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1 om D-salicin (2-(hydroxymethyl)phenyl beta-D-glucopyranoside).
2 -glucosidase enzyme assay, resorufin alpha-d-glucopyranoside.
3 the alpha anomer over the beta anomer of the glucopyranoside.
4 grow on glucose nor transport methyl-alpha-D-glucopyranoside.
5 ric in the nonionic detergent n-octyl-beta-D-glucopyranoside.
6 e, 2-phenylethanol, and 2-phenylethyl-beta-d-glucopyranoside.
7 in-3-O-beta-D-glucoside, luteolin-7-O-beta-D-glucopyranoside.
8 in transporter solubilized by n-Octyl beta-D-glucopyranoside.
9 ract and the nonionic detergent octyl-beta-d-glucopyranoside.
10 and 3,4,3'-tri-O-methylflavellagic acid 4'-O-glucopyranoside.
11 ere systematically disrupted by octyl-beta-D-glucopyranoside.
12 enic substrate, 4-methylumbelliferyl-alpha-D-glucopyranoside.
13 methyl-alpha-D-glucoside and related alpha-D-glucopyranosides.
14 to salicin, amygdalin, and many bitter beta-glucopyranosides.
16 )-4-hydroxymethyl-phenyl-6-O-caffeoyl-beta-d-glucopyranoside (1) was isolated and identified together
18 t, Ins(1,4,5)P3 and (2-hydroxyethyl)-alpha-D-glucopyranoside 2',3, 4-trisphosphate, an adenophostin A
19 corresponding d-enantiomers, methyl alpha-d-glucopyranoside 2,3,6-trisphosphate and methyl alpha-d-g
20 l-Glucose-derived ligands, methyl alpha-l-glucopyranoside 2,3,6-trisphosphate and methyl alpha-l-g
21 oside 2,3,6-trisphosphate and methyl alpha-l-glucopyranoside 2,4,6-trisphosphate, are also active, wh
23 -O-beta-D-glucopyranosyl(1" --> 6')-O-beta-D-glucopyranoside (2) together with four know compounds: c
24 te-based analogues, (2-hydroxyethyl)-alpha-D-glucopyranoside-2',3,4-trisphosphate and alpha,alpha'-tr
25 -O-[alpha-L-rhamnopyranosyl-(1 --> 4)-beta-D-glucopyranoside]-26-O-beta-D-glucopyranoside were found
26 yl-(1-->4)-[alpha-L-fucosyl-(1-->6) ]-beta-D-glucopyranoside (2a), has been synthesized in 14 steps f
28 hydroxy-6,3'-dimethoxy-isoflavone-7-O-beta-d-glucopyranoside (4) and 7,5'-dihydroxy-6,3'-dimethoxy-is
29 ompounds: caffeic acid (3), diosgenin beta-D-glucopyranoside (4), rutin (5), and quercetin 3-O-alpha-
31 (1-->2)-beta-d-galactopyranosyl 26-O-beta-d-glucopyranoside (4a,4b), (22S)-cholesta-1beta,3beta,16be
32 hypothesis that 4-methylumbelliferyl alpha-d-glucopyranoside (4MalphaG), a small, neutral dye molecul
33 l)-2-azido-4-O-benzyl-2-deoxy-1-thio-alpha-d-glucopyranoside (5), which is protected in such a way th
34 alphaGlc6P) and 4-methylumbelliferyl-alpha-D-glucopyranoside 6-phosphate (4MU alphaGlc6P) were hydrol
35 The substrate analogs p-nitrophenyl-alpha-D-glucopyranoside 6-phosphate (pNP alphaGlc6P) and 4-methy
36 luorogenic substrates, p-nitrophenyl-alpha-D-glucopyranoside 6-phosphate and 4-methylumbelliferyl-alp
37 ncentrations of intracellular methyl-alpha-D-glucopyranoside 6-phosphate are toxic, and cell growth i
39 ing the in vivo hydrolysis of methyl-alpha-D-glucopyranoside 6-phosphate to yield glucose 6-phosphate
40 6-phosphate and 4-methylumbelliferyl-alpha-D-glucopyranoside 6-phosphate were used for the discontinu
41 MalH and PagL cleaved p-nitrophenyl-alpha-d-glucopyranoside 6-phosphate with comparable efficiency,
42 chromogenic substrate p-nitrophenyl-alpha-d-glucopyranoside 6-phosphate, but whether hydrolysis refl
43 (5), 3,3',4-tri-O-methylellagic acid-4'-O-d-glucopyranoside (6), and 1,3-O-diferuloylglycerol (8), A
45 NPbetaGlc6P) and 4-methylumbelliferyl-beta-D-glucopyranoside-6-phosphate (4MUbetaGlc6P), respectively
46 fluorogenic substrates, p-nitrophenyl-beta-D-glucopyranoside-6-phosphate (pNPbetaGlc6P) and 4-methylu
48 7-O-(7,8-dihydro-p-hydroxycinnamoyl)-bet a-d-glucopyranoside (7) and four saponins, named licoricesap
