ライフサイエンスコーパス: methyl

1 Approximately 500 Tg of 2-methyl-1,3-butadiene (isoprene) is emitted by deciduous

2 2-Butanone and 3-methyl-1-butanol were identified in Lactococcus lactis s

3 flours presented the highest contents of 3/2-methyl-1-butanol, acetoin and organic acids.

4 with 2,2-dimethyl-6-t-butyl-dimethyl-silyoxy-methyl-1-cyclo-hexanone to give a vinyl cyclohexanol der

5 Yb; L(1): 1,4,7-tris[(6-carboxypyridin-2-yl)methyl]-1,4,7-triazacyclononane), taking into account th

6 ethylenediamine (EDA), piperazine (PPZ), and methyl 2,2-bis(aminomethyl)propionate (COOMe) cores.

7 ructurally related pentacyclic triterpenoids methyl 2-cyano-3,12-dioxoolean-1,9-dien-28-oate [bardoxo

8 A methyl 2-oxoester, with a short chain carrying a naphtha

9 en-28-oate [bardoxolone-methyl (Bar-Me)] and methyl 2-trifluoromethyl-3,11-dioxoolean-1,12-dien-30-oa

10 nes [1-((2'-lithiochloromethyldimethylsilyl)-methyl)-2-(methoxymethyl)-pyrrolidine], thus enabling th

11 t CYP11B1 inhibitor 5-((5-methylpyridin-3-yl)methyl)-2-phenylpyridine Ref 7 (IC50= 2 nM) exhibited pr

12 sis, cooked fruit notes were identified as 3-methyl-2,4-nonanedione, gamma-nonalactone and gamma-deca

13 the preparation of the regioisomer (S)-N(1)-methyl-2-[2'-(3''-methoxy-4''-hydroxyphenyl)ethyl]-1,2,3

14 ctural revision of (-)-galipeine to (S)-N(1)-methyl-2-[2'-(3''-methoxy-4''-hydroxyphenyl)ethyl]-1,2,3

15 fied from the headspace of infected hosts, 3-Methyl-2-buten-1-ol (prenol) and 3-Hydroxy-2-butanone (A

16 methoxy-poly (ethylene glycol)-block-poly (2-methyl-2-carboxyl-propylene carbonate-graft-SMART-graft-

17 y vinylogous aldol reaction between methyl-5-methyl-2-furoate and aldehydes or ketones is described.

18 Thus, we introduced the enantiopure (R)-2-methyl-2-isocyano-3-(tritylthio)propanoate as a novel cl

19 coccus and higher levels of 2-butanone and 4-methyl-2-pentanone compared to CTRLs.

20 des fragilis, Sutterella, Lachnospiraceae, 4-methyl-2-pentanone, 1-butanol, and 2-butanone could disc

21 ions and the chelating/bridging ligand alpha-methyl-2-pyridine-methanol.

22 igorously with the standard slurry solvent N-methyl-2-pyrrolidinone (NMP), indicating it is not compa

23 clization to afford (1R,5S,7S)-7-[(benzyloxy)methyl]-2-tosyl-6-oxa-2-azabicyclo[3.2.1]octane in a hig

24 (0.86%), pregan,20-one-2hydroxy,5,6,epox-15-methyl (3.45%), hexa-decanoicacid (8.19%), 9,O-ctadeceno

25 Derivatives of (2-methyl-3-biphenylyl)methanol exhibit the structures capp

26 The presence of the 2-methyl-3-butyn-2-ol (alkynol) moiety was important for b

27 crobial strains that produce either chiral 2-methyl-3-hydroxy acids (1.1 +/- 0.2 g L(-1)) or branched

28 her KR(0) domains is, as predicted, a (2R)-2-methyl-3-ketoacyl-ACP intermediate, came from a newly de

29 ed in the generation of C2-epimerized (2S)-2-methyl-3-ketoacyl-ACP intermediates.

30 nerates exclusively the corresponding (2R)-2-methyl-3-ketopentanoyl-ACP (7a) product.

