ライフサイエンスコーパス: ethoxy

1 coupling of acetaldehyde with excess surface ethoxy.

2 iophene-2-carboxamide, 5-methoxy-3-(1-methyl ethoxy)-1-oxide (PD 144795) block the induction of p53 a

3 1,2,4-dithiazolidine-3,5-dione (DtsNH) and 3-ethoxy-1,2,4-dithiazoline-5-one (EDITH) as effective sul

4 1,2,4-dithiazolidine-3,5-dione (DtsNH) and 3-ethoxy-1,2,4-dithiazoline-5-one (EDITH) as effective sul

5 3-ethoxy-1,2,4-dithiazoline-5-one (EDITH) was recently int

6 erences in the ability of N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ) to irreversibly inact

7 To determine if N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ), a carboxyl group act

8 onaphthalene (7-OH-DPAT), 1-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ), or fluphenazine were

9 esistant to alkylation by 1-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ), which readily alkyla

10 the receptor inactivator N-ethoxy-carbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ; 50 nmol/0.5 ml one da

11 d with [14C]acetate using N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline as the coupling agent.

12 dopamine antagonist EEDQ (N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline), into nucleus accumbens but

13 using [1-14C]acetate and N-ethoxy-carbonyl-2-ethoxy-1,2-dihydroquinoline.

14 the six-membered monocyclic phosphoester, 2-ethoxy-1,3,2-dioxaphosphinane 2-oxide.

15 action of 4,5-dimethyl-2-(2-oxo-1,2-diphenyl)ethoxy-1,3,2-dioxaphospholane, bearing a carboxyl group

16 5-Substituted-2-ethoxy-1,3,4-oxadiazoles were conveniently prepared thro

17 thyl-6-benzyloxy-3Z,5E-hexadienoyl)- 1-aza-2-ethoxy-1,3-butadiene (40) undergoes cycloaddition to pro

18 an exclusive 6-endo-dig iodocyclization of 3-ethoxy-1-(2-alkoxyphenyl)-2-yn-1-ols and 5-endo-dig iodo

19 ahydrofuran as a solvent, and initiated by 1-ethoxy-1-(trimethylsiloxy)-1,3-butadiene (ETSB), our met

20 d with 2-methyl-1-naphthylboronic acid and 2-ethoxy-1-naphthylboronic acid.

21 oxygen influenced the rise of the level of 3-ethoxy-1-propanol only.

22 ar fatty acids, alcohols, ethyl esters and 3-ethoxy-1-propanol.

23 xymethane (DEM) and 2-[2-(2,2-difluoroethoxy)ethoxy]-1,1,1-trifluoroethane (F5DEE).

24 itial lead, T3.5 (3-chloro-6-(2-diethylamino-ethoxy)-10-(2-diethylamino-ethyl)-acridone), demonstrate

25 4) (from 6 treated with FeSO4.7H2O) forms 12-ethoxy-11,12-dihydro-6H-6,12-methanodibenzo[b,f][1,5]thi

26 , 2-propynyl-17alpha-methylestradiol (39), 2-ethoxy-17-(1'-methylene)estra-1,3,5(10)-triene-3-ol (50)

27 ylene)estra-1,3,5(10)-triene-3-ol (50) and 2-ethoxy-17alpha-methylestradiol (51) showed similar or gr

28 thymidine (6) and deprotection of 15 gave 4'-ethoxy-2',3'-dideoxydidehydrothymidine (7).

29 Reduction of 11 gave 4'-ethoxy-2',3'-dideoxythymidine (6) and deprotection of 15

30 ement fluorinated processing aid perfluoro(2-ethoxy-2-fluoroethoxy)-acetic acid ("EEA"), were measure

31 ed gallium(III) complex, gallium(III)-(bis(3-ethoxy-2-hydroxy-benzylidene)-N,N'-bis(2,2-dimethyl-3- a

32 nd trans-[5,5'-(1,2-ethanediyl diimino)bis(2-ethoxy-2-methyl-3-oxo-4-pentenyl)]bis[dimethyl(3- methox

