ライフサイエンスコーパス: isopropyl

1 Unoprostone isopropyl (1.25 muM) had no effect on PG receptors, and

2 2-Isopropyl-1,3,5-trimethylbenzene is used as a comparable

3 of the chlorotitanium enolate of N-acetyl 4-isopropyl-1,3-thiazolidine-2-thione to five-membered, N-

4 um enolates from protected N-hydroxyacetyl-4-isopropyl-1,3-thiazolidine-2-thiones to dimethyl and dib

5 ckel-catalyzed alkylation of chiral N-acyl-4-isopropyl-1,3-thiazolidine-2-thiones using a commerciall

6 With a less hindered R2 group, lithium (S)-N-isopropyl-1-((triisopropylsilyl)oxy)propan-2-amide forms

7 g of the lithiated amides derived from (S)-N-isopropyl-1-((triisopropylsilyl)oxy)propan-2-amine, (R)-

8 2-fluoro-4-methanesulfonyl-phenyl)-{6-[4-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-pipe ridin-1-yl]-5-nitr

9 ydroxytetrahydro-2H-pyran-2-carboxamido)-24-isopropyl-18-methyl-17,20,23,26,29-pe ntaoxo-4,7,10,13-t

10 N-Isopropyl-1H-indole-2-carboxamide (3) displayed alloster

11 A series of 3-substituted-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amines have been

12 Our best prodrug 6 (isopropyl 2-(6-acetamido-2-(adamantane-1-carboxamido)hex

13 (N4Py(2Ar3))(CH3CN)](ClO4)2 (3) reacted with isopropyl 2-iodoxybenzoate to give the C-F hydroxylated

14 alene; 1,2,4-trimethylbenzene; alpha-pinene; isopropyl 2-methylbutanoate; cymene; 2,6-dimethyl-1,6-oc

15 ecular probes for this study, derivatives of isopropyl 2-O-benzyl-4,6-O-benzylidene-alpha-d-idopyrano

16 thesis of a highly toxic bicyclophosphate, 4-isopropyl-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane 1-o

17 ted to target gene enhancers in both ligand [isopropyl-2-(1,3-dithietane-2-ylidene)-2-[N-(4-methylthi

18 roots, like (3S,3aS,7aR)-wine lactone and 3-isopropyl-2-methoxypyrazine.

19 hydroxy-alpha-(or beta-)thujone, 5-hydroxy-5-isopropyl-2-methyl-2-cyclohexen-1-one, 4,10-dehydrothujo

20 ition of chiral 2,2'-(2,6-pyridinediyl)bis(4-isopropyl-2-oxazoline) (iPr-Pybox) to a self-assembled C

21 oactivity-guided isolation of 3-(octahydro-9-isopropyl-2H-benzo[h]chromen-4-yl)-2-methylpropyl benzoa

22 CAAC = (5 R,6 S)-2-(2,6-diisopropylphenyl)-6-isopropyl-3,3,9-trimethyl-2-azaspiro[4.5]decan-2-ylidene

23 lorophenyl)-1,1-dimethylurea and 5-dibromo-6-isopropyl-3-methyl-1,4-benzoquinone resulted in a distur

24 ns by reducing the PQ pool using 5-dibromo-6-isopropyl-3-methyl-1,4-benzoquinone.

25 2S,2'S)-1,1'-(pentane-1,5-diylbis(oxy))bis(N-isopropyl-3-methylbutan-2-amine) 10 is a monomer.

26 2S,2'S)-1,1'-(heptane-1,7-diylbis(oxy))bis(N-isopropyl-3-methylbutan-2-amine) 9 are dimers, whereas d

27 hose resulting from hydrogen substitution by isopropyl (3d), isobutyl (3f), cyclopentyl (3g), and pyr

28 PE1 inhibitor, N-(3-(benzo[d]thiazol-2-yl)-6-isopropyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridin-2- yl)a

29 ents among the four "Delta2-thujenes", two 1-isopropyl-4-methylbicyclo[3.1.0]hex-2-enes [(-)-cis-1 an

30 Use of 2-isopropyl-4-nitrophenylsulfonyl chloride is critical to

31 f electron-rich N-alkyl-substituted imine, N-isopropyl-(4-methyl)benzilidene amine (9), was accompani

