ライフサイエンスコーパス: octyl

1 non-eugenol [NE] or 2-octyl cyanoacrylate [2-octyl]).

2 Vth = 62 V, I(on)/I(off) = 10(3); N,N'-bis(n-octyl)-1,6,7,12-tetrachloroperylene-3,4:9,10-bis(dicarbo

3 10(5); N,N'-bis(n-octyl)-1,7- and N,N'-bis(n-octyl)-1,6-dibromoperylene-3,4:9,10-bis(dicarboximide) (

4 10(5); N,N'-bis(n-octyl)-1,7- and N,N'-bis(n-octyl)-1,6-dicyanoperylene-3,4:9,10-bis(dicarboximide) (

5 Vth = 55 V, I(on)/I(off) = 10(5); N,N'-bis(n-octyl)-1,7- and N,N'-bis(n-octyl)-1,6-dibromoperylene-3,

6 , Vth = 28, I(on)/I(off) = 10(5); N,N'-bis(n-octyl)-1,7- and N,N'-bis(n-octyl)-1,6-dicyanoperylene-3,

7 solutions, with R(+) as the 1-bicyclo[2.2.2]octyl, 1-adamantyl, or 3-homoadamantyl cation.

8 rocarbenes (ROCCl), with R = 1-bicyclo[2.2.2]octyl, 1-adamantyl, or 3-homoadamantyl, or by the ring e

9 actant probe molecules MG-butyl-1 (2) and MG-octyl-1 (3), which contain an n-butyl and an n-octyl cha

10 of the dicationic imidazolium salt 3,3'-di-n-octyl-1,1'-(1,3-phenylenedimethylene)diimidazolium 1,5-n

11 nhibition of Icmt by 2-[5-(3-methylphenyl)-1-octyl-1H-indol-3-yl]acetamide (cysmethynil).

12 e inhibitor of Icmt, 2-[5-(3-methylphenyl)-1-octyl-1H-indol-3-yl]acetamide (cysmethynil).

13 ple, beta-H elimination of (Phebox)Ir(OAc)(n-octyl) (2-Oc) proceeded on a time scale of minutes at -1

14 ,4-bis(9,9'-bis(8"-(N,N,N-trimethylammonium)-octyl)-2'-fluorenyl)benzene tetrabromide (C8) is reporte

15 gn principle, three PDI acceptors, N,N-bis(n-octyl)-2,5,8,11-tetra(n-hexyl)-PDI (Hexyl-PDI), N,N-bis(

16 11-tetra(n-hexyl)-PDI (Hexyl-PDI), N,N-bis(n-octyl)-2,5,8,11-tetraphenethyl-PDI (Phenethyl-PDI), and

17 phenethyl-PDI (Phenethyl-PDI), and N,N-bis(n-octyl)-2,5,8,11-tetraphenyl-PDI (Phenyl-PDI), were synth

18 The crystal structure of N,N-bis(n-octyl)-2,5,8,11-tetraphenylperylene-3,4:9,10-bis(dicarbo

19 -14 V, I(on)/I(off) = 10(3); and N,N'-bis(n-octyl)-2,6-dicyanonaphthalene-1,4,5,8-bis(dicarboximide)

20 Vth = 37 V, I(on)/I(off) = 10(4); N,N'-bis(n-octyl)-2-cyanonaphthalene-1,4,5,8-bis(dicarboximide) (ND

21 the BCNA 3-(2'-deoxy-beta-D-ribofuranosyl)-6-octyl-2,3-dihydrofuro[2,3-d]pyrimidin- 2-one (Cf1368) 4-

22 cid synthase-AMPK inhibitor C75 (3-carboxy-4-octyl-2-methylenebutyrolactone trans-4-carboxy-5-octyl-3

23 calcium signaling, including 8-(diethylamino)octyl-3,4,5-trimethoxybenzoate and 2-aminoethoxydiphenyl

24 cellular Ca2+ mobilization, 8-(diethylamino)-octyl-3,4,5-trimethoxybenzoate hydrochloride, inhibited

25 ellular Ca(2+) channel (8-(N,N-diethylamino)-octyl-3,4,5-trimethoxybenzoate), CaM (N-(6-aminohexyl)-5

26 h the combined presence of [8-(diethylamino)-octyl-3,4,5-trimethoxybenzoate, HCl] (TMB), an inhibitor

27 ichloroaniline, and sea-nine (4,5-dichloro-2-octyl-3-isothiazolone)).