33 tions by using eosin Y as the catalyst and N-ethoxy-2-methylpyridinium tetrafluoroborate as the oxida

34 rboxamide (1) to lead compound 6-methyl-N-(4-ethoxy-2-nitrophenyl)pyridine-3-carboxamide (10), with a

35 Compounds 1 and 6-chloro-N-(4-ethoxy-2-nitrophenyl)pyridine-3-carboxamide (8), a more

36 ication of compound (Z)-4-chloro-3-(5-((3-(2-ethoxy-2-oxoethyl)-2,4-dioxothiazolidin-5-ylidene)methyl

37 , ethyl-2-amino-6-(3,5-dimethoxyphenyl)-4-(2-ethoxy-2-oxoethyl)-4H-chromene-3-carbo xylate) (CXL017),

38 of ethyl 2-amino-6-cyclopentyl-4-(1-cyano-2-ethoxy-2-oxoethyl)-4H-chromene-3-carbox ylate (1, HA 14-

39 ethyl 2-amino-6-(3',5'-dimethoxyphenyl)-4-(2-ethoxy-2-oxoethyl)-4H-chromene-3-carboxyla te (5q, CXL01

40 alogue of ethyl 2-amino-6-bromo-4-(1-cyano-2-ethoxy-2-oxoethyl)-4H-chromene-3-carboxylate (6, HA 14-1

41 nduced by ethyl 2-amino-6-bromo-4-(1-cyano-2-ethoxy-2-oxoethyl)-4H-chromene-3-carboxylate (HA14-1), a

42 we have demonstrated that ethyl 2-amino-4-(2-ethoxy-2-oxoethyl)-6-phenyl-4H-chromene-3-carboxylate (5

43 ibitors [ethyl [2-amino-6-bromo-4-(1-cyano-2-ethoxy-2-oxoethyl)]-4H-chromene-3-carboxylate (HA14-1),

44 Rac-2-ethoxy-3 octadecanamido-1-propylphosphocholine (a protei

45 ll phenolic units blocked, and a dimer, 1-(4-ethoxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)propane-1,3-

46 dinyl]-5-hexyn-1-ol dihydrochloride and 4-(5-ethoxy-3-pyridinyl)-N-methyl-(3E)-3-buten-1-amine difuma

47 and 5-endo-dig iodocyclization of 1-alkoxy-4-ethoxy-3-yn-1,2-diols, respectively.

48 are the synthesis and characterization of an ethoxy/3,5-(CF(3))(2)C(6)H(3)-substituted 2,3:10,11-dibe

49 2-(R)-{1-(R)-[3,5-bis(trifluoromethyl)phenyl]ethoxy}-3-(R)-(3,4-difluor ophenyl)-4-(R)-tetrahydro-2H-

50 target daunomycin glucuronide, N-[(4"RS)-4"-ethoxy-4"-(sodium 1"'-O-beta-D-glucopyranuronate)butyl]d

51 benzodioxolane-5-carboxylic acid 3'-bromo-5'-ethoxy-4'-hydroxybenzylidene-hydrazide), an analog of co

52 in or doxorubicin with methyl 1-O-[(1'RS)-1'-ethoxy-4'-oxobutyl]-2,3,4-tri-O-acetyl-beta-D- glucopyra

53 These efforts led to compound ( R)-2-((2-ethoxy-4-(1-methylpiperidin-4-yl)phenyl)amino)-7-ethyl-5

54 thoxy-4-(trifluoromethyl)coumarin (7-MFC), 7-ethoxy-4-(trifluoromethyl)coumarin (7-EFC), 7-benzyloxy-

55 owed the highest catalytic efficiency with 7-ethoxy-4-(trifluoromethyl)coumarin (7-EFC), followed by

56 The 7-ethoxy-4-(trifluoromethyl)coumarin O-deethylation activi

57 the substrate benzphetamine, the K(m) for 7-ethoxy-4-(trifluoromethyl)coumarin, or the benzphetamine

58 Morlin (7-ethoxy-4-methyl chromen-2-one) was discovered in a scree

59 dation of the marker fluorogenic substrate 7-ethoxy-4-trifluoromethylcoumarin (7-EFC).

