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

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

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

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

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

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

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

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

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

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

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

23 2S,2'S)-1,1'-(pentane-1,5-diylbis(oxy))bis(N-isopropyl-3-methylbutan-2-amine) 10 is a monomer.

24 2S,2'S)-1,1'-(heptane-1,7-diylbis(oxy))bis(N-isopropyl-3-methylbutan-2-amine) 9 are dimers, whereas d

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

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

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

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

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

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

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

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

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

34 60 degrees C for 12 h formed 3-isobutyryl-2-isopropyl-5-methylfuran in 77% isolated yield.

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

36 (1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5 H)-one (AMG 221).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

51 3-(3-Cyclopentyloxy-4-methoxy-benzyl)-8-isopropyl-adenine V11294 (1) has been identified as a le

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

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

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

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

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

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

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

59 The isopropyl alcohol adsorption simulations indicate that D

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

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

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

63 Using isopropyl alcohol and water mixtures, detection limits a

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

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

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

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

68 mechanism of the alkylation of m-cresol with isopropyl alcohol in scCO(2) using Nafion SAC-13 as the

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

85 ed solvent and subsequent precipitation with isopropyl alcohol.

86 Reactions of isopropyl alpha-lithioisobutyrate (2) with suitable deag

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

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

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

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

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

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

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

94 bitor, Y27632, or NHE1 blocker, S-(N-ethyl-N-isopropyl) amiloride, respectively) blocks NHE1 phosphor

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

96 5-(N-Ethyl-N-isopropyl)amiloride (EIPA) and soluble THY-1 blocked HCM

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

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

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

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

101 1 h) and NHE activity was measured as ethyl-isopropyl-amiloride (EIPA)-sensitive 22Na uptake.

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

103 )/H(+) transport, as demonstrated by ethyl-N-isopropyl-amiloride-inhibitable, intracellular alkaliniz

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

105 4-(Benzothiazol-6-ylamino)-6-(benzyl-isopropyl-amino)-[1,3,5]triazin-2-ol (14d) exhibited low

106 These analogues with the amino acid 4-(N-isopropyl)-aminomethylphenylalanine (IAmp) at position 9

107 ional conformational constraint (IAmp = 4-(N-isopropyl)-aminomethylphenylalanine).

108 d, Nal = 3-(2-naphthyl)-alanine, IAmp = 4-(N-isopropyl)-aminomethylphenylalanine, SRIF = somatostatin

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

110 In a comparison of a series of N-alkyl-N-isopropyl analogues, activity decreased in the order CH3

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 X-ray crystal structure of 9a shows that the isopropyl and phenyl groups are mutually cis and that th

116 tolyl moiety is oriented s-trans to both the isopropyl and phenyl groups.

117 of little steric interaction between the cis isopropyl and phosphorus substituent in 9a, 11a, and 12a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 g growth, but, shortly after the addition of isopropyl beta-d-thiogalactopyranoside, Y-EI became bipo

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

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

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

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

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

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

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

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

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

151 ene under the control of a tightly regulated isopropyl-beta-d-thiogalactopyranoside (IPTG)-inducible

152 An isopropyl-beta-D-thiogalactopyranoside (IPTG)-inducible

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

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

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

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

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

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

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

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

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

162 Upon induction of alginate production with isopropyl-beta-D-thiogalactopyranoside, the DeltaalgL mu

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

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

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

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

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

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

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

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

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

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

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

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

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

176 /mol (methyl cation/benzene) to 31 kcal/mol (isopropyl cation/methanol).

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

178 ules each of CHCl(3), 1,2-dichloroethane, or isopropyl chloride.

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

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

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

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

183 1, 2:1, and 10:1 for the methyl, benzyl, and isopropyl derivatives 7a,b, 8a,b, and 9a,b, respectively

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

202 orientation of the tolyl moiety s-cis to the isopropyl group in 9b, 12b, and 13.

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

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

205 In contrast, isopropyl group inversion during formylation of menthone

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

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

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

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

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

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

212 The endo-isopropyl group was installed by selective hydrogenation

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

243 50) in HDAC inhibition, 16 nM), of which the isopropyl moiety was favorable in interacting with this

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

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

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

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

248 N-[4-(thien-3-ylethynyl) phenyl] amine and N-isopropyl-N-(4-{[4-(thien-3-ylethynyl) phenyl]ethynyl}ph

249 ylamido)titanium, Ti[N(CH(3))(2)](4), with N-isopropyl-N-[4-(thien-3-ylethynyl) phenyl] amine and N-i

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

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

252 2,4,6-cycloheptatrien-1-one, 2,7-dihydroxy-4-isopropyl (NSC 18806) IC50 = 4.8 +/- 2.5 microM] exhibit

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

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

255 potentially ambident RNH[N(O)NO](-) ion (R = isopropyl or cyclohexyl) has been shown to occur at the

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

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

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

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

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

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

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

270 yl-piperidin-4-yloxy)-benzonitriles and 4-(1-isopropyl-piperidin-4-yloxy)-benzylamines have been prep

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

272 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

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

274 The crystal structure of the isopropyl reagent, i-Pr(CHB(11)Me(5)Br(6)), has been det

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

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

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

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

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

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

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

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

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

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

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

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

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

288 3BH3, R2NHBH3, and RNH2BH3 where R = methyl, isopropyl, tert-butyl, and cyclohexyl) and rhodium catal

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

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

291 Isopropyl-thiazole ((iPr)Th) represents a new addition t

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

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

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

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

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

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

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

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

300 es C6H3-2,6(C6H3-2,6-Pri2)2 and Pr indicates isopropyl] with a slight excess of potassium graphite ha