ライフサイエンスコーパス: dimethylamine

1 CoM methylation with monomethylamine but not dimethylamine.

2 ted methyl-CoM formation from both mono- and dimethylamine.

3 se that converts metformin to guanylurea and dimethylamine.

4 ations of sulphuric acid, water, ammonia and dimethylamine.

5 y catalyses the NADPH-dependent oxidation of dimethylamine.

6 nzymes that hydrolyze ADMA to citrulline and dimethylamine.

7 alyte to the boron center and elimination of dimethylamine.

8 nt of a propargylic azide in the presence of dimethylamine.

9 on was applied to remove the main byproduct, dimethylamine.

10 hylate coenzyme M during methanogenesis from dimethylamine.

11 was optimal for coenzyme M methylation with dimethylamine.

12 dimethylamine and formaldehyde (1 TMAO --> 1 dimethylamine + 1 formaldehyde), confirming that it enco

13 and acetate) and 8 significantly decreased (dimethylamine, 4-DTA, creatinine, ascorbate, 2-hydroxyis

14 ylaminopropylamine-amidoamine-oleamidopropyl dimethylamine, alkyl glucosides, budesonide-hydrocortiso

15 The dimethylamine analogue LY333531 (1), (S)-13-[(dimethylam

16 In pH 7-10 waters amended with 10 uM total dimethylamine and 800 ueq Cl(2).L(-1) dichloramine (NHCl

17 ioxide to methanol via tandem catalysis with dimethylamine and a homogeneous ruthenium complex.

18 Thus, BDMA is thought to be transformed to dimethylamine and benzoic acid via debenzylation.

19 ynthesis of N,N-dimethylformamide (DMF) from dimethylamine and CO(2)/H(2) via blocking reaction pathw

20 mbinant Escherichia coli can convert TMAO to dimethylamine and formaldehyde (1 TMAO --> 1 dimethylami

21 tive demethylation of trimethylamine to form dimethylamine and formaldehyde.

22 herically important trimethylamine (TMA) and dimethylamine and generalized by the study of the larger

23 and catalyzes the hydrolysis of metformin to dimethylamine and guanylurea with a catalytic efficiency

24 was maintained in the presence of a benzylic dimethylamine and hydrosilanes, overriding the establish

25 Both dimethylamine and isopropylamine volatilized when aqueou

26 pathways for the ammonolysis of glyoxal with dimethylamine and methylamine by using metadynamics simu

27 ater dimer for the reactions of glyoxal with dimethylamine and methylamine display the lowest free en

28 roplet ammonolysis reactions of glyoxal with dimethylamine and methylamine were more feasible and occ

29 The mtbA gene was required for dimethylamine and monomethylamine (MMA) utilization and

30 itiating methanogenesis from trimethylamine, dimethylamine and monomethylamine possess a novel residu

31 These results indicate MtbB1 demethylates dimethylamine and specifically methylates the corrinoid

32 esis of N,N-dimethylaniline derivatives from dimethylamines and aryl triflates.

33 ween cis and trans compounds or between N, N-dimethylamines and primary amines.

34 The release was initiated by a mild base, dimethylamine, and accelerated by microwave radiation.

35 e, 2-oxoglutarate, valine, maltose, leucine, dimethylamine, and choline with high VIP scores could di

36 bstitutions include the C2 primary amide, C4 dimethylamine, and the C12a tertiary alcohol.

37 and 20a-c with liquid ammonia, methylamine, dimethylamine, and thiourea furnished several interestin

38 ve chemotactic responses toward methylamine, dimethylamine, and trimethylamine but did not display si

39 We find that methylamine, dimethylamine, and trimethylamine undergo molecular chem

40 of water molecules to ammonia, methylamine, dimethylamine, and trimethylamine, and their respective

41 on from: methanol, acetate, monomethylamine, dimethylamine, and trimethylamine.

42 for select VOCs including dimethyl sulfide, dimethylamine, and trimethylamine.

