ライフサイエンスコーパス: dimethyl

1 f cyclopentadiene with dimethyl fumarate and dimethyl 1,1-ethylenedicarboxylate.

2 on complex [Fe(btz)3](3+) (where btz is 3,3'-dimethyl-1,1'-bis(p-tolyl)-4,4'-bis(1,2,3-triazol-5-ylid

3 boxylate (11), 1,10-phenanthroline (12), 2,9-dimethyl-1,10-phenanthroline (13), or 4,7-diphenyl-1,10-

4 )(dmp)2TFSI2/1 (0.93 V vs SHE, dmp = bis(2,9-dimethyl-1,10-phenanthroline).

5 acids 1-10 with cyclohexa-1,3-diene and 2,3-dimethyl-1,3-butadiene (several cycloadducts characteriz

6 = N,N'-bis(2,6-dialkylphenyl)-1,4-diaza-2,3-dimethyl-1,3-butadiene) carrying nearly unperturbed nitr

7 zed metal-organic framework comprised of 2,2-dimethyl-1,3-diaminopropane (dmpn) appended to the Mg(2+

8 -trimethyl-1,3-dioxane (TMD) and 2-ethyl-5,5-dimethyl-1,3-dioxane (2EDD) which impart a distinctive s

9 oating the Li metal surface with poly((N-2,2-dimethyl-1,3-dioxolane-4-methyl)-5-norbornene-exo-2,3-di

10 , linalool, and the two homoterpenes (E)-3,8-dimethyl-1,4,7-nonatriene (DMNT) and (E,E)-4,8,12-trimet

11 ) [(Fl)DAB = N,N'-bis(pentafluorophenyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene; TFA = trifluoroacetate

12 [(Fl)DAB is N,N'-bis(pentafluorophenyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene; TFA is trifluoroacetat

13 3,6-dimethyl-1,4-dioxan-2-one to (3R,6R)-3,6-dimethyl-1,4-dioxan-2-one falls to 3:2.

14 eat (R)-(+)-PO, the formation of (3S,6R)-3,6-dimethyl-1,4-dioxan-2-one occurs, while at higher temper

15 higher temperatures the ratio of (3S,6R)-3,6-dimethyl-1,4-dioxan-2-one to (3R,6R)-3,6-dimethyl-1,4-di

16 ne; isopropyl 2-methylbutanoate; cymene; 2,6-dimethyl-1,6-octadiene; 3-methyloctane; 1-(1,4-dimethyl-

17 A structural analog of choline, 3,3-dimethyl-1-butanol (DMB), is shown to non-lethally inhib

18 the formation of an amine side product, N,N'-dimethyl-1-phenyl-1-(o-tolyl)methanamine.

19 The spin-trap reagents, 5,5-dimethyl-1-pyrroline N-oxide (DMPO) and 2-ethoxycarbonyl

20 Using the spin trap, 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), hydroxyl radical ((

21 SO4(.-) was determined by a DMPO (5,5-dimethyl-1-pyrroline-N-oxide) spin-trapping EPR method a

22 Here we used [(13)C]itaconate and dimethyl [(13)C]itaconate (DMI) to probe itaconate metab

23 ,5-a]pyridin-3-yl)-2-pyrimidinyl]amino}-3,5- dimethyl-1H-pyrazol-1-yl)-1-piperidinyl]-2-hydroxy-1-pro

24 l hit compound (Z)-5-((1-(4-bromophenyl)-2,5-dimethyl-1H-pyrrol-3-yl)methylene)thiazolidine-2,4- dion

25 ne (9), 4,4'-dimethoxy-2,2'-bipyridine (10), dimethyl 2,2'-bipyridine-4,4'-dicarboxylate (11), 1,10-p

26 H2)](+) where NN = 2,2'-bipyridine (8), 4,4'-dimethyl-2,2'-bipyridine (9), 4,4'-dimethoxy-2,2'-bipyri

27 t of [B{3,5-(CF3)2C6H3}4]AgFe(CO)5 with 4,4'-dimethyl-2,2'-bipyridine (Me2Bipy) and Fe(CO)5 afforded

28 m-catalyzed borylation of pyrene, using 4,4'-dimethyl-2,2'-bipyridine as the ligand, in the presence

29 ))(dmby)2TFSI2/1 (0.97 V vs SHE, dmby = 6,6'-dimethyl-2,2'-bipyridine) and Cu((II/I))(tmby)2TFSI2/1 (

30 )2(poly(vinylimidazole))10Cl](+) or [Os(4,4'-dimethyl-2,2'-bipyridine)2(poly(vinylimidazole))10Cl](+)

31 cosylated enzyme coimmobilized with [Os(4,4'-dimethyl-2,2'-bipyridine)2(poly(vinylimidazole))10Cl](+)

32 4'-Dihydro-1'(2H)-naphthalen-1'-ylidene)-3,7-dimethyl-2,3,6-o ctatrienoinic acid (UAB30) is currently

33 adding n-type dopant 2-(2-methoxyphenyl)-1,3-dimethyl-2,3-dihydro-1H-benzoimidazole.

