ライフサイエンスコーパス: ethylamine

1 midite ligand derived from (R)-1-(2-naphthyl)ethylamine.

2 ds great promise for practical production of ethylamine.

3 the auxiliary is S-(6-methoxynaphth-2-yl)-1-ethylamine.

4 s coupled with their further inactivation by ethylamine.

5 h pathways are unable to grow appreciably on ethylamine.

6 ergoes a nucleophilic addition by 1 equiv of ethylamine.

7 he K212Q enzyme is activated 4-fold by added ethylamine.

8 each component and by reducing the amount of ethylamine.

9 with a solution-phase nucleophile, ferrocene ethylamine.

10 nomalonate, 2-aminoisobutyrate, alanine, and ethylamine.

11 -substituted 3-[(N-Boc-2-carboxyethyl)phenyl]ethylamines.

12 )-3BrMBA(2)PbI(4) [3BrMBA = 1-(3-bromphenyl)-ethylamine].

13 tions of benzotriazole and 2-(pyrrol-1-yl)-1-ethylamine (1) with formaldehyde and glutaric dialdehyde

14 unds, such as N-monomethyl-2-(1-naphthyloxy)-ethylamine (11; Ki = 26 nM), that display significantly

15 ethoxy-phenyl)-ethyl]-tetrahydro-furan-2-yl}-ethylamine (14) and 2-{5-[3-(5-fluoro-2-methoxy-phenyl)-

16 thoxy-phenyl)-propyl]-tetrahydro-furan-2-yl}-ethylamine (15) were both individually linked to the PDE

17 lorophenyl)ethyl]-N-methyl-2-(1-pyrrolidinyl)ethylamine (2).

18 thesis of the marine sponge 2,3'-bis(indolyl)ethylamine (2,3'-BIEA) alkaloid ( )-gelliusine E was per

19 monohydrated cluster of 2-(2-fluoro-phenyl)-ethylamine (2-FPEA) by mass-selected resonance-enhanced

20 ctions of benzotriazole (4), 2-(arylsulfanyl)ethylamines 3, or 2-phenoxyethylamine (11) with 2,5-dime

21 Condensation of 2-(3-methyl-1H-indol-1-yl)ethylamine (7) with benzotriazole and formaldehyde gave

22 paeaH(2) bis(pyridyl-6-methyl-2-carboxylate)-ethylamine)), a ligand forming a stable soluble aqueous

23 ere treated with MTSEA (methanethiosulfonate ethylamine), a thiol-specific reagent that implants a po

24 nd the growth substrate was then switched to ethylamine, a condition where the cell must make a sudde

25 of sodium cyanide and (S)-1-(4-methoxyphenyl)ethylamine affords highly crystalline (S,S)-alpha-aminon

26 an internal (gamma-thialysine) or external (ethylamine) aldimine followed by the slow formation of t

27 sis (2.5- and 8-fold effects on k(cat) using ethylamine and benzylamine as substrates), the same muta

28 Unlike methylamine, the larger substrates ethylamine and benzylamine give normal turnover with E40

29 ansenula polymorpha (HPAO-1) in complex with ethylamine and benzylamine have been determined to resol

30 laced in an aqueous solution containing 2.8% ethylamine and heated to form nanometer-sized SiO2 parti

31 ecies does not react with phenylhydrazine or ethylamine and is stable toward pH buffer exchange, long

32 ed valine to protonated base for dimers with ethylamine and propylamine, respectively, from which a G

33 o mediate a memory response on reexposure to ethylamine and to secrete IFN-gamma in response to bacte

34 amine-functionalized TREN-bis(1,2-HOPO)-TAM-ethylamine and TREN-bis(1-Me-3,2-HOPO)-TAM-ethylamine li

35 ity of C-H bonds at the terminal position of ethylamines and ethers results from a combination of att

36 from pteroic acid, 2,2'-(ethylenedioxy)-bis(ethylamine), and t-Bu-protected DTPA.

37 cluding acetaldehyde, carbon dioxide, water, ethylamine, and other aldehyde- and imine-containing spe

38 yramine, p-methoxyphenethylamine, 2-(p-tolyl)ethylamine, and p-fluorophenethylamine generated the cor

39 organic cations methylamine, dimethylamine, ethylamine, and trimethylamine are permeant through the

40 ysed transamidation of gluten proteins using ethylamine as amine nucleophile, substantial amounts of

41 ues employing enantiopure (1-naphthalen-1-yl)ethylamine as chiral precursor are described.