28 l-2-methylenebutyrolactone trans-4-carboxy-5-octyl-3-methylenebutyrolactone) prevented fructose inhib

29 m bis[(trifluoromethyl)sulfonyl] amide and 1-octyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]

30 siting a thin film of ionic liquid, either 1-octyl-3-methylimidazolium bromide ([OMIm][Br]) or 1-octy

31 mmonium dicyanamide ([Aliquat][DCA]) and 1-n-octyl-3-methylimidazolium dicyanamide ([Omim][DCA]) insi

32 DDTC) followed by dispersion with 40 mg of 1-octyl-3-methylimidazolium hexafluorophosphate ([C(8)mim]

33 For DC18C6 in 1-octyl-3-methylimidazolium hexafluorophosphate, the alkal

34 rphosphate was added and a water-insoluble 1-octyl-3-methylimidazolium hexafluorphosphate was formed

35 t, an aqueous solution of the ionic liquid 1-octyl-3-methylimidazolium tetrafluorborate and sodium he

36 -methylimidazolium bromide ([OMIm][Br]) or 1-octyl-3-methylimidazolium thiocyanate ([OMIm][SCN]), ont

37 The results are compared to those for 4-octyl-4'-cyanobiphenyl (8CB) which, in addition to adopt

38 By confining the LC 4'-octyl-4-cyanobiphenyl in mum-sized rectangular channels

39 e 1-substituted: 1, methyl; 2, n-hexyl; 3, n-octyl; 4, n-octadecyl; and 5, cholestanyloxycarbonylmeth

40 ly(2-(4,4'-didodecyl-2,2'-bithiophen-5-yl)-4-octyl-4H-bisthieno[3,2-b:2',3'-d]p yrrole) (P6) thin fil

41 '-diphospho-5-fluoro-N-acetylglucosamine and octyl 5-fluoro-N-acetylglucosamine, have been synthesize

42 lated model studies on the silabicyclo[2.2.2]octyl (5+, 6+, 5a+, and 6a+), silanorbornyl (7+ and 8+),

43 w Zealand parsnips contain higher amounts of octyl acetate, a floral volatile used by webworms for or

44 issue using ammonium sulphate precipitation, octyl agarose, and heparin agarose chromatography.

45 5)-alpha-d-Araf-(1-->5)-alpha-D-Araf with an octyl aglycon.

46 roxymethyl)pyrrolidinediol (ADP-HPD) and 8-n-octyl-amino-ADP-HPD.

47 On the other hand, N-octyl aminocyclitols having the nitrogen substituents in

48 Nortestosterone analogues bearing 11beta-octyl and 11beta-decyl side-chains bind tightly to recom

49 Galf-(1-->5)-beta-D-Galf-(1-->6)-beta-D-Galf-octyl and beta-D-Galf-(1-->6)-beta-D-Galf-(1-->5)-beta-D

50 ffeates of medium alkyl chain length (butyl, octyl and dodecyl) added resulted in a better oxidative

51 oxytyrosyl (HT) ethers (ethyl, butyl, hexyl, octyl and dodecyl) in rat brain slices.

52 The method is applied with alkyl-modified (n-octyl and n-octadecyl) and perfluorinated (alkyl and phe

53 orothiophenes containing straight (hexyl and octyl) and branched (2-ethylhexyl) alkyl groups.

54 es of varying structure (biphenyl, naphthyl, octyl, and hexadecyl).

55 cemic by mixture", "racemic by synthesis", n-octyl, and n-dodecyl groups was synthesized.

56 aused by their degradation products (such as octyl- and nonylphenol) has raised interest in the envir

57 y, a quantitative method for the analysis of octyl- and nonylphenol, and their ethoxylates (1-5) in w

58 e 3-substituted: 6, methyl; 7, n-hexyl; 8, n-octyl; and 9, n-octadecyl.

