ライフサイエンスコーパス: ethyl

1 erved in some patients receiving telotristat ethyl.

2 Both electronically and sterically diverse ethyl 1,2,3,4-tetrahydroisoquinolone-3-carboxylates were

3 d a dichloromethane/toluene solvent mixture, ethyl 1-thio-beta-d-glucosyl disaccharide donors having

4 (1.93; 95% CI: 0.70, 5.30), and chlorimuron ethyl (1.74; 95% CI: 1.02, 2.96), although monotonic exp

5 nversion of the related metabolite (1S,6R)-5-ethyl-1,6-dihydroxycyclohexa-2,4-diene-1-carboxylic acid

6 ained microbial-associated volatiles, with 2-ethyl-1-hexanol and 2-nonanone - both detected by bees -

7 -methyl-2-[2'-(3''-methoxy-4''-hydroxyphenyl)ethyl]-1,2,3,4-tetrahydroqui noline is reported, the (1)

8 -methyl-2-[2'-(3''-hydroxy-4''-methoxyphenyl)ethyl]-1,2,3,4-tetrahydroqui noline, the originally prop

9 -methyl-2-[2'-(3''-methoxy-4''-hydroxyphenyl)ethyl]-1,2,3,4-tetrahydroqui noline.

10 n-2-yl)-ethynyl 5'-methyl 9 (MRS7292) and 5'-ethyl 10 (MRS7232) esters enhanced binding at DAT (EC50

11 molecule 5 (CEACAM5) for tumor delivery of 7-ethyl-10-hydroxycamptothecin (SN-38), in an expanded pha

12 ery of the anticancer agents cisplatin and 7-ethyl-10-hydroxycamptothecin to esophageal cancer cells

13 hree C20 (cochlearenine, paniculamine, and N-ethyl-1alpha-hydroxy-17-veratroyldictyzine) natural prod

14 In this study, ethyl 2-(4-(acryloyloxy)-3-formylphenyl)-4-methylthiazol

15 same molecule was examined using 3-diazo-1-(ethyl 2-diazomalonyl)indolin-2-one under rhodium(II) cat

16 eless, branched hydroxylated esters, such as ethyl 2-hydroxy-3-methylbutanoate and ethyl 2-hydroxy-4-

17 uch as ethyl 2-hydroxy-3-methylbutanoate and ethyl 2-hydroxy-4-methylpentanoate were the only compoun

18 lin, acetic acid, nor-furaneol, guaiacol and ethyl 2-methylbutanoate.

19 the addition of cyclic enolates derived from ethyl 2-oxo-cyclopentanecarboxylate 2 to phosphorated 2H

20 hyl-3-cyclohexen-1-yl)ethanone; terpinolene; ethyl 2-phenylacetate; naphthalene and 7 unknown compoun

21 3-position of the aniline ring, we generated Ethyl (2-amino-3-fluoro-4-((4-(trifluoromethyl)benzyl)am

22 A room-temperature ionic liquid, 1-ethyl-2,3-dimethylimidazolium bis(trifluoromethanesulfon

23 after TSPO blockade with XBD173 (N-benzyl-N-ethyl-2-(7-methyl-8-oxo-2-phenylpurin-9-yl)acetamide) to

24 uxin (IAA) and an auxin-inhibitor (a-(phenyl ethyl-2-one)-indole-3-acetic acid (PEO-IAA)), together w

25 2+) (PaPy3 = N,N-bis(2-pyridylmethyl)amine-N-ethyl-2-pyridine-2-carboxamide) and the S = 0 [Fe(PaPy3)

26 ged over 12 weeks were -0.81 for telotristat ethyl 250 mg ( P < .001) and 0.69 for telotristat ethyl

27 reductions per day for placebo, telotristat ethyl 250 mg, and telotristat ethyl 500 mg were -0.9, -1

28 d 42% of patients given placebo, telotristat ethyl 250 mg, and telotristat ethyl 500 mg, respectively

29 herapy received (1:1:1) placebo, telotristat ethyl 250 mg, or telotristat ethyl 500 mg three times pe

30 5'-Methyl 25 and ethyl 26 esters potently antagonized 5HT2Rs with moderat

31 The catalytic reaction of ethyl 3-(trimethylsilyl)propiolate and methyl 4-formylbe

32 Photolysis of ethyl 3-azido-4,6-difluorobenzoate at room temperature i

33 ated and subjected to a Perkow reaction with ethyl 3-chloropyruvate.

