ライフサイエンスコーパス: 1-propanol

1 glyoxal, a toxic byproduct of glycolysis, as 1-propanol.

2 [3H]phosphatidylpropanol in the presence of 1-propanol.

3 e formed from monomeric and dimeric adsorbed 1-propanol.

4 e precursor of 3-phenylpropanal and 3-phenyl-1-propanol.

5 adation are propionaldehyde, propionate, and 1-propanol.

6 ay of zirconium(IV)-n-propoxide solutions in 1-propanol.

7 y acids, alcohols, ethyl esters and 3-ethoxy-1-propanol.

8 sses between 96% (R) and 75% (S) of 1-phenyl-1-propanol.

9 n tetramethoxyquinolizine 9 with neat 3-iodo-1-propanol.

10 r and acetonitrile--water in the presence of 1-propanol.

11 f various concentrations of 2-amino-3-phenyl-1-propanol.

12 enantiomeric composition of 2-amino-3-phenyl-1-propanol.

13 ase liquid chromatography in the presence of 1-propanol.

14 sted acid-catalyzed gas-phase dehydration of 1-propanol (0.075-4 kPa) was studied on zeolite H-MFI (S

15 min using a mobile phase of 0.05M SDS - 7.5% 1-propanol - 0.5% triethylamine buffered at pH 3, runnin

16 rences using mobile phase of 0.05M SDS/12.5% 1-propanol/0.5% triethylamine at pH 3, running at 1mL/mi

17 electrooxidation of four alcohols (ethanol, 1-propanol, 1-butanol, and 1-pentanol) to the correspond

18 C1 column and elution with a 2:1 mixture of 1-propanol:1-butanol.

19 o afford the corresponding (S)-1-substituted 1-propanols 10a-n with a mean enantiomeric excess of 92%

20 Microwave reactions of 2-amino-2-methyl-1-propanol (2) or 2-aminoethanethiol hydrochloride (4) w

21 After baking, 2,3-butanedione, 1-propanol, 2-methyl-1-propanol, 3/2-methyl-1-butanol an

22 h of the alcohol chain (C1-C3) and geometry (1-propanol, 2-propanol) as well as their polarity on the

23 , such as type and concentration of alcohol (1-propanol, 2-propanol, and ethanol), type of salt (sodi

24 ng 1 to 100 mM 2-nitroethanol (2ne), 2-nitro-1-propanol (2nprop), and 3-nitro-2-pentanol (3n2pent) at

25 nitroalcohols (2-nitroethanol [2ne], 2-nitro-1-propanol [2nprop]), and 3-nitro-2-pentanol [3n2pent]).

26 -OH terminating head group, i.e., 3-mercapto-1-propanol (3-MPL), 6-mercapto-1-hexanol (6-MHL), 8-merc

27 la using 1-propanol, ethyl acetate, 2-methyl-1-propanol, 3-methyl-1-butanol and 2-methyl-1-butanol an

28 ntent of 1-propanol, ethyl acetate, 2-methyl-1-propanol, 3-methyl-1-butanol and 2-methyl-1-butanol wa

29 asted samples with the exception of 2-methyl-1-propanol, 3-methyl-1-butanol and 2-phenylethyl alcohol

30 aking, 2,3-butanedione, 1-propanol, 2-methyl-1-propanol, 3/2-methyl-1-butanol and ethyl octanoate wer

31 d poly(1,5-pentanediol diacrylate-co-3-amino-1-propanol) ('536') at a 25 polymer-to-DNA weight-to-wei

32 2(R)-d-erythro-2-(N-myristoylamino)-1-phenyl-1-propanol, a ceramidase inhibitor, and TNFalpha, a homo

33 a covalently linked monolayer of 3-mercapto-1-propanol, a modified surface that blocks the oxidation

34 than for the primary amines 2-amino-2-methyl-1-propanol (AMP) and monoethanolamine (MEA) and the tert

35 (DEA) carbamate as well as 2-amino-2-methyl-1-propanol (AMP) carbamate were obtained in crystalline