59 e carrier trapping observed in films of N-(n-octyl)arylene diimides occurs at a molecular reduction p

60 from spinach and further solubilised using n-octyl beta-D-glucopyranoside (OctGlc) and n-dodecyl beta

61 the presence of the non-ionic detergents, n-octyl beta-D-glucopyranoside (octyl glucoside) and Trito

62 etinal rod outer segment disk lipids using n-octyl beta-d-glucopyranoside and the detergent dialysis

63 However, in the presence of n-octyl beta-d-glucopyranoside, a nonionic lipid mimicking

64 measure intersubunit distances in detergent (octyl beta-d-glucopyranoside, OGP) purified and OMM boun

65 -barrel protein transporter solubilized by n-Octyl beta-D-glucopyranoside.

66 of Bcl-xL treated with the mild detergent n-Octyl beta-D-Maltoside (OM).

67 ositol 4,5-bisphosphate in the presence of n-octyl beta-glucopyranoside but not cetyltriethylammonium

68 bsence of detergents or in the presence of n-octyl beta-glucopyranoside or Triton X-100, but not in t

69 bacteriochlorophylls (BChls) in micelles of octyl beta-glucoside (OG) into complexes with spectral p

70 nges in the CD spectrum of VDAC suspended in octyl beta-glucoside also are reversible.

71 hen VDAC is suspended at room temperature in octyl beta-glucoside at pH < 5 or in sodium dodecyl sulf

72 dichoism (CD) spectrum of VDAC suspended in octyl beta-glucoside is similar to those of bacterial po

73 Heating VDAC in octyl beta-glucoside or in liposomes results in thermal

74 osomal membranes by the nonionic detergent n-octyl- beta-glucopyranoside; the soluble fraction was lo

75 yl sulfate (SDS) or the nonionic detergent n-octyl-beta-D-glucopyranoside (betaOG).

76 Saccharide surfactants, such as n-octyl-beta-d-glucopyranoside (NOG), are widely used to s

77 e, we show a profound inhibitory effect of n-octyl-beta-d-glucopyranoside (OG), the detergent used fo

78 aphy step (MonoS) in the non-ionic detergent octyl-beta-D-glucopyranoside (OG).

79 detergents, sodium dodecyl sulfate (SDS), n-octyl-beta-D-glucopyranoside (OGP), and Zwittergent 3-14

80 structure, is occupied by two molecules of n-octyl-beta-D-glucopyranoside and represents the phosphol

81 Increasing concentrations of the detergent octyl-beta-d-glucopyranoside decreased rates of nitroalk

82 ic receptor a 20-fold larger affinity toward octyl-beta-d-glucopyranoside in CDCl(3), demonstrating t

83 ion chromatography in the presence of 0.2% n-octyl-beta-D-glucopyranoside yields a molecular weight o

84 embrane (L-alpha-lysophosphatidylcholine and octyl-beta-D-glucopyranoside) and activated by cholester

85 dopsin in a bilayer environment perturbed by octyl-beta-D-glucopyranoside) and under fully solubilizi

86 branes treated with the nonionic detergent n-octyl-beta-d-glucopyranoside, suggesting that perturbati

87 erse and dimeric in the nonionic detergent n-octyl-beta-D-glucopyranoside.

88 lar lipid extract and the nonionic detergent octyl-beta-d-glucopyranoside.

89 k membranes were systematically disrupted by octyl-beta-D-glucopyranoside.

90 solubilized from rat liver microsomes with n-octyl-beta-D-glucoside and reconstituted into proteolipo

91 Although detergents such as n-octyl-beta-D-glucpyranoside can efficiently solubilize t

92 cted in Triton X-100 at 37 degrees C or in n-octyl-beta-D-glycoside at 4 degrees C (representative of

93 dimethyl-3-ammonio-1-propanesulfonate, and n-octyl-beta-d-thioglucopyranoside, respectively.

94 The octyl-beta-glucoside ghost extracts from both P4.2-defic

95 ce-cold TX-100 or when treated with ice-cold octyl-beta-glucoside instead of TX-100.

96 g of nonintegral proteins, solubilization in octyl-beta-glucoside, and anion exchange chromatography.

97 y (TPA), and the extractability of band 3 by octyl-beta-glucoside, the latter being a nonionic deterg

98 The nonionic detergent octyl-beta-glucoside, which does not disturb band 3-cyto

99 r separation by isoelectric focusing with an octyl-bonded capillary.

