ライフサイエンスコーパス: glucopyranoside

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1 om D-salicin (2-(hydroxymethyl)phenyl beta-D-glucopyranoside).

2 ric in the nonionic detergent n-octyl-beta-D-glucopyranoside.

3 ract and the nonionic detergent octyl-beta-d-glucopyranoside.

4 and 3,4,3'-tri-O-methylflavellagic acid 4'-O-glucopyranoside.

5 in transporter solubilized by n-Octyl beta-D-glucopyranoside.

6 ere systematically disrupted by octyl-beta-D-glucopyranoside.

7 enic substrate, 4-methylumbelliferyl-alpha-D-glucopyranoside.

8 -glucosidase enzyme assay, resorufin alpha-d-glucopyranoside.

9 the alpha anomer over the beta anomer of the glucopyranoside.

10 grow on glucose nor transport methyl-alpha-D-glucopyranoside.

11 to salicin, amygdalin, and many bitter beta-glucopyranosides.

12 methyl-alpha-D-glucoside and related alpha-D-glucopyranosides.

13 The K0.5 for alpha-methyl-d-glucopyranoside (0.2 mM) was similar to that for SGLT1,

14 )-4-hydroxymethyl-phenyl-6-O-caffeoyl-beta-d-glucopyranoside (1) was isolated and identified together

15 measuring the uptake of alpha-methyl-D-[14C]glucopyranoside ([14C]alphaMDG).

16 t, Ins(1,4,5)P3 and (2-hydroxyethyl)-alpha-D-glucopyranoside 2',3, 4-trisphosphate, an adenophostin A

17 -O-beta-D-glucopyranosyl(1" --> 6')-O-beta-D-glucopyranoside (2) together with four know compounds: c

18 te-based analogues, (2-hydroxyethyl)-alpha-D-glucopyranoside-2',3,4-trisphosphate and alpha,alpha'-tr

19 -O-[alpha-L-rhamnopyranosyl-(1 --> 4)-beta-D-glucopyranoside]-26-O-beta-D-glucopyranoside were found

20 yl-(1-->4)-[alpha-L-fucosyl-(1-->6) ]-beta-D-glucopyranoside (2a), has been synthesized in 14 steps f

21 Vanillin-(6'-O-galloyl)-O-beta-D-glucopyranoside, 3,4,5-trimethoxyphenyl-(6'-O-galloyl)-O

22 hydroxy-6,3'-dimethoxy-isoflavone-7-O-beta-d-glucopyranoside (4) and 7,5'-dihydroxy-6,3'-dimethoxy-is

23 ompounds: caffeic acid (3), diosgenin beta-D-glucopyranoside (4), rutin (5), and quercetin 3-O-alpha-

24 mall molecule, 4-methyl-umbelliferyl-alpha-d-glucopyranoside (4-MalphaG).

25 (1-->2)-beta-d-galactopyranosyl 26-O-beta-d-glucopyranoside (4a,4b), (22S)-cholesta-1beta,3beta,16be

26 hypothesis that 4-methylumbelliferyl alpha-d-glucopyranoside (4MalphaG), a small, neutral dye molecul

27 l)-2-azido-4-O-benzyl-2-deoxy-1-thio-alpha-d-glucopyranoside (5), which is protected in such a way th

28 alphaGlc6P) and 4-methylumbelliferyl-alpha-D-glucopyranoside 6-phosphate (4MU alphaGlc6P) were hydrol

29 The substrate analogs p-nitrophenyl-alpha-D-glucopyranoside 6-phosphate (pNP alphaGlc6P) and 4-methy

30 luorogenic substrates, p-nitrophenyl-alpha-D-glucopyranoside 6-phosphate and 4-methylumbelliferyl-alp

31 ncentrations of intracellular methyl-alpha-D-glucopyranoside 6-phosphate are toxic, and cell growth i

32 em using the chromogenic p-nitrophenyl alpha-glucopyranoside 6-phosphate as substrate.

33 ing the in vivo hydrolysis of methyl-alpha-D-glucopyranoside 6-phosphate to yield glucose 6-phosphate

34 6-phosphate and 4-methylumbelliferyl-alpha-D-glucopyranoside 6-phosphate were used for the discontinu

35 MalH and PagL cleaved p-nitrophenyl-alpha-d-glucopyranoside 6-phosphate with comparable efficiency,

36 chromogenic substrate p-nitrophenyl-alpha-d-glucopyranoside 6-phosphate, but whether hydrolysis refl

37 (5), 3,3',4-tri-O-methylellagic acid-4'-O-d-glucopyranoside (6), and 1,3-O-diferuloylglycerol (8), A

38 oromethanesulfonyl-2,3,4-tri-O-benzyl beta-D-glucopyranoside (6).