32 Zr, Hf; Ox(R) = 4,4-dimethyl-2-oxazoline, 4S-isopropyl-5,5-dimethyl-2-oxazoline, 4S-tert-butyl-2-oxaz

33 cation of (3 R,5 R)-7-[2-(4-fluoro-phenyl)-4-isopropyl-5-(4-methyl-benzylcarbamoyl)-2 H-pyrazol-3-yl]

34 use of a photoreactive analog of propofol, 2-isopropyl-5-[3-(trifluoromethyl)-3H-diazirin-3-yl]phenol

35 we use a photoreactive analog of propofol (2-isopropyl-5-[3-(trifluoromethyl)-3H-diazirin-3-yl]phenol

36 Thymol (2-isopropyl-5-methylphenol) is the main monoterpene phenol

37 (1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5 H)-one (AMG 221).

38 Optically pure trans-3-isopropyl-5-vinylcyclopentene (5) is the final, strongly

39 The lead prodrug, isopropyl 6-diazo-5-oxo-2-(((phenyl(pivaloyloxy)methoxy)

40 +)-trans-2] and two isomers, exo- and endo-3-isopropyl-6-methylbicyclo[3.1.0]hex-2-ene [(+)-exo-3 and

41 on of the 5-sulfanyl group, we synthesized 3-isopropyl-7-[4-(2-pyridyl)benzyl]amino-1(2) H-pyrazolo[4

42 Significantly, 7alpha-isopropyl-7-deoxypodophyllotoxin (20), without any hydro

43 re identified, such as 3-(2-hydroxybenzyl)-5-isopropyl-8-methyl-2H-chromen-2-one (12, PSB-SB-489, IC5

44 Thus, 2-amino-6-cyclohexylmethoxy-8-isopropyl-9H-purine adopts a "reverse" binding mode wher

45 thyl isobutyrate, ethyl 2-methylbutyrate and isopropyl acetate were also significantly higher, while

46 ethyl 2-methylbutyrate), 3-methyl-1-butanol, isopropyl acetate, and finally the two sulfides dimethyl

47 yl acrylamide) (PNIPAM) and in its monomer N-isopropyl acrylamide (NIPAM) in solution across the LCST

48 udy, we report a lightly cross-linked (2%) N-isopropyl acrylamide (NIPAm) synthetic polymer NP (50-65

49 oits the thermosensitive characteristic of N-isopropyl acrylamide (NIPAm) to transition phases when p

50 N-Isopropyl acrylamide (NIPAM), N,N-dimethyl acrylamide (D

51 igh density terminally functionalized poly(N-isopropyl acrylamide) 'brush' layer is grown by surface

52 Poly(N-isopropyl acrylamide) (PNIPAAm) is a well-known 'smart'

53 tudy molecular changes in the polymer poly(N-isopropyl acrylamide) (PNIPAM) and in its monomer N-isop

54 n hybrid gels of thermally responsive poly(N-isopropyl acrylamide) copolymer networks containing iron

55 cs of a cancer drug (prodigiosin) frompoly-n-isopropyl-acrylamide (P(NIPA))-based gels.

56 3-(3-Cyclopentyloxy-4-methoxy-benzyl)-8-isopropyl-adenine V11294 (1) has been identified as a le

57 rs synthesized from N-isopropyl valinol or N-isopropyl alaninol were lithiated with n-butyllithium in

58 , but only 2 of the 4 studies found that 70% isopropyl alcohol (e.g., alcohol wipes or soaks) eradica

59 tants of the hydride-transfer reactions from isopropyl alcohol (i-PrOH) to an NAD(+) model, 9-phenylx

60 obs)) of the hydride-transfer reactions from isopropyl alcohol (i-PrOH) to two NAD(+) analogues, 9-ph

61 soamyl or butyl nitrite in mixed solvents of isopropyl alcohol (IPA) and water at 25+/-1 degrees C.

62 thylene blue (MB) as the probe compound, and isopropyl alcohol (IPA) as the standard.