49 However, in the presence of n-octyl beta-d-glucopyranoside, a nonionic lipid mimicking detergent, a
50 e, and the allyl 2-acetamido-2-deoxy-alpha-D-glucopyranoside acceptor as compared to the wild-type en
51 yl-L-cysteinyl)amido-2-deoxy-(alpha, beta)-D-glucopyranoside (AcCySmB-GlcN) was at least 10(3) lower
52 avage of the model substrate 4-nitrophenyl-D-glucopyranoside, achieving a turnover number ~9% of that
53 e acids (H4MP-G), along with gallic-4-O-beta-glucopyranoside acid (AG-G), 3-indolyl-(2R)-O-beta-d-gly
55 -G) and 2-hydroxy-4-methylpentanoic-2-O-beta-glucopyranoside acids (H4MP-G), along with gallic-4-O-be
56 zylidene-2-deoxy-2-trichloroacetamido-beta-D-glucopyranoside afforded the corresponding 4-O-benzoyl-6
57 nsporter 1 (SGLT1) substrate, methyl-alpha-D-glucopyranoside (alpha-MGP), stimulated release, whereas
58 afford 6-O-tetradecanoyl-alpha-d-cholesteryl glucopyranoside (alphaCAG) of Helicobacter pylori and th
60 f three cholesteryl-6-O-phosphatidyl-alpha-D-glucopyranosides (alphaCPG) unique to Helicobacter pylor
61 ethylene glycol, mannitol and alpha-methyl-D-glucopyranoside (alphaMDG) by control oocytes and by ooc
63 function of external Na+ and alpha-methyl-D-glucopyranoside (alphaMG) concentrations were consistent
64 -Reg(S20E), QEP, DFMO, and/or alpha-methyl-d-glucopyranoside (AMG), and measured AMG uptake, glucose-
65 s, 1,1,1,3,3,3-hexafluoropropan-2-yl alpha-d-glucopyranoside and 1,6-anhydro-beta-D-glucopyranose.
67 orm 1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside and acetate, the fourth overall step in
68 fo-2-acetamido-2-deoxy derivatives of beta-D glucopyranoside and beta-D-galactopyranoside were prepar
71 th, yielding higher levels of O-ethyl beta-d-glucopyranoside and d-glucose, and lower levels of malic
74 lly with a glucosidase, (Z)-3-hexenyl beta-D-glucopyranoside and linalyl beta-D-glucopyranoside were
75 representative carbohydrates, methyl alpha-D-glucopyranoside and methyl alpha-D-galactopyranoside.
76 ferol-3-O-beta-D-glucopyranosyl-(1-2)-beta-D-glucopyranoside and quercetin-3-O-beta-D-glucopyranosyl-
77 alues for the substrate p-nitrophenyl-beta-D-glucopyranoside and reduced sensitivity to competitive i
78 occupied by two molecules of n-octyl-beta-D-glucopyranoside and represents the phospholipid-binding
80 ter segment disk lipids using n-octyl beta-d-glucopyranoside and the detergent dialysis (DD) and rapi
81 -catalyzed hydrolysis of p-nitrophenyl-alpha-glucopyranoside and the lipoprotein lipase-catalyzed est
82 pha-lysophosphatidylcholine and octyl-beta-D-glucopyranoside) and activated by cholesterol enrichment
83 ilayer environment perturbed by octyl-beta-D-glucopyranoside) and under fully solubilizing conditions
84 4,5-trimethoxyphenyl-(6'-O-galloyl)-O-beta-D-glucopyranoside, and (6R,9R)-3-oxo-alpha-ionol-9-O-(6'-O
85 rom the corresponding (13)C-labeled methyl D-glucopyranosides, and multiple NMR J-couplings (J(HH), J
86 pyranosides, the alpha-sialosides, the alpha-glucopyranosides, and the beta-arabinofuranosides with a
89 not active with 4-methylumbelliferyl-alpha-D-glucopyranoside as the substrate and it did not bind to
92 tion, glycogen, D-xylose, and methyl-alpha-D-glucopyranoside assimilation, and growth at 35 degrees C
93 l 6-C-substituted 2-acetamido-2-deoxy-beta-D-glucopyranosides (beta-D-GlcNAc monosaccharides 1a-3a an
95 crystal growth, the additive n-heptyl-beta-d-glucopyranoside, binds near the activation function heli
96 cetin-3-O-beta-D-glucopyranosyl-(1-2)-beta-D-glucopyranoside, both of which were absent from the tepa
97 bisphosphate in the presence of n-octyl beta-glucopyranoside but not cetyltriethylammonium bromide.
