-hydroxy-3-nitrophenyl)acetyl-chicken gamma-globulin (CGG) + anti-C

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

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

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

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

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

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

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

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

72 The key nitrophenyl alanine intermediates are prepared enantiose

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

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

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

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

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

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

79 serum albumin (M6P-BSA) by phosphorylating p-nitrophenyl-alpha-d-mannopyranoside, reducing its nitro

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

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

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

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

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

85 existing at room temperature, 5-methyl-2-[(2-nitrophenyl)amino]-3-thiophenecarbonitrile (ROY) is the

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

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

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

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

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

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

92 On the other hand, a 2-nitrophenyl and a 2-thienyl derivative were ineffective

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

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

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

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

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

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

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

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

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 es beta-galactosidase for cleavage of both 4-nitrophenyl-beta-d-galactopyranoside and 4-nitrophenyl-2

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

128 (16)O(18)O-labeled methyl, ethyl, phenyl, p-nitrophenyl, diethyl p-nitrophenyl, triphenyl, and di-te

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

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

131 Caged-Ca(2+) compounds such as nitrophenyl-EGTA (NP-EGTA) and DM-nitrophen (DMn) are ex

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 in astrocytes, induced by uncaging Ca(2+), o-nitrophenyl-EGTA, increased action potential-driven spon

135 ion of ureas possessing 1-naphthylenyl and 4-nitrophenyl end groups separated by either one or two ph

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

137 ase substrates, thymidine 5'-monophosphate p-nitrophenyl ester and p-nitrophenylphosphorylcholine, bu

138 0 muM inhibited thymidine 5'-monophosphate p-nitrophenyl ester hydrolysis by NPP1 and NPP3 by >90% an

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

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

141 as judged from the rate of hydrolysis of a p-nitrophenyl ester of thymidine monophosphate, also remai

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

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

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

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

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

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

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

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

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

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

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

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

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

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

156 rkably, the uncaging cross section of a 1-(2-nitrophenyl)ethyl (NPE)-caged coumarin is 6600 at wavele

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

173 2-Nitrophenyl isocyanide is introduced as a convertible is

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

205 Activation parameters for 4-chloro-3-nitrophenyl phenyl sulfate and 4-nitrophenyl phenyl sulf

206 4-chloro-3-nitrophenyl phenyl sulfate and 4-nitrophenyl phenyl sulfate gave the following respective

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

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

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

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

214 ate profiles for the hydrolysis of diethyl p-nitrophenyl phosphate (I) and diethyl p-chlorophenyl pho

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

232 The metal complex of the p-nitrophenyl phosphate monoester was found to hydrolyze b

233 By contrast, the hydrolysis of uncomplexed p-nitrophenyl phosphate occurs by a very loose transition

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

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

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

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

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

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

240 y, the metal complex of the diester methyl-p-nitrophenyl phosphate was found to hydrolyze via a two-s

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

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

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

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

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

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

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

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

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

250 ring of alkaline phosphatase hydrolysis of p-nitrophenyl phosphate.

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

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

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

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

255 Pretreatment of cp70 cells with bis-(p-nitrophenyl) phosphate, an esterase inhibitor, before VE

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

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

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

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

260 p-nitrophenyl phosphonate-conjugated fluorochromes, includ

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

282 (15(V/K) refers to the nitro group in p-nitrophenyl sulfate).

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

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

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

286 O-Nitrophenyl,sulfenyl-adrenocorticotropin, which produces

287 o-Nitrophenyl sulfoxides were found to be efficient synthe

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

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

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

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

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

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

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

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

296 A spectrophotometric assay (4-nitrophenyl-trans-2,3-epoxy-3-phenylpropyl carbonate, NE

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

298 hyl, ethyl, phenyl, p-nitrophenyl, diethyl p-nitrophenyl, triphenyl, and di-tert-butyl ethyl phosphat

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

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

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