ライフサイエンスコーパス: choline chloride

1 from incorporations of deuterated methyl-D9-choline chloride.

2 nt (choline chloride: citric acid), and only choline chloride.

3 ic solvent comprising magnesium chloride and choline chloride.

4 ectrolyte of 3 M potassium hydroxide and 2 M choline-chloride.

5 t (Postnatal Days [PD] 4-9) and treated with choline chloride (0, 10, 50, or 100 mg/kg) from PD 10-30

6 idant constituents from hazelnut pomace, and choline chloride:1,2-propylene glycol (CC-PG) was determ

7 subcutaneous injections of saline vehicle or choline chloride (100 mg/kg/day) from PD 11-20, PD 21-30

8 Substitution of NaCl with choline chloride (120 mM) produced a marked suppression

9 Choline chloride-2-naphthol and choline chloride-thymol-

10 between analytes (hydrogen bond donors) and choline chloride (a hydrogen bond acceptor) supported in

11 Intriguingly, choline chloride, a commercial salt taste enhancer, is a

12 epended on Cl(-) rather than Na(+) Moreover, choline chloride, an established salt taste enhancer, wa

13 inhibitory compounds, (1-pentylthiocarbonyl)choline chloride and (1-heptylthiocarbonyl)choline chlor

14 ADESs formed by the hydrogen bond acceptors (choline chloride and betaine) and the hydrogen bond dono

15 cantly inhibited by replacement of NaCl with choline chloride and by sulfobromophthalein-GSH, neither

16 Novel chitosan (Ch) films containing choline chloride and citric acid mixture as plasticizer

17 Choline chloride and diverse hydrogen bond donors were u

18 ic solvent (DES) systems based on mixture of choline chloride and either urea or ethylene glycol.

19 g agents in a DES formed from the mixture of choline chloride and ethylene glycol.

20 o acids in the most common DESs, formed from choline chloride and ethylene glycol.

21 howed that 57% of water in NaDES composed of Choline Chloride and Glycerol (1:2) as extraction solven

22 stablished that the solvent synthesized from choline chloride and malic acid provided highest extract

23 The NADES, consisting of choline chloride and oxalic acid (1:1), was screened out

24 ding deep eutectic solvent (DES) composed of choline chloride and phenol (1:2).

25 Choline chloride and phenol in a 1:2 M ratio was used as

26 p eutectic solvent (DES) formed by mixing of choline chloride and phenol was used as an extraction so

27 ry for lead (II) extraction was obtained for choline chloride and phenol with a 1:2 M ratio.

28 dding dithizone (DZ) into DES, prepared from choline chloride and phenol.

29 ceived, daily for 4 weeks, a diet containing choline chloride and UMP (a uridine source) and/or DHA b

30 Nine different NaDES composed of choline chloride as a hydrogen bond acceptor and organic

31 A second infusion of methyl-D9-choline chloride at day 5 clearly indicated continued ac

32 ES for proposed extraction was performed and choline chloride-based DES containing oxalic acid as a h

33 us of this study was to evaluate whether six choline chloride-based natural deep eutectic solvents (N

34 NaCl buffer, but was not affected in 100 mM choline chloride buffer.

35 ere measured in Na+-containing and Na+-free (choline chloride) buffers using cells grown on gelatin-c

36 NaCl, sucrose, mannitol, sodium acetate, and choline chloride but not urea.

37 ions [3H]-1-methyl-4-phenylpyridium and [3H]-choline chloride, but did not transport other classes of

38 Deep eutectic solvents based on choline chloride, carboxylic acids, urea, and polyols we

39 ytes exposed to increasing concentrations of choline chloride (CC) and D,L-methionine (DLM).

40 f deep eutectic solvents (DES) prepared with choline chloride ([Ch]Cl) and carboxylic acids for pheno

41 p Eutectic Solvents (NADES) systems based on choline chloride (ChCl) as a hydrogen bond acceptor (HBA

42 Different combinations of DES consisting of choline chloride (ChCl) in various mixing ratios with su

43 of (hetero)aromatic halides and triflates in choline chloride (ChCl)-based deep eutectic solvents (DE

44 iency (k(cat) /K(M) ) increase in 30 % (v/v) choline chloride (ChCl): acetamide and 4.1-fold in 95 %

45 logy to maximize phenolic recovery (80 % v/v choline chloride-citric acid NaDES in water, 30 mL/g sol

46 line chloride: lactic acid (1:3)) and DES5 ((Choline chloride: citric acid (1:1)).

47 Choline Chloride: Citric Acid (1:2) with 50 % ethanol wa

48 citric acid, natural deep eutectic solvent (choline chloride: citric acid), and only choline chlorid

49 eutectic solvents (NADES), a combination of choline chloride:citric acid was selected because of its

50 ls in deep eutectic solvents (DESs) based on choline chloride combined with alcohols/ureas.

51 In this finding, choline chloride could be used as a novel, green and pro

52 given an s.c. injection of either saline or choline chloride daily on postnatal days (PD) 15-26.

53 , male Sprague-Dawley rats were exposed to a choline chloride deficient (DEF), sufficient (CON), or s

54 The replacement of NaCl with choline chloride did not down-regulate gamma-subunit exp

55 /kgH2O) for 48 h by replacement of NaCl with choline chloride did not prevent the up-regulation of th

56 ith the hypothesis that supplementation with choline chloride during early development leads to an in

57 Choline chloride-Ethylene glycol (1:2) with 40% V/V wate

58 The choline chloride-extracted complex contained the highest

59 irst experiment, rats were supplemented with choline chloride from conception until weaning.