63 rasonic assisted liquid phase exfoliation in isopropyl alcohol (IPA) using polyvinyl pyrrolidone (PVP

64 Ethanol (EtOH), isopropyl alcohol (IPA), and propylene glycol (PG) incre

65 The isopropyl alcohol adsorption simulations indicate that D

66 Continuous exposure of either TTIP or isopropyl alcohol after the first cycle shows unlimited

67 duces Cr(VI) via a termolecular complex with isopropyl alcohol and Cr(VI), but its efficacy in soils

68 ted, or aliphatic aldehydes 2a-i mediated by isopropyl alcohol and employing a cyclometalated iridium

69 The addition of isopropyl alcohol and tartaric acid to soils enhances th

70 Using isopropyl alcohol and water mixtures, detection limits a

71 nic framework upon adsorption of benzene and isopropyl alcohol are gained from computer simulations.

72 mol%) which can be employed, and the use of isopropyl alcohol as both a solvent and formal reductant

73 cluded that both sodium hypochlorite and 70% isopropyl alcohol eliminated HSV.

74 onitoring system (DAAMS) sampling tubes with isopropyl alcohol extraction and isotope dilution using

75 alcohol plus tincture of iodine rather than isopropyl alcohol plus povidone-iodine.

76 were observed when skin was disinfected with isopropyl alcohol plus tincture of iodine rather than is

77 s are shown to yield [RuCl(H)(H2)(PCy3)2] in isopropyl alcohol solutions, while 3-phenylindenylidene

78 reaction of three of the aryl radicals with isopropyl alcohol were found to correlate linearly with

79 In this procedure, 200 microL aliquots of isopropyl alcohol were repeatedly dropped onto the film

80 efficient H atom donors (methanol, ethanol, isopropyl alcohol) favor products arising from a net red

81 tment (no soil +12 mM tartaric acid + 0.29 M isopropyl alcohol) reduced 0.37 mM Cr(VI) (19%) in 99 h.

82 tendency of an alcohol (methanol > ethanol > isopropyl alcohol) to move toward the silica surface, th

83 ms can be caused by sodium hypochlorite, 70% isopropyl alcohol, 3% hydrogen peroxide, ethyl alcohol,

84 In addition, acetate, isopropyl alcohol, and concentrations of acetone that oc

85 l, 2,2,2-trifluoroethanol, n-propyl alcohol, isopropyl alcohol, and tert-butyl alcohol at 25, 35, and

86 Ethanol, 70% isopropyl alcohol, dilute bleach, and mechanical cleanin

87 When ODI CL reagents (H(2)O(2) in isopropyl alcohol, ODI in ethyl acetate) were injected i

88 ater, dimethyl sulfoxide, methanol, ethanol, isopropyl alcohol, tert-butyl alcohol, tetrahydrofuran,

89 ciencies for two substrates, cyclohexane and isopropyl alcohol, were measured for 23 structurally dif

90 lay a role in the dehydration of off-gassing isopropyl alcohol.

91 hol by switching from methanol to ethanol to isopropyl alcohol.

92 ed solvent and subsequent precipitation with isopropyl alcohol.

93 Diamidine 1 and di( N-isopropyl)amidine 45, administered at 4 x 1 mg/kg, exhib

94 nt currents were insensitive to 10 muM ethyl-isopropyl amiloride or 100 muM 4,4'- diisothiocyanatosti

95 and three analogues - benzamil, 5-(N-ethyl-N-isopropyl) amiloride (EIPA) and hexamethyleneamiloride (

96 reatment with the NHE inhibitor 5-(N-ethyl-N-isopropyl) amiloride (EIPA) resulted in a robust inhibit

97 her macropinocytosis inhibitor, 5-(N-ethyl-N-isopropyl) amiloride (EIPA).

98 RVI were inhibited by 10microM 5-(N-ethyl-N-isopropyl) amiloride or 10microM 5-(N-methyl-N-isobutyl)

99 g Na/H exchange (luminal 10 mum 5-(N-ethyl-N-isopropyl) amiloride or 25 mum HOE694) slows restitution

100 olamide (ACTZ, a CA inhibitor), 5-(N-Ethyl-N-isopropyl)amiloride (EIPA) (Na(+)/H(+) exchange blocker)

101 5-(N-Ethyl-N-isopropyl)amiloride (EIPA) and soluble THY-1 blocked HCM

102 oride and the related compound 5'-(N-ethyl-N-isopropyl)amiloride (EIPA) but not to HOE694.

103 h a macropinocytosis inhibitor, 5-(N-ethyl-N-isopropyl)amiloride, or Rab5/Rab4 depletion with small i

104 Furthermore, 50 mum of 5-(N-ethyl-N-isopropyl)-amiloride (EIPA), a specific inhibitor for Na

105 r by its more potent derivative 5-(N-ethyl-N-isopropyl)-amiloride hydrochloride.