60 to rotate upward to give testosterone and 7-ethoxy-4-trifluoromethylcoumarin access to the heme, whi

61 sed on the H(2)O(2)-dependent oxidation of 7-ethoxy-4-trifluoromethylcoumarin, and identification of

62 S)-5-{(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy}-4-(4-fluorop henyl)octahydro-2H-isoindol-2-yl]cy

63 ed that one potent salicylaldehyde analog, 3-ethoxy-5,6-dibromosalicylaldehyde, is a non-competitive

64 imidine derivatives as well as 2-(4-benzyl-3-ethoxy-5-methyl-1H-pyrazol-1-yl)-5-methylpyridine, we de

65 e iterative process that, from 2-(4-benzyl-3-ethoxy-5-methyl-1H-pyrazol-1-yl)pyrimidine, led to 2-(4-

66 dyl compound STS-E412 (2-[2-(4-chlorophenoxy)ethoxy]-5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine),

67 nzodioxol-4-yl)-7-[2-(4-methylpiperazin-1-yl)ethoxy]-5-(tetrahy dro-2H-pyran-4-yloxy)quinazolin-4-ami

68 romodiphenyl ether (6,6'-diMeO-BDE194) and 6-ethoxy-6'-methoxy-2,2',3,3',4,4',5,5'-octabromodiphenyl

69 stradiol, 2-ethoxy-6-oximinoestradiol, and 2-ethoxy-6-methoximinoestradiol.

70 2',2'-trifluoroethoxy)-6-oximinoestradiol, 2-ethoxy-6-oximinoestradiol, and 2-ethoxy-6-methoximinoest

71 bin, the steroid derivative 17beta-acetoxy-2-ethoxy-6-oxo-B-homo-estra-1,3,5(10)-trien-3-ol, and cycl

72 the identification of 4-(2-(azetidin-2(S)-yl)ethoxy)-7-chloro-2-oxo-3-(3,4,5-trimethylphenyl)-1, 2-di

73 formation of 2-(2-(1H-benzo[d]imidazol-1-yl)ethoxy)acetaldehyde (12) and 2-(1H-benzo[d]imidazol-1-yl

74 es contain an N-terminal 2-(2-(2-aminoethoxy)ethoxy)acetic acid (PEG) moiety that makes them cell per

75 ptide, poly(N(epsilon)-2-[2-(2-methoxyethoxy)ethoxy]acetyl-lysine) (1), has been studied using optica

76 A(2A) receptor agonist 2-[2-(4-chlorophenyl)ethoxy]adenosine (MRE0094).

77 Reactions with ethoxy alkynes are performed at 120-130 degrees C, where

78 de metho-p-toluenesulfonate (CMCT), and beta-ethoxy-alpha-ketobutyraldehyde (kethoxal, KT) are widely

79 -benzoimidazole-5-carboxylic acid (2-hydroxy-ethoxy)-amide (AZD6244/ARRY142886), 2-(4-morpholinyl)-8-

80 ne 1 (diethyl (1-(tert-butyl(1-(pyridin-4-yl)ethoxy)amino)-2,2-dimethylpropyl)phosphonate) and its N(

81 in and inhibit its polymerization, and its 2-ethoxy analogue is even more potent.

82 Ethoxy and acetate are identified as two key reaction in

83 The presence of ethoxy and methoxy end groups indicates both methoxide a

84 The involvement of ethoxy and phosphinoyl radicals in the photoreaction has

85 The formation of three of them (methoxy, ethoxy and propoxy adducts) has not been reported yet.

86 The 5'-methoxy, 5'-ethoxy, and 5'-butoxy analogs of 2,5,6-trichloro-1-(beta

87 rone, imipramine and 3-beta-[2-(diethylamino)ethoxy]androst-5-en-17-one (U18666A) strongly inhibited

88 ht to reside in close proximity to the pro-S-ethoxy arm of the paraoxon substrate, was mutated to arg

89 Ethoxy aryl ethers, including ethoxybenzene, also underg

90 Pioglitazone (5-(4-(2-(5-ethyl-2-pyridyl)ethoxy)benzyl)-2,4-thiazolidinedione, 2) is a prototypic

91 d the propoxy group of 2c was preferred over ethoxy, butoxy, or pentoxy.