31 ty changes were confirmed using biotinylated methyl-3-nitro-4-(piperidin-1-ylsulfonyl) benzoate (NPSB

32 t hit compound, N-[4-(diethylamino)phenyl]-5-methyl-3-phenylisoxazole-4-carboxamide (3, IC50 = 3 muM)

33 r of the roasted meat aroma, i.e., (2S,3R)-2-methyl-3-thioacetate tetrahydrofuran, is reported as wel

34 lable in gram quantities in good yields from methyl 4(or 3)-hydroxy-3(or 4)-benzyloxybenzoate.

35 on of ethyl 3-(trimethylsilyl)propiolate and methyl 4-formylbenzoate shows first-order dependence on

36 and evaluation of N-(5-fluoropyridin-2-yl)-6-methyl-4-(pyrimidin-5-yloxy)picolinamide (27, VU0424238)

37 One such compound, 4-(6-methoxy-2-methyl-4-(quinolin-4-yl)-9H-pyrimido[4,5-b]indol-7-yl)-3

38 ic spine morphology, alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) to N-methyl-D-a

39 AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid)-subtype ionotropic gl

40 ibuted to increased alpha-amino-3-hydroxyl-5-methyl-4-isoxazole-propionate (AMPA) throughput.

41 e compounds blocking alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor and mam

42 Ac spine density and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR)-mediat

43 , lysosomes regulate alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor levels at the

44 elated with synaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid-type glutamate receptor

45 n primary dopaminergic neurons potentiated 1-methyl-4-phenyl pyrinidium (MPP(+))-induced neuronal dea

46 d, monkeys were rendered parkinsonian with n-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and dy

47 Although the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) mouse

48 a mouse model of Parkinson's disease using 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP).

49 ine dinucleotide, methylnicotinamide, and N1-methyl-4-pyridone-5-carboxamide, that can be used as val

50 N-Methylation of methyl 5-hydroxynicotinate followed by reaction with a d

51 Other compounds like pentanal and 6-methyl-5-hepten-2 one arose from blanching and boiling.

52 3-methylbutanal, 3-hydroxy-2-butanone, and 6-methyl-5-hepten-2-one.

53 , alpha-citral, hexanal, 3-hexen-1-ol, and 6-methyl-5-hepten-2-one; Fraction 2 was described as a "fr

54 tch induced by acidic citrate, but not alpha-methyl-5-hydroxytryptamine, chloroquine, compound 48/80,

55 the doubly vinylogous aldol reaction between methyl-5-methyl-2-furoate and aldehydes or ketones is de

56 In contrast, S-1-methyl-5-propyl-5-(m-trifluoromethyl-diazirinylphenyl) b

57 CMPF (2-(2-carboxyethyl)-4-methyl-5-propylfuran-3-carboxylic acid) is a metabolite

58 we review the pro- and anti-viral effects of methyl-6-adenosine in distinct viral life cycles, the ro

59 e B. cereus sensu lato group produce CDP-3-C-methyl-6-deoxy sugars for the formation of cereose-conta

60 d confirmed the highly potent antiandrogen 4-methyl-7-diethylaminocoumarin (C47) and two derivatives

61 [h]chromen-4-yl)-2-methylpropyl benzoate and methyl 8-(2-(benzoyloxy)-ethyl)-hexahydro-4-((E)-pent-2-

62 -Methoxybenzyl)-9-((tetrahydro-2H-pyran-4-yl)methyl)-8,9,10,11-tetrahydropyri do[4',3':4,5]thieno[3,2

63 g synthetic pathways for production of alpha-methyl acids in Escherichia coli using these enzymes all

64 ies in the Morita-Baylis-Hillman reaction of methyl acrylate with benzaldehyde derivatives.

65 id poly-(o-phenylene ethynylene)-block-poly-(methyl acrylate) block copolymers.

66 generated in ca. 90% yield on metathesis of methyl acrylate, styrene, or ethylene in the presence of

67 tes formed by nucleophilic attack of PCy3 on methyl acrylate.