34 xceeding 90% from ethyl 3-hydroxypropanoate (ethyl 3-HP) via dehydration and nitrilation with ammonia

35 achieves ACN molar yields exceeding 90% from ethyl 3-hydroxypropanoate (ethyl 3-HP) via dehydration a

36 8-016 (N-(2-((bis(4-fluorophenyl)methyl)thio)ethyl)-3-phenylpropan-1-amine) was selected for further

37 fect of the small molecule pan-PHD inhibitor ethyl-3,4-dihydroxybenzoate (EDHB) on liver regeneration

38 fect of the small molecule pan-PHD inhibitor ethyl-3,4-dihydroxybenzoate (EDHB) on liver regeneration

39 reversed by the collagen synthesis inhibitor ethyl-3,4-dihydroxybenzoate.

40 Fg) onto the pCB-coated surface via simple 1-ethyl-3-(3-(dimethylamino)propyl)-carbodiimide and N-hyd

41 mercially available peptide coupling agent 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide (EDC).

42 Therefore, chemical crosslinking by 1-ethyl-3-(3-dimethylaminopropyl) and carbodiimide/N-hydro

43 Ts led to a high immobilization density of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) activ

44 The use of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide HCl (EDC) h

45 zed onto screen printed electrode by using 1-Ethyl-3-(3-dimethylaminopropyl)-carbodiimide and N-Hydro

46 terocycles led to the identification of 6-(1-ethyl-3-(quinolin-8-yl)-1H-pyrazol-5-yl)pyridazin-3-amin

47 re of two imidazolium-based ionic liquids, 1-ethyl-3-methylimidazolium acetate [C2MIM][OAc] and 1-eth

48 The SILM contained 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonly)im

49 ted in acetonitrile and two ionic liquids, 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)am

50 n the room temperature ionic liquid (RTIL) 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)im

51 The RTILs studied were 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)im

52 and room-temperature ionic liquid (RTIL), 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)im

53 methylimidazolium acetate [C2MIM][OAc] and 1-ethyl-3-methylimidazolium octanoate [C2MIM][OOct].

54 thyl-1-butanol, pyrazine, 2-ethylpyrazine, 2-ethyl-3-methylpyrazine, 2-vinylpyrazine, 3-hydroxy-2-but

55 We also investigated the novel use of ethyl-3-phenylprop-2-enoate (ethyl cinnamate) as a nonto

56 a-[1-[2,6-dimethoxy-4-(2-propen-1-yl)phenoxy]ethyl]-3,4-dimethoxy-1-acetate, (3) odoratisol A, phenol

57 H-indol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl]ethyl}-3-methylb enzene-1-sulfonamide) exhibited a broad

58 o-6-methyl-2-oxocyclohex-3-en-1-oate (E121), ethyl 4-(4'-bromophenyl)amino-6-methyl-2-oxocyclohex-3-e

59 ve activity of five anilino enaminones E139, ethyl 4-(4'-chlorophenyl)amino-6-methyl-2-oxocyclohex-3-

60 -methyl-2-oxocyclohex-3-en-1-oate (E138) and ethyl 4-(4'-fluorophenyl)amino-6-methyl-2-oxocyclohex-3-

61 N-methyl and N-ethyl 4-MA were substrates at NET, whereas N-propyl and

62 The determination of ethyl [4-oxo-8-(3-chlorophenyl)-4,6,7,8-tetrahydroimidaz

63 ydro-5-(4-hydroxyphenyl)-4-pentylfuran-3-yl)-ethyl-4-hydroxybenzoate (1), 2-2-[(4-hydroxybenzoyl)-oxy

64 xybenzoate (1), 2-2-[(4-hydroxybenzoyl)-oxy]-ethyl-4-methoxy-4-2-[(4-methylpentyl)oxy]-3,4-dihydr o-2

65 ities of novel derivatives of 2-(2-benzamido)ethyl-4-phenylthiazole (1), which had been identified as

66 re, and electrophysiological evaluation of 1-ethyl-4-phenylthiomorpholin-1-ium triflate, a weak parti

67 n results in the regioselective formation of ethyl 5,7-difluoro-4-azaspiro[2.4]hepta-1,4,6-triene-1-c

68 seven novel and two reported analogues of 6-(ethyl(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2

69 yl-5-oxohexyl) phthalate (MEOHP) and mono (2-ethyl-5-hydroxyhexyl) phthalate (MEHHP).