92 onyl)-1-(2-chloroethyl)-2-[[1-(4-nitrophenyl)ethoxy]carb onyl]hydrazine (KS119), requires enzymatic n

93 terification, [1,2]-H and [1,5]-methoxy- and ethoxy carbonyl shift, and finally aromatization to yiel

94 4'-(3-methyl-4-(((1(R)-(3-(11)C-methylphenyl)ethoxy)carbonyl)amino)isoxazol-5 -yl)-[1,1'-biphenyl]-4-

95 gral injection of the receptor inactivator N-ethoxy-carbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ; 50

96 UDP-galactosamine using [1-14C]acetate and N-ethoxy-carbonyl-2-ethoxy-1,2-dihydroquinoline.

97 xtracted higher levels of wood compounds and ethoxy-compounds were higher in the 68%-ethanol distilla

98 The diphenyl-substituted 3-ethoxy cyclobutanone rearranges itself by intramolecular

99 A cascade ring opening of 3-ethoxy cyclobutanones followed by a double cyclization s

100 ctivation of the two smallest carbocycles, 3-ethoxy cyclobutanones, and donor-acceptor cyclopropanes

101 Changing 11-methoxy for 11-ethoxy decreased the binding affinity slightly, and this

102 target-to-nontarget ratio than compounds 1 (ethoxy derivative) and 2 (propoxy derivative).

103 N-Ethyl-N-ethoxy-dithiocarbamato-N-(99m)Tc ((99m)Tc-N-NOET) is a n

104 port activity of MDR1 Pgp with ((67/68)Ga-[3-ethoxy-ENBDMPI])(+) may enable noninvasive SPECT/PET mon

105 thyl-3- amino-propyl)ethylenediamine) (Ga-[3-ethoxy-ENBDMPI])(+), as a candidate SPECT ((67)Ga) and g

106 (1R-1-benzo thiophen-5-yl-2[2-diethylamino)-ethoxy] ethanol hydrochloride (T-588) prevented long-ter

107 ist, 2-{2-[4-(3-phenoxybenzyl)piperazin-1-yl]ethoxy}ethanol (ZK 756326), for the CC chemokine recepto

108 ch as poly(2-(3,3'-bis(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)-[2,2'-bithiophen]-5-yl)thieno[3,2-b]thiop

109 omeric bis-N,N'-(2-(2-(2-(2-thioacetylethoxy)ethoxy)ethoxy)ethyl)perylenetetracar boxylic diimide.

110 with (E)-4-(2-(6-(2-(2-(2-(18)F-fluoroethoxy)ethoxy)ethoxy)pyridin-3-yl)vinyl)-N-methy l benzenamine

111 (E)-4-(2-(6-(2-(2-(2-(18)F-fluoroethoxy)ethoxy)ethoxy)pyridin-3-yl)vinyl)-N-methy l benzenamine

112 anediamine, 1,8-octanediamine, 2-[2-(2-amino-ethoxy)-ethoxy]-ethylamine, homospermidine, and homosper

113 [2-{2-([(18)F]fluoroethoxy)-ethoxy}-ethoxy] -ethoxy)-ethoxy}-ethoxy]-quinazoline-6-yl-acrylamide ([(1

114 -[2-{2-((18)F-fluoroethoxy)-ethoxy}-ethoxy]- ethoxy)-ethoxy}-ethoxy]-quinazoline-6-yl-acrylamide) ((1

115 [2-{2-(2-[2-{2-([(18)F]fluoroethoxy)-ethoxy}-ethoxy] -ethoxy)-ethoxy}-ethoxy]-quinazoline-6-yl-acryla

116 est compound, zinc (2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]acetate)(2), extends the lifetime of symme

117 -butyl-4-hydroxy-5-methylphenyl)propanoyloxy]ethoxy]ethoxy]ethyl-3-(3-tert-butyl-4-hydroxy-5-methylph