68 NH and methyl, alkyl, aralkyl, vinyl, cyano, aryl and N-heteroa

69 The primary outcome measure was methyl aminolevulinate-induced PPIX fluorescence accumul

70 pretreated with non-AFXL (median, 2898 AU), methyl aminolevulinate-treated controls (median, 2254 AU

71 CN and purified using alumina and quaternary methyl ammonium solid-phase extraction cartridges.

72 Using methyl-ammonium lead bromide perovskite nanocrystals (PN

73 Methyl analogue 45 has an even more selective profile.

74 it of detection) to 7.3 ng/m(3) for azinphos-methyl, and < LOD to 0.8 ng/m(3) for azinphos-methyl-oxo

75 outdoor exposures to chlorpyrifos, azinphos-methyl, and oxygen analogs in a rural agricultural commu

76 hosphorus pesticides: chlorpyrifos, azinphos-methyl, and their oxygen analogs at 14 farmworker and 9

77 nternal and external double bonds, number of methyl- and ethyl- functional groups, molecular weight,

78 of 44 Michael acceptors and their calculated methyl anion affinities, particularly when solvation by

79 odel allowed us to show unambiguously that a methyl appears bigger than a chlorine and gave the follo

80 inol amide, and were completely prevented by methyl-arachidonoyl-fluorophosphate and palmostatin B, a

81 Proteins with methyl arginine residues are also enriched at the tip an

82 While the methyl asparagusic acid-derived hydrogels are highly dyn

83 Here, we present Methyl Assignment by Graph Matching (MAGMA), for the aut

84 ocine ring and an unprecedented 2-dimethyl-3-methyl-azetidine ring.

85 ,12-dioxoolean-1,9-dien-28-oate [bardoxolone-methyl (Bar-Me)] and methyl 2-trifluoromethyl-3,11-dioxo

86 Based on laboratory studies, we report that methyl benzoate (MB), a naturally-occurring compound in

87 Treatment of HSV-1-infected Vero cells with methyl beta-cyclodextrin from 2 to 9 h postentry reduced

88 and increased to approximately 79 pN/mum by methyl-beta-cyclodextrin treatment to sequester membrane

89 chromium (VI) and organic pollutants (using methyl blue (MB) as an example) removal, and the removal

90 Thermolysis of the methyl-borylamide (NacNac(NMe2))Sc(Me){NHB(NAr'CH)2} (18

91 lectivity for forming products with an alpha-methyl branch using a propionyl-CoA extender unit.

92 ed cavity that facilitates binding of the C2 methyl branch.

93 hed and abandoning gas fumigation containing methyl bromide resulted in the recurrence of an almost f

94 This is related to a different gas product (methyl bromide, MeBr) removal mechanism, changing from c

95 renoid diphosphates, such as (E)-4-hydroxy-3-methyl-but-2-enyl diphosphate (HMBPP), are ligands of th

96 vitamin C from day 0 to day 6 of storage (3-methyl butane nitrile) and temperature (limonene) are id

97 hosphate (N(2) -alkyl-dGTP) derivatives with methyl, butyl, benzyl, or 4-ethynylbenzyl substituents w

98 enone 1,2-addition of a new TEMPO carbamate methyl carbanion.

99 d with a second peripheral (4-chlorobiphenyl)methyl (CBP) addition to the vancomycin disaccharide to

100 Xanthan, locust bean, guar and carboxy methyl cellulose significantly enhanced Bostwick consist

101 ifferent ingredients (guar, xanthan, carboxy methyl cellulose, locust bean gums, potato fiber, milk,

102 using ground-based measurements of methane, methyl chloroform, and the C(13)/C(12) ratio in atmosphe

103 Methyl-coenzyme M reductase (MCR), found in strictly ana

104 NMR correlations, we have identified novel N-methyl-containing amines and amides, primary amides, and

105 der caused by mutations in the gene encoding methyl CpG binding protein 2 (MeCP2) that occur sporadic

106 n the gene encoding the transcription factor Methyl CpG Binding Protein 2 (MECP2).