43 dimethylamido ligands, which are retained as dimethylamines, and generation of a titanium imido compl

44 para-Dimethylamine- and para-pyrrolidine-substituted arylazop

45 have also been determined for methylamine-, dimethylamine-, and trimethylamine-borane, Me(n)H(3-n)N.

46 lus methylotrophus that has been grown up on dimethylamine; and (e) a discrete inhibitory substrate-b

47 ndicate that carbon dioxide, methylamine and dimethylamine are major degradation products of glyphosa

48 DMA(x) PbI(3) (MA is methylamine and DMA is dimethylamine) are defect density and carrier recombinat

49 The increase in dimethylamine arises entirely from enthalpy, contrary to

50 When generated in dimethylamine as solvent, the carbene undergoes preferre

51 t stabilizing species, including ammonia and dimethylamine, as well as oxidation products of pinanedi

52 ent methylation of CoM and the production of dimethylamine at specific activities of up to 600 nmol/m

53 r at the 6-position and a secondary amide of dimethylamine at the 2'-position.

54 nthracyclines, and structures containing N,N-dimethylamine at the reducing sugar prove that are more

55 ic acid together with two bases (ammonia and dimethylamine), at the CLOUD chamber at CERN.

56 und to increase the basicity of methylamine, dimethylamine, benzylamine, and N,N-dimethylaniline.

57 und to increase the basicity of methylamine, dimethylamine, benzylamine, N,N-dimethylaniline, 2-methy

58 ction of (NHC)Mg(N(SiMe(3) )(2) )(2) (1) and dimethylamine borane yields the tris(amide) adduct (NHC-

59 e2](-), MgAB) is prepared by the reaction of dimethylamine-borane with methylmagnesium chloride.

60 cules methylamine-borane, MeH(2)N.BH(3), and dimethylamine-borane, Me(2)HN.BH(3), have been investiga

61 re generated by hydride abstraction from N,N-dimethylamine boranes Ar(CH(2))(n)NMe(2)BH(3) using Ph(3

62 xpressed at low levels on methanol, TMA, and dimethylamine but was significantly upregulated on monom

63 Facile acetylation of dimethylamine by acetaldehyde occurs with high selectivi

64 tor/mol of 24-kDa polypeptide and stimulated dimethylamine:coenzyme M methyl transfer 3.4-fold in a c

65 icated high specificity of MtbB1 and MtbC in dimethylamine:coenzyme M methyl transfer activity.

66 nsfer reaction replaced proteins involved in dimethylamine:coenzyme M methyl transfer indicated high

67 e the sole protein requirements for in vitro dimethylamine:coenzyme M methyl transfer.

68 ray diffraction analysis of select mono- and dimethylamine containing phases suggests that the number

69 Although the molar NDMA yields from five N,N-dimethylamine-containing precursors varied between 1.4%

70 tbC and MtbA were used to assay and purify a dimethylamine:corrinoid methyltransferase, MtbB1.

71 (MA) and ammonia (AM) with MG, but not from dimethylamine (DA) with the MG mixture under acidic cond

72 indicating MtbB1 carries an active site for dimethylamine demethylation and corrinoid methylation.

73 hase (cesium iodide, glycine) and gas-phase (dimethylamine, dimethylnapthylamine) analytes as well as

74 n applied at an equimolar molar ratio, while dimethylamine (DMA) allowed neutral dicamba to remain de

75 e the concentration of trimethylamine (TMA), dimethylamine (DMA) and methylamine (MA) in fish.

76 eir decomposition products reacting with (i) dimethylamine (DMA) and/or (ii) chlorinated unsymmetrica

77 During ozonation tests in DI water using dimethylamine (DMA) as model precursor, the NDMA yield s

78 ric acid (SA) concentrations the presence of dimethylamine (DMA) at mixing ratios of several parts pe

79 ines by forming adduct ions that have lost a dimethylamine (DMA) molecule ([M + H + TDMAB - HN(CH(3))

80 zonolysis of alpha-pinene in the presence of dimethylamine (DMA) was investigated in a flow tube reac