100 Several compounds, especially those with octyl chain at O-4'' and/or O-6'' positions on the ring

101 tyl-1 (3), which contain an n-butyl and an n-octyl chain, respectively, and a charged headgroup simil

102 le) 1-adamantyl chloride and 1-bicyclo[2.2.2]octyl chloride ion pairs were not independent of their R

103 2-tert-butyl-3-phenyl-2,3-diazabicyclo[2.2.2]octyl-containing charge-bearing units that are doubly li

104 periodontal dressings (non-eugenol [NE] or 2-octyl cyanoacrylate [2-octyl]).

105 Thus ozonolysis of octyl cyclobutene-1-carboxylate followed by sodium chlor

106 -DHC8-Cer), and a new ceramide derivative, N-octyl-D-erythro-sphingosine (D-e-C8-Ceramine), to induce

107 n surfactants n-dodecyl-beta-D-maltoside and octyl-D-glucoside, but they also significantly stabilize

108 mogeneous solutions of FhaC solubilized in n-octyl-d17-betaD-glucoside and on a variant devoid of the

109 t-8-(n-C(8)H(17))B(10)H(11)](2)(2-), of 6-(n-octyl)decaborane have been established by single-crystal

110 nalogues (where substituent = methyl, hexyl, octyl, decyl, dodecyl, and phenyl) in high yield.

111 2',3'-d]pyrroles (where substituent = hexyl, octyl, decyl, tert-butyl, and p-hexylphenyl) in good yie

112 mperature 1H NMR studies on the more soluble octyl derivative 2 show that there is a distinct change

113 ynthesized and compared to 5b, the analogous octyl derivative containing a phosphodiester linkage bet

114 ates-di(2-ethylhexyl) phthalate (DEHP), di-n-octyl-, di-iso-butyl-, di-n-butyl-, butylbenzyl-, and di

115 sted of alpha-hexyl, alpha-heptyl, and alpha-octyl dibenzyl ketones that yielded large amounts of Nor

116 onfirmed that the new species was P,P'-(di-n-octyl) dihydrogen pyrophosphonic acid (PPA).

117 r than the ones with medium and long chains (octyl, dodecyl, hexadecyl and eicosyl).

118 rhodamine 19 butyl ester (C4R1), whereas the octyl ester (C8R1) was of poor effect.

119 ,4,5-trimethoxybenzoic acid 8-(diethylamino)-octyl ester (TMB-8) and 2-[(2-bis-[carboxymethyl]amino-5

120 ,5-bis(trifluoromethyl)phenyl)thioureido and octyl ester substituents.

121 terminating the polymerization of norbornene octyl ester with a CA-based chain-terminator or by the r

122 d butyl ester, [6,6]-phenyl-C61-butyric acid octyl ester, [6,6]-bis(phenyl)-C61-butyric acid methyl e

123 3,4,5-trimethoxybenzoic acid 8-[diethylamino]octyl ester, an intracellular Ca2+ antagonist, did not c

124 Longer (butyl-octyl) esters adopt increasingly coiled conformations th

125 -diene), 1,2-dichlorobenzene, or nitrophenyl octyl ether (1-(2-nitrophenoxy)octane) was studied using

126 Use of the detergent pentaoxyethylene octyl ether (C8E5) is a great advantage, since its micel

127 ed: dioctyl sebacate (DOS) and o-nitrophenyl octyl ether (NPOE).

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

129 thylhexyl) sebacate (DOS)- and 2-nitrophenyl octyl ether (o-NPOE)-plasticized ISE membranes).

130 ide) membrane plasticized with o-nitrophenyl octyl ether (PVC-NPOE) is here measured by a novel appro

131 d selected Fluka plasticizers (2-nitrophenyl octyl ether and 2-ethylhexyl sebacate).

132 Using 2-nitrophenyl octyl ether as the supported liquid membrane (SLM) for E

133 nyl chloride) plasticized with o-nitrophenyl octyl ether in a 1:2 mass ratio may be used for the dete

134 containing the polar plasticizer nitrophenyl octyl ether in the absence of ionic additive exhibited n

135 PVC membrane plasticized with 2-nitrophenyl octyl ether was supported on a gold electrode modified w

136 accumulation time, 40 s; SLM, 2-nitrophenyl octyl ether+10% tris-(2-ethylhexyl) phosphate+10% di-(2-

137 ide) membrane plasticized with 2-nitrophenyl octyl ether.