107 rodevelopmental disorder in which the MECP2 (methyl CpG-binding protein 2) gene is mutated.

108 Here, we focus on methyl-CpG binding protein 2 (MECP2) restoration for RTT

109 Methyl-CpG binding proteins play an essential role in tr

110 Proteins containing a methyl-CpG-binding domain (MBD) bind methylated DNA and

111 In the presence of the MeCP2 methyl-CpG-binding domain (MBD), however, DNA methylatio

112 Suppressor of Mek null (Smek) interact with methyl-CpG-binding domain 3 (Mbd3) and the complex plays

113 Mutations in the X-linked gene encoding methyl-CpG-binding protein 2 (MeCP2) cause Rett syndrome

114 isorder caused primarily by mutations in the methyl-CpG-binding protein 2 (MECP2) gene, which encodes

115 The methyl-CpG-binding protein 2 (MeCP2) protein is an epige

116 The Rett-syndrome-associated methyl-CpG-binding protein 2 (MeCP2) selectively binds m

117 The TET enzymes catalyze conversion of 5-methyl cytosine (5mC) to 5-hydroxymethyl cytosine (5hmC)

118 Here, we examine the genome-wide, C(5) -Methyl-cytosine (m5C) methylome and its correlation to g

119 DNA cytosine methylation and methyl-cytosine binding domain (MBD) containing proteins

120 ific DNA methyl transferases and spontaneous methyl-cytosine deamination.

121 The activation of the N-methyl D-aspartate receptor (NMDAR) is controlled by a g

122 KYNA depletion then leads, in an N-methyl D-aspartate receptor (NMDAR)-dependent manner, to

123 vel glutamatergic compound that acts as an N-methyl-D-aspartate (NMDA) modulator with glycine-like pa

124 ethyl-4-isoxazole propionic acid (AMPA) to N-methyl-D-aspartate (NMDA) ratios, and matrix metalloprot

125 ne) has been used successfully to quantify N-methyl-d-aspartate (NMDA) receptor binding in humans.

126 nic motoneuron expression of glutamatergic N-methyl-D-aspartate (NMDA) receptors and decreased expres

127 N-methyl-d-aspartate (NMDA) receptors are glutamate- and g

128 Activation of extrasynaptic N-methyl-d-aspartate (NMDA) receptors causes neurodegenera

129 netic approaches, we find that ablation of N-methyl-D-aspartate (NMDA) receptors during postnatal dev

130 Competitive antagonists against N-methyl-D-aspartate (NMDA) receptors have played critical

131 totoxicity, mediated by overstimulation of N-methyl-D-aspartate (NMDA) receptors, is a mechanism that

132 aocular) unimNPs with the glutamate analog N-methyl-d-aspartate (NMDA), which is excito-toxic and ind

133 subset of antibody-positive patients, anti-N-methyl-d-aspartate receptor (5 patients), had normal MRI

134 nd are linked to underlying dysfunction of N-methyl-D-aspartate receptor (NMDAR)-mediated neurotransm

135 tibodies-especially antibodies against the N-methyl-D-aspartate receptor (NMDAR)-more commonly than d

136 N-methyl-D-aspartate receptor activation requires the bind

137 ggests a single sub-anesthetic dose of the N-methyl-D-aspartate receptor antagonist ketamine may work

138 The N-methyl-D-aspartate receptor hypofunction model of schizo

139 ations for understanding D-serine-mediated N-methyl-D-aspartate receptor plasticity in the amygdala a

140 ct subdivisions of ACC with different AMPA/N-methyl-D-aspartate receptor profiles.