106 1 h) and NHE activity was measured as ethyl-isopropyl-amiloride (EIPA)-sensitive 22Na uptake.

107 1), and inhibition of NHE1 with 5'-N-ethyl-N-isopropyl-amiloride blocks H/R induced apoptosis, indica

108 with cofactors provided by the host cell and isopropyl amine added as the amine donor.

109 4-(Benzothiazol-6-ylamino)-6-(benzyl-isopropyl-amino)-[1,3,5]triazin-2-ol (14d) exhibited low

110 -p-phenylene diamine (PD), and its ethyl and isopropyl analogues are discussed.

111 compounds, especially 26 and 22, bearing a 3-isopropyl and 3-iodine group, respectively, exhibited hi

112 The parent polyether and its isopropyl and ethyl esters were all shown to be highly e

113 Unoprostone isopropyl and M1 activated sustained iberiotoxin (IbTX)-

114 Prostones, unoprostone isopropyl and M1, are potent AL-8810-insensitive, stereo

115 g at the iso and anteiso positions, terminal isopropyl and sec-butyl, respectively, do not alter CACI

116 lexible Lewis pairs with P(O)R2 (R = phenyl, isopropyl) and BMes2 (Mes = 2,4,6-trimethylphenyl) funct

117 ir SN2 reactions of methyl, ethyl, n-propyl, isopropyl, and allyl halides with LiX.E, LiX.2E, and LiX

118 kyl-N,N-dimethylbenzylamines (alkyl = ethyl, isopropyl, and benzyl) to the phthalimide N-oxyl radical

119 effects for the reactions of methyl, ethyl, isopropyl, and tert-butyl iodide with cyanide ion in the

120 tions of BrO(-) with RCl (R = methyl, ethyl, isopropyl, and tert-butyl) were measured using a tandem

121 eactions of fluorene-4-carboxylic acid and 4-isopropyl- and 4-ethylbenzoic acid also gave high rates

122 a C-terminal methyl ester along with ethyl-, isopropyl-, and benzyl-ester analogs in good yield.

123 ing an alkyldiazirinyl moiety for one of the isopropyl arms but in the meta position.

124 established transfer dehydrogenation from an isopropyl aryl substituent to either the enyne or diyne

125 [Ncy(R), where R is 2-naphthyl, methyl, and isopropyl] at positions 1, 4, 7, and 10 were synthesized

126 rganocatalytic reaction of aldehydes with di-isopropyl azodicarboxylate leads to an intermediate carb

127 on fork helicases were fully tolerant of the isopropyl backbone modification, irrespective of strand.

128 R groups, with isopropylamine (IPA)/NO (R = isopropyl) being the smallest examined to date.

129 tion of cationic (alpha-diimine)Ni-ethyl and isopropyl beta-agostic complexes, which are key intermed

130 d anti-repressors that respond to the ligand isopropyl beta-d-1-thiogalactopyranoside (anti-LacI).

131 es not require optimization and does not use isopropyl beta-d-1-thiogalactopyranoside (IPTG) inductio

132 ble by the small non-pharmacologic molecule, Isopropyl beta-D-1-thiogalactopyranoside (IPTG) that has

133 Using a library of isopropyl beta-D-1-thiogalactopyranoside (IPTG)-inducibl

134 nduction to wild-type LacI with its inducer, isopropyl beta-D-1-thiogalactopyranoside (IPTG).

135 nd its interplay with the lac operon inducer isopropyl beta-D-1-thiogalactopyranoside (IPTG, which in

136 ation constant for the competitive inhibitor isopropyl beta-d-1-thiogalactopyranoside is extracted us

137 t culture times following the induction with isopropyl beta-d-1-thiogalactopyranoside, from which the

138 n Luria-Bertani (LB) broth supplemented with isopropyl beta-d-thiogalactopyranoside (IPTG), we were a

139 rpoS from flacp was dependent on the inducer isopropyl beta-D-thiogalactopyranoside and was unaffecte

140 nts (NDelta150 and NDelta150/CDelta24) using isopropyl beta-D-thiogalactopyranoside-free autoinductio

141 upon induction of the lac operon genes using isopropyl beta-D-thiogalactopyranoside.