39 NPbetaGlc6P) and 4-methylumbelliferyl-beta-D-glucopyranoside-6-phosphate (4MUbetaGlc6P), respectively

40 fluorogenic substrates, p-nitrophenyl-beta-D-glucopyranoside-6-phosphate (pNPbetaGlc6P) and 4-methylu

41 the chromogenic analog, p-nitrophenyl-beta-D-glucopyranoside-6P.

42 7-O-(7,8-dihydro-p-hydroxycinnamoyl)-bet a-d-glucopyranoside (7) and four saponins, named licoricesap

43 However, in the presence of n-octyl beta-d-glucopyranoside, a nonionic lipid mimicking detergent, a

44 e, and the allyl 2-acetamido-2-deoxy-alpha-D-glucopyranoside acceptor as compared to the wild-type en

45 yl-L-cysteinyl)amido-2-deoxy-(alpha, beta)-D-glucopyranoside (AcCySmB-GlcN) was at least 10(3) lower

46 zylidene-2-deoxy-2-trichloroacetamido-beta-D-glucopyranoside afforded the corresponding 4-O-benzoyl-6

47 nsporter 1 (SGLT1) substrate, methyl-alpha-D-glucopyranoside (alpha-MGP), stimulated release, whereas

48 afford 6-O-tetradecanoyl-alpha-d-cholesteryl glucopyranoside (alphaCAG) of Helicobacter pylori and th

49 Both cholesteryl alpha-d-glucopyranoside (alphaCG) and cholesteryl alpha-d-galact

50 f three cholesteryl-6-O-phosphatidyl-alpha-D-glucopyranosides (alphaCPG) unique to Helicobacter pylor

51 ethylene glycol, mannitol and alpha-methyl-D-glucopyranoside (alphaMDG) by control oocytes and by ooc

52 C5 increased the alpha-methyl-D-glucopyranoside (alphaMDG) uptake up to 20-fold above th

53 function of external Na+ and alpha-methyl-D-glucopyranoside (alphaMG) concentrations were consistent

54 s, 1,1,1,3,3,3-hexafluoropropan-2-yl alpha-d-glucopyranoside and 1,6-anhydro-beta-D-glucopyranose.

55 orm 1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside and acetate in MSH biosynthesis.

56 orm 1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside and acetate, the fourth overall step in

57 fo-2-acetamido-2-deoxy derivatives of beta-D glucopyranoside and beta-D-galactopyranoside were prepar

58 4), The detergents n-nonyl-beta-D-glucopyranoside and Cymal-5 have exceptional delipidatin

59 th, yielding higher levels of O-ethyl beta-d-glucopyranoside and d-glucose, and lower levels of malic

60 elease, which was mimicked by methyl alpha-D-glucopyranoside and galactose but not fructose.

61 ythritol, 2-C-methyl-d-erythritol 4-O-beta-d-glucopyranoside and linalool.

62 lly with a glucosidase, (Z)-3-hexenyl beta-D-glucopyranoside and linalyl beta-D-glucopyranoside were

63 representative carbohydrates, methyl alpha-D-glucopyranoside and methyl alpha-D-galactopyranoside.

64 ferol-3-O-beta-D-glucopyranosyl-(1-2)-beta-D-glucopyranoside and quercetin-3-O-beta-D-glucopyranosyl-

65 alues for the substrate p-nitrophenyl-beta-D-glucopyranoside and reduced sensitivity to competitive i

66 occupied by two molecules of n-octyl-beta-D-glucopyranoside and represents the phospholipid-binding

67 ty was quantified using p-nitrophenol-beta-d-glucopyranoside and SIM isoflavone extracts.

68 ter segment disk lipids using n-octyl beta-d-glucopyranoside and the detergent dialysis (DD) and rapi

69 -catalyzed hydrolysis of p-nitrophenyl-alpha-glucopyranoside and the lipoprotein lipase-catalyzed est

70 pha-lysophosphatidylcholine and octyl-beta-D-glucopyranoside) and activated by cholesterol enrichment

71 ilayer environment perturbed by octyl-beta-D-glucopyranoside) and under fully solubilizing conditions

72 4,5-trimethoxyphenyl-(6'-O-galloyl)-O-beta-D-glucopyranoside, and (6R,9R)-3-oxo-alpha-ionol-9-O-(6'-O

73 rom the corresponding (13)C-labeled methyl D-glucopyranosides, and multiple NMR J-couplings (J(HH), J

74 pyranosides, the alpha-sialosides, the alpha-glucopyranosides, and the beta-arabinofuranosides with a

75 beta-glucopyranosides are ubiquitous in nature, with many hav

76 us 4, 500 s-1 mM-1 with p-nitrophenyl-beta-D-glucopyranoside as substrate).