34 ew general tool, Fmoc-Ddae-OH, N-Fmoc-1-(4,4-dimethyl-2,6-dioxocyclo-hexylidene)-3-[2-(2-aminoethoxy)

35 xyphenyl)decyl]-1,2-benzenediol; 8-[(2E)-3,7-dimethyl-2,6-octadien-1-yl]-5-hydroxy-2,8-dimethyl-6-(3-

36 opride), and serotonin transporter (11)C-N,N-dimethyl-2-(-2-amino-4-cyanophenylthio) benzylamine ([(1

37 ure the test-retest reliability of (11)C-N,N-dimethyl-2-(2'-amino-4'-hydroxymethylphenylthio)benzylam

38 Interaction of 4,5-dimethyl-2-(2-oxo-1,2-diphenyl)ethoxy-1,3,2-dioxaphospho

39 dimethylisoxazol-5-yl)sulfamoyl)-phenyl)-6,8-dimethyl-2-(pyridin-2- yl)quinoline-4-carboxamide], a se

40 eights (100.1 g/mol), 4-aminopiperidine, 3,3-dimethyl-2-butanone (pinacolone) and methylisobutyl keto

41 with TON > 8000 for the hydrogenation of 2,3-dimethyl-2-butene.

42 ry of N-(biphenyl-3-ylmethyl)-2-(4-ethyl-6,6-dimethyl-2-oxomorpholin-3-yl)acetamide (87), which, in a

43 's cytotoxicity was tested using MTT (2-(4,5-dimethyl-2-thiazolyl)-3,5-diphenyl-2H-tetrazolium bromid

44 Dye as 5,5'-(1-propen-1-yl-3-ylidene)bis[1,3-dimethyl-2-thio-barbituric acid].

45 ective hydrolysis and transesterification of dimethyl 3-benzamidophthalates into the corresponding ca

46 ter including, amongst others, 4-hydroxy-2,5-dimethyl-3(2H)-furanone (furaneol), vanillin, (E)-4,5-ep

47 hereas, in oil roasted almonds 4-hydroxy-2,5-dimethyl-3(2H)-furanone, 2,3-pentanedione, methional and

48 ve step in the biosynthesis of 4-hydroxy-2,5-dimethyl-3(2H)-furanone, a major component in the charac

49 cluding the key compound HDMF [4-hydroxy-2,5-dimethyl-3(2H)-furanone] contribute to the flavor of the

50 a catalyst [Co(II)N4H(MeCN)](2+) (N4H = 2,12-dimethyl-3,7,11,17-tetraazabicyclo[11.3.1]heptadeca-1(17

51 methyl-1,6-octadiene; 3-methyloctane; 1-(1,4-dimethyl-3-cyclohexen-1-yl)ethanone; terpinolene; ethyl

52 uding an azocine ring and an unprecedented 2-dimethyl-3-methyl-azetidine ring.

53 he selenosemicarbazone, 2-acetylpyridine 4,4-dimethyl-3-selenosemicarbazone (Ap44mSe), and its iron a

54 ovel anti-tumor agent di-2-pyridylketone 4,4-dimethyl-3-thiosemicarbazone (Dp44mT) overcomes MDR.