36 with 1-phenyl-2-palmitoylamino-3-morpholino-1-propanol, an inhibitor of glucosylceramide synthesis,

37 -threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol, an inhibitor of several glucosphingolipid sy

38 he formation of 3-methyl-1-butanol, 2-methyl-1-propanol and 3-(methylsulfanyl)-propanal, whereas hexa

39 Plant tissue is extracted in aqueous 1-propanol and mixed with dichloromethane.

40 -threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol and phospholipase C), we demonstrated that PS

41 opionate accumulated stoichiometrically when 1-propanol and propionaldehyde were added to butane- and

42 ed primarily by conversion to propionate and 1-propanol and secondarily due to volatility.

43 Replacement of ethanol with 1-propanol and use of a surfactant increased the signal.

44 quence of the competitive adsorption between 1-propanol and water.

45 itor D-erythro-2-tetradecanoylamino-1-phenyl-1-propanol and, to a much lesser extent, by L-cycloserin

46 The influence of methanol, ethanol, 1-propanol, and 2-propanol and K(3)PO(4), K(2)HPO(4) or

47 ns of different alcohols (methanol, ethanol, 1-propanol, and 2-propanol) adsorbed into Cu-BTC thin fi

48 3-Phenylpropanal, 3-phenyl-1-propanol, and benzyl alcohol were identified as potent

49 ter seems to be inhibited in the presence of 1-propanol, and partitioning is the predominant solute r

50 ment of CdSe nanocrystals (NCs) in a 3-amino-1-propanol (APOL)/water (v/v = 10:1) mixture at 80 degre

51 of dibenzoquinolizines 9 and 14 with 3-halo-1-propanols are highly cis-selective (94-100% cis), resu

52 ments showed that 3-phenylpropanal, 3-phenyl-1-propanol, benzyl alcohol, methyl 3-phenylpropionate, m

53 -threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol), C9DGJ (N-nonyl-deoxygalactonojirimycin) or

54 esis, 1-phenyl-2-palmitoylamino-3-morpholino-1-propanol, completely abolished the formation of lipid-

55 roxyphenyl)-2-(4-hydroxy-4-phenylpiperidino)-1-propanol (CP 101,606).

56 roxyphenyl)-2-(4-hydroxy-4-phenylpiperidino)-1-propanol (CP-101,606, 1) is a recently described antag

57 ,2R)-D-erythro-2-(N-myristoylamino)-1-phenyl-1-propanol (D-erythro-MAPP).

58 -threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (D-PDMP) (an inhibitor of glucosylceramide sy

59 threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (D-PDMP), an inhibitor of glucosylceramide sy

60 d by D-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (D-PDMP), an inhibitor of UDP-galactose:gluco

61 -threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (D-PDMP), solubilized in vehicle (5% Tween-80

62 -threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (D-PDMP).

63 The inhibition by 1-propanol-d7 (CD3CD2CD2OH) was significantly lower than

64 th [residual hGH]1-propanol-h7/[residual hGH]1-propanol-d7 = 1.95 at 30% (v/v) 1-propanol, reflecting

65 lectivity was developed using 3-diethylamino-1-propanol (deapH) in lieu of BnOH and NEt(3).

66 Interestingly, 1-propanol, delta-butyrolactone and ethyl lactate concen

67 (BV2), of which dimercaprol (2,3-dimercapto-1-propanol (DMP)) was found to be the most effective com

68 edioxy)phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol (EtDO-P4), the glucosylceramide (GlcCer) synt

69 The content of 1-propanol, ethyl acetate, 2-methyl-1-propanol, 3-methyl

70 ver, gold, aged and extra-aged tequila using 1-propanol, ethyl acetate, 2-methyl-1-propanol, 3-methyl

71 mplicit water as well as explicit hexane and 1-propanol for the nanomer.