60 )H]palmitic acid, [(3)H]oleic acid, or [(3)H]choline chloride from differentiated THP-1 monocytic cel

61 iet with adequate amounts of choline (1 g/kg choline chloride) from conception until weaning of offsp

62 better than conventional solvent were DES1 (Choline chloride: glycerol (1:2)), DES2 (Choline chlorid

63 DES was formulated with choline chloride: glycerol at 1: 2 M ratio.

64 ere, we investigated acetophenone in a (1:2) choline chloride:glycerol (ChCl:Gly) DES solution by exp

65 igation of intermicellar interactions in 1:2 choline chloride:glycerol and 1:2 choline bromide:glycer

66 e) and an antibody (immunoglobulin G) in 1:2 choline chloride:glycerol and 1:2 choline chloride:urea

67 t effective solvent for phenolic recovery in Choline Chloride:Glycerol and Urea:Glycerol solvents, ac

68 l or a natural deep eutectic solvent (NADES; choline chloride:glycerol, 1:2 mol/mol).

69 ted for bovine serum albumin in hydrated 1:2 choline chloride:glycerol.

70 olvent for the extraction of phytochemicals, choline chloride:glycerol:citric acid-based NADES can be

71 nt composed of a 4:1 mixture of glycerol and choline chloride (glycholine), is now described.

72 Here, we develop a trifunctional choline chloride/glyoxylic acid (ChCl/GA) binary deep eu

73 The isosmotic replacement of NaCl with choline chloride had no effect in I(A) kinetics demonstr

74 the thermophysical results, the solvent with choline chloride had the most compact fluid structure.

75 ts with a choline supplemented diet (5 mg/kg choline chloride in AIN76A) prenatally on embryonic days

76 ods rats were fed a standard diet (1.1 mg/kg choline chloride in AIN76A); control rats consumed only

77 ernal choline supplementation (ChS; 5.0 g/kg choline chloride) in two generations (Gen) of APP/PS1 mi

78 ular Na+ with either N-methyl-D-glucamine or choline chloride increased the ERK1/2 stimulation in res

79 were randomized to supplemental choline (as choline chloride) intakes of 550 mg/d (500 mg/d d0-choli

80 ing solution was replaced isosmotically with choline chloride inward currents were abolished at all p

81 7 and then returned to a control diet (1.1 g choline chloride/kg).

82 A choline chloride + lactic acid (1:1) natural deep eutect

83 Six NADES composed of choline chloride, lactic acid, citric acid, glucose, and

84 five NADES containing binary combinations of choline chloride, lactic acid, fructose, and sucrose.

85 S1 (Choline chloride: glycerol (1:2)), DES2 (Choline chloride: lactic acid (1:3)) and DES5 ((Choline

86 We show that systematic addition of choline chloride leads to microscopic heterogeneities th

87 Choline chloride-malonic acid DESs exhibited reduced vis

88 es in either NaCl medium (Na+-containing) or choline chloride medium (Na+-free) at 37 degrees C and 4

89 after 1 hour of incubation in NaCl medium or choline chloride (Na(+)-free) medium containing tracer G

90 hloride) or not supplemented (CON; 1.1 mg/kg choline chloride) on embryonic days 12-17.

91 produced in vitro were cultured with 1.8 mM choline chloride or control medium.

92 ned on a choline-supplemented diet (5.1 g/kg choline chloride) or a control, unsupplemented diet with

93 diet supplemented with choline (SUP; 5 mg/kg choline chloride) or not supplemented (CON; 1.1 mg/kg ch

94 hows a systematic study of the impact of DES choline chloride/p-toluenesulfonic acid and DES choline

95 line chloride/p-toluenesulfonic acid and DES choline chloride/p-toluenesulfonic acid-water in the aza

96 ew magnetic nano gel (MNG) was prepared from choline chloride/phenol deep eutectic solvent and magnet

97 Choline chloride:phenol-based DES showed the best result

98 g deep eutectic solvents (DESs) derived from choline chloride, plant phenolic acids, and formic acid

99 te buffer saline, sodium perchlorate, and in choline chloride plus oxalic acid, using analytical dete

100 Solvents of choline chloride-propionic acid (ChPA, molar ratio 1:2)

101 The results revealed that choline chloride-propylene glycol emerged as the optimal

102 09 and 1.02 +/- 0.06 in 0.3 M NaCl and 0.3 M choline chloride, respectively, at substrate concentrati

103 m tonicity with NaCl, sucrose, mannitol, and choline chloride stimulated S100A4 expression, whereas u

104 Choline chloride-2-naphthol and choline chloride-thymol-ethanol DESs are used as a dual-

105 ibitory property, whereas the supernatant of choline chloride-treated R36A, containing CBPs, was mark

106 e-CA/BET; tartaric acid/betaine-TA/BET; urea/choline chloride-UR/ChCl) coupled with autoclaving (121

107 eously, the reaction could be carried out in choline chloride urea as a natural deep eutectic solvent

108 A choline chloride/urea eutectic mixture is also used in t

109 The nanostructure of a series of choline chloride/urea/water deep eutectic solvent mixtur

110 G) in 1:2 choline chloride:glycerol and 1:2 choline chloride:urea follow a re-entrant behavior with

111 nce in a deep eutectic solvent (2:1 urea and choline chloride), utilizing various orthophosphate sour

112 water (1:2:3 M ratio), XoCH, and citric acid:choline chloride:water (1:1:6 M ratio), CiCH.

113 in the agro-food field were studied: xylitol:choline chloride:water (1:2:3 M ratio), XoCH, and citric

114 two DESs have been characterized: d-glucose:choline chloride:water (GCH) and d-glucose:citric acid:w

115 l)choline chloride and (1-heptylthiocarbonyl)choline chloride, were calculated from kinetic data and

116 ts inhibitory activity, we incubated R36A in choline chloride, which selectively strips CBPs from its