98 rom 1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside by ligation with cysteine followed by ac
99 l precursor was prepared from methyl alpha-d-glucopyranoside by the biomimetic procedure of Bender an
100 lysed the hydrolysis of p-nitrophenyl-beta-D-glucopyranoside, cello-oligosaccharides, beta-linked glu
101 of nonionic detergents of the n-alkyl-beta-D-glucopyranoside class on the ordering of lipid bilayers
102 O-[alpha-L-rhamnopyranosyl-(1 --> 4)]-beta-d-glucopyranoside (compound 1) exhibited the best protecti
103 of the bioactive compound corotoxigenin-3-O-glucopyranoside; conversely, calotropin significantly de
104 tyl-1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside deacetylase (MshB) catalyzes the hydroly
105 tyl-1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside deacetylase (MshB) catalyzes the hydroly
107 concentrations of the detergent octyl-beta-d-glucopyranoside decreased rates of nitroalkene reaction
108 alactopyranosyl-(1->3)-2-acetamido-2-deoxy-d-glucopyranoside derivatives bearing a unique azide funct
109 MEG (methyl-6-O-(N-heptyl-carbamoyl)-alpha-D-glucopyranoside) detergent extraction in concert with hi
111 ide (NAG), deacetyl nomilinic acid 17-beta-D-glucopyranoside (DNAG), obacunone 17-beta-D-glucopyranos
113 Recently, epi-dihydrophaseic acid-3'-O-beta-glucopyranoside (epi-DPA-G) and astilbin, two molecules
114 EWL), while Apigenin and Apigenin 5-O-Beta-D-Glucopyranoside exhibited significant binding energy aga
115 3-galactoside and methyl gallate 3-O-beta-d-glucopyranoside, Ficus capensis (Cape fig) the most 3-CQ
118 benzyl-3,6-O-(di-tert-butylsilylene)-alpha-D-glucopyranoside gave alpha/beta mixtures with standard N
120 to 1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside (GlcN-Ins) and is the major thiol produc
121 d to 1D-myo-inosityl 2-amino-2-deoxy-alpha-D-glucopyranoside (GlcN-Ins) and is the predominant thiol
122 1D-myo-inosityl 2-acetamido-2-deoxy-alpha-D-glucopyranoside (GlcN-Ins), and is the major low-molecul
123 with 1D-myo-inosityl 2-amino-2-deoxy-alpha-D-glucopyranoside; GlcN-Ins) catalyzed by MshC to produce
124 1-D-myo-inosityl-2-acetamido-2-deoxy-alpha-D-glucopyranoside (GlcNAc-Ins), a hypothetical mycothiol b
126 serine, methionine, threonine, methyl alpha-glucopyranoside, glucose, penicillamine, valinol, phenyl
128 d by sugars with specificity: methyl alpha-D-glucopyranoside > D-glucose > D-galactose >> D-mannitol.