77 not active with 4-methylumbelliferyl-alpha-D-glucopyranoside as the substrate and it did not bind to

78 or the complexes formed by both 2 and 3 with glucopyranosides, as determined by Job plots.

79 tion, glycogen, D-xylose, and methyl-alpha-D-glucopyranoside assimilation, and growth at 35 degrees C

80 l 6-C-substituted 2-acetamido-2-deoxy-beta-D-glucopyranosides (beta-D-GlcNAc monosaccharides 1a-3a an

81 DS) or the nonionic detergent n-octyl-beta-D-glucopyranoside (betaOG).

82 crystal growth, the additive n-heptyl-beta-d-glucopyranoside, binds near the activation function heli

83 cetin-3-O-beta-D-glucopyranosyl-(1-2)-beta-D-glucopyranoside, both of which were absent from the tepa

84 bisphosphate in the presence of n-octyl beta-glucopyranoside but not cetyltriethylammonium bromide.

85 rom 1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside by ligation with cysteine followed by ac

86 l precursor was prepared from methyl alpha-d-glucopyranoside by the biomimetic procedure of Bender an

87 lysed the hydrolysis of p-nitrophenyl-beta-D-glucopyranoside, cello-oligosaccharides, beta-linked glu

88 of nonionic detergents of the n-alkyl-beta-D-glucopyranoside class on the ordering of lipid bilayers

89 O-[alpha-L-rhamnopyranosyl-(1 --> 4)]-beta-d-glucopyranoside (compound 1) exhibited the best protecti

90 tyl-1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside deacetylase (MshB) catalyzes the hydroly

91 tyl-1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside deacetylase (MshB) catalyzes the hydroly

92 tyl-1-d-myo-inosityl-2-amino-2-deoxy-alpha-d-glucopyranoside deacetylase) activity.

93 concentrations of the detergent octyl-beta-d-glucopyranoside decreased rates of nitroalkene reaction

94 MEG (methyl-6-O-(N-heptyl-carbamoyl)-alpha-D-glucopyranoside) detergent extraction in concert with hi

95 g 2',4'-dintrophenyl-2-fluoro-2-deoxy-beta-D-glucopyranoside did not reduce PNG hydrolysis.

96 ide (NAG), deacetyl nomilinic acid 17-beta-D-glucopyranoside (DNAG), obacunone 17-beta-D-glucopyranos

97 de and dinitrophenol-2-deoxy-2-fluoro-beta-D-glucopyranoside (DNP2FGlc).

98 tyl-1-d-myo-inosityl-2-amino-2-deoxy-alpha-d-glucopyranoside) for MshB.

99 benzyl-3,6-O-(di-tert-butylsilylene)-alpha-D-glucopyranoside gave alpha/beta mixtures with standard N

100 to 1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside (GlcN-Ins) and is the major thiol produc

101 d to 1D-myo-inosityl 2-amino-2-deoxy-alpha-D-glucopyranoside (GlcN-Ins) and is the predominant thiol

102 1D-myo-inosityl 2-acetamido-2-deoxy-alpha-D-glucopyranoside (GlcN-Ins), and is the major low-molecul

103 with 1D-myo-inosityl 2-amino-2-deoxy-alpha-D-glucopyranoside; GlcN-Ins) catalyzed by MshC to produce

104 1-D-myo-inosityl-2-acetamido-2-deoxy-alpha-D-glucopyranoside (GlcNAc-Ins), a hypothetical mycothiol b

105 1D-myo-inosityl 2-acetamido-2-deoxy-alpha-D-glucopyranoside (GlcNAc-Ins).

106 serine, methionine, threonine, methyl alpha-glucopyranoside, glucose, penicillamine, valinol, phenyl

107 The formation of beta-D-glucopyranosides (glucuronides) by the UDP-glucuronosylt

108 d by sugars with specificity: methyl alpha-D-glucopyranoside > D-glucose > D-galactose >> D-mannitol.