72 2CD2OH) was significantly lower than that by 1-propanol-h7 with [residual hGH]1-propanol-h7/[residual

73 han that by 1-propanol-h7 with [residual hGH]1-propanol-h7/[residual hGH]1-propanol-d7 = 1.95 at 30%

74 The presence of a small amount of 1-propanol has been shown to affect mainly the polarity

75 -1-phenyl-2-hexadecanoylamino-3 -pyrrolidino-1-propanol-HC l (glucosylceramide synthase), which deple

76 -Threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol.HCI (PDMP), a glucosylceramide synthase and L

77 threo-1-phenyl-2-decanolylamine-3-morpholino-1-propanol HCl, an inhibitor of glucosylceramide synthas

78 -threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol-HCl, also results in a significant decrease i

79 -threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol.HCl (PDMP), a glucosylceramide synthase and L

80 d, and 3-methylbutanoic acid; 3-(methylthio)-1-propanol; hexanoic acid; beta-damascenone; and ethyl-3

81 dium and that inhibition of PA production by 1-propanol inhibited secretion.

82 anti-Lewisite, also known as 2,3-dimercapto-1-propanol) inhibits S6K1 phosphorylation and stabilizes

83 nd significantly changes the wine content in 1-propanol, isobutanol, acetaldehyde, 1,1-diethoxiethane

84 -threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (L-PDMP) in two mouse models of Parkinsonism

85 mationally restricted version of the 3-amino-1-propanol moiety common to the many previously describe

86 Water stabilizes the adsorbed 1-propanol monomer significantly more than the eliminati

87 1-propanol stabilizes the adsorbed state of 1-propanol more than the elimination transition state.

88 etitive adsorption isotherms of rac-1-phenyl-1-propanol on cellulose tribenzoate were measured by com

89 influenced the rise of the level of 3-ethoxy-1-propanol only.

90 hreo-1-phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol (P4), or reduction of CD82 expression by RNA

91 und, 1-phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol (P4), was made.

92 hreo-1-phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol (P4).

93 ibitor 1-phenyl-2-decanoylamino-3-morpholino-1-propanol (PDMP) resulted in the production of virus pa

94 -threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (PDMP), increased caspase activity to the sam

95 threo-1-phenyl-2-decanoylamino-3-morpholino- 1-propanol (PDMP), shifted the steady-state distribution

96 -threo 1-phenyl-2-decanoylamino-3-morpholino-1-propanol (PDMP), which inhibits acid ceramidase or glu

97 o resolution of racemic mixtures of 1-phenyl-1-propanol (PP) was studied by varying time, temperature

98 threo-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol (PPMP), an inhibitor of glucosylceramide synt

99 or 1-phenyl-2-hexadecanoylamino-3-morpholino-1-propanol (PPMP), blocked target membrane glycosphingol

100 bitor 1-phenyl-2-palmitoylamino-3-morpholino-1-propanol (PPMP, 5.0 micromol/L, 4 days) decreased gang

101 r 1-phenyl-2-hexadecanoylamino-3-pyrrolidino-1-propanol (PPPP) each partially inhibited the ability o

102 reo-1-phenyl-2-(palmitoylamino)-3-morpholino-1-propanol, prevented the increase of GlcCer in cDMEM cu

103 sidual hGH]1-propanol-d7 = 1.95 at 30% (v/v) 1-propanol, reflecting a kinetic isotope effect close to

104 The stronger adsorption of 1-propanol relative to water indicates that the reduced

105 In a similar manner, an excess of 1-propanol stabilizes the adsorbed state of 1-propanol m

106 -threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol, the percentage of trajectories exhibiting co

107 ified 2-butanol, 2-butanone, 2-pentanone and 1-propanol to be possibly elevated in the ALF stage.

108 hreo-1-phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol) treatment or by knockdown of CD9 by the RNA

109 Quaternization of 14 with 3-chloro-1-propanol under Finkelstein conditions generated cis-di

110 ency of methanol, acetonitrile, ethanol, and 1-propanol used as modifiers in packed-column SFC.

111 be inhibited by the presence of >/=28% (v/v) 1-propanol which appears (i) to perturb the metal-bindin

112 isfavored omega-hydroxy metabolite, 2-phenyl-1-propanol, with product stereoselectivity for the (S)-e