70 ono (2-ethylhexyl) phthalate (MEHP), mono (2-ethyl-5-oxohexyl) phthalate (MEOHP) and mono (2-ethyl-5-

71 hexyl) phthalate] metabolites {MEOHP [mono(2-ethyl-5-oxohexyl) phthalate] and SigmaDEHP} were associa

72 250 mg ( P < .001) and 0.69 for telotristat ethyl 500 mg ( P < .001).

73 bo, telotristat ethyl 250 mg, or telotristat ethyl 500 mg three times per day orally during a 12-week

74 o, telotristat ethyl 250 mg, and telotristat ethyl 500 mg were -0.9, -1.7, and -2.1, respectively.

75 o, telotristat ethyl 250 mg, and telotristat ethyl 500 mg, respectively.

76 5 patients subsequently received telotristat ethyl 500 mg.

77 Reactions of ethyl 6-indolyl-2,4-dioxo-5-hexenoate with nucleophiles

78 ave a series of 7-[2-(alkyl- or arylsulfanyl)ethyl]-7-deaza-2'-deoxyadenosines in 45-85% yields.

79 We found an association between chlorimuron ethyl, a herbicide introduced in 1986, and lung cancer t

80 eliminary studies suggested that telotristat ethyl, a tryptophan hydroxylase inhibitor, reduces bowel

81 the major volatiles excepting acetaldehyde, ethyl acetate and acetoine, whereas the application of o

82 ed on silica gel with a mixture of n-hexane, ethyl acetate and ammonia.

83 tannins, exhibited the highest acetaldehyde, ethyl acetate and C6-compounds levels, and had increased

84 he effect of treatment with petroleum ether, ethyl acetate and n-butanol extracts of rhubarb in a rat

85 1.5) increased the acetaldehyde, ethanol and ethyl acetate concentration, regardless of the fruit mat

86 ogenic microbes, have been isolated from the ethyl acetate extract of B. amyloliquefaciens.

87 Ethyl acetate extraction and LC-MS/MS analysis were used

88 trix solid phase dispersion and a dispersive ethyl acetate extraction were compared.

89 al techniques, such as QuEChERS and buffered ethyl acetate extraction, this method provided superior

90 s (bcAR) and methylalkylresorcinols (mAR) in ethyl acetate extracts of quinoa.

91 dation of ethanol are 1,1-diethoxyethane and ethyl acetate formed from condensation of acetaldehyde o

92 The ethyl acetate fraction of red seaweed Hypnea musciformis

93 nalysis were used to identify the bio-active ethyl acetate fraction.

94 Effects of I. fumosorosea and cell-free ethyl acetate fractions derived from the fungus on the B

95 y the effect of pH on phenol extraction with ethyl acetate from the aqueous phase of hydrothermally t

96 yl propionate from hydroxyethyl acrylate and ethyl acetate from vinyl acetate, respectively.

97 the fungal mycelium as well as by cell-free ethyl acetate fungal extracts.

98 ines to oximes using m-CPBA as an oxidant in ethyl acetate is described.

99 ological disorders, and the concentration of ethyl acetate was below the odour threshold.

100 compounds, amyl alcohols, ethyl lactate and ethyl acetate were quantitatively relevant in all of the

101 s of some solvents (water, ethanol, acetone, ethyl acetate), used as pure or in binary and ternary mi

102 ymatic reaction, quercetin is extracted with ethyl acetate, and subsequently oxidized under basic con

103 number could produce significant amounts of ethyl acetate, arabinitol, glycerol and acetate in addit

104 ile compounds, with increment in ethanol and ethyl acetate, but far below the odour threshold.