129 pounds, 2-hydroxy-3-methylpentanoic-2-O-beta-glucopyranoside (H3MP-G) and 2-hydroxy-4-methylpentanoic
131 actions isolated from homogenates with octyl glucopyranoside had cholesterol and sphingomyelin conten
132 s of nonionic detergents, the n-alkyl-beta-D-glucopyranosides, have on the phase behavior of hydrated
133 ty and the ability to acidify methyl-alpha-D-glucopyranoside helped recognize E. gallinarum and incre
134 ) by TPG hydrolyzing of (Z)-3-hexenyl-beta-D-glucopyranoside, hexanyl-beta-D-glucopyranoside (HGP), b
135 xenyl-beta-D-glucopyranoside, hexanyl-beta-D-glucopyranoside (HGP), benzyl-beta-D-glucopyranoside, pr
136 Michaelis-Menten parameters of 4-nitrophenyl glucopyranoside hydrolysis by sweet almond beta-glucosid
137 copyranosyl-(1-->2)-galactopyranosyl-(1-->2)-glucopyranoside, identified as potential taxonomic marke
138 20-fold larger affinity toward octyl-beta-d-glucopyranoside in CDCl(3), demonstrating the superior r
139 date for noncovalent 1:1 binding of an alpha-glucopyranoside in chloroform (Ka = 212,000 +/- 27,000 M
140 plexation of glutaric acid and beta-methyl d-glucopyranoside in chloroform were investigated through
141 2-phenylethylamine and 2-phenylethyl-beta-d-glucopyranoside in planta, whereas PtAAS1 likely contrib
142 n increased sensitivity to many bitter beta -glucopyranosides in the presence of the N172 allele.
145 ty B medium supplemented with methyl-alpha-D-glucopyranoside (investigational), motility S medium, mo
146 dines 40 and 41 starting from methyl alpha-d-glucopyranoside is described and will be used as a templ
147 etin-3-O-(6-O-alpha-l-rhamnopyranosyl-beta-d-glucopyranoside) is usually assessed by means of high pe
148 -(N-acetyl-L-cysteinyl)amido-2-deoxy-alpha-D-glucopyranoside, is an unusual conjugate of N-acetylcyst
149 onoid glucosides, that is, limonin 17-beta-D-glucopyranoside (LG), nomilin 17-beta-D-glucopyranoside
150 R)-3-oxo-alpha-ionol-9-O-(6'-O-galloyl)-beta-glucopyranoside (macarangioside E) were isolated and ide
151 were: alpha-methyl-4-[F-18]-fluoro-4-deoxy-d-glucopyranoside (Me-4FDG), a substrate for SGLTs; 4-deox
154 alog, alpha-methyl-4-deoxy-4-[(18)F]fluoro-D-glucopyranoside (Me4FDG), which is not transported by GL
155 y (13)C-labeled methyl 2-deoxy-2-acetamido-d-glucopyranoside (MeGlcNAc) anomers were investigated, le
156 y (13)C-labeled methyl 2-deoxy-2-formamido-d-glucopyranoside (MeGlcNFm) anomers provided standard (1)
158 inose (ARA), acidification of methyl-alpha-D-glucopyranoside (MGP), and rapid motility (RM), for diff
159 -(N-acetyl-l-cysteinyl)amido-2-deoxy-alpha-d-glucopyranoside (MSH or AcCys-GlcN-Ins), to act against
161 ucopyranoside (NG), nomilinic acid 17-beta-D-glucopyranoside (NAG), deacetyl nomilinic acid 17-beta-D
162 ta-d-galactopyranosyl-(1-->4)-1-thio-beta -d-glucopyranoside; Neu5Acalpha2,3LacbetaSPh, and the corre
163 ta-D-glucopyranoside (LG), nomilin 17-beta-D-glucopyranoside (NG), nomilinic acid 17-beta-D-glucopyra
164 ccharide surfactants, such as n-octyl-beta-d-glucopyranoside (NOG), are widely used to solubilize or
165 yranoside (OG), and obacunoic acid 17-beta-D-glucopyranoside (OAG) were investigated using a quadrupl
166 lactopyranosyl)-2-trichlo roacetamido-beta-D-glucopyranoside, obtained by regioselective reductive op
167 and further solubilised using n-octyl beta-D-glucopyranoside (OctGlc) and n-dodecyl beta-D-maltoside
168 of the non-ionic detergents, n-octyl beta-D-glucopyranoside (octyl glucoside) and Triton X-100R-PC (
169 -glucopyranoside (DNAG), obacunone 17-beta-D-glucopyranoside (OG), and obacunoic acid 17-beta-D-gluco
170 ermine the respective CMCs of n-octyl beta-d-glucopyranoside (OG), n-dodecyl beta-d-maltopyranoside (
171 profound inhibitory effect of n-octyl-beta-d-glucopyranoside (OG), the detergent used for LeuT crysta
173 sodium dodecyl sulfate (SDS), n-octyl-beta-D-glucopyranoside (OGP), and Zwittergent 3-14 (Z3-14).