55 The compound, di-2-pyridylketone 4,4-dimethyl-3-thiosemicarbazone (Dp44mT), has been shown to

56 tein (Pgp) substrate, di-2-pyridylketone-4,4-dimethyl-3-thiosemicarbazone (Dp44mT), induces lysosomal

57 emicarbazones, namely di-2-pyridylketone 4,4-dimethyl-3-thiosemicarbazone and di-2-pyridylketone 4-cy

58 ependent on NDRG1 for di-2-pyridylketone 4,4-dimethyl-3-thiosemicarbazone, but was independent of thi

59 By using methyl viologen (N,N'-dimethyl-4,4'-bipyridinium) to shuttle electrons to nitr

60 *) (MV refers to methyl viologen, i.e., N,N'-dimethyl-4,4'-bipyridinum) engage in weak radical-radica

61 lated, but more-electron-rich derivative 9,9-dimethyl-4,5-diazafluorene (Me2DAF) simplifies the equil

62 dicationic -[P(H2Im)2](+2) unit (H2Im = 1,3-dimethyl-4,5-dihydroimidazol-2-ylidene) and a -PPh2 grou

63 conformation of the N-substituted trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine (1) class of opio

64 astereoselective cyclization promoted by N,N-dimethyl-4-aminopyridine.

65 ning aromatic compounds, 4-cyanoaniline, N,N-dimethyl-4-cyanoaniline (DMABN), sotalol (a beta-blocker

66 of a recent interesting attempt in which 6,7-dimethyl-4-hydroxy-2-mercaptopteridine was reported as a

67 erisation and cyclisation of acetol into 2,5-dimethyl-4-hydroxy-tetrahydrofuran-3-one was found to be

68 V)(O) (SR-TPA)(NCMe)](2+) (SR-TPA = tris(3,5-dimethyl-4-methoxypyridyl-2-methy)amine), the excitation

69 (L)2](ClO4)3 (4) models (where, L = tris(3,5-dimethyl-4-methoxypyridyl-2-methyl)amine) (TPA*)).

70 4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-thioxoimida zolidin-1-yl)-2-fluoropheny

71 4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin -1-yl)-2-fluoro-N-(7

72 e Strecker reaction from (4S,5S)-5-amino-2,2-dimethyl-4-phenyl-1,3-dioxane.

73 Both (S,S) and (R,R) enantiomers of 5,6-dimethyl-5,6-dihydro-1,4-dithiin-2,3-dithiolate (dm-dddt

74 onvenient for arylated or heteroarylated 5,5-dimethyl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazoles.

75 rowth, we identified 6-(2-methoxyphenyl)-1,3-dimethyl-5-phenyl-1H-pyrrolo[3,4-d]pyrimidine-2,4(3 H,6

76 ,7-dimethyl-2,6-octadien-1-yl]-5-hydroxy-2,8-dimethyl-6-(3-methyl-2-bute n-1-yl)-2H-1-benzopyran-4,7(

77 eacts with acetone with the formation of 3,3-dimethyl-6-phenyl-2,3-dihydro-1,2,4-triazin-4-oxide (7')

78 reaction of vinyl magnesium bromide with 2,2-dimethyl-6-t-butyl-dimethyl-silyoxy-methyl-1-cyclo-hexan

79 6aR,9R,10aR)-1-hydroxy-9-(hydroxymethyl)-6,6-dimethyl-6a,7,8,9,10,10a-h exahydro-6H-benzo[c]chromen-3

80 sis and characterization of new cationic N,N-dimethyl[70]fulleropyrrolidinium iodide derivatives that

81 pplements into the riboflavin precursor, 6,7-dimethyl-8-ribityllumazine, with yields up to 40%.

82 carbaldehyde and tetrazolo[1,5-a]quinoline-3-dimethyl acetal at room temperature in methanol as solve

83 propylphenyl)-imidazol-2-ylidene borane with dimethyl acetylenedicarboxylate gives 80% yield of a sta

84 They also reacted with quinones and dimethyl acetylenedicarboxylate to form adducts with hig

85 EDs) composed of three emitters (2,7-bis(9,9-dimethyl-acridin-10-yl)-9,9-dimethylthioxanthene-S,S-dio

86 Branched alkylation with N,N-dimethyl acrylamide was successfully applied to the alky

87 somerized isopentenyl pyrophosphate (IPP) to dimethyl allyl pyrophosphate (DMAPP) and vice versa.

88 lity formed diagnostic adducts that had lost dimethyl amine (DMA).

89 f ketones using a commercially available 2,2-dimethyl aminooxyacetic acid auxiliary.