81 The bonding of the trimethylamine (TMA) and dimethylamine (DMA) with crystalline silicon surfaces ha

82 and secondary alkylamines: methylamine (MA), dimethylamine (DMA), and ethylamine (EA), have been dete

83 Both the initial products decompose to dimethylamine (DMA), and the mechanism of further decomp

84 lization from solid (BAMPA) on glass as with dimethylamine (DMA), diglycolamine (DGA), and N,N-bis(3-

85 reactions of MSA with trimethylamine (TMA), dimethylamine (DMA), methylamine (MA), and ammonia over

86 retinol, essential fatty acids, methionine, dimethylamine (DMA), trimethylamine, and trimethylamine-

87 including ammonia (NH(3)), amines (including dimethylamine, DMA, and diethylamine, DEA), alkyl nitrat

88 (NPh)(dpma)](2) (3) on removal of the labile dimethylamine donors.

89 of this parent fluorophore by replacing its dimethylamine electron-donating group with conformationa

90 m chloride) (polyDADMAC) and epichlorohydrin-dimethylamine (Epi-DMA), are commonly used by water util

91 shown that the organic cations methylamine, dimethylamine, ethylamine, and trimethylamine are permea

92 An N,N-Dimethylamine ethylimino-appended triazole-linked calix[

93 flow protocol for the in situ generation of dimethylamine from DMF followed by nucleophilic aromatic

94 ncluding glucose, leucine, choline, betaine, dimethylamine, fumaric acid, citric acid, 3-hydroxyisova

95 ylate takes the place of the more common C-4 dimethylamine functionality, making SsfX3 the first acyl

96 and nucleophilic aromatic substitution with dimethylamine gave puromycin aminonucleoside [9-(3-amino

97 the stoichiometric removal of one O2 per N,N-dimethylamine group of the precursor indicating that the

98 site of protonation (opposite the auxiliary dimethylamine group), the geometry of the hydrazone (E),

99 base catalysis from ammonia, methylamine and dimethylamine have been examined.

100 centrations of taurine, creatinine, adenine, dimethylamine, histidine, N-Acetyl aspartate, and glucos

101 -oxides, amides, and some amines via loss of dimethylamine in a Fourier transform ion cyclotron reson

102 n derived from the study of acetaldehyde and dimethylamine in combination with previous work, allowin

103 Induction of frmRAB, detection of dimethylamine in culture medium and formaldehyde product

104 noid bound to MtbC or free cob(I)alamin with dimethylamine, indicating MtbB1 carries an active site f

105 ency concurrent with facile incorporation of dimethylamine into the former O-linked sites.

106 The neutral loss of dimethylamine is also observed.

107 Instead, surprisingly, (azidomethyl)dimethylamine is generated with good reproducibility.

108 The dimethylamine is proposed to play a dual role in this sy

109 the experiments involving sulfuric acid and dimethylamine, it was possible to study the appearance t

110 onths of storage, while choline derivatives, dimethylamine, lactate, and most of the free amino acids

111 betaine (LAPB) (1% aq.); and lauramidopropyl dimethylamine (LAPDMA) (0.05% aq.), which is an impurity

112 gut microbiota (lower choline, betaine, and dimethylamine levels in PBC) were significantly differen

113 yhippuric acid, and decreased creatinine and dimethylamine levels were the major explanations for the

114 (2)O production rates ranked in the order of dimethylamine < methylamine < ammonia and decreased with

115 ighly mass efficient (PMI = 9.1), and excess dimethylamine may be recovered (93% recovery, 51% decrea

116 Etn, MeEtn, Me2Etn, methylamine (MeNH2), and dimethylamine (Me2NH) were studied.

117 thanol, acetone, formaldehyde, dibutylamine, dimethylamine, methylamine, carbon monoxide, and nitroge

118 -2, 3-dihydro-1H-benzoimidazol-2-yl) phenyl) dimethylamine (N-DMBI) (-2.36 eV), which can result in a

119 hyl-2,3-dihydro-1H-benzoimidazol-2-yl)phenyl)dimethylamine (N-DMBI), the highest thermoelectric perfo

120 hyl-2,3-dihydro-1H-benzoimidazol-2-yl)phenyl dimethylamine (N-DMBI-H), and augmented with density fun

121 substitution with four different amines: N,N-dimethylamine, N-methylamine, ammonia, and morpholine.