142 ded, fully functional, and binds the inducer isopropyl beta-d-thiogalactoside with the same affinity

143 In contrast, reagents bearing, for example, isopropyl, beta-styryl, and anisyl moieties undergo effi

144 ch as N-acyl-L-homoserine lactones (AHLs) or isopropyl-beta-D-thio-galactopyranoside (IPTG) can be ut

145 The addition of isopropyl-beta-D-thio-galactoside (IPTG) destabilizes bu

146 d activity in vivo when overproduced from an isopropyl-beta-D-thiogalactopyranoside (IPTG)-inducible

147 synthesis of KinA is under the control of an isopropyl-beta-d-thiogalactopyranoside (IPTG)-inducible

148 indicated that clone lambda-A8 expressed an isopropyl-beta-d-thiogalactopyranoside (IPTG)-inducible

149 Inducing pilT expression with isopropyl-beta-D-thiogalactopyranoside partially rescues

150 Growth of the mutant in the absence of isopropyl-beta-d-thiogalactopyranoside resulted in cell

151 up to 5 mM of phenol and tyrosol using IPTG (isopropyl-beta-D-thiogalactopyranoside) as inducer.

152 inant virus in which F18 expression is IPTG (isopropyl-beta-d-thiogalactopyranoside) dependent, we de

153 free-citrate transport was observed in IPTG (isopropyl-beta-d-thiogalactopyranoside)-induced or -unin

154 and analyzed their activities using an IPTG (isopropyl-beta-d-thiogalactopyranoside)-inducible artifi

155 onate pathway genes is regulated by an IPTG (isopropyl-beta-D-thiogalactopyranoside)-inducible promot

156 An IPTG (isopropyl-beta-d-thiogalactopyranoside)-inducible rpsO t

157 R in B. burgdorferi, we constructed an IPTG (isopropyl-beta-d-thiogalactopyranoside)-regulated bosR s

158 which A21L gene expression was regulated by isopropyl-beta-d-thiogalactopyranoside, was constructed.

159 In this strain, an isopropyl-beta-D-thiogalactopyranoside-inducible copy of

160 less, overexpression of RelA protein from an isopropyl-beta-d-thiogalactopyranoside-inducible promote

161 infectious virus formation were dependent on isopropyl-beta-D-thiogalactopyranoside.

162 hen A6 expression was induced by the inducer isopropyl-beta-D-thiogalactoside (IPTG), iA6 replicated

163 usion of sucrose and betaine, in addition to isopropyl-beta-d-thiogalactoside (IPTG), to the growth m

164 rioxa-1-phosphabicyclo[2.2.2]octane 1-oxide (Isopropyl Bicyclophosphate or IPBCP) were discovered usi

165 on fungicides (ametoctradin, benthiavalicarb-isopropyl, boscalid, cyazofamid, dimethomorph, fenhexami

166 the internal rotation of benzene around the isopropyl C-H bond in sevoflurane, producing detectable

167 te; (ii) use of a new crystalline and stable isopropyl calcium sulfinate reagent ensuring robust prep

168 s with iodomethane, benzophenone and N,N'-di-isopropyl carbodiimide and by density functional theory.

169 he OH moiety and the radical centered on the isopropyl carbon in 2b and the bulkiness of the isopropy

170 bon of the GeOC moiety into a methyl-aryl or isopropyl carbon to form six-membered ring products.

171 This transformation is enabled by isopropyl carbonate anhydrides, which serve as both an a

172 -) with methyl chloride, ethyl chloride, and isopropyl chloride were found to occur by an additional

173 aminopimelic acid (after derivatization with isopropyl chloroformate), and the mycolic acids by liqui

174 urvata catalyzes the C-C bond cleavage of an isopropyl-CoA side chain from the D-ring of the steroid

175 '-R-carbamoylmethyl)amine (H(5)2R), where R=isopropyl, cyclopentyl, and (S)-(-)-alpha-methylbenzyl.

176 Deuterating the individual leucine residues (isopropyl-d(7)) permits the use of solid-state deuterium

177 Media composition and isopropyl-d-thiogalactosidase induction were optimized t

178 The 4-isopropyl dichloroacetic acid ester 3b reacts with N3- t

179 cemic isopropanesulfinamide from inexpensive isopropyl disulfide and recycling of the isopropanesulfi

180 ] (dtc: di-butyldithiocarbamate (1); dtp: di-isopropyl dithiophosphate (2)) were synthesized from the

181 inhibition of their enzymatic hydrolysis by isopropyl dodecylfluorophosphonate (IDFP).

