ライフサイエンスコーパス: gluco

1 configuration binding more tightly than the gluco.

2 cosidase enzymes and compared with natural d-gluco-1-deoxynojirimycin (DNJ).

3 terification of the epoxide derived from the gluco-[13]-macro-dilactone.

4 ontaining mixed-valent Fe1(III)(mu-OH(-))(mu-GluCO(2)(-))(2)Fe2(II) and Fe1(II)(mu-GluCO(2)(-))(2)Fe2

5 -))(mu-GluCO(2)(-))(2)Fe2(II) and Fe1(II)(mu-GluCO(2)(-))(2)Fe2(III)-OH(-) cores.

6 lactose, (2) 2-acetamido-2-deoxy-3-O-(beta-D-gluco-4-enepyranosyluronic acid)-4-O-sulfo-D-galactose,

7 ose, and (3) 2-acetamido-2-deoxy-3-O-(beta-D-gluco-4-enepyranosyluronic acid)-6-O-sulfo-D-galactose,

8 harides, (1) 2-acetamido-2-deoxy-3-O-(beta-D-gluco-4-enepyranosyluronic acid)-D-galactose, (2) 2-acet

9 Intestinal infusion with di(glucos-6-yl)poly(ethylene glycol) 600 led to induction o

10 membrane impermeable d-glucose analogue, di(glucos-6-yl)poly(ethylene glycol) 600, was synthesized a

11 model compounds that mimic alpha-gluco, beta-gluco, alpha-allo, and beta-allo 2-acetamido-2-deoxy-D-a

12 Non-digestible dietary galacto- and gluco-alpha-(1,6)-oligosaccharides from legumes and star

13 s were established for the synthesis of beta-gluco and alpha- and beta-manno-configured phostones of

14 ituted iminosugars of both configurations (D-gluco and L-ido) with the aim to introduce structural fe

15 previous work, we synthesized a series of D-gluco and L-ido-configured iminosugars N-modified with a

16 ity of both lectins to differentiate between gluco and manno diastereomers was diminished in the C-gl

17 ly different stereoselectivities in both the gluco and manno, but not the galacto series.

18 nd to the alpha and beta anomers of methyl D-gluco- and D-galactopyranoside as guests.

19 oducts of catalysis and in complex with both gluco- and galacto-configured inhibitors O-(2-acetamido-

20 sets of interaction were maintained with the gluco- and galacto-configured inhibitors, the inhibition

21 ve evolved to discriminate primarily between gluco- and galactopyranosides.

22 ercise in mammals, with hepatic and muscular gluco- and glyconeogenesis contributing to a lesser exte

23 g finger protein-1 (MuRF1) protected against gluco- and lipotoxicity-induced apoptosis.

24 Both GTDF and metformin protected against gluco- and lipotoxicity-induced osteoblast apoptosis, an

25 ammonium phosphonite-borane complexes in the gluco- and manno-like series have been developed from P(

26 roved strategy for the synthesis of P-chiral gluco- and manno-phosphonite-borane complexes is describ

27 O-benzyl-4,6-O-benzylidene-protected 3-deoxy-gluco- and mannopyranosyl thioglycosides is highly stere

28 2 and BPS were metabolized into a variety of gluco- and sulfo-conjugated metabolites.

29 inding protein which recognizes alpha-linked gluco-and manno-pyranosyl groups of polysaccharide chain

30 stereoselectivity of couplings to galacto-, gluco-, and mannopyranosyl thioglycosides, otherwise pro

31 Previously, antibodies specific to a gluco-asparagine (N-Glc) glycopeptide, CSF114(N-Glc), we

32 nts in four model compounds that mimic alpha-gluco, beta-gluco, alpha-allo, and beta-allo 2-acetamido

33 llenging glycosidic linkages including alpha-gluco, beta-manno, and beta-rhamno have seen obtained wi

34 nd WP400 (2'-bromo-4'-epidaunorubicin, alpha-gluco configuration), is significantly less cytotoxic.

