2,5-Deoxyfructosazine, a D-glucosamine derivative, inhibits T-cell interleukin-2 production better than D-glucosamine. - Wikidata - wikimedia - TriplyDB

2,5-Deoxyfructosazine, a D-glucosamine derivative, inhibits T-cell interleukin-2 production better than D-glucosamine.

2,5-Deoxyfructosazine, a D-glucosamine derivative, inhibits T-cell interleukin-2 production better than D-glucosamine.

http://www.wikidata.org/entity/Q37378455

about

Total synthesis and determination of the absolute configuration of a natural analgesic: crotonine.Glucosamine condensation catalyzed by 1-ethyl-3-methylimidazolium acetate: mechanistic insight from NMR spectroscopy.

P2860

Q46096087-44910C37-097D-4DEE-AF93-339857EB4F13 Q51807320-F269C043-1939-47BB-9B22-B35E0154E0D0

P2860

2,5-Deoxyfructosazine, a D-glucosamine derivative, inhibits T-cell interleukin-2 production better than D-glucosamine.

http://www.wikidata.org/entity/Q37378455

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 07 September 2007

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

2,5-Deoxyfructosazine, a D-glu ...... ion better than D-glucosamine.

@en

2,5-Deoxyfructosazine, a D-glu ...... ion better than D-glucosamine.

@nl

type

label

2,5-Deoxyfructosazine, a D-glu ...... ion better than D-glucosamine.

@en

2,5-Deoxyfructosazine, a D-glu ...... ion better than D-glucosamine.

@nl

prefLabel

2,5-Deoxyfructosazine, a D-glu ...... ion better than D-glucosamine.

@en

2,5-Deoxyfructosazine, a D-glu ...... ion better than D-glucosamine.

@nl

P1433

Q37378455-C383F1D9-60B6-4029-AFF7-74253B8C085E

P1476

Q37378455-C727C3C4-5DA3-49BB-A39D-2F05F066FE80

P2093

Q37378455-14666F13-B770-4101-B1AF-1B94FC328B01

Q37378455-15A13E3C-CD38-494E-A84A-F7387104F5C7

Q37378455-58BE000F-78FE-420C-8589-E85EFB7E1491

Q37378455-DDA35BE0-409A-4E15-AF66-4904CFDA93B8

P2860

Q37378455-0C6994B9-6C14-4D53-99A6-3E14588F6408

Q37378455-2128AD7E-AF9C-42F4-A8F7-62D402A56904

Q37378455-2B3BDB73-B134-4ECC-8B8B-A668D0EF523A

Q37378455-2EDEBA06-CF70-4406-8A50-C1390C2873CE

Q37378455-394E211B-F016-461E-8F1F-7B1184C1A643

Q37378455-39786318-CC4D-4B37-983D-43B3F53E7DC4

Q37378455-3F20F22D-52BF-4F6E-BE00-DD8942A99828

Q37378455-42F4C67D-3224-4998-8F2C-D4F43DE8E77C

Q37378455-441201C0-BD77-43A0-A18B-3C7EEA589FCF

Q37378455-65650A7F-BA53-4ECB-B7C2-ACDF1088F07C

P304

Q37378455-9114F801-CA95-44E9-88FB-BAF853802654

P31

Q37378455-66685720-430E-4C80-8EBC-670454BB044F

P356

Q37378455-9FDD1CF5-2D91-4AF4-B579-5734119EC676

P433

Q37378455-314AD8C1-5778-4E1E-96AB-4CBA1A1A4FE5

P478

Q37378455-9753BFB4-5B70-4BDE-AD0B-19CB96312842

P50

Q37378455-D0B6B60D-5A5C-4CD4-AD45-BC8CD7CC4127

P577

Q37378455-4E7B3980-E6C9-4DB8-A7DC-B8270F7BC049

P5875

Q37378455-86328993-2933-4FAF-90FC-5EE9895B7265

P698

Q37378455-FB17557C-B757-45BF-8A59-A390EB059383

P921

Q37378455-152447bf-76fe-4c0a-ae8d-4a4bfa821c49

P932

Q37378455-DC672887-9217-42F0-BD75-62A5D9B187E4

P356

J.CARRES.2007.08.025

P1433

Carbohydrate Research

P1476

2,5-Deoxyfructosazine, a D-glu ...... ion better than D-glucosamine.

@en

P2093

Aiping Zhu

http://www.w3.org/2001/XMLSchema#string

Andrea Clark

http://www.w3.org/2001/XMLSchema#string

Howard R Petty

http://www.w3.org/2001/XMLSchema#string

Ji-Biao Huang

http://www.w3.org/2001/XMLSchema#string

P2860

The hexosamine signaling pathway: deciphering the "O-GlcNAc code"

Small-scale analysis of O-linked oligosaccharides from glycoproteins and mucins separated by gel electrophoresis.

The hexosamine biosynthesis pathway negatively regulates IL-2 production by Jurkat T cells.

Microanalysis of N-linked oligosaccharides in a glycoprotein by capillary liquid chromatography/mass spectrometry and liquid chromatography/tandem mass spectrometry.

Increased flux through the hexosamine biosynthesis pathway inhibits glucose transport acutely by activation of protein kinase C.

Use of porous graphitic carbon coupled with mass detection for the analysis of polar phenolic compounds by liquid chromatography.

Inhibitory actions of glucosamine, a therapeutic agent for osteoarthritis, on the functions of neutrophils.

On-line high-performance liquid chromatography/mass spectrometric characterization of native oligosaccharides from glycoproteins.

Immunosuppressive effects of glucosamine.

Structure-retention diagrams of ceramides established for their identification.

P304

2745-2749

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1016/J.CARRES.2007.08.025

http://www.w3.org/2001/XMLSchema#string

P433

18

http://www.w3.org/2001/XMLSchema#string

P478

342

http://www.w3.org/2001/XMLSchema#string

P50

P577

2007-09-07T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

5951360

http://www.w3.org/2001/XMLSchema#string

P698

17892867

http://www.w3.org/2001/XMLSchema#string

P921

P932

2758268

http://www.w3.org/2001/XMLSchema#string