118 -[2-{2-(2-[2-{2-((18)F-fluoroethoxy)-ethoxy}-ethoxy]- ethoxy)-ethoxy}-ethoxy]-quinazoline-6-yl-acryla

119 o]-7-{2-[2-{2-(2-[2-{2-([(18)F]fluoroethoxy)-ethoxy}-ethoxy] -ethoxy)-ethoxy}-ethoxy]-quinazoline-6-y

120 no]-7-(2-[2-{2-(2-[2-{2-((18)F-fluoroethoxy)-ethoxy}-ethoxy]- ethoxy)-ethoxy}-ethoxy]-quinazoline-6-y

121 (18)F]fluoroethoxy)-ethoxy}-ethoxy] -ethoxy)-ethoxy}-ethoxy]-quinazoline-6-yl-acrylamide ([(18)F]F-PE

122 (18)F-fluoroethoxy)-ethoxy}-ethoxy]- ethoxy)-ethoxy}-ethoxy]-quinazoline-6-yl-acrylamide) ((18)F-PEG(

123 ement of N-[2-[2-[2-[(N-biotinylcaproylamino)ethoxy)ethoxyl]-4-[2-(trifluoromethyl)-3H-dia zirin-3-yl

124 lamide and hydrophilic 2-[2-(2-methoxyethoxy)ethoxy]ethyl acrylate.

125 these compounds (methyl 2-[1-(2-nitrophenyl)ethoxy]ethyl phosphate, 9) was studied in detail by a co

126 ne, 1,8-octanediamine, 2-[2-(2-amino-ethoxy)-ethoxy]-ethylamine, homospermidine, and homospermine cov

127 ylglycine-block-poly-N-2-(2-(2-methoxyethoxy)ethoxy)ethylglyci ne (pNeh-b-pNte) and poly-N-decylglyci

128 ylglycine-block-poly-N-2-(2-(2-methoxyethoxy)ethoxy)ethylglycine (pNdc-b-pNte) with 18 monomer units

129 ylglycine-block-poly-N-2-(2-(2-methoxyethoxy)ethoxy)ethylglycine (pNdc-b-pNte) with volume fraction o

130 ock copolymers, poly(N-2-(2-(2-methoxyethoxy)ethoxy)ethylglycine)-block-poly(N-(2-ethylhexyl)glyc ine

131 reactive reagent (18)F-(2-(2-(2-fluoroethoxy)ethoxy)ethylsulfonyl)ethane ((18)F-DEG-VS) was facilely

132 ons, with the PdCo(x) alloy surface favoring ethoxy formation, a critical precursor for further C-C b

133 Replacing a methoxy pendant with a fluoro-ethoxy group and introducing deuterium atoms suppressed

134 nteraction between the 4-substituent and the ethoxy group at the 3-position.

135 group at the 3-position, 2-(2(S)-azetidinyl)ethoxy group at the 4-position, and N-4-pyrimidinylcarbo

136 A chloro and ethoxy group at the meta- and para-positions, respective

137 Instead, the H transfer from the ethoxy group in the anion radical, followed by extrusion

138 The role of groups attached through an ethoxy group to the 4-position of the naphthalene and di

139 of the 29 NHOCs likely containing methoxy or ethoxy groups on a benzene or benzene-methanol backbone

140 the methoxy groups on DME with larger-sized ethoxy groups, the resulting 1,2-diethoxyethane (DEE) sh

141 000 via the intermediacy of node methoxy (or ethoxy) groups formed from methanol (or ethanol).

142 Methoxy (or ethoxy) groups on node vacancy sites are converted to a

143 ntial methylation of a methoxy group to form ethoxy, i-propoxy, s-butoxy, and t-butoxy groups on a p-

144 -2-(4-methylpiperazin+ ++- 1-yl)thiazol-4-yl]ethoxy inverted question markphenyl)propionic acid (24)

145 symmetric mixture of methyl, methoxy, ethyl, ethoxy, isopropoxy, phenyl, phenoxy, cyclohexyl, and cyc

146 umaranones via the corresponding O-silylated ethoxy ketals.