141 st common and was predicted best when both N-methyl-D-aspartate receptor-IgG and aquaporin-4-IgG coex

142 ferences in the pharmacological profile of N-methyl-d-aspartate receptors (NMDAR) in the NAc core, TL

143 interaction between synaptic activation of N-methyl-D-aspartate receptors (NMDARs) and intrinsic osci

144 synaptic accumulation of GluN2B-containing N-methyl-D-aspartate receptors (NMDARs) and pathological p

145 N-methyl-D-aspartate receptors (NMDARs) are glycoproteins

146 N-methyl-d-aspartate receptors (NMDARs) are heterotetramer

147 The significant role played by N-methyl-d-aspartate receptors (NMDARs) in both the pathop

148 ent firing of 'Delay cells' is mediated by N-methyl-d-aspartate receptors and weakened by cAMP-PKA-po

149 of both alpha7 nicotinic acetylcholine and N-methyl-D-aspartate receptors.

150 nic state in vitro and in vivo after NMDA (N-methyl-d-aspartate) damage in young mice.

151 ited by MK-801, a specific pore blocker of N-Methyl-D-aspartic acid receptor (NMDAR) channels, and th

152 By measuring N-methyl-d-aspartic acid receptor (NMDAR)-driven calcium r

153 henylalanine-derived tetramic acid and (R)-2-methyl-deca-6E,8E-dienal.

154 N1-methyl-deoxyadenosine (1-MeA) is formed by methylation o

155 were the 6-methoxy, 6-methylsulfanyl, and 6-methyl derivatives, which were highly active to cancer c

156 Once deposited, mCA is bound by the methyl-DNA-binding protein MECP2 and functions in a rheo

157 Maintenance of proper levels of the methyl donor S-adenosylmethionine (SAM) is critical for

158 tion with S-adenosylmethionine, the reactive methyl donor, and by reaction with alkylating agents.

159 urthermore, bacterially induced reduction of methyl-donor availability influenced global DNA methylat

160 ices based on [6,6]-phenyl-C61 -butyric acid methyl ester (PC61 BM).

161 yl-thiophene) (P3HT)-phenyl-C61-butyric acid methyl ester (PCBM) mixture, and found to predict morpho

162 matic polyketide natural product zincophorin methyl ester has attracted significant attention from sy

163 ide synthase with N(omega) -nitro-l-arginine methyl ester.

164 400 admixture combinations for the oxidative methyl esterification of 1-octanol at 60 degrees C in me

165 ethane" ((13)C-TrEnDi), which results in the methyl esterification of all acidic sites and the conver

166 t are highly effective for aerobic oxidative methyl esterification of primary alcohols.

167 L/h and a process yield of 0.27 g-fatty acid methyl esters/g-glucose, which constitutes a 25% improve

168 er 3-(1H-imidazol-4-yl)propyl-(4-iodophenyl)-methyl ether (iodoproxyfan), which are strongly consiste

169 a blend formation with poly(ethylene glycol) methyl ether (mPEG) to prevent its leaching out from the

170 ortho-, meta- and para-Hydroxymethylaniline methyl ethers 3-5-OMe and acetyl derivatives 3-5-OAc wer

171 solvent free strategy to functionalize aryl methyl ethers through direct nucleophilic substitution o

172 ludes the use of benzyl methyl ethers, vinyl methyl ethers, and unbiased anisole derivatives, thus re

173 wide scope, which includes the use of benzyl methyl ethers, vinyl methyl ethers, and unbiased anisole

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

175 The hormone methyl farnesoate binds to the MfR to regulate various a

176 methyl farnesoate, and that the presence of methyl farnesoate stimulates dissociation of Met multime

177 highly dynamic in controlling the action of methyl farnesoate through temporal variation in its expr

178 et proteins self-associate in the absence of methyl farnesoate, and that the presence of methyl farne

179 mM s(-1) on para-nitrophenyl-acetate, and on methyl-ferulate, the value was 27 times higher.