90 raarsenic marine metabolite arsenicin A, the dimethyl analogue 2 and four isomeric methylene homologu

91 The dioctyl, dimethyl, and dibenzyl derivatives also show distinctive

92 rsenosugars and their metabolites (including dimethyl arsenate (DMA), thio-dimethylarsinoylethanol (t

93 Pd(PPh)3)4 and dimethyl barbituric acid.

94 13)C-methyl]l-methionine implicated an alpha-dimethyl-beta-keto acid intermediate in the biosynthesis

95 cubation of the chemically synthesized alpha-dimethyl-beta-keto acid with a purified recombinant flav

96 thers (MeO-BDEs) and chlorinated methyl- and dimethyl bipyrroles (MBPs and DMBPs) were the most abund

97 ts are additive, for example, a 2,6-diiodo-B-dimethyl BODIPY photocage features quantum yields of 28%

98 on graphite electrodes in Ethylene Carbonate/Dimethyl Carbonate (1:1), 1 M LiPF6 as an electrolyte.

99 olutions in a binary ethylene carbonate (EC)-dimethyl carbonate (DMC) 1:1 v/v solvent mixture, obtain

100 as been designed for the direct synthesis of dimethyl carbonate (DMC) from methanol and carbon dioxid

101 lO4 in 1:1 (v/v) ethylene carbonate (EC) and dimethyl carbonate (DMC).

102 he reaction parameters highlights the use of dimethyl carbonate as a preferred polymerization solvent

103 It was observed that the dimethyl carbonate is only formed when the electrode is

104 ion of methanol with CO for the synthesis of dimethyl carbonate on metallic electrodes at low overpot

105 oxy groups that can further react with CO to dimethyl carbonate.

106 Unreactive by itself, the Mo-dimethyl catecholate analogue reduces O(2) in the presen

107 Using 2,2-dimethyl cyclohexanone as the starting compound, (+)-ant

108 ompounds tested were 1-propylmercaptan (PM), dimethyl disulfide (DMDS), diallyl disulfide (DADS), pro

109 Dimethyl disulfide and methyl thioacetate were important

110 functional electrolyte system incorporating dimethyl disulfide as a co-solvent that enables a new el

111 e, pentane, 3-methylfuran, 2-ethylfuran, and dimethyl disulfide from wild rocket with different initi

112 n, the reaction of diynols with an excess of dimethyl disulfide in the presence of NBS gave the 4-met

113 ion, and the release of dimethyl sulfide and dimethyl disulfide was related to the total aerobic bact

114 S1 and RP-RS2, the predominant odorants were dimethyl disulfide, dimethyl trisulfide, and hexanal.

115 unds, such as methanethiol, diethyl sulfide, dimethyl disulfide, methional and dimethyl trisulfide, i

116 Dimethyl sulphide, dimethyl disulphide, dimethyl trisulphide 2-propylthiazo

117 By using ferbam (ferric dimethyl-dithiocarbamate) as an indicator molecule that

118 OP pesticides, specifically diethyl (DE) and dimethyl (DM) phosphate metabolites, were measured in ur

119 Discrete endo,exo-norbornenyl dialkylesters (dimethyl DME, diethyl DEE, di-n-butyl DBE) were strategi

120 The representative compounds DMAC (N,N'-dimethyl), DPAC (N,N'-diphenyl), and FlPAC (N-phenyl-N'-

121 Starting from dimethyl (E)-2-{[(1-tert-butoxycarbonyl)-1H-indol-3-yl]m

122 nty-four times more effective than l-cystine dimethyl ester (CDME) in increasing the metastable super

123 fter the evaluation of the reactivity of the dimethyl ester derivative with various primary amines, t

124 le-1,2,5-tricarboxylic acid tert-butyl ester dimethyl ester with electrophiles such as methyl chlorof

125 for one-step conversion of synthesis gas to dimethyl ether (DME) was imaged simultaneously and in si

126 ed reactions, the dehydration of methanol to dimethyl ether and the total methane oxidation reactions

127 of CO2 to formate/formic acid, methanol, and dimethyl ether are thoroughly reviewed, with special emp

128 Intact poly(ethylene glycol) dimethyl ether is identified as the electrolyte degradat

129 ouble Baeyer-Villiger reaction of quinizarin dimethyl ether is viable, directly providing the dibenzo

130 The products, methanol, dimethyl ether, and CO2, were desorbed with the passage

131 ls including syngas, methanol, formaldehyde, dimethyl ether, heavier hydrocarbons, aromatics, and hyd

132 ethyl carbonate (EMC), poly(ethylene glycol) dimethyl ether, poly(ethylene glycol) ethyl methyl ether

133 Poly(N-(3-dimethyl(ferrocenyl)methylammonium bromide)propyl acryla

134 itrophenol and [DMF.H(+)](CF3SO3(-))) (DMF = dimethyl-formamide) or electron (decamethylferrocene (Fc