138 Lipophilic (butyl and octyl) ethers blocking the phenolic hydroxyl (3-OH) of A

139 lated ProDOPs (43a, 43b, and 43c) containing octyl, ethylhexyl, and dioctyl substituents appended to

140 ionizing power are very similar to those for octyl fluoroformate, suggesting that the addition step o

141 6-(4-bromophenoxy)hexyl or 8-(4-bromophenoxy)octyl fragment at N(1) position.

142 on donors NADH and NADPH and is sensitive to octyl gallate (Ogal), a plastidial terminal oxidase inhi

143 ity fractions isolated from homogenates with octyl glucopyranoside had cholesterol and sphingomyelin

144 ains (DIGs)/ caveolae, were solubilized by n-octyl glucoside (NOG, 1%) at 4 degrees C, and contained

145 sulfhydryl-specific spin label, purified in octyl glucoside (OG), and reconstituted into palmitoylol

146 ubilized in sodium dodecyl sulfate (SDS) and octyl glucoside (OG), respectively.

147 EYPC/cholate = 1.2 in 0.15 M NaCl, and EYPC/octyl glucoside = 0.13 in 0.15 M NaCl all form highly ov

148 Octyl glucoside accelerated the dissociation rate by 3-5

149 At pH 8.5 in the presence of octyl glucoside and Ca2+ both forms exhibited a broad co

150 oluble in solutions containing the detergent octyl glucoside and formed high molecular mass oligomers

151 omal lysoplasmalogenase was solubilized with octyl glucoside and purified 500-fold to near homogeneit

152 nd both nonionic and ionic amphiphilic CPEs (octyl glucoside and sodium lauryl sulfate, respectively)

153 Their segregation between octyl glucoside and the detergent and aqueous phases of

154 at obtained by using lytic concentrations of octyl glucoside but more sensitive to inhibition by cell

155 Here, octyl glucoside extraction of cells was used to identify

156 AO B was performed using protein prepared by octyl glucoside extraction.

157 bacillus subsp. M3 were extracted with 1.25% octyl glucoside in the presence of 0.4% Escherichia coli

158 d-free receptor, solubilized in thermostable octyl glucoside micelles, exhibited a cooperative transi

159 sed in Escherichia coli and refolded in beta-octyl glucoside micelles.

160 concentration (1,2-dioleoyl-sn-glycerol) in octyl glucoside mixed micelles when the surface substrat

161 A single beta-octyl glucoside molecule outlines a possible receptor bi

162 aced with nondissociating detergents such as octyl glucoside or cholic acid.

163 hange when dodecyl maltoside was replaced by octyl glucoside or octyl glucoside-phospholipid-mixed mi

164 GLUT1 forms a multimeric complex in octyl glucoside that dissociates upon addition of reduct

165 retinae by immunoaffinity chromatography in octyl glucoside was reconstituted into liposomes prepare

166 detergents, n-octyl beta-D-glucopyranoside (octyl glucoside) and Triton X-100R-PC (Triton).

167 differential effects of detergents (CHAPS vs octyl glucoside), we have shown that this direct interac

168 The addition of mannose 6-phosphate or octyl glucoside, a nonionic detergent containing a sugar

169 polipoprotein A-II and its complex with beta-octyl glucoside, a widely used lipid surrogate.

170 UCP1 was folded in octyl glucoside, as indicated by its high helical conten

171 e tested a range of detergents as follows: n-octyl glucoside, dodecyl maltoside, Triton X-100, Tween

172 , other detergents such as polydocanol, W-1, octyl glucoside, dodecyl maltoside, Tween 20, and sodium

173 inhibited by Nonidet P-40, Triton X-100, or octyl glucoside, even at concentrations up to 0.3%.

174 During BAX activation with n-octyl glucoside, it has been shown that BAX forms high m

175 ic changes, observed in the presence of beta-octyl glucoside, might provide clues to the structural b

176 Triton X-100, Triton X-114, NP-40, Brij-35, octyl glucoside, octyl thioglucoside, and lauryl maltosi

177 In Triton and octyl glucoside, plots of specific activity versus molec

178 Bacillus subtilis QST713, and the detergent octyl glucoside, respectively, with the detergent C12EO8

179 Typical detergents such as C(12)EO(8), octyl glucoside, SDS, and lauryl maltoside initiate memb

180 Isolated from human blood platelets in octyl glucoside, the alphaIIbbeta3 complex behaved as an

181 dized glutathione and the nonionic detergent octyl glucoside, the G protein regained considerable nat

182 of this epitope was observed in W-1, Chaps, octyl glucoside, Tween 20, and Brij 35.