109 Responses to methyl alpha-D-glucopyranoside had a higher threshold, commensurate wit

110 actions isolated from homogenates with octyl glucopyranoside had cholesterol and sphingomyelin conten

111 s of nonionic detergents, the n-alkyl-beta-D-glucopyranosides, have on the phase behavior of hydrated

112 ty and the ability to acidify methyl-alpha-D-glucopyranoside helped recognize E. gallinarum and incre

113 Michaelis-Menten parameters of 4-nitrophenyl glucopyranoside hydrolysis by sweet almond beta-glucosid

114 copyranosyl-(1-->2)-galactopyranosyl-(1-->2)-glucopyranoside, identified as potential taxonomic marke

115 20-fold larger affinity toward octyl-beta-d-glucopyranoside in CDCl(3), demonstrating the superior r

116 date for noncovalent 1:1 binding of an alpha-glucopyranoside in chloroform (Ka = 212,000 +/- 27,000 M

117 plexation of glutaric acid and beta-methyl d-glucopyranoside in chloroform were investigated through

118 n increased sensitivity to many bitter beta -glucopyranosides in the presence of the N172 allele.

119 ric acid or three molecules of beta-methyl d-glucopyranoside inside.

120 Mimetic 3 and all the glucopyranoside intermediates generated in its synthesis

121 ty B medium supplemented with methyl-alpha-D-glucopyranoside (investigational), motility S medium, mo

122 dines 40 and 41 starting from methyl alpha-d-glucopyranoside is described and will be used as a templ

123 etin-3-O-(6-O-alpha-l-rhamnopyranosyl-beta-d-glucopyranoside) is usually assessed by means of high pe

124 -(N-acetyl-L-cysteinyl)amido-2-deoxy-alpha-D-glucopyranoside, is an unusual conjugate of N-acetylcyst

125 onoid glucosides, that is, limonin 17-beta-D-glucopyranoside (LG), nomilin 17-beta-D-glucopyranoside

126 R)-3-oxo-alpha-ionol-9-O-(6'-O-galloyl)-beta-glucopyranoside (macarangioside E) were isolated and ide

127 were: alpha-methyl-4-[F-18]-fluoro-4-deoxy-d-glucopyranoside (Me-4FDG), a substrate for SGLTs; 4-deox

128 alog, alpha-methyl-4-deoxy-4-[(18)F]fluoro-D-glucopyranoside (Me4FDG), which is not transported by GL

129 y (13)C-labeled methyl 2-deoxy-2-acetamido-d-glucopyranoside (MeGlcNAc) anomers were investigated, le

130 y (13)C-labeled methyl 2-deoxy-2-formamido-d-glucopyranoside (MeGlcNFm) anomers provided standard (1)

131 When methyl-alpha-D-glucopyranoside (MGP) molecules are reacted with hexamet

132 inose (ARA), acidification of methyl-alpha-D-glucopyranoside (MGP), and rapid motility (RM), for diff

133 -(N-acetyl-l-cysteinyl)amido-2-deoxy-alpha-d-glucopyranoside (MSH or AcCys-GlcN-Ins), to act against

134 -(N-acetyl-L-cysteinyl)amido-2-deoxy-alpha-D-glucopyranoside (MSH or AcCys-GlcN-Ins).

135 ucopyranoside (NG), nomilinic acid 17-beta-D-glucopyranoside (NAG), deacetyl nomilinic acid 17-beta-D

136 ta-d-galactopyranosyl-(1-->4)-1-thio-beta -d-glucopyranoside; Neu5Acalpha2,3LacbetaSPh, and the corre

137 ta-D-glucopyranoside (LG), nomilin 17-beta-D-glucopyranoside (NG), nomilinic acid 17-beta-D-glucopyra

138 ccharide surfactants, such as n-octyl-beta-d-glucopyranoside (NOG), are widely used to solubilize or

139 yranoside (OG), and obacunoic acid 17-beta-D-glucopyranoside (OAG) were investigated using a quadrupl

140 lactopyranosyl)-2-trichlo roacetamido-beta-D-glucopyranoside, obtained by regioselective reductive op

141 and further solubilised using n-octyl beta-D-glucopyranoside (OctGlc) and n-dodecyl beta-D-maltoside

142 of the non-ionic detergents, n-octyl beta-D-glucopyranoside (octyl glucoside) and Triton X-100R-PC (

143 -glucopyranoside (DNAG), obacunone 17-beta-D-glucopyranoside (OG), and obacunoic acid 17-beta-D-gluco

144 profound inhibitory effect of n-octyl-beta-d-glucopyranoside (OG), the detergent used for LeuT crysta

145 noS) in the non-ionic detergent octyl-beta-D-glucopyranoside (OG).

146 sodium dodecyl sulfate (SDS), n-octyl-beta-D-glucopyranoside (OGP), and Zwittergent 3-14 (Z3-14).