135 Dimethyl fumarate (DMF) (BG-12, Tecfidera) is a fumaric

136 We show here that dimethyl fumarate (DMF) dose-dependently induces mitocho

137 of this study was to explore the efficacy of dimethyl fumarate (DMF) in preventing disease reactivati

138 Dimethyl Fumarate (DMF) is an FDA approved anti-oxidativ

139 Dimethyl fumarate (DMF) is indicated for the treatment o

140 We investigated the effects of dimethyl fumarate (DMF) on CTCL cells in vitro and in vi

141 Dimethyl fumarate (DMF) possesses anti-inflammatory prop

142 To address this need, we examined whether dimethyl fumarate (DMF), an anti-inflammatory drug alrea

143 modifiers, including sulforaphane (SFN) and dimethyl fumarate (DMF), are unable to induce a similar

144 Fumaric acid esters, including dimethyl fumarate (DMF, Tecfidera; Biogen, Cambridge, MA

145 Dimethyl fumarate (DMF; trade name Tecfidera) is an oral

146 Alder cycloadditions of cyclopentadiene with dimethyl fumarate and dimethyl 1,1-ethylenedicarboxylate

147 ents-natalizumab, fingolimod, teriflunomide, dimethyl fumarate, and alemtuzumab-with regard to their

148 ls and anti-inflammatory mediators, that is, dimethyl fumarate, phosphodiesterase 4, and leukotriene

149 are reduced by fingolimod, alemtuzumab, and dimethyl fumarate, whereas natalizumab disproportionally

150 treat cancer and the multiple sclerosis drug dimethyl fumarate.

151 hitosan promoted the formation of esters and dimethyl furfural in very short time after coating, whil

152 -W routes lie in (1) the location of the gem-dimethyl group (with respect to the 1-acetal unit) at th

153 Four of the ligands possess a C(4)-gem-dimethyl group and four a C(4)-gem-diphenyl group adjace

154 The results indicate that a dimethyl group at C4 as well as a C9,C19 cyclopropane gr

155 Reinstallation of the trans-olefin and gem-dimethyl group present in bryostatin 1 in Merle 48 resul

156 methylation can precede condensation in gem-dimethyl group producing PKS modules.

157 nal chemists have elegantly employed the gem-dimethyl group to obtain clinically useful drugs and to

158 o provide synthetic methods to install a gem-dimethyl group.

159 ystal structure shows that the squaraine gem-dimethyl groups force a relatively wide separation betwe

160 Solution-state studies show that the gem-dimethyl groups in 3,3-dimethylindoline squaraine dyes a

161 secondary homopropargyl alcohols bearing gem-dimethyl groups.

162 enes toward 5' ends, and histone H3 lysine 4 dimethyl (H3K4me2) extended farther upstream of start si

163 Using this approach, dimethyl-histone H3 and p53 proteins have been synthesiz

164 Radical trifluoromethylation of aryl N,N-dimethyl hydrazones using TBAI as an initiator and Togni

165 3-carbomethoxycarbazole was synthesized from dimethyl indolylmethylenesuccinate in four steps.

166 odium 4-amino-3,5-dinitropyrazolate (5) with dimethyl iodide yielded bis(4-amino-3,5-dinitropyrazolyl

167 (1 mol %) in the asymmetric hydrogenation of dimethyl itaconate.

168 anoRPLC-MS/MS), called mass defect-based N,N-dimethyl leucine (mdDiLeu) labeling.

169 of diverse nucleophiles (e.g., indoles, N,N-dimethyl-m-anisidine, 2-ethylpyrrole, and 2-methylallyls

170 , while an inhibitor of succinate oxidation, dimethyl malonate (DMM), promotes an anti-inflammatory o

171 ives, which allows for the convenient use of dimethyl malonate as a methylene synthon.

172 tocol for the asymmetric Michael addition of dimethyl malonate to various alpha,beta-unsaturated carb

173 yl methacrylate as a comonomer, and ethylene dimethyl methacrylate (EDMA) as a cross-linker.

174 In nitrogen, protonated forms of dimethyl methyl phosphonate (DMMP) and methyl phosphonic

175 e have selectively detected three compounds, dimethyl methyl phosphonate (DMMP), cyclotrimethylene tr

176 HN films and tested for their sensitivity to dimethyl methylphosphonate (a nerve agent simulant).

177 man (GD) (and their less reactive simulants, dimethyl methylphosphonate (DMMP)) as well as mustard (H

178 and decomposition of a nerve-agent simulant, dimethyl methylphosphonate (DMMP), on UiO-66, UiO-67, MO

179 atalyst has been shown to react readily with dimethyl methylphosphonate (DMMP).

