ライフサイエンスコーパス: ethylamine

1 h pathways are unable to grow appreciably on ethylamine.

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

3 ergoes a nucleophilic addition by 1 equiv of ethylamine.

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

5 each component and by reducing the amount of ethylamine.

6 s coupled with their further inactivation by ethylamine.

7 with a solution-phase nucleophile, ferrocene ethylamine.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

45 00-fold molar excess of methanethiosulfonate ethylamine, demonstrating that Cys(439) is either at the

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

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

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

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

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

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

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

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

54 > 1-propylamine > pyridine > triethylamine > ethylamine > methylamine > diethylamine > tert-butylamin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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