105 s, with increased citronellol, acetaldehyde, ethyl acetate, dicarboxylic acids esters, benzenoids, fu

106 equires a combined elution with methanol and ethyl acetate, especially for increasing the recovery of

107 Extractions were performed with ethyl acetate, ethanol, water and ethanol:water to devel

108 s, based on pressurized liquid extraction by ethyl acetate, followed by selective identification and

109 sor for preparation of (13) C hyperpolarized ethyl acetate-1-(13) C, which provides a convenient vehi

110 Chemical investigation of ethyl acetate-methanol extract of the venerid bivalve cl

111 d with hexane to be further partitioned into ethyl acetate.

112 e moment - hexane: 0.0, diethyl ether: 2.80, ethyl acetate: 4.40, methanol: 5.10 and water: 9.0D) wer

113 lpha-[1-[2,6-dimethoxy-4-(2-propenyl)phenoxy]ethyl]- acetate, (5) licarin C; benzofuran,2,3-dihydro-7

114 econdary amines, the aza-Michael addition to ethyl acrylate occurs preferentially according to a 1,2-

115 of 6,6-spiroepoxycyclohexa-2,4-dienones with ethyl acrylate, radical cyclization and 1,3-acyl shift i

116 ear-quantitative ACN yields (98 +/- 2%) from ethyl acrylate.

117 70% isopropyl alcohol, 3% hydrogen peroxide, ethyl alcohol, water immersion, ultraviolet light, and h

118 50 = 10 nM) inhibitor N-(3,4-dimethoxyphenyl)ethyl amide (WOBE437) exerted pronounced cannabinoid rec

119 of the aspartic protease inhibitor hydroxyl-ethyl-amine-based scaffold compound 49c.

120 yl-4-phenylpyrimidin-2-yl)[2-(2-pyridylamino)ethyl]amine analogues which are inhibitors of human glyc

121 ing of a wide range of amines, which include ethyl amines, azetidines, pyrrolidines, piperidines, aze

122 uorophore (7-diethylamino-3-((((2-maleimidyl)ethyl)amino)carbonyl) coumarin) placed at the same posit

123 Ethionine, an S-ethyl analog of the amino acid methionine, is known to i

124 e formation of these compounds, especially 4-ethyl and 4-vinyl derivatives of phenol and guaiacol wer

125 rgets of existing drugs, including icosapent ethyl and adipocyte fatty-acid-binding protein.

126 demonstrated by the synthesis of non-natural ethyl and benzyl congeners of deoxyamphimedine and amphi

127 aracterization of cationic (alpha-diimine)Ni-ethyl and isopropyl beta-agostic complexes, which are ke

128 ntial methylations of a methyl group to form ethyl and isopropyl groups but remarkably also sec-butyl

129 Benzyl, methyl, ethyl, and isopropyl esters are essentially unreactive u

130 3, bisphenol A, the sum of parabens (methyl, ethyl, and propyl parabens), 2,5-dichlorophenol, and tri

131 trazol-5-yl)propa-1,2-diene and 3-methyl-, 3-ethyl- and 3-benzyl derivatives undergo microwave-induce

132 -methoxyguaiacol and guaiacol, followed by 4-ethyl- and 4-vinylguaiacol.

133 A suite of MPs (methyl-, ethyl-, and propylsyringol) and deconjugated PAH metabol

134 disproportionation reaction with 1 equiv of ethyl arene formed for each equivalent of diarylbutadien

135 confirmed by direct dynamics simulations for ethyl as residue and attributed to the dynamics of elimi

136 4-Nitro-N-[2-(2-phenylsulfanylethylamino)ethyl]benzamide hydrochloride is the most potent inhibit

137 t (18)F-6-(3-fluoropropyl)-3-(2-(azepan-1-yl)ethyl)benzo[d]thiazol-2(3H)-one ((18)F-FTC-146).

138 ing locked-nucleic-acid (LNA) or constrained-ethyl-bicyclic-nucleic-acid ((S)-cEt) modifications much

139 3.3 kcal mol(-1) for potassium fluoride plus ethyl bromide reaction model.

140 mice with the neurotoxin N-(2-chloroethyl)-N-ethyl-bromobenzylamine (DSP-4) starting at 2 months of a

141 anoate, ethyl tetradecanoate, hexyl acetate, ethyl butanoate and ethyl isobutanoate).

