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 avior of sucrose in aqueous ionic liquids {1-octyl-3-methyl imidazolium bromide and 1-octyl-3-methyl

29 {1-octyl-3-methyl imidazolium bromide and 1-octyl-3-methyl imidazolium chloride} solutions have been

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

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

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

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

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

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

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

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

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

39 ster linkages, including 2-butyl, 2-hexyl, 3-octyl, 4-trifluoromethyl cyclohex-1-yl, hexadecyl, and 4

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

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

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

43 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

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

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

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

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

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

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

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

51 The log K(MW) values for the octyl analogues increase in the order H(CH(2))(8)SO(3)(-

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

53 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

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

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

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

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

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

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

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

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

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

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

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

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

66 iments to determine the respective CMCs of n-octyl beta-d-glucopyranoside (OG), n-dodecyl beta-d-malt

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

98 et surface tensions for nonionic surfactants octyl-beta-D-thioglucopyranoside and Tween20 with solubl

99 surfactant (either sodium dodecyl sulfate or octyl-beta-D-thioglucopyranoside) using a stroboscopic i

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

101 , the {Mo(154)} species in the presence of n-octyl-beta-glucoside (C8G1), widely used as a surfactant

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

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

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

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

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

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

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

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

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

111 2-tert-butyl-3-phenyl-2,3-diazabicyclo[2.2.2]octyl-containing charge-bearing units that are doubly li

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

113 oup, a high viscosity blend of n-butyl and 2-octyl cyanoacrylate was applied until hemostasis was ach

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

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

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

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

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

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

120 2',3'-d]pyrroles (where substituent = hexyl, octyl, decyl, tert-butyl, and p-hexylphenyl) in good yie

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

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

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

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

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

126 tyl-p-benzoquinone, diphenylamine, 4,4'-di-t-octyl diphenylamine, 2,4-dihydroxybenzophenone, and 2-hy

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

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

129 ,4,5-trimethoxybenzoic acid 8-(diethylamino)-octyl ester (TMB-8) and 2-[(2-bis-[carboxymethyl]amino-5

130 ,5-bis(trifluoromethyl)phenyl)thioureido and octyl ester substituents.

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

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

133 3,4,5-trimethoxybenzoic acid 8-[diethylamino]octyl ester, an intracellular Ca2+ antagonist, did not c

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

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

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

137 standard EME system comprising 2-nitrophenyl octyl ether (NPOE) as SLM and 10 mM HCl as sample/accept

138 2-Nitrophenyl octyl ether (NPOE) was dexterously employed as both supp

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

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

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

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

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

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

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

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

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

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

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

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

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

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

153 6-(4-bromophenoxy)hexyl or 8-(4-bromophenoxy)octyl fragment at N(1) position.

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

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

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

157 aethylene glycol dodecyl ether (C(12)EO(8)), octyl glucoside (OG), and dodecyl maltoside.

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

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

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

161 Octyl glucoside accelerated the dissociation rate by 3-5

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

203 and extraction of the washed membranes with octyl glucoside.

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

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

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

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

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

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

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

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

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

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

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

215 vel diazo compounds containing a fluorinated octyl group and boron-dipyrromethene (BODIPY) chromophor

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

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

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

219 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

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

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

222 -3,4:9,10-bis(dicarboximide) having either n-octyl groups (octyl-tpPDI) or hydrogen atoms (H-tpPDI) a

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

224 gauche rather than anti conformations of the octyl groups.

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

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

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

228 mentation of the Irg1-itaconate axis using 4-octyl itaconate (4-OI) beneficially remodeled advanced p

229 4-Octyl itaconate (4-OI) is a derivative of the Krebs cycl

230 olved in fatty acid oxidation in following 4-octyl itaconate (4-OI) treatment in vitro.

231 Here we show that 4-octyl itaconate (4-OI), a chemical derivative of the Kre

232 behind the antiviral effects of exogenous 4-octyl itaconate (4-OI), a derivative of itaconate, again

233 4-Octyl itaconate (4-OI), a derivative of the endogenous m

234 4-Octyl itaconate (4-OI), a derivative of the Krebs cycle-

235 trast, exogenous cell permeable itaconate, 4-octyl itaconate (OI) attenuated PM-induced inflammation

236 iously, we reported that administration of 4-octyl itaconate to lupus-prone mice abrogated immune dys

237 red by the endogenous itaconate derivative 4-octyl itaconate, suggesting that synthetic XPO1 inhibito

238 Further, we uncover that NRF2 agonists 4-octyl-itaconate (4-OI) and the clinically approved dimet

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

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

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

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

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

244 Octyl-modified SiO2 NPs, though initially more aggregate

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

246 ,1-b][3,8]phenanthroline-1,3,6(2H)-trione, 2-octyl (NDI-1T).

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

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

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

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

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

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

253 C), phthalate plasticizers such as hexadecyl octyl oxalate gave rise to the most abundant ions.

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

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

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

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

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

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

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

261 erse association between late pregnancy di-n-octyl phthalate (DNOP) exposure and nonverbal IQ.

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

263 had >0.1% diisobutyl phthalate (DiBP), di-n-octyl phthalate (DnOP), and diisononyl phthalate (DiNP),

264 iBP], di-isononyl phthalate [DiNP], and di-n-octyl phthalate [DOP] increased in California pregnant w

265 For example, a 1-SD increase in Edi-n-octyl phthalate metabolites was associated with increase

266 phthalate, di-(2-ethylhexyl) phthalate, di-n-octyl phthalate, diisononyl phthalate, diisodecyl phthal

267 DCHP; di(2-ethylhexyl) phthalate, DEHP; di-n-octyl phthalate, DNOP; diisononyl phthalate, DINP; and d

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

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

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

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

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

273 These were able to bind to Octyl-Sepharose and could be released by detergent, whil

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

291 hin films, H-tpPDI is more slip-stacked than octyl-tpPDI and has intermolecular hydrogen bonds to its

292 Transient absorption spectroscopy shows that octyl-tpPDI exhibits strong mixing between its singlet e

293 dicarboximide) having either n-octyl groups (octyl-tpPDI) or hydrogen atoms (H-tpPDI) attached to its

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

295 N-octyl-tributylammonium and -triethylammonium also blocke

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

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

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

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

300 ta-NiS composites using nickel alkyl (ethyl, octyl) xanthate precursors.