42 s contracts with a decrease in k(cat) (using ethylamine as the substrate) of 125-fold.

43 rs and the amount of 2,2'-(ethylenedioxy)bis(ethylamine) as cross-linking reagent.

44 ragment identified, (S)-1-(4-isopropylphenyl)ethylamine, binds to the Lck SH2 domain better than the

45 paeaH(2)=bis(pyridyl-6-methyl-2-carboxylate)-ethylamine), biologically produced U(V) persisted in aqu

46 O)2(mu-OAc)](ClO4)2 (4, bpea = bis(2-pyridyl)ethylamine), [(bpea)2Mn2(IV/IV)(mu-O)2(mu-OAc)](ClO4)3 (

47 ialic acid) were coupled with 2-(dansylamido)ethylamine by reductive amination.

48 galactose) were modified with 2-(dansylamido)ethylamine by reductive amination.

49 silicon and germanium surfaces modified with ethylamine (CH(3)CH(2)NH(2)) and aniline (C(6)H(5)NH(2))

50 (STM) data for alpha-ketoester/1-(1-naphthyl)ethylamine complexes on Pt(111) reveal a tumbling motion

51 The tri(2-hexanamido)ethylamine core IL series proved to be very interesting

52 thylamine core, and (4) D = tri(2-hexanamido)ethylamine core; to which three identical imidazolium or

53 activity at 5HT(1B/1D) receptors than their ethylamine counterparts.

54 with exceptional affinity to tris-(triazole ethylamine) cryptophane, a previously unsynthesized wate

55 riments with deuterated N-nitroso-N-methyl-N-ethylamine demonstrated that the lower KIEs associated w

56 00-fold molar excess of methanethiosulfonate ethylamine, demonstrating that Cys(439) is either at the

57 : iodoacetamide (IAM), N,N-dimethyl-2-chloro-ethylamine (DML), and (3-acrylamidopropyl)-trimethyl amm

58 : methylamine (MA), dimethylamine (DMA), and ethylamine (EA), have been determined using the techniqu

59 ssivation molecules, 2,2'-(ethylenedioxy)bis(ethylamine) (EDA)-CDots and 3-ethoxypropylamine (EPA)-CD

60 alysts, Cu nanoparticles exhibit the highest ethylamine Faradaic efficiency (~96%) at -0.29 V versus

61 catalysts and discover Pd/C exhibits a 43.8% ethylamine Faradaic efficiency at the current density of

62 onstrated on Cu at 100 mA cm(-2) with an 86% ethylamine Faradaic efficiency.

63 ration, 2,6-diformylpyridine and 2,2'-oxybis(ethylamine) form a dynamic combinatorial library of at l

64 eacts at normal pressure with methylamine or ethylamine, forming N-alkylpyridinium salts.

65 the two series, as well as the fact that the ethylamine fragment in 2 approximates a gauche conformat

66 gulatory mechanisms controlling them, making ethylamine growth a useful condition to study the regula

67 he same relative reactivity of methylamine > ethylamine > ammonia.

68 > 1-propylamine > pyridine > triethylamine > ethylamine > methylamine > diethylamine > tert-butylamin

69 lorophenyl)ethyl]-N-methyl-2-(1-pyrrolidinyl)ethylamine) > 4-IPBS > haloperidol > (+)-pentazocine > D

70 h a flexible linker, 2,2'-(ethylenedioxy)bis(ethylamine), has been synthesized and characterized.

71 octanediamine, 2-[2-(2-amino-ethoxy)-ethoxy]-ethylamine, homospermidine, and homospermine covalently

72 he presence of l-alanine or of l-alanine and ethylamine in place of l-lysine.

73 Additionally, the inclusion of ethylamine in the reactions of K274A yields the N-ethyl

74 pea)(4)](n+) (bpea = N,N-bis(2-pyridylmethyl)ethylamine) in two oxidation states, Mn(IV)(4) and Mn(II

75 The transamination reaction of ethylamine is 75-fold slower than that of alanine.

76 time, the extent of reaction with ferrocene ethylamine is not homogeneous throughout the thickness o

77 d the 3-aminocyclobutyl group as a potential ethylamine isostere.

78 nzenesulfonyl)amino-N-(4-chlorocinnamyl)-N-m ethylamine (KN-93).

79 M-ethylamine and TREN-bis(1-Me-3,2-HOPO)-TAM-ethylamine ligands have been synthesized and attached to

80 )), but the pH-dependent coordination of the ethylamine moiety occurs in the pH range of 6-8 (log K(M

81 at the shifted modes are associated with the ethylamine moiety of R6G.

