ライフサイエンスコーパス: 1-propanol

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

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

3 rages acid-catalyzed Si-O bond exchange with 1-propanol.

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

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

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

7 droxymethyl group (-CH(2)OH) of the produced 1-propanol.

8 r couple with CO leading to the formation of 1-propanol.

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

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

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

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

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

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

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

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

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

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

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

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

21 pt, this was evaluated on methanol, ethanol, 1-propanol, 1-pentanol, and 1-octanol using a commercial

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

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

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

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

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

27 es of volatile compounds and fusel alcohols (1-propanol, 2-propanol, acetone, and acetaldehyde) was f

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

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

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

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

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

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

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

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

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

37 o 1-hexnaol, the intercalation rate peaks in 1-propanol (80 times faster than the slowest case in met

38 2(R)-d-erythro-2-(N-myristoylamino)-1-phenyl-1-propanol, a ceramidase inhibitor, and TNFalpha, a homo

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

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

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

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

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

44 treated with dithiol ligands (2,3-dimercapto-1-propanol and 2,3-dimercapto-1-propanesulfonic acid sod

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

46 substrates with 3-C-(a,B-d,l-glycopyranosyl)1-propanol and C-(a-d,l-glycopyranosyl)methanol structur

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

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

49 th a mixture of two amines, 2-amino-2-methyl-1-propanol and piperazine (CESAR1).

50 thylbutanol- and 2-methylbutanoate (2MB) and 1-propanol and propanoate (PROP) esters.

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

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

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

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

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

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

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

58 3-Phenylpropanal, 3-phenyl-1-propanol, and benzyl alcohol were identified as potent

59 rophilic asthma, the combination of nonanal, 1-propanol, and hexane had a classification performance

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

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

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

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

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

65 hyl octanoate, ethyl decanoate, 3-methylthio-1-propanol, carvone, benzyl alcohol and nonanoic acid) w

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

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

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

69 ,2R)-D-erythro-2-(N-myristoylamino)-1-phenyl-1-propanol (D-erythro-MAPP).

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

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

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

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

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

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

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

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

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

79 ate as the hydrogen bond acceptor mixed with 1-propanol (DES-1), 1,3-propanediol (DES-2) and 1,2,3-pr

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

81 edioxy)phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol (EtDO-P4) greatly reduced GSL and monosialote

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

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

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

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

86 2CD2OH) was significantly lower than that by 1-propanol-h7 with [residual hGH]1-propanol-h7/[residual

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

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

89 -1-phenyl-2-hexadecanoylamino-3 -pyrrolidino-1-propanol-HC l (glucosylceramide synthase), which deple

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

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

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

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

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

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

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

97 the formation of 2-propanol, propylene, and 1-propanol involving the oxidation of Fe(II) to Fe(III)

98 dehyde, only a minor fraction (up to 36%) of 1-propanol is from this pathway, and the majority of it

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

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

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

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

103 1-propanol stabilizes the adsorbed state of 1-propanol more than the elimination transition state.

104 o-1,3-propanediol (NT = nitrotriol), 2-nitro-1-propanol (NP)] against 5 different microbial pathogens

105 ons using different proportions of lecithin, 1-propanol, olive oil and water to examine their abiliti

106 ying 5 g microemulsion composed of lecithin: 1-propanol: olive oil: water (53.33:26.67:10:10 wt%) res

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

122 igher production of C(3) oxygenates, such as 1-propanol, propionaldehyde, and allyl alcohol, compared

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

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

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

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

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

128 ch primarily formed 3-(methylamino)-1-phenyl-1-propanol (TP 166) and 4-(trifluoromethyl)phenol, by hy

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

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

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

132 he production of C3 oxygenates (propanal and 1-propanol) via the heterogeneous hydroformylation react

133 acids and bases up to pK(a) 10 in 50% (v/v) 1-propanol/water, 50% (v/v) dimethyl sulfoxide/water, an

134 ely, 2-methyl-1-propyl acetate, and 2-methyl-1-propanol were observed to be correlated with the ferme

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

136 tinctly favors the production of acetate and 1-propanol, while *CO(L) favors ethylene and ethanol for

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