183 ivatives) and the glycoacyl chain detergent, octyl glucoside, with egg yolk phosphatidylcholine (EYPC

184 -disc" model for bile salt-EYPC micelles and octyl glucoside-EYPC micelles principally because the nu

185 old increases barbed end nucleation sites in octyl glucoside-permeabilized platelets by 3-fold, enabl

186 maltoside was replaced by octyl glucoside or octyl glucoside-phospholipid-mixed micelles.

187 analyses showed that the oligomeric state of octyl glucoside-solubilized GlpF varies: low ionic stren

188 alpha(i-2) also resist extraction with 0.1 m octyl glucoside.

189 and extraction of the washed membranes with octyl glucoside.

190 ods is activation with detergents, such as n-octyl glucoside.

191 One of them is 0.5% n-octyl glucoside/0.5% trifluoroacetic acid.

192 maleimide, the samples were solubilized with octyl glucoside/cholate and the subunit a was purified v

193 In either octyl glucoside/lipid or dodecylmaltoside/lipid micelles

194 to micelles composed of the detergents beta-octyl-glucoside (BOG) and SDS.

195 bserved a significantly lower Delta(1-43)A-I/octyl-glucoside complex partial specific volume than tha

196 toskeletal proteins, though its retention in octyl-glucoside-treated platelets and ultrastructural ob

197 v Victory) root PM in an active form with 1% octyl-glucoside.

198 A synthetic hydrophobic octyl glucuronoside was used to characterize the GDP-man

199 The (5-F)-GlcNAc beta-octyl glycoside acceptor, however, is an excellent subst

200 mine their binding abilities toward a set of octyl glycosides.

201 Bacillus subtilis, which were immobilized in octyl-glyoxyl silica and glyoxyl-silica supports, respec

202 recently reported that the attachment of an octyl group at the O-4'' position of kanamycin B convert

203 e, N-alkylacetamide, (alkyl=butyl, hexyl and octyl group) in chloroform.

204 in the NE group, and 1986 microg/ml in the 2-octyl group).

205 or the NE group and 8.78 microg/ml for the 2-octyl group); by the end of day 1 levels were < or = 2 m

206 n the study; 13 in the NE group, 13 in the 2-octyl group, and 6 in the group taking oral doxycycline.

207 for the NE group and 148 microg/ml for the 2-octyl group.

208 of the eight possible configurations of the octyl groups was found in homochiral hexagonal networks.

209 gauche rather than anti conformations of the octyl groups.

210 ate the binding of indolactam(V) (ILV), 7-(n-octyl)-ILV, 8-(1-decynyl)benzolactam(V) (benzolactam), a

211 proved isozyme selectivity relative to the n-octyl-ILV.

212 The commonly used IL 1-methyl-3-octyl imidazolium chloride ([OMIM][Cl]) was added at var

213 nds contained pentyl, hexyl, or hexanoyl and octyl lipid chains at the sn-1 and sn-2 positions of the

214 alkylamines (NH2R', R' = n-butyl, n-hexyl, n-octyl) (</=0.01 carboxylates nm(-2)).

215 c mice that included: a sunscreen containing octyl methoxycinnamate and benzophenone-3 with a sun pro

216 ntained the established ultraviolet B filter octyl methoxycinnamate, whereas the other contained tere

217 tyl ammonium bromide (TBAB)-modified Nafion; octyl-modified linear polyethyleneimine (C8-LPEI); and c

218 Octyl-modified SiO2 NPs, though initially more aggregate

219 Alkyl chain derivatives (octyl mycophenolate, MPA-C8E; octadecyl mycophenolate, M

220 ,1-b][3,8]phenanthroline-1,3,6(2H)-trione, 2-octyl (NDI-1T).

221 y measured or estimated formation yields for octyl nitrates and hydroxyoctyl nitrates, 93 +/- 15% of

222 ifferent surface functionalization (propyl-, octyl-, octadecyl-trimethoxysilane and esterification) w

223 rs (methyl, ethyl, propyl, butyl, hexyl, and octyl) of estradiol were obtained from 3-O-benzyl-17beta

224 f average molecular weight 2,000 or 5,000, N-octyl-oligo-oxyethylene, or dodecanol.