82 everal primary amines including methylamine, ethylamine, n-propylamine, n-butylamine, and 1,5-diamino

83 ctures (where M = Zn, Cd; Q = S, Se; and L = ethylamine, n-propylamine, n-butylamine, n-amylamine, n-

84 The adsorption of 1-(1-naphthyl)ethylamine (NEA) on platinum surfaces has been character

85 this effect is explored on a R-1-(1-naphthyl)ethylamine (NEA)-modified Pd(111) model catalyst where t

86 Levels of tryptamine and beta-phenyl-ethylamine never exceeded 50 and 29 mg/kg, respectively.

87 The use of a small primary amine such as ethylamine or bromoethylamine in the assay system leads

88 Ethylamine or methylamine chains were introduced at C2,

89 rophenoxy)propyl)-1,1-dimethyl-2-(2-nephthyl)ethylamine] or Ca(2+) (o) removal.

90 ed methylamine oxidation and Y305A-catalyzed ethylamine oxidation are comparable, while profiles of Y

91 Under optimal conditions, we achieve an ethylamine partial current density of 846 mA cm(-2).

92 using a new amine monomer, 2-(pyridyldithio)-ethylamine (PDA).

93 ethoxy-phenyl)-ethyl]-tetrahydro-furan-2-yl}-ethylamine)-pen tyl]-4,5,8,8a-tetrahydro-2H-phthalazin-1

94 The PC2A-EA ligand with an ethylamine pendant arm was found to form a thermodynamic

95 mTAAR1) for structural modifications in the ethylamine portion of 1.

96 anine, a precursor of the nonpeptide antigen ethylamine, primed peripheral blood gammadelta T cells t

97 oropyruvate, MTFP, and (R)-(+)-1-(1-naphthyl)ethylamine, (R)-NEA, on Pt(111) was studied using scanni

98 re favorable than for respective glycine and ethylamine reactions.

99 n cysteine mutants with methanethiosulfonate ethylamine revealed that [(3)H]dihydrotetrabenazine bind

100 ine building block, (S)-1-(pentafluorophenyl)ethylamine (S-2), which was found to be highly compatibl

101 Further exploration of the cycloalkanol ethylamine scaffold, of which venlafaxine ( 1) is a memb

102 report an electrocatalytic route to produce ethylamine selectively through an electroreduction of ac

103 computational study, which suggests the high ethylamine selectivity on Cu is due to the moderate bind

104 respect to the rotameric conformation of the ethylamine side chain and the distance between the amino

105 be a good strategy for rigidification of the ethylamine side chain only for tryptamines that bind to

106 composed of an imidazole ring attached to an ethylamine side chain.

107 rum is diagnostic of the conformation of the ethylamine side chain.

108 Pictet-Spengler cyclizations of pyrrolyl 2-ethylamine substituted at the pyrrole nitrogen are signi

109 During growth on ethylamine, the EMC pathway operates as a linear pathway

110 compared to 0.45 for propanone and 0.70 for ethylamine, the first time that such large hydrogen bond

111 studies, whereby binding of 2-(4-aminophenyl)ethylamine to the in situ generated [(L1)Pd(p-tolyl)](+)

112 Exogenous addition of ethylamine to the K42A variant leads to a neglible recov

113 ized polyesters with 2,2'-(ethylenedioxy)bis(ethylamine) to give well-defined nanoparticles with narr

114 Ethylamine transamination is inhibited 4-fold by Al(3+)

115 cell-type-specific analysis of glutamate and ethylamine (two precursors of theanine biosynthesis) met

116 es, such as 2-aryl-2,2-difluoroethanols and -ethylamines, under mild conditions.

117 nearly to WT values as the concentration of ethylamine was increased.

118 hly enantiopure (1-aryl)- and (1-naphthyl)-1-ethylamines were synthesized by the borane-mediated redu

119 ) alpha-(DMEN)PbBr4 (DMEN = 2-(dimethylamino)ethylamine), which adopts a unique corrugated layered st

120 atinum supported catalysts of 1-(1-naphthyl)-ethylamine, which is used as a chiral modifier in hydrog

121 cted with phenyl chloroformate and then with ethylamine, which provides a mild and efficient means of

122 pathway have a partial defect for growth on ethylamine, while mutants lacking both pathways are unab

123 alkylamine position within 2-(4-aminophenyl)ethylamine with [Pd(cinnamyl)Cl](2)/L1 and 4-chlorotolue