174 subunit distances in detergent (octyl beta-d-glucopyranoside, OGP) purified and OMM bound forms by a
175 d AglA recognized glucose and methyl-alpha-D-glucopyranoside, only AglA accepted other alpha-D-glucos
176 to lead to beta-d-galactopyranosyl-(1->3)-d-glucopyranoside or beta-d-galactopyranosyl-(1->3)-2-acet
178 etergents or in the presence of n-octyl beta-glucopyranoside or Triton X-100, but not in the presence
181 ays were conducted with p-nitrophenyl-beta-d-glucopyranoside (PNPG) and demonstrate that the Cu-HisPi
183 ium cation-attached alpha- and beta-O-methyl-glucopyranoside precursor ions, formed by electrospray i
184 -beta-D-glucopyranoside (HGP), benzyl-beta-D-glucopyranoside, prunasin and geranyl-beta-D-glucopyrano
185 tigated the capacity of quercetin-3-O-beta-d-glucopyranoside (Q3G) isolated from Echinophora cinerea
187 Y, binding of a galactopyranoside, but not a glucopyranoside, results in a decrease in distance on th
188 1-pentyl-beta-D-maltoside and n-octyl-beta-D-glucopyranoside revealed highly homogeneous oligomers an
189 ing using 5-bromo-4-chloro-3-indolyl-alpha-D-glucopyranoside revealed that the acidic alpha-glucosida
190 Application to methyl alpha- and beta-D-glucopyranosides reveals different rotameric distributio
191 ted to access 2-aryl/alkenyl-methylene-alpha-glucopyranoside scaffolds via a three-step sequence incl
192 uronides to corresponding J-couplings in the glucopyranosides showed that more pervasive changes occu
193 e encoding a taste receptor for bitter beta -glucopyranosides, shows significant association with alc
194 d with the nonionic detergent n-octyl-beta-d-glucopyranoside, suggesting that perturbation of the int
195 nce aesculin, 6,7-dihydroxycoumarin-6-O-beta-glucopyranoside, suppresses inflammation, we asked wheth
197 en cyclohexenyl-based carbasugars of alpha-d-glucopyranoside that we show are good covalent inhibitor
198 rous experimental studies have shown that in glucopyranosides the omega-torsion angle (O(6)-C(6)-C(5)
199 l was compared against that of thymol-beta-D-glucopyranoside, the latter being resistant to absorptio
200 (1-->3)-2-deoxy-2-trichlor oacetamido-beta-d-glucopyranoside, the product of site-specific enzymatic
201 anes by the nonionic detergent n-octyl- beta-glucopyranoside; the soluble fraction was loaded at pH 7
202 tyl-1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside to form 1-D-myo-inosityl-2-amino-2-deoxy
203 tyl-1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside to form 1-D-myo-inosityl-2-amino-2-deoxy
204 he intrinsic reactivity, for 4,6-O-protected glucopyranosides (trans-diols) as well as 4,6-O-protecte
206 acid production was reduced by thymol-beta-D-glucopyranoside treatment, indicating that fermentation
207 opyranosyl-(1-->4)-2,3,6-tri-O -sulfo-beta-d-glucopyranoside, tridecasodium salt (PG545, 18) as a cli
208 including MG-1655, accumulate methyl-alpha-D-glucopyranoside via the phosphoenolpyruvate-dependent gl
211 t time that vanillin-(6'-O-galloyl)-O-beta-D-glucopyranoside was identified and the first time that m
212 zation (CTI) in methyl 2-deoxy-2-acylamido-d-glucopyranosides was investigated by (1)H and (13)C NMR
213 1 --> 4)-beta-D-glucopyranoside]-26-O-beta-D-glucopyranoside were found as key bitter contributors af
214 yl beta-D-glucopyranoside and linalyl beta-D-glucopyranoside were identified as aroma precursors in P
215 d its nonmetabolizable analog methyl alpha-D-glucopyranoside were measured with 33-ms time resolution
216 , ocotillone, and beta-sitosterol 3-O-beta-D-glucopyranoside, were also isolated and characterized.
217 allyl 2,6-dideoxy-2-N-trifluoroacetyl-beta-d-glucopyranoside when addressing the feasibility of synth
219 2-phenylethylamine and 2-phenylethyl-beta-d-glucopyranoside, whereas the emission of 2-phenylethanol
220 zylidene-2-deoxy-2-trichloroacetamido-beta-d-glucopyranoside with 3,4,6-tri-O-acetyl-2-O-bromoacetyl-
222 raphy in the presence of 0.2% n-octyl-beta-D-glucopyranoside yields a molecular weight of approximate