142 etic derivative, the N-(1-carbamoyl-2-phenyl-ethyl) butyramide, FBA, have been demonstrated to be pro

143 east squares regression (PLSR) revealed that ethyl caprylate (1.000), trans-geraniol (0.995), ethyl i

144 , a multi-dose intraperitoneal injections of ethyl carbamate (urethane, 1 g/kg body weight) were esta

145 The exposure to furan, acrolein and ethyl carbamate through wine consumption may pose risks

146 toxic compounds (formaldehyde, acetaldehyde, ethyl carbamate, furan, furfural and acrolein) found in

147 es was studied to elucidate the formation of ethyl carbamates in the course of these procedures.

148 bioactive PUFA, with the lowest formation of ethyl carbamates in the process.

149 N-acylation/dehydrative cyclization between ethyl carbazate and N-acylbenzotriazoles in the presence

150 For example, for mono(2-ethyl-carboxy-propyl) phthalate (MECPP), a metabolite of

151 In contrast to the application of cream and ethyl cellulose nanocarriers, Dex was already detectable

152 k was to implant timolol maleate (TM) loaded ethyl cellulose nanoparticle-laden ring in hydrogel cont

153 ere developed, by dispersing TM encapsulated ethyl cellulose nanoparticles in acrylate hydrogel (fabr

154 In contrast, ethyl cellulose-ethanol injections of one-fourth the tum

155 nol within the tumor through the addition of ethyl cellulose.

156 Obeticholic acid (6alpha-ethyl-chenodeoxycholic acid, 6-ECDCA), a synthetic FXR a

157 at C-2 with a (1S)-phenyl-2-(phenylsulfanyl)ethyl chiral auxiliary.

158 Ethyl cinnamate rapidly cleared all tested organs, inclu

159 he novel use of ethyl-3-phenylprop-2-enoate (ethyl cinnamate) as a nontoxic solvent-based clearing re

160 Using ethyl cinnamate-cleared kidneys, we also quantified the

161 We performed experiments on ethyl crotonate and menthol, using three different types

162 ng step, a diastereoselective addition of an ethyl cuprate and an unusual strategy to install two add

163 -(7-cyano-1,2,3,4-tetrahydroisoquinolin-2-yl)ethyl]cyclohexyl]-1H- indole-2-carboxamide (SB269652), a

164 side chains undergo covalent modification by ethyl diazoacetate (EDA).

165 boxylate complexes and their reactivity with ethyl diazoacetate.

166 een a poorly selective cyclopropanation with ethyl diazoacetate.

167 lysis of 15 selected minor compounds (mainly ethyl dodecanoate, ethyl tetradecanoate, hexyl acetate,

168 Both telotristat ethyl dosages significantly reduced mean urinary 5-hydro

169 ds to the plant volatile compound pear ester ethyl-(E,Z)-2,4-decadienoate, while CpomOR6a responds to

170 Me), methylfolate, omega-3 (primarily EPA or ethyl-EPA), and vitamin D, with positive isolated studie

171 ied Kendrick mass defect filtering targeting ethyl-epicatechin (C17H16O6) units.

172 co-drug, butyric acid 2-(2-butyryloxyethoxy) ethyl ester (BA-DEG-BA), released active butyric acid wh

173 y physicochemical properties of ferulic acid ethyl ester (FAEE) encapsulated in sodium caseinate and

174 Glycine ethyl ester (GEE) and ammonium chloride served as replac

175 s on glucose uptake and Tetramethylrhodamine ethyl ester (TMRE) reports on mitochondrial membrane pot

176 ification studies confirmed stability of the ethyl ester of benzoate while the POC group was rapidly

177 The ethyl ester of OTA (OTC) could be identified in the same

178 to 35% (w/w) triglyceride oil and 30% (w/w) ethyl ester oil, respectively, can be directly compresse

179 Sacubitril is an ethyl ester prodrug of LBQ657, the active neprilysin (NE

180 odified alpha2,6-linked sialic acids through ethyl esterification, and alpha2,3-linked sialic acids v

181 on process in terms of volatiles, fatty acid ethyl esters (FAEEs) and pyropheophytins (PPPs) concentr

182 Fatty acid ethyl esters (FAEEs) are non-oxidative metabolites of et

183 bution of ethanol metabolites of FAs, ie, FA ethyl esters (FAEEs), to AP outcomes is unclear.