225 then be removed by using the mild detergents octyl oligooxyethelene (OPOE) or N,N-dimethyldodecylamin

226 O) energy level mainly due to the additional octyl on the D unit and downshifted lowest unoccupied mo

227 The molecule 4,4''''-di-n-octyl-p-quaterphenyl was synthesized in one step by a ni

228 ed viologen" isostructural with 4,4''''-di-n-octyl-p-quaterphenyl.

229 T response parameters as follows: N,N'-bis(n-octyl)perylene-3,4:9,10-bis(dicarboximide) (PDI-8): mu =

230 henyl-2-oxazolyl)benzene) and an extractant (octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxi

231 oused at the tip of a 25-mum capillary using octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxi

232 airs coordinated with the separations ligand octyl,phenyl,(N,N-diisobutylcarbamoyl)methylphosphine ox

233 The synthesis of poly[3-(4-n-octyl)-phenylthiophene] (POPT) from Grignard Metathesis

234 easured in all foods except beef [where di-n-octyl phthalate (DnOP) was the highest phthalate found],

235 teins solubilized with detergents (C12E8 and octyl-PoE) and supported by the following complementary

236 d from P. haemolytica by solubilization in N-octyl polyoxyl ethylene.

237 yzed by Lineweaver-Burk plots indicates that octyl protocatechuate is a competitive inhibitor and the

238 r (2a and 2b) of 11-cis-locked bicyclo[5.1.0]octyl retinal (retCPr) 2 was prepared and its conformati

239 The failure of the bound thioether analogue, octyl-SCoA, to elicit pK shifts to flavin and Glu376 sho

240 a Triton X-114-soluble fraction followed by octyl-Sepharose column chromatography and preparative hi

241 w method based on interactions of GroEL with octyl-Sepharose, it was demonstrated that Zn2+ binding s

242 ified by gel filtration on Sephadex G-50 and octyl-Sepharose.

243 Galf-(1-->6)-beta-D-Galf-(1-->5)-beta-D-Galf-octyl showed that Rv3792 gene product can transfer an ar

244 hiphilic motif represented by a lipophilic n-octyl side chain at position 1 and a positively charged

245 -functionalized BTA that contains two remote octyl side chains.

246 gadolinium(III) (Gd-DTPA) derivative with an octyl substituent, was synthesized and compared to 5b, t

247 UV-vis spectra reveal that the effect of octyl substituents on the onset of electronic absorption

248 onic receptors 1 and 2 containing p-tolyl or octyl substituents, respectively, have been synthesized,

249 h charge-carrier mobilities of the hexyl and octyl-substituted P34AT produce power conversion efficie

250 SPSo), sodium octanesulfonate (SOSo), sodium octyl sulfate (SOS), and sodium dodecyl sulfate (SDS)].

251 cetyltrimethylammonium bromide (CTAB)/sodium octyl sulfonate catanionic vesicles, K =.7 k(B)T, sugges

252 compounds and X-ray structural data for the octyl-, tert-butyl-, and p-hexylphenyl-functionalized co

253 ithiohpene and 2,1,3-benzothiadiazole with 6-octyl-thieno[3,2-b]thiophene as a pi-bridge unit are syn

254 distannyl-DTG derivative with 1,3-dibromo-N-octyl-thienopyrrolodione (TPD) results in an alternating

255 iton X-114, NP-40, Brij-35, octyl glucoside, octyl thioglucoside, and lauryl maltoside, with high rec

256 asted to the deficient performance of poly(3-octyl-thiophene) (POT) for carbonate detection.

257 and of Au(111) covered by monolayers of the octyl-triazatriangulenium molecule.

258 N-octyl-tributylammonium and -triethylammonium also blocke

259 le, an 11-month-old sensor based on 50 mol % Octyl-triEOS exhibits more than 4-fold greater sensitivi

260 than 400% whereas a sensor based on 50 mol % Octyl-triEOS remains stable (RSD = 4%).

261 based on spin-coated n-octyltriethoxysilane (Octyl-triEOS)/tetraethylorthosilane (TEOS) composite xer

262 results show that certain [Ru(dpp)3]2+-doped Octyl-triEOS/TEOS composites form uniform, crack-free xe