182 les and substrates, the pan-lipase inhibitor isopropyl dodecylfluorophosphonate was employed for comp

183 eries of 9-dihydro-9-acetamido-N-desmethyl-N-isopropyl erythromycin A analogues and related derivativ

184 coupling of phosphorochloridate of L-alanine isopropyl ester (13) with FMCA gave its phosphoramidate

185 The 4-isopropyl ester 2b predominantly undergoes ordinary acid

186 ignments are inconsistent with an N-terminal isopropyl ester and point instead to a 3-methylbutanoyl

187 ponding carboxylic acid by reaction with the isopropyl ester of methionine (MIPE), mediated by carbod

188 4) receptor agonist 3,7-dithia PGE(1) and an isopropyl ester prodrug thereof reduced IOP in monkeys.

189 A single dose of 3,7-dithia PGE(1) isopropyl ester, at a 0.01% or 0.1% dose, decreased IOP

190 e demonstrate that arginine, as its N-acetyl isopropyl ester, is amenable to GC analysis using a 15 m

191 ahydrocyclopenta[b]indol-2-yl)car bamic acid isopropyl ester, LY2452473, is a promising treatment of

192 dine ring, while the other is attached to an isopropyl ester.

193 The most stable compound (5c, methyl-POM-DON-isopropyl-ester) was evaluated in monkeys, where it achi

194 Benzyl, methyl, ethyl, and isopropyl esters are essentially unreactive under these

195 g assay demonstrate that while the ethyl and isopropyl esters manifest near-wild-type activity, the b

196 polyether analogue, along with its ethyl and isopropyl esters.

197 of spiroindolenine isomers were washed with isopropyl ether after flash chromatography, the major is

198 ine substituents (R = tert-butyl rather than isopropyl) favor chelation.

199 e isobars in a mixture, alfentanil and ortho-isopropyl furanyl fentanyl, is demonstrated without leng

200 hand to specifically grab with R842, and its isopropyl group as legs to stand on I846 and L843.

201 The orientation of the isopropyl group at the liquid/vapor interface in 2-propa

202 Selective, individual deuteration of the isopropyl group in each leucine residue was used to prob

203 .39) that was predicted to interact with the isopropyl group in the N1 position of the benzodiazepine

204 In contrast, isopropyl group inversion during formylation of menthone

205 facial selectivity, with attack trans to the isopropyl group leading to the [4 + 2] product and cis a

206 ray diffraction study of 6b reveals that the isopropyl group of the menthone ketal influences the pos

207 exo-norbornylamine at the 2-position and an isopropyl group on the 5-position are potent 11beta-HSD1

208 propyl carbon in 2b and the bulkiness of the isopropyl group prevent the necessary rotation to form E

209 These metabolites contain an isopropyl group proposed to be formed using CysS, a coba

210 anges in the molecular susceptibility of the isopropyl group stretches were derived in the laboratory

211 The endo-isopropyl group was installed by selective hydrogenation

212 ids loss of configurational integrity at the isopropyl group, giving hydroxymethylenementhone 12.

213 m abstraction (HAA) from an imido aryl ortho isopropyl group, or from 1,4-cyclohexadiene, respectivel

214 cle (4) through dehydrogenation of a pendant isopropyl group.

215 he herbicides is largely due to the ethyl or isopropyl group.

216 ctivation of one methyl group of each of the isopropyl groups at the 2- and 6-positions.

217 ylations of a methyl group to form ethyl and isopropyl groups but remarkably also sec-butyl and t-but

218 The ligands with isopropyl groups H(4)1iPr and H(5)2iPr were combined wit

219 ur by displacement, but preferential loss of isopropyl groups in the phenylketene reaction with diiso

220 o the direct, regioselective introduction of isopropyl groups into complex, biologically active molec

221 re seen between the dichloro complex 2b with isopropyl groups on phosphorus, which appeared to exist

222 Fs can be improved by periodic decoration of isopropyl groups on their backbones.

223 line ligands that enable desymmetrization of isopropyl groups via palladium insertion into the C(sp(3

224 TPyzPzs with isopropyl groups were found to be the best derivatives i

225 Trans-unoprostone isopropyl had no effects.

226 en phosphines with small cyclohexyl- (Cy) or isopropyl- ((i)Pr) groups and the tris-silylated cluster

227 ethylene as a byproduct ([(i)Pr2Im] = 1,3-di(isopropyl)imidazole-2-ylidene).