122 channel that contains a bound n-dodecyl-N,N-dimethylamine-N-oxide detergent molecule.

123 ractions are enhanced in LDAO (n-dodecyl-N,N-dimethylamine-N-oxide), whereas the interaction of AmtB-

124 be blocked by the addition of n-dodecyl-N,N-dimethylamine-N-oxide.

125 rization function (GP(ex)) of 6-dodecanoyl-2-dimethylamine-naphthalene (LAURDAN), which is sensitive

126 state-of-the-art descriptions of ammonia and dimethylamine new particle formation (NPF) pathways and

127 Monomethylamine (NH(2)CH(3)), dimethylamine (NH(CH(3))(2)), and trimethylamine (N(CH(3

128 Neither dimethylamine nor monomethylamine served as the substrat

129 Cross-linkers optimally possessed tertiary dimethylamine or piperazine groups and potential bufferi

130 itiating methanogenesis from trimethylamine, dimethylamine, or monomethylamine by various Methanosarc

131 mega-bromo groups with ammonia, methylamine, dimethylamine, or trimethylamine provided peptides conta

132 ting methane formation from monomethylamine, dimethylamine, or trimethylamine, respectively, in certa

133 erases with specificity for monomethylamine, dimethylamine, or trimethylamine.

134 Inclusion of the detergent lauryl dimethylamine oxide (LDAO) improves protease and helicas

135 espond differently in the presence of lauryl dimethylamine oxide (LDAO) in the assay medium.

136 during assay, and less stimulated by lauryl dimethylamine oxide (LDAO).

137 ases containing ammonium acetate with lauryl-dimethylamine oxide are most universal for characterizin

138 displays a far-UV CD spectrum (in 1% lauryl dimethylamine oxide at pH 6-8) similar to that of bacter

139 oxide, whereas this concentration of lauryl dimethylamine oxide inhibits the mutant complex by 25%.

140 resence of the zwitterionic detergent lauryl dimethylamine oxide, increasing concentrations of urea r

141 complex is stimulated 4-fold by 0.1% lauryl dimethylamine oxide, whereas this concentration of laury

142 ction of the resultant epoxycarbinol 32 with dimethylamine produced the aminohydroxy pyranose 33a.

143 The specific chemicals included 2,4-D dimethylamine salt, methomyl, imidacloprid, and alpha-(p

144 The introduction of a dimethylamine side chain has significantly enhanced the

145 electron-donating hydroxyl groups in the N,N-dimethylamine side chain.

146 Using a dimethylamine substituent as a reporter, DeltaG(*) was m

147 esulting from a loss of conjugation with the dimethylamine substituent.

148 The dimethylamine substrate forms part of a highly polarized

149 eversibly bind large quantities of mono- and dimethylamine through framework-to-coordination polymer

150 Methyl transfer from dimethylamine to coenzyme M was reconstituted in vitro f

151 cell extracts to convert monomethylamine and dimethylamine to methyl-CoM was lost almost entirely by

152 and (iii) peroxynitrite reaction with total dimethylamine (TOTDMA) to NDMA or decomposition to nitri

153 We found that dimethylamine, triethylamine, tetraethylammonium, tetrab

154 N-Nitroso-dimethylamine was detected in all examined products in t

155 Acetate, butyrate and propionate along with dimethylamine were important for the distinction between

156 e, but levels of hippurate, methylamine, and dimethylamine were not significantly lower in patients w

157 dant oxidation products of alpha-pinene, and dimethylamine were selected to study the formation of N-

158 200 ms) due to the reaction with eliminated dimethylamine, which acts as a nucleophile in the case o

159 enamine derived from phenylacetaldehyde and dimethylamine with 2-cyclohexenone to give a mixture of

160 al studies of the reaction of piperidine and dimethylamine with the same aryl halides using the polar