147 ropoxy versus the 2-(6-methylamino-2-pyridyl)ethoxy) led to improved activity toward alpha(v)beta(3).

148 with cyclic basic amine groups attached via ethoxy linkages at the C-8 position were the most active

149 2(S)-azetidinylmethoxy]pyridine (A-85380), 5-ethoxy-metanicotine (TC-2559), cytisine, and 3-Br-cytisi

150 on that proceeds through C-H addition of the ethoxy methyl group followed by beta-aryl oxide eliminat

151 ing up with 2-tetrahydropyranyloxy methyl or ethoxy methyl have been shown to follow the alternative

152 arib from the protected N-[2-(trimethylsilyl)ethoxy]methyl (SEM) arylboronate ester precursor in a 17

153 We study poly(3-{[2-(2-methoxyethoxy)ethoxy]methyl}thiophene-2,5-diyl) (P3MEEMT), a new polyt

154 dazole (8a) was condensed with [2-(benzyloxy)ethoxy]-methyl chloride (9) and [1,3-bis(benzyloxy)-2-pr

155 The purified ethoxy methylphosphonyl oximes formed during the reactiv

156 Reactivation of both ethoxy methylphosphonyl- and diethylphosphoryl-AChE by t

157 ryl oximes formed during reactivation of the ethoxy methylphosphonyl-AChE conjugate by LuH6 and TMB4

158 nyl oximes formed during the reactivation of ethoxy methylphosphonyl-AChE conjugate with LuH6 and TMB

159 hich the reduction of the DEC molecule to an ethoxy moiety plays a key role.

160 olyl-2H-pyrazol-3-yl)-3-[4-(2-morpholin-4-yl-ethoxy)n aphthalen-1-yl]urea (BIRB 796), an inhibitor of

161 Bis(N-ethoxy,N-ethyldithiocarbamato)nitrido technetium (V) ((9

162 99mTc-(N-ethoxy-N-ethyl-dithiocarbamato)nitrido (N-NOET) is a via

163 N-Ethoxy-N-ethyl-dithiocarbamato-nitrido-(99m)Tc ((99m)Tc-

164 -independent perfusion tracer such as (bis(N-ethoxy-N-ethyldithiocarbamato)nitrido (99m)Tc(V)) ((99m)

165 g adduct after quenching in methanol; for [1-ethoxy-(N-ethoxycarbonyl)formimidoyl](N'-methyl-N'-pheny

166 ed conditions stop at the (chlorocarbonyl)[1-ethoxy-(N-ethoxycarbonyl)formimidoyl]disulfane intermedi

167 The most potent antiviral compound was the p-ethoxy-o-fluorobenzoyl chloropyridyl ester (PSB-21110, 2

168 h a specific nucleophile reactive inhibitor, ethoxy oleoyl fluorophosphonate, identified S241 as the

169 In general, a 3-ethoxy or 3-isopropoxy substituent on the pyridine ring,

170 stion mark4-[2-(5-methyl-2-phenyloxazol-4-yl)ethoxy]phen yl inverted question mark ethylamino)benzoic

171 th oxygen ([6-hydroxy-3-[4-[2-(1-piperidinyl)ethoxy]phenoxy]-2-(4-hydroxyphenyl)]b enzo[b]thiophene h

172 zoxifene ([6-hydroxy-3-[4-[2-(1-piperidinyl)-ethoxy]phenoxy]-2-(4-methoxyphenyl)]be nzo[b]thiophene)

173 he reaction is catalytic for p-methoxy and p-ethoxy phenyl azides, while no azoarene is observed for

174 estion mark4-[2-(methylpyridin-2-ylamino+ ++)ethoxy ]phenyl inverted question markpropionic acid (18)

175 romobenzyloxy)-4-[4-(2-naphthalen-1-yl-2-oxo-ethoxy)phenyl]p iperidine) has been studied using steady

176 uestion mark4-[2-(benzoxazol-2-ylmethylamino)ethoxy]phenyl inverted question mark-(2S)-((2- benzoylph