35 The galacto/gluco configurational change takes place at the level of

36 Gluco-configured macro-dilactones gave the R, R epoxide,

37 ls have revealed an inverse relation between gluco-corticoid levels and hippocampus volumes.

38 Their D-gluco-counterparts are also potent inhibitors of intesti

39 ner-like intake of glucose during subsequent gluco-deprivation.

40 was acetylated prior to isolation while the gluco-dialdehyde afforded a mixture of three stereoisome

41 The reduced affinity of D-gluco-dihydroacarbose (K1 = 10(-8) M) relative to acarbo

42 var. X100 with the pseudotetrasaccharides D-gluco-dihydroacarbose and acarbose have been refined to

43 ic contacts between the nonreducing end of D-gluco-dihydroacarbose and the catalytic water perturb Wa

44 ational distortion of the first residue of D-gluco-dihydroacarbose is consistent with the generation

45 In the case of D-gluco-dihydroacarbose the shift in the position of the 6

46 f the nonreducing end of both acarbose and D-gluco-dihydroacarbose toward a more axial position.

47 configuration, ranging from 1.5 to 13, with gluco exhibiting the smallest ratio and gulo the largest

48 ide derivative of the 6-O-methyl-D-glycero-L-gluco-heptopyranose residue found in the Campylobacter j

49 we show that WcaGNCTC is not necessary for L-gluco-heptose synthesis and does not affect its producti

50 dation for elucidation of the more complex L-gluco-heptose synthesis pathway of Campylobacter jejuni

51 /C5 epimer generated by MlghB and produces L-gluco-heptose via stereospecific C4 reductase activity.

52 ycosyl residue, 3-acetimidoylamino-3-deoxy-d-gluco-hexuronic acid was identified and characterized, a

53 sions of these to a range of heparin-related gluco-ido disaccharide building blocks (various C-4 prot

54 at small intestine to study the secretion of gluco-insulinotropic peptide (GIP), glucagon-like peptid

55 ced by E. coli, while beta-glucosidase (beta-gluco) is produced by Enterococcus spp.

56 heless, the degree of acetylation of xylan, (gluco)mannan, and xyloglucan as well as overall cell wal

57 the identification of GDP-D-erythro-alpha-D-gluco-octose (GDP-D-alpha-D-octose) as a key intermediat

58 leading to the identification of D-erythro-D-gluco-octose 8-phosphate as a key intermediate.

59 tose, and resulted in the synthesis of novel gluco-oligosaccharides in which alpha1,3-linked glucosyl

60 Soaking with isomaltotriose or gluco-oligosaccharides led to structures in which isomal

61 fd-glucosyl units from sucroseto dextrans or gluco-oligosaccharides via the formation of alpha-(1-->2

62 4-Amino-3-(d-gluco-pentitol-1-yl)-4,5-dihydro-1,2,4-triazole-5-thione

63 increase hemolymph glucose, an indication of gluco-privation, but instead of increasing feeding it ei

64 -4-hydroxymethyl)-phenyl-6-O-caffeoyl-beta-d-gluco-pyranoside (2), protocatechuic acid (3), gallic ac

65 alpha-D-glucopyranosyl-(6d --> 1e)-O-alpha-D-gluco-pyranoside (6) along with two known compounds n-he

66 It is unclear, however, if hepatic gluco-regulation is altered in G4Tg mice in the basal, n

67 bolism in G4Tg mice and to determine whether gluco-regulatory adaptations exist in the non-insulin-st

68 ake in extra-hepatic sites provoke important gluco-regulatory adaptations in the liver.

69 the relaxation of this torsion angle in the gluco series.

70 tive providing the alpha-C-glycosides in the gluco-series and the beta-C-glycosides in the manno-seri

71 lylation and a triflate inversion to set the gluco-stereochemistry in addition to Luche reduction and

72 ing beta-selective glucosylation followed by gluco to manno epimerization at a late stage of the synt