180 The aryl/methyl fragmentation selectivities for phenyltrimethylst

181 mpounds, carotenoids, organic acids, hydroxy methyl furfural (HMF) and other quality parameters of to

182 tigated in the presence of gallic acid (GA), methyl gallate (MG), MG/GA combinations (75:25, 50:50, a

183 zylglutathione cyclopentyl diester (pBBG) or methyl-gerfelin (MeGFN)) reduced immobility in the TST a

184 bone H-bond impairing modifications (alpha)N-methyl Gln or l-Pro at key positions within betaHP.

185 Subsequent introduction of the methyl group and functional group transformation complet

186 cence and excellent photostability, (b) an N-methyl group at each end of the squaraine core that ensu

187 hat results from the enzymatic addition of a methyl group at the fifth carbon of the cytosine base.

188 Conversely, the introduction of a methyl group at the methylene hinge connecting the 6-ami

189 hen compared to the analogous dye containing methyl group away from donor.

190 the KMT family catalyze the transfer of the methyl group from S-adenosylmethionine (SAM) to lysine r

191 rom the beta-position of the thiazole to the methyl group in the product.

192 isotope effect), whereas deuteration of the methyl group induces a normal secondary isotope effect.

193 horizontal lineNTol species deprotonates the methyl group of the NacNac ligand.

194 pulsive force and presence of the additional methyl group on the backbone.

195 A dye containing methyl group on the donor side exhibited blue shift in a

196 y to overcome this obstacle is to remove the methyl group on these modified bases prior to cDNA synth

197 ed set of genes encoding the upper branch of methyl group oxidation to CO2 as well as membrane-bound

198 substitution at a bridgehead position with a methyl group produced a quadricyclane that thermally rev

199 rsible synthesis of acetyl-CoA from CO and a methyl group through a series of nickel-based organometa

200 al SAM enzyme catalyzing the conversion of a methyl group to a t-butyl group.

201 only catalyzes sequential methylations of a methyl group to form ethyl and isopropyl groups but rema

202 cterized protein that oxidizes the pyocyanin methyl group to formaldehyde and reduces the pyrazine ri

203 Methyltransferases add a methyl group to mRNA while demethylases remove methyl gr

204 st likely be attributed to the exchange of a methyl group.

205 lex regulatory feedback network between free methyl groups and genomic imprinting at birth.-Tserga, A

206 (SAM), which is the major cellular donor of methyl groups for protein modification.

207 The nitroxides are designed to have the methyl groups further away from the N-O spin site to dec

208 possesses four mPEG-3 groups replacing four methyl groups in the tert-butyl groups at the 3- and 6-p

209 he distance between the nitroxide moiety and methyl groups is effective in lengthening Tm at T > 70 K

210 acking motif with the electron-poor ammonium methyl groups occupying the electron-rich cavity of the

211 ivities by functionalization of enantiotopic methyl groups under mild conditions.

212 The angular methyl groups were attached by electrophilic cyclopropan

213 m (1)H/(13)C NMR probes at isoleucine delta1 methyl groups, which facilitated (1)H/(13)C methyl TROSY

214 thyl group to mRNA while demethylases remove methyl groups.

215 the fast and reversible deuteration of the 2-methyl H of the imidazolium cation followed by D transfe

216 ard selective monohalogenation of methane to methyl halides or their in situ oligomerization to highe

217 All four esters (methyl, hexyl, dodecyl and octadecyl dihydrocaffeates) e

218 xytyrosol and its biological metabolite, 3-O-methyl-hydroxytyrosol, also known as homovanillyl alcoho

219 tions with methane that result in a discrete methyl intermediate where the formal oxidation state (FO

220 Methyl iodide is a toxic halocarbon with diverse industr

221 tes from the corresponding alpha-substituted methyl iodides.

222 Samples were diluted in methyl isobutyl ketone.

223 des along with their (omega)-linked or alpha-methyl isomers and ethanolamide derivatives, as well as

224 oliar applications of phenylalanine (Phe) or methyl jasmonate (MeJ) could improve the synthesis of se

225 Exposure to methyl jasmonate (MeJA) and methyl salicylate (MeSA) vap

226 tebark pine needle transcriptomes, following methyl jasmonate (MeJA) treatment using RNA-seq.

