ライフサイエンスコーパス: mannopyranoside

1 e furanosylation of p-nitrophenyl 6-O-acetyl mannopyranoside.

2 yl 3,6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside.

3 lglucosamine to 3-0-alpha-D-mannopyranosyl-D-mannopyranoside.

4 the buffer containing 500 mM alpha-methyl-D-mannopyranoside.

5 60-fold higher affinity than methyl-alpha-D-mannopyranoside.

6 nnose-GPs was blocked by free methyl-alpha-D-mannopyranoside.

7 is efficiently antagonized by biaryl alpha-d-mannopyranosides.

8 o- and fucopyranosides and 2,3-O-unprotected mannopyranosides.

9 xybenzyl 2,6-dideoxy-2-iodo-3-C-methyl-alpha-mannopyranoside (11).

10 de, lactulose, 4-O-beta-D-galactopyranosyl-D-mannopyranoside, 3-O-beta-D-galactopyranosyl-D-arabinose

11 The SAMs present mixtures of alpha-D-mannopyranoside (a ligand that promotes the adhesion of

12 labeled parasites on a p-aminophenyl alpha-D-mannopyranoside-agarose column.

13 une response elicited against methyl alpha-d-mannopyranoside and also bound equivalently to a dodecap

14 O-carbonyl-4, 6-O-benzylidene-1-thia-alpha-D-mannopyranoside and ethyl 3-O-benzoyl-4, 6-O-benzylidene

15 -dimethoxybutane-2', 3'-diyl)-1-thia-alpha-D-mannopyranoside and its sulfoxide, following activation

16 yl 3,6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside and to a series of asparagine-linked oli

17 yl 3,6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside, and are a useful model system for addre

18 -->6)-[alpha-D-mannopyranosyl-(1-->6)](7) -D-mannopyranoside, and the glycosyl donor C(50) -polypreno

19 he direct stereocontrolled synthesis of beta-mannopyranosides are presented.

20 ol released/min/mg with p-nitrophenyl-beta-D-mannopyranoside as substrate.

21 f the sPLA2 receptor, p-amino-phenyl-alpha-D-mannopyranoside BSA, also induced an increase in cPLA2 a

22 direct and stereoselective synthesis of beta-mannopyranosides by anomeric O-alkylation has been devel

23 Analogous results were obtained with mannopyranoside derivatives with either 4,6-O-benzyliden

24 but having no detectable affinity for alpha-mannopyranosides, for certain architectural arrangements

25 atalyzed hydrolysis of 4-nitrophenyl alpha-d-mannopyranoside in aqueous media has been studied by the

26 lds anomerically pure 2,3-di-O-benzyl-beta-D-mannopyranosides in excellent yield.

27 Numerous alpha-d-mannopyranosides, including alpha-d-heptyl mannose (HM),

28 Methyl alpha-D-mannopyranoside inhibited the growth of A. castellanii b

29 yl 3,6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside is presented.

30 rolled synthesis of the 3-amino-3-deoxy-beta-mannopyranosides is achieved by means of thioglycoside d

31 uce p-isothiocyanatophenyl-6-phospho-alpha-d-mannopyranoside (itcM6P) for conjugation with BSA.

32 sides are first used to introduce the beta-d-mannopyranoside linkage in high yield and stereoselectiv

33 P-aminophenyl-alpha-d-mannopyranoside (MAN), a kind of mannose analog, was con

34 t the crystal growth faces of methyl alpha-D-mannopyranoside (MDM), a representative pyranose sugar,

35 enhancement in affinity over methyl alpha-d-mannopyranoside (MeMan).

36 enyl-labeled substrate p-nitrophenyl-alpha-D-mannopyranoside (MNP), and indoxyl phosphate were found

37 ose (PYG) and PYG with 100 mM methyl alpha-D-mannopyranoside or galactose.

38 SA) by phosphorylating p-nitrophenyl-alpha-d-mannopyranoside, reducing its nitro group, and reacting

39 es using the new substrate resorufin alpha-d-mannopyranoside (Res-Man).

40 roup present at the O-2 position of a single mannopyranoside residue, followed by glycosylation with

41 al 3,6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside residues to ConA and DGL were subjected

42 al 3,6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside residues to the lectin concanavalin A (C

43 Dimeric analogs possessing terminal alpha-D-mannopyranoside residues, and di-, tri-, and tetrameric

44 l 3, 6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside residues, which is the core trimannoside

45 lexibility and length between terminal alpha-mannopyranoside residues.

46 yl-4, 6-O-benzylidene-1-deoxy-1-thia-alpha-D-mannopyranoside S-oxide is treated with triflic anhydrid

47 dosis fibroblasts, and p-nitrophenyl-alpha-D-mannopyranoside substrates.

48 d applied to the 4,6-O-benzylidene-protected mannopyranoside system.

49 for the synthesis of divalent biaryl-linked mannopyranosides that was subsequently generalized towar

50 the 2-deoxy-beta-glycopyranosides, the beta-mannopyranosides, the alpha-sialosides, the alpha-glucop

51 nii trophozoites are grown in methyl-alpha-D-mannopyranoside, they are induced to secrete a novel 133

52 yl 3,6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside to ConA and DGL are linear with slopes n

53 yl 3,6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside (trimannoside) have been determined at n

54 , 3, 6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside was determined by isothermal titration m

55 l 3, 6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside, which contains two of the most commonly

56 y, 3,6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside, which is present in all asparagine-link

57 , 3, 6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside, which is present in asparagine-linked c