147 subunit distances in detergent (octyl beta-d-glucopyranoside, OGP) purified and OMM bound forms by a

148 d AglA recognized glucose and methyl-alpha-D-glucopyranoside, only AglA accepted other alpha-D-glucos

149 Results suggest that thymol-beta-D-glucopyranoside or similar beta-glycosides may be able t

150 etergents or in the presence of n-octyl beta-glucopyranoside or Triton X-100, but not in the presence

151 ing either thioglucose, 2'-aminoethyl beta-d-glucopyranoside, or aminophlorizin.

152 ose, and the nonmetabolizable methyl alpha-D-glucopyranoside, or with fructose.

153 d increase in the k(cat)/K(m) for pNP-beta-d-glucopyranoside (pNPG) was identified.

154 ium cation-attached alpha- and beta-O-methyl-glucopyranoside precursor ions, formed by electrospray i

155 tigated the capacity of quercetin-3-O-beta-d-glucopyranoside (Q3G) isolated from Echinophora cinerea

156 roducing a chemical tagging strategy for the glucopyranoside residue.

157 Y, binding of a galactopyranoside, but not a glucopyranoside, results in a decrease in distance on th

158 ing using 5-bromo-4-chloro-3-indolyl-alpha-D-glucopyranoside revealed that the acidic alpha-glucosida

159 Application to methyl alpha- and beta-D-glucopyranosides reveals different rotameric distributio

160 uronides to corresponding J-couplings in the glucopyranosides showed that more pervasive changes occu

161 e encoding a taste receptor for bitter beta -glucopyranosides, shows significant association with alc

162 d with the nonionic detergent n-octyl-beta-d-glucopyranoside, suggesting that perturbation of the int

163 nce aesculin, 6,7-dihydroxycoumarin-6-O-beta-glucopyranoside, suppresses inflammation, we asked wheth

164 that of 2, displaying higher affinities for glucopyranosides than for other monosaccharides.

165 rous experimental studies have shown that in glucopyranosides the omega-torsion angle (O(6)-C(6)-C(5)

166 l was compared against that of thymol-beta-D-glucopyranoside, the latter being resistant to absorptio

167 (1-->3)-2-deoxy-2-trichlor oacetamido-beta-d-glucopyranoside, the product of site-specific enzymatic

168 anes by the nonionic detergent n-octyl- beta-glucopyranoside; the soluble fraction was loaded at pH 7

169 tyl-1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside to form 1-D-myo-inosityl-2-amino-2-deoxy

170 tyl-1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside to form 1-D-myo-inosityl-2-amino-2-deoxy

171 Thymol-beta-D-glucopyranoside treatment (1 mM) did not reduce C. coli

172 acid production was reduced by thymol-beta-D-glucopyranoside treatment, indicating that fermentation

173 opyranosyl-(1-->4)-2,3,6-tri-O -sulfo-beta-d-glucopyranoside, tridecasodium salt (PG545, 18) as a cli

174 including MG-1655, accumulate methyl-alpha-D-glucopyranoside via the phosphoenolpyruvate-dependent gl

175 Dinosylated alpha-d-glucopyranoside was directly transformed into alpha-d-al

176 benzyl-3,6-O-(di-tert-butylsilylene)-alpha-D-glucopyranoside was found to be alpha-selective.

177 t time that vanillin-(6'-O-galloyl)-O-beta-D-glucopyranoside was identified and the first time that m

178 zation (CTI) in methyl 2-deoxy-2-acylamido-d-glucopyranosides was investigated by (1)H and (13)C NMR

179 1 --> 4)-beta-D-glucopyranoside]-26-O-beta-D-glucopyranoside were found as key bitter contributors af

180 yl beta-D-glucopyranoside and linalyl beta-D-glucopyranoside were identified as aroma precursors in P

181 d its nonmetabolizable analog methyl alpha-D-glucopyranoside were measured with 33-ms time resolution

182 , ocotillone, and beta-sitosterol 3-O-beta-D-glucopyranoside, were also isolated and characterized.

183 The method is also applicable to the glucopyranosides when high alpha-selectivity is observed

184 zylidene-2-deoxy-2-trichloroacetamido-beta-d-glucopyranoside with 3,4,6-tri-O-acetyl-2-O-bromoacetyl-

185 n-Alkyl-beta-D-glucopyranosides with alkyl chains with 6, 7, 8, and 10

186 raphy in the presence of 0.2% n-octyl-beta-D-glucopyranoside yields a molecular weight of approximate

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