180 el for 4'-pentyl-4-biphenylcarbonitrile, and dimethyl methylphosphonate to metal cation models repres

181 e agent (CWA) simulants trimethyl phosphate, dimethyl methylphosphonate, and diisopropyl methylphosph

182 or and limits of detection for acetonitrile, dimethyl methylphosphonate, diisopropyl methyl phosphona

183 n act as stable fluorescent water sensors, a dimethyl modified MOF exhibits a temperature dependent p

184 The gem-dimethyl moiety is a structural feature frequently found

185 However, s-BuLi converted the dimethyl N-Boc-phosphoramidate derived from 1-phenylethy

186 LiTMP metalated dimethyl N-Boc-phosphoramidates derived from 1-phenyleth

187 plex alpha-[Fe(II)(CF3SO3)2(mcp)] (mcp=(N,N'-dimethyl-N,N'-bis(2-pyridylmethyl)-1,2-cis-diaminocycloh

188 ed biosensor (annexin B12-Cys101,Cys260-N,N'-dimethyl-N-(iodoacetyl)-N'-(7-nitrobenz-2-oxa-1,3-diazol

189 is a disolvated symmetric dimer in DMEA, N,N-dimethyl-n-butylamine, and N-methylpyrrolidine.

190 ns of nitramine, N-methyl nitramine, and N,N-dimethyl nitramine with anhydrous HF and the superacids

191 Introduction of a gem-dimethyl on the 6-position of the morpholin-2-one core l

192 As a result, the hydrogenation of dimethyl oxalate (DMO) to ethylene glycol, an important

193 amolecular insertion reaction to produce 5,5-dimethyl oxazolidinone.

194 MS, of dopamine (DA), tyrosine (Tyr) and N,N-dimethyl-p-phenylenediamine (DMPA), were evaluated using

195 source of ethane was found to be an unstable dimethyl Pd(IV) complex (dpms)Pd(IV)Me2(OH) (7), which c

196 vo in splenic DC following administration of dimethyl PGE2 in conjunction with LPS.

197 one (Rosi) or prostaglandin E2 analog (16,16-dimethyl PGE2) to adipose tissue vasculature.

198 GDH inhibitor + PGE2 or metabolism-resistant dimethyl-PGE2 resulted in preterm cervical ripening and

199 three diethyl phosphate (SigmaDEP) and three dimethyl phosphate (SigmaDMP) metabolites of OP pesticid

200 etermined by quantum chemistry methods using dimethyl phosphate as a model.

201 This pathway uses soluble dimethyl polysulfides and lithium organosulfides as inte

202 eto intermediate to yield an alpha,alpha-gem-dimethyl product, a new programing feature among HRPKSs.

203 om BM cells pulsed in vitro for 2 hours with dimethyl prostaglandin E2 were functionally similar to t

204 ine-reactive mass defect-based chemical tag, dimethyl pyrimidinyl ornithine (DiPyrO), that is compact

205 cals were spin-trapped via reaction with 5,5-dimethyl-pyrroline N-oxide at different electrochemical

206 idly, we have fabricated a microchip in poly(dimethyl siloxane) (PDMS) by soft lithography process.

207 agnesium bromide with 2,2-dimethyl-6-t-butyl-dimethyl-silyoxy-methyl-1-cyclo-hexanone to give a vinyl

208 n a straightforward manner in two steps from dimethyl squarate.

209 GNP dimers linked with an organic molecule (dimethyl suberimidate) as the interacting species.

210 Dimethyl succinate, the inactive analog of DMF that lack

211 Here we present dimethyl sulfate (DMS) mutational profiling with sequenc

212 otides and then detects these events through dimethyl sulfate (DMS) probing and mutational profiling.

213 ins generally have higher reactivity to DMS (dimethyl sulfate), a chemical that covalently modifies a

214 sulfoniopropionate (DMSP) cleavage, yielding dimethyl sulfide (DMS) and acrylate, provides vital carb

215 Dimethyl sulfide (DMS) is produced in large quantities a

216 methanethiol (MeSH), ethanethiol (EtSH), and dimethyl sulfide (DMS) were assessed in wines post-bottl

217 P lyases cleave DMSP, producing acrylate and dimethyl sulfide (DMS), a climate-active gas with roles

218 Oceans dominate emissions of dimethyl sulfide (DMS), the major natural sulfur source.

219 ntermediates in the atmospheric oxidation of dimethyl sulfide (DMS), was generated by flash pyrolysis

220 BlMGL) produced the sulfur volatile compound dimethyl sulfide (DMS).

221 sms(2,3) and the major precursor for gaseous dimethyl sulfide (DMS).