184 hich also set specific limits for fatty-acid ethyl esters (FAEEs).

185 alysed, in particular fatty acids, alcohols, ethyl esters and 3-ethoxy-1-propanol.

186 endoplasmic reticulum to generate fatty acid ethyl esters and fatty alkanes with tailored chain lengt

187 FAEEs and FAs, with oleic acid (OA) and its ethyl esters being the most abundant.

188 In addition, (1)H NMR data suggest that the ethyl esters form inclusion complexes with beta-cyclodex

189 tive maceration displayed higher contents of ethyl esters of branched acids and cinnamates.

190 developments in higher alcohol acetates and ethyl esters of branched acids during ageing.

191 esulted in significantly slower synthesis of ethyl esters of branched acids, whereas varietal thiols

192 e without maceration showed higher levels of ethyl esters of fatty acids and higher alcohol acetates.

193 ndividual higher alcohol acetates (HAAs) and ethyl esters of straight chain fatty acids (EEFAs) at th

194 Probes modified with ethyl esters preferentially label genetically modified c

195 25-40% (w/w) omega-3 oil as triglycerides or ethyl esters were prepared utilizing a direct compaction

196 In traditional Chilean sparkling wines, ethyl esters were significantly higher, while acetic est

197 of an interaction between wine proteins and ethyl esters, the effects induced by these fermentative

198 trongly affected by the presence of selected ethyl esters.

199 rotein removal, as recently demonstrated for ethyl esters.

200 d for the amperometric detection of paraoxon-ethyl, fenitrothion and chlorpyrifos ranging from 1.0 an

201 F254 HPTLC plates with a solvent mixture of ethyl formate, formic acid, water, toluene 30/4/3/1.5 (v

202 external double bonds, number of methyl- and ethyl- functional groups, molecular weight, and number o

203 ontingency management intervention using the ethyl glucuronide (EtG) alcohol biomarker resulted in in

204 d quantification of a metabolite of ethanol, ethyl glucuronide (EtG).

205 using a metabolite expressed in human sweat, Ethyl Glucuronide.

206 hiophenols with 1,2-biselectrophiles such as ethyl glyoxalate and diethyl oxalate in aqueous medium l

207 orward condensation of this sulfinamide with ethyl glyoxylate provided the N-perfluorobutanesulfinyl

208 ransformation involving a primary carbamate, ethyl glyoxylate, and various types of nucleophiles is r

209 erature (1)H NMR spectroscopy indicates fast ethyl group exchange between Ar(C2H5)SnSn(C2H5)Ar (Ar =

210 dem oxidation and amidation of an unreactive ethyl group.

211 an antifungal polyketide that bristles with ethyl groups mounted onto a caged heterotricyclic core.

212 n unusual strategy to install two additional ethyl groups that makes use of a thiocarbonyl ylide gene

213 adecyloxyethyl benzyl 9-[(2-phosphonomethoxy)ethyl]guanine (ODE-Bn-PMEG) as an active compound which

214 propyl benzoate and methyl 8-(2-(benzoyloxy)-ethyl)-hexahydro-4-((E)-pent-2-enyl)-2H-chromene-6-carbo

215 and beta-damascenone, 3-methylbutyl acetate, ethyl hexanoate and 3-MHA were deemed to be important, i

216 the intra-oral release of aliphatic esters (ethyl hexanoate).

217 decanoate and -dodecanoate, but decreased by ethyl-hexanoate.

218 signaling than hH3R445: 2-(1H-imidazol-5-yl)ethyl imidothiocarbamate (imetit), proxyfan, and iodopro

219 rolled phase III study evaluated telotristat ethyl in this setting.

220 ecanoate, hexyl acetate, ethyl butanoate and ethyl isobutanoate).

221 om 4-alkyl-N,N-dimethylbenzylamines (alkyl = ethyl, isopropyl, and benzyl) to the phthalimide N-oxyl

222 l caprylate (1.000), trans-geraniol (0.995), ethyl isovalerate (-0.994) and benzyl carbinol (0.993) a

223 a total of 13 slurry-borne odorants ((methyl ethyl ketone (MEK), isobutyl alcohol (i-BuAl), benzene (

224 the major volatile compounds, amyl alcohols, ethyl lactate and ethyl acetate were quantitatively rele

225 utanol, acetaldehyde, 1,1-diethoxiethane and ethyl lactate.

