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1 mnopyranose, beta-D-galactopyranose, alpha-L-glucopyranose).
2 pha-d-glucopyranoside and 1,6-anhydro-beta-D-glucopyranose.
3 ced with the sugar 2,3-diamino-2,3-dideoxy-d-glucopyranose.
4 lative stereochemistry of 4,6-O-ethylidene-d-glucopyranose.
5 yl)-(1->4)-O-alpha-D-glucopyranosyl-(1->4)-D-glucopyranose.
6 2,6-dimethoxyphenol; and 1,6-anhydro-beta-D-glucopyranose.
8 do-3-O-[(R)-3-hydroxy-hexadecanoyl]-alpha-d-glucopyranose (11) and 2-deoxy-6-O-[2-deoxy-3-O-[(R)-3-h
9 henolic compounds 1-O-trans-cinnamoyl-beta-d-glucopyranose (2), ellagic acid (3), myricetin (4), quer
10 NO donors NOC-18 and N-(2-deoxy-alpha,beta-d-glucopyranose-2-)-N2-acetyl-S-nitroso-d,l-penicillaminam
11 ne derivative of D-glucose,3-deoxy-3,3-azi-D-glucopyranose (3-DAG), and studied its interaction with
12 to-C(o) ratio 0.89 +/- 0.07 for 3-O-methyl-d-glucopyranose (3OMG) ranged widely (0.72-1.04, n = 26).
13 tamido-1,3,6-tri-O-acetyl-4-deoxy-4-fluoro-D-glucopyranose [4-F-GlcNAc]) to alter HECA-452 expression
14 el compounds, 6-deoxytetra-O-galloyl-alpha-D-glucopyranose (43) and tetra-O-galloyl-alpha-D-xylopyran
15 hyl citrate (1), sinapic aldehyde 4-O-beta-d-glucopyranose (5), 3,3',4-tri-O-methylellagic acid-4'-O-
17 loro-6-deoxy-1,2,3,4-tetra-O-galloyl-alpha-D-glucopyranose (80) exhibits a significantly higher gluco
18 ucopyranosyl)-1,6-di-O-pentadecanoyl-alpha-D-glucopyranose a novel fatty acid derivative (2) were iso
19 tamido-1,3,6-tri-O-acetyl-4-deoxy-4-fluoro-D-glucopyranose) action by contrasting the effects on sial
21 ,3,4-tri-O-acetyl-2-amino-2,6-dideoxy-beta-d-glucopyranose and allyl 2-amino-2,6-dideoxy-beta-d-gluco
22 we have computationally docked alpha/beta-D-glucopyranose and alpha/beta-(1-->2)-, alpha/beta-(1-->3
23 -(beta-D-glucopyranosyl)-1-O-octanoyl-beta-D-glucopyranose and asperulosidic acid, extracted from the
24 a-glucopyranose to its equilibrium with beta-glucopyranose, and these were converted into unidirectio
25 te 2, 4-diacetamido-2, 4, 6-trideoxy-alpha-D-glucopyranose (BacAc(2)) is found in a variety of eubact
27 nprotected 2-deoxy glycosyl cations in the d-glucopyranose, d-galactopyranose, and l-arabinofuranose
28 their respective high-energy 1-O-acyl-beta-D-glucopyranose derivatives is followed by transfer of the
29 The synthesis of a variety of new 1-thio-D-glucopyranose derivatives oxidized at the sulfur atom is
31 troso-2,3,4, 6-tetra-O-acetyl-1-alpha,beta-D-glucopyranose ester (24) were evaluated against subcutan
32 of-beta-1,6 linked 2,3-dideoxy-2,3-diamno-d-glucopyranose further modified with galacturonic acid in
33 ranosyluronic acid, GlcNp is 2-amino-2-deoxy-glucopyranose, GlcAp is glucopyranosyluronic acid, S is
34 lecules containing 2,3-diamino-2,3-dideoxy-d-glucopyranose (GlcN3N) units in place of glucosamine, do
35 y of the alpha- and beta-anomeric forms of D-glucopyranose in water using deuterium conformational eq
36 yl)-(1->4)-O-alpha-D-glucopyranosyl-(1->4)-D-glucopyranose is produced from dTDP-4-amino-4,6-dideoxy-
37 y that PGG (1,2,3,4,6-penta-O-galloyl-beta-D-glucopyranose) is a CMG2 inhibitor with antiangiogenic a
38 on, the inverted product, 1,6-anhydro-beta-D-glucopyranose, is formed by intramolecular capture of a
41 UDP 2-acetamido-3-amino-2,3-dideoxy-alpha-d-glucopyranose or UDP-GlcNAc3N), characterized in the pre
42 s of poly-(1-6)-beta-glucotriosyl-(1-3)-beta-glucopyranose (PGG) glucan, a biological-response modifi
43 alpha- and beta-anomers of penta-O-galloyl-D-glucopyranose (PGG), 2 and 3, act as insulin mimetics th
44 al origin, 1,2,3,4,6-penta- O-galloyl-beta-d-glucopyranose (PGG), binds to capillary morphogenesis ge
45 des, poly-(1-6)-beta-glucotriosyl-(1-3)-beta-glucopyranose (PGG)-glucan and Bacteroides fragilis poly
46 involved in binding, but play a role in the glucopyranose ring distortion necessary for catalysis.
47 n invariant protein conformation, the beta-D-glucopyranose ring in the betaG1P TSA complexes (step 1)
48 depolymerization via ring contraction of the glucopyranose ring to the glucofuranose ring occurs with
49 degrees change in two dihedral angles of the glucopyranose ring toward a half-chair conformation.
50 e force-induced chair-to-boat transitions of glucopyranose rings are responsible for the characterist
51 n elasticity caused by the conversion of its glucopyranose rings from the chair to the boat conformat
53 as alpha,beta-trehalose, which connects its glucopyranose rings via a (1-->1) linkage in an axial, e
54 l protecting group arrays cyclization in the glucopyranose series is more rapid than in the mannopyra
56 ejuni 2,4-diacetamido-2,4,6-trideoxy-alpha-d-glucopyranose, termed N,N'-diacetylbacillosamine (Bac2,4
57 s levoglucosan and 1,4:3,6-dianhydro-alpha-D-glucopyranose to a common intermediate with calculated b
58 licyl chloride with 2,3,4,6-tetra-O-benzyl-D-glucopyranose to give [[(2,3,4,6-tetra-O-benzyl-D-glucop
59 on the rate constants for approach of alpha-glucopyranose to its equilibrium with beta-glucopyranose
61 2-acetamido-4-amino-2, 4, 6-trideoxy-alpha-D-glucopyranose (UDP-4-amino-sugar) to form UDP-BacAc(2).
63 rom six, seven, and eight alpha-1,4-linked d-glucopyranose units and are industrially produced on ton
64 ndrimers containing 8, 12, 16, and 24 beta-D-glucopyranose units at the periphery, have been synthesi
65 delta-CD (formed from nine alpha-1,4-linked glucopyranose units) has received very little attention.
68 ng ligand, Beta-1, 2,3,4,6-Penta-O-Galloyl-D-Glucopyranose was reported to be a naturally occurring t
69 nhydrosugar levoglucosan (1,6-anhydro-beta-d-glucopyranose), which can be converted to glucose 6-phos
70 ackbone containing mostly 3-substituted beta-glucopyranose with 4-substituted glucopyranosyluronic ac