227 on whitebark pine needles demonstrated that methyl jasmonate (MeJA)-triggered transcriptome re-progr

228 ichomes under normal conditions, addition of methyl jasmonate, a biotic stress hormone, induced expre

229 neral process that involved a 12,13-olefinic methyl ketone as a starting material obtained by ozonoly

230 me c by replacing tyrosine 48 with p-carboxy-methyl-l-phenylalanine (pCMF).

231 lvement, Wistar rats were treated with alpha-methyl-L-tyrosine and tyrosol.

232 By combining the use of highly methyl-labeled protein with experimentally determined in

233 nt cysLT) or the selective CysLT2R agonist N-methyl LTC4 to allergen sensitized wild-type mice marked

234 os, pups and dams were collected for choline/methyl metabolite measurements, immunoblotting or gene e

235 r materials calcium sulfate (CaSO4) and poly methyl methacrylate (PMMA).

236 ased monomers and the photopolymerization of methyl methacrylate and made it possible to determine th

237 ulk polymerization using methacrylic acid or methyl methacrylate as monomer and ethylene glycol dimet

238 0 succinate (TPGS), Polysorbate 80, and poly(methyl methacrylate) (PMMA) as analytes.

239 ces, i.e., nitrocellulose, polystyrene, poly(methyl methacrylate), and poly(butyl methacrylate), poly

240 noethyl methacrylate, butyl methacrylate and methyl methacrylate, E) to enhance vancomycin encapsulat

241 e determined the mutation spectrum caused by methyl methanesulfonate (MMS), and showed that MMS also

242 oped in this study, the reactivity between S-methyl methanethiosulfonate (MMTS) with persulfide was u

243 of new compounds like pentadecanoicacid; 14-methyl-methylester etc.

244 el human mitochondrial KMT that introduces a methyl modification into a metabolic enzyme and whose ac

245 distinct viral life cycles, the role of 2' O-methyl modifications in RNA stability and innate immune

246 N)2Cu(II)2(O2(2-))](2+) ((S)P(MeAN), MeAN: N-methyl-N,N-bis[3-(dimethylamino)propyl]amine) that featu

247 To date, a single molecule, 4-methyl-N-9H-xanthen-9-yl-benzenesulfonamide (AH-7614), h

248 Using N-methyl-N-nitro-N-nitroso-guanidine mutagenesis and selec

249 an active component of Cassia seed, in an N-methyl-N-nitrosourea (MNU)-induced mouse model of RP.

250 An efficient synthesis of methyl nicotinates/6-halonicotinates by the domino isome

251 The reactions of nitramine, N-methyl nitramine, and N,N-dimethyl nitramine with anhydr

252 We present methyl NMR analysis of the BiP chaperone cycle that reve

253 ethyl, and < LOD to 0.8 ng/m(3) for azinphos-methyl-oxon.

254 Triclosan, methyl paraben, and propyl paraben concentrations were q

255 s sp. based optical microplate biosensor for methyl parathion (MP) was good as it detected multiple s

256 on, thiamethoxam, trifluralin, carbaryl, and methyl parathion.

257 d 21 healthy individuals (HC) received alpha-methyl-paratyrosine (AMPT) over 24 h to achieve catechol

258 )F-fluoronicotinamid o)butanamido)butanamido)methyl)phenyl)-3-(naphthalen-2-ylmethyl)-1,4,12-trioxo-2

259 In nitrogen, protonated forms of dimethyl methyl phosphonate (DMMP) and methyl phosphonic acid (MP

260 ile, dimethyl methylphosphonate, diisopropyl methyl phosphonate in positive polarity and carbon dioxi

261 ms of dimethyl methyl phosphonate (DMMP) and methyl phosphonic acid (MPA) exhibit the reduced mobilit

262 is worldwide, produces a CPS with a unique O-methyl phosphoramidate (MeOPN) modification on specific

263 hin in the muscle of mdx mouse through a 2'O-methyl phosphorothioate-mediated splicing modulation.