226 111)In-DOTA or (125)I-iodo-((4-hydroxyphenyl)ethyl) maleimide (HPEM).

227 allylpiperazine (1-ALPP) or 2-(dimethylamino)ethyl methacrylate (DMAEMA), in combination with 2-hydro

228 al micelles with a LC poly(2-(perfluorooctyl)ethyl methacrylate (PFMA) core via a fragmentation-therm

229 te branched selectivity is even achieved for ethyl methacrylate, which enables the introduction of a

230 rnary carbon was achieved by alkylation with ethyl methacrylate.

231 [2-(dimethylamino)ethyl methacrylate] (DMAEMA) was homopolymerized or copo

232 ively charged compound [2-(trimethylammonium)ethyl] methane thiosulfonate bromide (MTS-ET) increased

233 lines, TG01 and TG10, were generated through ethyl methanesulfonate mutagenesis.

234 ccessful symbiotic infection, we screened an ethyl methanesulfonate mutagenized population of Lotus j

235 A subset of an ethyl methanesulfonate mutagenized population of soybean

236 was affected in tomato RNA interference and ethyl methanesulfonate-cus1 mutants.

237 In the ethyl methanesulfonate-induced mutant hcf222-1, the accu

238 the thioreactive agent 2-((trimethylammonium)ethyl) methanethiosulfonate (MTSET).

239 olarization, whereas [2-(trimethyl ammonium) ethyl] methanethiosulfonate chloride modification of I52

240 cement of peptide negative ionization, while ethyl methanoate showed the best results.

241 tions of formaldehyde, 2,2-dimethylpropanal, ethyl methanoate, and 2-phenyl-2-oxoethanal as the negat

242 Ethyl methoxyacetate was found as a suitable acyl donor

243 When EC is paired with ethyl methyl carbonate (EMC), poly(ethylene glycol) dime

244 lycol) dimethyl ether, poly(ethylene glycol) ethyl methyl ether, and poly(ethylene glycol) are found

245 ile dimethyl sulfoxide, dimethyl sulfone and ethyl methyl sulfone were responsible for 'sulfurous' ar

246 In an N-ethyl-N-nitrosaurea mutagenesis screen, we have now gene

247 ian locomotor output cycles Kaput delta 19 N-ethyl-N-nitrosoure (ENU) mutation (ClockDelta19) are use

248 We conducted a sensitized N-ethyl-N-nitrosourea (ENU) mutagenesis screen for dominan

249 A hitherto unidentified N-ethyl-N-nitrosourea (ENU)-induced mutation affects dorsa

250 We describe a novel N-ethyl-N-nitrosourea (ENU)-induced mutation, early doors

251 We have utilized N-ethyl-N-nitrosourea mutagenesis to generate pedigrees of

252 Using N-ethyl-N-nitrosourea, a novel recessive mutation named se

253 N-Ethyl-N-nitrosourea-induced (ENU-induced) missense mutat

254 notype-altering mutations from a screen of N-ethyl-N-nitrosourea-induced mutants.

255 Here, we report a novel, N-ethyl-N-nitrosourea-induced mutation that causes a gain

256 oly(I:C)) resulting from three independent N-ethyl-N-nitrosourea-induced mutations in host cell facto

257 The recessive N-ethyl-N-nitrosourea-induced phenotype toku is characteri

258 neration germline mutant mice derived from N-ethyl-N-nitrosourea-mutagenized grandsires for intestina

259 -methyl-1-propanol, 3/2-methyl-1-butanol and ethyl octanoate were evaporated whereas the other volati

260 n of beta-glucanase enhanced the increase of ethyl octanoate, but produced a decrease in the contents

261 e, p-cymene, limonene, alpha-terpinolene and ethyl octanoate, were targeted.