228 ons with either imidazole nitrogen, 1e, a di(isopropyl)imidazolyl analogue of 1b was made along with

229 cation of the nerve agent metabolites ethyl, isopropyl, isobutyl, cyclohexyl, and pinacolyl methylpho

230 Effects of cis-unoprostone isopropyl, its primary metabolite M1, trans-unoprostone

231 Studies of the pivalaldehyde-methyl isopropyl ketone rearrangement and the benzopinacol to p

232 ketones with a propargyl borolane and the N-isopropyl-l-proline ligand is presented.

233 provided efficient access to the related N-1 isopropyl lactam series.

234 its primary metabolite M1, trans-unoprostone isopropyl, latanoprost free acid, and fluprostenol were

235 entified as palmitic acid (a fatty acid) and isopropyl laurate (a fatty acid ester), respectively.

236 lic glycopeptides, iso-butylmercaptoquinine, isopropyl macrocyclic oligosaccharides, and pai-electron

237 id and reliable method for quantifying DMMP, isopropyl methoxypyrazine (IPMP), secbutyl methoxypyrazi

238 limination followed by cyclometalation of an isopropyl methyl group, demonstrating an overall transfe

239 G was used to probe the reorientation of the isopropyl methyl groups of l-leucine at the air-water in

240 porous/impermeable surfaces were 60-103% for isopropyl methylphosphonate (IMPA), GB degradate; 61-91%

241 acid (PMPA; hydrolysis product of soman) and isopropyl methylphosphonic acid (IMPA; hydrolysis produc

242 However, the desymmetrization of ubiquitous isopropyl moieties by organometallic catalysts has remai

243 s a key interaction between Glu202 and the O-isopropyl moiety of sarin.

244 the formation of hydrogen bonds between the isopropyl molecules and the framework.

245 xternal nonpolar solvents, n-heptane (n-Hp), isopropyl myristate (IPM), and methyl laurate (ML) were

246 Nanoemulsion formulations composed of isopropyl myristate and Tween 80 encapsulating a fluores

247 ations, i.e., middle-chain triglycerides and isopropyl myristate.

248 Palladium-catalyzed oxidation of isopropyl N-acetyl-alpha-d-glucosamine (GlcNAc) is used

249 he equilibrium binding of three isocyanides, isopropyl, n-butyl, and benzyl, to the two major human H

250 ve novel hexameric peptoids decorated with N-isopropyl, N-isobutyl, and N-benzyl substituents.

251 indolinones has been presented from 2-halo-N-isopropyl-N-alkylbenzamide substrates and KO(t)Bu by the

252 o acids were converted to NACME and N-acetyl-isopropyl (NAIP) esters; the latter established derivati

253 2,4,6-cycloheptatrien-1-one, 2,7-dihydroxy-4-isopropyl (NSC 18806) IC50 = 4.8 +/- 2.5 microM] exhibit

254 al amide base complex consisting of an (S)-N-isopropyl-O-triisopropylsilyl valinol ligand and lithium

255 l group of N-methylaniline is replaced by an isopropyl or a phenyl group, trisolvated monomers are fo

256 tution patterns (including hydrogen, methyl, isopropyl or tert-butyl groups) were used for the synthe

257 he quinone derivative 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone (DBMIB), a known inhibitor of t

258 ds the quinone analog 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone (DBMIB), and the oxidized form

259 of the quinone analog 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone (DBMIB).