222 of tissue disintegration, and the release of dimethyl sulfide and dimethyl disulfide was related to t

223 Significant amounts of dimethyl sulfide are emitted from cruciferous vegetables

224 controlled to release increasing amounts of dimethyl sulfide as the supply of DMSP exceeds cellular

225 While transgenic lines emitted dimethyl sulfide from leaves and roots, no sulfur-contai

226 usly shunts as much as 59% of DMSP uptake to dimethyl sulfide production.

227 avage pathway to the climatically active gas dimethyl sulfide(3,4).

228 es of domoic acid, a marine algal toxin, and dimethyl sulfide, a volatile precursor to cloud condensa

229 reased hydrogen sulfide (H2S), methanethiol, dimethyl sulfide, and carbon disulfide concentrations.

230 tron ionization (EI) were: carbonyl sulfide, dimethyl sulfide, carbon disulfide, 2-methylthiophene, 3

231 terised by a high level of sulfur compounds (dimethyl sulfide, ethanethiol), and ester and alcohol co

232 y, the release of acetone, carbon disulfide, dimethyl sulfide, nitromethane, pentane, 3-methylfuran,

233 um carbonate precipitation and production of dimethyl sulfide, often blooms in mid-latitude at the be

234 erexpressing methionine-gamma-lyase produced dimethyl sulfide.

235 te with levels of isoprene, monoterpenes, or dimethyl sulfide.

236 idney bean' aroma, while dimethyl sulfoxide, dimethyl sulfone and ethyl methyl sulfone were responsib

237 at 3.1 V, with O being trapped in a form of dimethyl sulfone in the electrolyte.

238 dabrafenib with the MEK inhibitor trametinib dimethyl sulfoxide (CombiDT therapy) increases response

239 f 1,2-dibromoethane (extraction solvent) and dimethyl sulfoxide (disperser solvent) was injected rapi

240 e approach strategically involves the use of dimethyl sulfoxide (DMSO) acting as an organic solvent f

241 , we found that CSOD can tolerate up to 3.9% dimethyl sulfoxide (DMSO) and up to 10% serum, which sho

242 sphate buffer saline solution containing 10% dimethyl sulfoxide (DMSO) at 21 degrees C.

243 Dimethyl sulfoxide (DMSO) disrupts the hydrogen-bond net

244 nfected HepG2/NTCP cells was attributable to dimethyl sulfoxide (DMSO) in culture medium, NTCP overex

245 oreover, a medium comprised of Ficoll 70 and dimethyl sulfoxide (DMSO) in presence or absence of feta

246 Dimethyl sulfoxide (DMSO) is a common solvent and biolog

247 Dimethyl sulfoxide (DMSO) is a promising solvent for thi

248 Dimethyl sulfoxide (DMSO) or sulfide ligands have positi

249 e Kubota's Medium (KM) supplemented with 10% dimethyl sulfoxide (DMSO), 15% human serum albumin (HSA)

250 r, when the media contains a small amount of dimethyl sulfoxide (DMSO), the adduct is able to move to

251 loxifene (cRbm20(DeltaRRM)-raloxifene), with dimethyl sulfoxide (DMSO)-injected mice (cRbm20(DeltaRRM

252 nsitized with 5% ammonium persulfate (AP) or dimethyl sulfoxide (DMSO).

253 chelating agent in a common organic solvent, dimethyl sulfoxide (DMSO).

254 Dimethyl sulfoxide 2 M was used as cryoprotector for slo

255 o NTCP overexpression, genotype D virus, and dimethyl sulfoxide added to culture medium.

256 Dimethyl sulfoxide and polyurethane were assigned as sur

257 Experimental data of ethanol and dimethyl sulfoxide are shown as proof-of-concept.

258 CDC) protocol using iodine as a catalyst and dimethyl sulfoxide as an oxidant under green chemistry c

259 ed using iodine as a catalyst (30 mol %) and dimethyl sulfoxide as an oxidant under metal-free reacti

260 ionalization of imidazo[1,2-a]pyridines with dimethyl sulfoxide as the carbon synthon (CH2) using H2O

261 oped automation-friendly reactions to run in dimethyl sulfoxide at room temperature.