262 e, acetoin, acetic acid, isobutyric acid and ethyl octanoate, were the main volatile compounds in dou

263 e groups: 1-hexanol in meat aged for 15days, ethyl- octanoate and 2-pentylfuran in meat aged for 22da

264 ty was slightly increased by the addition of ethyl-octanoate, -decanoate and -dodecanoate, but decrea

265 25 degrees C to yield Sn2(Ar((i)Pr6))2R2(R = ethyl or t-butylethyl), which exist either as a symmetri

266 = 1.51; 95% CI: 1.03, 2.23), and chlorimuron ethyl (OR = 1.45; 95% CI: 1.01, 2.07) compared with neve

267 Similar associations were observed between ethyl paraben (EP) and couple fecundity for both partner

268 ciated with altered respiratory health, with ethyl-paraben and bisphenol A exhibiting some consistenc

269 Ethyl-paraben was associated with increased asthma rate

270 Ethyl-paraben, bisphenol A, 2,5-dichlorophenol, and DIDP

271 16-fold against methyl-parathion, malathion, ethyl-paraoxon, and methyl-paraoxon, respectively.

272 In Brazil, the PFOS-precursor N-ethyl perfluorooctane sulfonamide (EtFOSA) is used in Su

273 The observed metabolites in fish were N-ethyl perfluorooctane sulfonamidoacetic acid, perfluoroo

274 olymerization of monomer bis[2-(methacryloxy)ethyl] phosphate in pores of the host membranes, poly(pr

275 components, including bis[2-methacryloyloxy)ethyl]-phosphate (2MP) as acidic monomer and trimethylbe

276 of substituted cinnamic and styrenyl allylic ethyl phosphates.

277 esponding isoxazolones with 4-fold excess of ethyl propiolate under basic conditions at ambient tempe

278 ously inaccessible intermediates, trapped by ethyl propiolate, were obtained by reacting correspondin

279 thening the amine substituent from methyl to ethyl, propyl, and butyl produced a stepwise decrease in

280 micals triclosan, triclocarban, and methyl-, ethyl-, propyl-, and butylparaben in the dust microbiome

281 e hydrogenation of alpha-keto esters such as ethyl pyruvate.

282 CF3)2)3] featuring a mesityl (R = Mes) or an ethyl (R = Et) substituent initiate the living ring-open

283 ing the same samples, biomarkers of alcohol (ethyl sulfate) and tobacco (trans-3'-hydroxycotinine) us

284 s-2-(5-phenylacetamido-1,2,4-thiadiazol-2-yl)ethyl sulfide (BPTES) and the related molecule CB-839, b

285 f the sulfur mustard simulant, 2-chloroethyl ethyl sulfide (CEES).

286 formed selectively to nontoxic 2-chloroethyl ethyl sulfoxide and vinyl ethyl sulfoxide using nearly s

287 oxic 2-chloroethyl ethyl sulfoxide and vinyl ethyl sulfoxide using nearly stoichiometric 3 % aqueous

288 d minor compounds (mainly ethyl dodecanoate, ethyl tetradecanoate, hexyl acetate, ethyl butanoate and

289 ide derivatives, characterized as (E)-12-(17-ethyl-tetrahydro-16-hydroxy-15-(methyl pentanoate)-14-ox

290 m these mutants, three VSCs - ethanethiol, S-ethyl thioacetate and diethyl disulfide - increased prop

291 Ethyl thioacetate was a key precursor to EtSH, with a ma

292 uded: brain tumor studies using (18)F-fluoro-ethyl-tyrosine ((18)F-FET) (n = 31) and (68)Ga-DOTANOC (

293 if led to the identification of isoquinoline ethyl urea 13 as a promising starting point for fragment

294 Screening around the minimal ethyl urea binding motif led to the identification of is

295 n readily available N-[(2-benzoyloxy-1-tosyl)ethyl]urea with sodium enolates of beta-oxoesters or 1,3

296 pounds, 4-(3-(2-(4-substitued piperazin-1-yl)ethyl)ureido)benzenesulfonamides, showed low nanomolar i

297 mall molecules: the technique uses a special ethyl-vinyl acetate film functionalized with strong cati

298 EC consisting of a bromide catholyte and an ethyl viologen anolyte with the addition of tetrabutylam

299 tostatin analogs, treatment with telotristat ethyl was generally safe and well tolerated and resulted

300 ery stable aryl halides along with potassium ethyl xanthate as an odorless sulfur surrogate.