260 tosynthetic inhibitor 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone but this induction requires the

261 the herbicide DBMIB (2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone), a well-known inhibitor of pho

262 esis was sensitive to 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone, a cytochrome b6f complex inhib

263 unctional groups, including carboxyl, amine, isopropyl, phenethyl, and tert-butylphenethyl groups, an

264 HB(trip)(2) (pin=pinacolato, trip=2,4,6-tri(isopropyl)phenyl) for 15 min is sufficient for efficient

265 ified the phenylurea BX430 (1-(2,6-dibromo-4-isopropyl-phenyl)-3-(3-pyridyl)urea, molecular weight =

266 opropyl) phosphate (TDCIPP), tris(1-chloro-2-isopropyl) phosphate (TCIPP), triphenyl phosphate (TPHP)

267 propyl) phosphate (BDCIPP)-tris(1,3-dichloro-isopropyl) phosphate (TDCIPP) and bis(2-chloroethyl) pho

268 Tris(1,3-dichloro-2-isopropyl) phosphate (TDCIPP) concentrations were higher

269 yl) phosphate (TCPP) and tris(1,3-dichloro-2-isopropyl) phosphate (TDCP)), four alkylated OPs (tri-n-

270 e flame retardants (FRs), tris (1,3-dichloro-isopropyl) phosphate (TDCPP) and Firemaster((R)) 550 (FM

271 cleanest reduction was observed with the tri-isopropyl phosphine cluster, to afford neutral iPr-[H12]

272 e selected member of the new series, 4-[4-(1-isopropyl-piperidin-4-yloxy)-benzyl]-morpholine (13g), w

273 ylphosphino)ethane fragment (alkyl = methyl, isopropyl) proceeds via initial exothermic formation of

274 here L: is:C[N(2,6-Pri2-C6H3)CH]2 and Pri is isopropyl} produces L:(Cl)Si-Si(Cl):L, a carbene-stabili

275 rked duplex DNA substrate harboring a single isopropyl PTE specifically positioned in the helicase-tr

276 possesses beta-C-H bonds (e.g., R = ethyl or isopropyl), results in formation of (PCP)Ir(H)(OAr), (PC

277 The tin(II) isopropyl-(S)-lactate complex, ((Me)BDI(DIPP))SnOCH(Me)C

278 treatment of ((Me)BDI(DIPP))Sn(NMe(2)) with isopropyl-(S)-lactate.

279 t specificity (kcat/Km) for steroids with an isopropyl side chain at C17, such as 3-oxo-23,24-bisnorc

280 dration of hydrophilic amide and hydrophobic isopropyl side groups, as well as molecular interactions

281 The most potent inhibitors contained a N(5)-isopropyl substituent on the C-ring.

282 C(4)-gem-diphenyl group adjacent to the C(5)-isopropyl substituent.

283 l icosahedron of pseudo-Ih symmetry (without isopropyl substituents) enables a structural/bonding com

284 l iron iminyl from aryl azides bearing ortho isopropyl substituents, ((tBu)L)FeCl((*)NC6H3-2,6-(i)Pr2

285 e bending of the linkers and the barrier for isopropyl-substituted derivative 10 was experimentally e

286 For the isopropyl-substituted ligand, [SiP(3)(iPr)], it has prov

287 hloronitriles, RCH(CN)Cl (R = methyl, ethyl, isopropyl, tert-butyl) were investigated both experiment

288 opropyl, tert-butyl), N-alkylazetidines (R = isopropyl, tert-butyl), and N-methylpyrrolidine.

289 observed for N-alkylaziridines (R = methyl, isopropyl, tert-butyl), N-alkylazetidines (R = isopropyl

290 3BH3, R2NHBH3, and RNH2BH3 where R = methyl, isopropyl, tert-butyl, and cyclohexyl) and rhodium catal

291 uence of carbon-based groups (methyl, ethyl, isopropyl, tert-butyl, phenyl, and 3,3,3-trifluoropropyl

292 SE(R*), along the simple series methyl/ethyl/isopropyl/tert-butyl are known to vary in spread and eve

293 groups (Phe-1 and Phe-2) and removal of the isopropyl-thiazole (IPT) moiety affect affinity, inhibit

294 ions are in good agreement with the data for isopropyl thiogalactoside (IPTG), but somewhat discrepan

295 agent to induce protein expression, such as isopropyl thiogalactoside.

296 ahedra with three nonsilyl substituents, tri-isopropyl tin in this case.

297 ladium cluster core of [Ge18Pd3] and six tri-isopropyl tin substituents.

298 ch to several sesterterpenoids containing an isopropyl trans-hydrindane system is presented.

299 h two major components being 3,5-dihydroxy-4-isopropyl-trans-stilbene (compound 1) and its stilbene e

300 t chiral diamino diethers synthesized from N-isopropyl valinol or N-isopropyl alaninol were lithiated