264 bPs, [3-(guanine-9-yl)-2-((2-phosphonoethoxy)methyl)propoxy]methylphosphonic acid, exhibited Ki value

265 nt couplings of the unpaired electron to the methyl protons that shorten Tm at T > 70 K in currently

266 sence of six odour-active compounds, being 2-methyl pyrazine the key aroma compound of this beverage.

267 rded compound 11 (N-[(1-benzyl-1H-indol-3-yl)methyl]pyridin-3-amine, VA012), which exhibited dose-dep

268 and (R)-2-(1-((2,3-dihydro-1H-imidazol-2-yl)methyl)pyrrolidin-3-yl)-5-fluoro-1H-benzo [d]imidazole (

269 trapyrrole that promotes catalysis through a methyl radical/Ni(ii)-thiolate intermediate.

270 The discovery of extremely halophilic, methyl-reducing methanogens related to haloarchaea provi

271 rometry (MS)-assisted strategy to assign the methyl resonances of methionine residues is presented.

272 ing (MAGMA), for the automatic assignment of methyl resonances.

273 The MBs are composed of 2'-O-methyl RNAs with a fully phosphorothioate-modified loop

274 idual components elicited varying responses; Methyl salicylate (MeSA) elicited the highest positive c

275 Exposure to methyl jasmonate (MeJA) and methyl salicylate (MeSA) vapours at 10 and 100micromoll(

276 nene, 2-methoxy-3-(1-methylpropyl)-pyrazine, methyl salicylate and tridecane.

277 2 to acetophenone was reduced, while that to methyl salicylate did not change.

278 phenolics, glucosinolates, sulphoraphane, Se-methyl selenocysteine and myrosinase in broccoli.

279 e genome-wide DNA methylation analysis using methyl-sequencing to measure changes between normal and

280 iloxane (D5, C10H30O5Si5), a cyclic volatile methyl siloxane (cVMS) found in consumer products, was s

281 Cyclic volatile methyl siloxanes (cVMS) are emitted to aquatic environme

282 factor S-adenosyl-l-Methionine (AdoMet) as a methyl source.

283 than that for the quadricyclane without the methyl substituent.

284 of which JJC8-016 (N-(2-((bis(4-fluorophenyl)methyl)thio)ethyl)-3-phenylpropan-1-amine) was selected

285 , but lengthening the amine substituent from methyl to ethyl, propyl, and butyl produced a stepwise d

286 o catalyze unconventional reactions, such as methyl transfer to electrophilic carbon atoms, sulfur to

287 ue of VTE4 (which encodes a gamma-tocopherol methyl transferase converting gamma-tocopherol into alph

288 an et al. found that mutation of the histone methyl transferase SEDT2 affects alternative splicing fa

289 ed that copy number elevations of catechol-O-methyl-transferase (COMT) or Tbx1, two genes encoded in

290 rRNA 2'-O-Me globally by inhibiting the rRNA methyl-transferase fibrillarin in human cells.

291 millions of years, driven by CG-specific DNA methyl transferases and spontaneous methyl-cytosine deam

292 ), acyl transfers (acetyl-CoA, carbamoyl-P), methyl transfers (SAM), prenyl transfers (IPP), glucosyl

293 Using methyl transverse relaxation-optimized NMR spectroscopy,

294 midate salt protecting strategy that employs methyl trifluoromethanesulfonate as a reversible alkylat

295 methyl groups, which facilitated (1)H/(13)C methyl TROSY NMR measurements with opposing ligands.

296 Here we report a methyl-TROSY based solution NMR study showing that the E

297 Methyl-TROSY-based NMR studies have previously revealed

298 By using methyl viologen (N,N'-dimethyl-4,4'-bipyridinium) to shu

299 chlorpyrifos and 35% of samples for azinphos-methyl were > LOD.

300 rein are the naturally occurring benzofurans methyl wutaifuranate, wutaifuranol, wutaifuranal, their