262 cells stably transfected with HBV DNA, while dimethyl sulfoxide could increase NTCP protein level des

263 hiafulvalene (TTF) in 1.0 m LiClO4 dissolved dimethyl sulfoxide electrolyte are reported.

264 copic study of oxygen reduction on gold in a dimethyl sulfoxide electrolyte containing phenol as a pr

265 o initiate the catalytic reduction of either dimethyl sulfoxide or trimethylamine N-oxide.

266 S from S-methylmethionine was obtained, with dimethyl sulfoxide producing significantly less DMS with

267 nd Michael acceptors have been determined in dimethyl sulfoxide solution at 20 degrees C.

268 s elusive, FRET experiments in formamide and dimethyl sulfoxide suggest that interactions between hyd

269 n affinities, particularly when solvation by dimethyl sulfoxide was taken into account by applying th

270 Interestingly, when dimethyl sulfoxide was used instead of Triton((R)) X-100

271 ts, we have utilized the chemical denaturant dimethyl sulfoxide which, in conjunction with a short th

272 The effect of two solvents (water and dimethyl sulfoxide) and two MALDI matrices (2,5-dihydrox

273 icity (attributed to an allergic reaction to dimethyl sulfoxide) in the 29 patients enrolled, who rec

274 dichlorido[(1,3-dibenzyl)imidazol-2-ylidene](dimethyl sulfoxide) platinum(II) 3a induced G2/M phase a

275 amin-related protein 1 inhibitor or vehicle (dimethyl sulfoxide).

276 ibuting to 'cooked kidney bean' aroma, while dimethyl sulfoxide, dimethyl sulfone and ethyl methyl su

277 vs presence of a hydroxyl radical scavenger (dimethyl sulfoxide, DMSO), and different pH values.

278 oxidative bromination using HBr paired with dimethyl sulfoxide, which serves as the oxidant as well

279 c conformations in a molar ratio of 1.5:1 in dimethyl sulfoxide.

280 (xDP and xFP) were prepared and dissolved in dimethyl sulfoxide.

281 s similar behavior to drugs pre-dissolved in dimethyl sulfoxide.

282 , which were compared with dissolved PhIP in dimethyl sulfoxide.

283 lues around 5000-8000 for water and 2000 for dimethyl sulfoxide; differences between samples were rev

284 cal methods revealed a decrease in ester and dimethyl sulphide (DMS) concentrations in the first few

285 the abundant production of methyl sulphides (dimethyl sulphide and methanethiol) in euxinic or H2S-ri

286 Dimethyl sulphide, dimethyl disulphide, dimethyl trisulp

287 onalized weak polyanion with a polycation in dimethyl sulphoxide (DMSO), the solution was applied und

288 Taking advantage of 3,5-dichloro-N-[1-(2,2-dimethyl-tetrahydro-pyran-4-ylmethyl)-4-fluoro-piperidin

289 time, a combination of L-amino acid, (R)-5,5-dimethyl thiazolidinium-4-carboxylate (L-DMTC) with simp

290 yridine-4-carboxaldehydes using formaldehyde dimethyl thioacetal monoxide (FAMSO), and application of

291 Here, we have shown that the histone dimethyl transferase WHSC1 critically drives indolent PT

292 rizontal lineCH2(OAr)(OTf), treatment of the dimethyl triflate precursor with the ylide H2CPPh3 produ

293 Herein, we use dimethyl trisulfide (DMTS) as a model compound to study

294 e: dipropyl disulfide, S-propyl thioacetate, dimethyl trisulfide, 1-octen-3-one, methional, dipropyl

295 redominant odorants were dimethyl disulfide, dimethyl trisulfide, and hexanal.

296 l sulfide, dimethyl disulfide, methional and dimethyl trisulfide, in contributing to 'cooked kidney b

297 Dimethyl sulphide, dimethyl disulphide, dimethyl trisulphide 2-propylthiazole and 2-s-butylthiaz

298 and %uAs metabolites [monomethyl (%uMMA(V)), dimethyl (%uDMA(V)), and inorganic (%iAs) species] and p

299 urbit[8]uril (CB[8]) and an auxiliary guest, dimethyl viologen, with high selectivity and equilibrium

300 mulation with the STING-dependent ligand 5,6-dimethyl xanthnone-4-acetic acid (DMXAA).