177 uestion mark4-[2-(Benzoxazol-2-ylmethylamino)ethoxy]phenyl inverted question mark-(2S)-((2- benzoylph

178 -[2-(5-methyl-2-pyridin-4-yloxazol+ ++- 4-yl)ethoxy]phenyl inverted question markpropionic acid (16)

179 l)methane, vis., 4-[2-(6-amino-9H-purin-9-yl)ethoxy]phenyl-4-[bis(2,2'-bithienyl)methane] or Ade-BTM,

180 -[4-[2-(5-methyl-2-thiophen-2-yl-oxazol-4-yl)ethoxy]phenyl]- 2-phenoxypropionic acid (2) for the trea

181 iodotamoxifen [2a,(E)-1-[4-(N-dimethylamino)-ethoxy]phenyl]-1-(4-iodophenyl)-2-phenyl -1-butene] with

182 droxyphenyl)-4-methyl-2-[4-[2-(1-piperidinyl)ethoxy]phenyl]-2H- 1-benzopyran-7-ol (EM652), and the am

183 roxybenzo[b]thien-3-yl] [4-[2-(1-piperidinyl)ethoxy]phenyl]methanone hydrochloride (2), is representa

184 arboxy-2-{4-[2-(5-methyl-2-phenyloxazol-4-yl)ethoxy]phenyl}ethy lamino)benzoic acid methyl ester) ((1

185 4-chloro-3-{5-methyl-3-[4-(2-pyrrolidin-1-yl-ethoxy)phenylamino]benzo[1,2,4]triaz in-7-yl}phenol ( 5)

186 diastereomeric cavitands comprise a 2,5-bis(ethoxy)pillar[6]arene core with one of six phenylene rin

187 6-dioxocyclo-hexylidene)-3-[2-(2-aminoethoxy)ethoxy]-pro pan-1-ol, a heterobifunctional traceless lin

188 zol-3-yl)-2-(1-methyl-1H-1,2,4-triazol-5-ylm ethoxy)pyrazolo[1,5-d][1,2,4]triazine (13) has been iden

189 uoroethoxy)-ethoxy}-ethoxy] -ethoxy)-ethoxy}-ethoxy]-quinazoline-6-yl-acrylamide ([(18)F]F-PEG6-IPQA)

190 uoroethoxy)-ethoxy}-ethoxy]- ethoxy)-ethoxy}-ethoxy]-quinazoline-6-yl-acrylamide) ((18)F-PEG(6)-IPQA)

191 iple, from a 1,2-hydrogen shift and/or a 1,2-ethoxy shift in the carbene, a deuterium labeling study

192 th a Si(100)-hydrogen terminated wafer, a Si-ethoxy (Si-OC2H5) surface intermediate forms due to DEC

193 well as FR E and Z isomers with methoxy and ethoxy side chains.

194 ligomers of the same length with and without ethoxy solubilizing groups reveals that both solubilized

195 derivative possessing two 2-(morpholin-4-yl)ethoxy substituents in nonperipheral positions.

196 Ethoxy substituents on the phenyl rings improve the solu

197 s (4-phenyl and 4-cyano with N-methoxy and N-ethoxy substituents) led to a consistent set of kinetic

198 Three 2-(morpholin-4-yl)ethoxy substituted phthalocyanines were synthesized and

199 hods are compared for the synthesis of the P-ethoxy-substituted 5-membered benzophostam.

200 surfaces indicates the equatorial form of 2-ethoxy tetrahydropyran is more sensitive to solvent than

201 uatorial anomers of the model carbohydrate 2-ethoxy tetrahydropyran to evaluate the level of theory r

202 ion of benzphetamine and O-deethylation of 7-ethoxy-trifluoromethylcoumarin as the WT did, whereas th

203 difference in effects of methyl, methoxy, or ethoxy), two side chains bearing 1-naphthyl groups, and

204 TX-series with a large number (n = 30-70) of ethoxy units, which were initially found to exhibit extr

205 acetaldehyde is due to the deprotonation of ethoxy, which can be further oxidized into acetate.