155-84-0 | Ac-Arg-OH

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$26.00	$18.00
5g	97%	in stock	$34.00	$24.00
25g	97%	in stock	$82.00	$58.00
100g	97%	in stock	$251.00	$176.00
500g	97%	in stock	$760.00	$532.00

Description

• Catalog Number: AA76968
• Chemical Name: Ac-Arg-OH
• CAS Number: 155-84-0
• Molecular Formula: C8H16N4O3
• Molecular Weight: 216.2376
• MDL Number: MFCD00019733
• SMILES: NC(=N)NCCC[C@@H](C(=O)O)NC(=O)C

Computed Properties

• Complexity: 261
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 4
• Rotatable Bond Count: 6
• XLogP3: -1.7

Literature

• Metabolic variation during development in culture of Leishmania donovani promastigotes.

  PLoS neglected tropical diseases 20111201

• Topical application of L-arginine blocks advanced glycation by ascorbic acid in the lens of hSVCT2 transgenic mice.

  Molecular vision 20110101

• Reaction of the butter flavorant diacetyl (2,3-butanedione) with N-α-acetylarginine: a model for epitope formation with pulmonary proteins in the etiology of obliterative bronchiolitis.

  Journal of agricultural and food chemistry 20101222

• Simultaneous chemical and photochemical protein crosslinking induced by irradiation of eye lens proteins in the presence of ascorbate: the photosensitizing role of an UVA-visible-absorbing decomposition product of vitamin C.

  Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20101028

• Guanidino compounds inhibit acetylcholinesterase and butyrylcholinesterase activities: effect neuroprotector of vitamins E plus C.

  International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 20101001

• Behaviour of 4-(-2-hydroxyethyl)-1-piperazineethanesulfonic acid under electrospray ionization mass spectrometry conditions.

  European journal of mass spectrometry (Chichester, England) 20100101

• The formation of argpyrimidine in glyceraldehyde-related glycation.

  Bioscience, biotechnology, and biochemistry 20080201

• Detection of kynurenine modifications in proteins using a monoclonal antibody.

  Journal of immunological methods 20070731

• Arginine improves protein elution in hydrophobic interaction chromatography. The cases of human interleukin-6 and activin-A.

  Journal of chromatography. A 20070622

• Isolation and identification of 5-methyl-imidazolin-4-one derivative as glyceraldehyde-derived advanced glycation end product.

  Bioscience, biotechnology, and biochemistry 20060601

• Effective elution of antibodies by arginine and arginine derivatives in affinity column chromatography.

  Analytical biochemistry 20051015

• Model studies on the influence of high hydrostatic pressure on the formation of glycated arginine modifications at elevated temperatures.

  Journal of agricultural and food chemistry 20050713

• 3-hydroxykynurenine-mediated modification of human lens proteins: structure determination of a major modification using a monoclonal antibody.

  The Journal of biological chemistry 20050610

• Identification of N7-(1-carboxyethyl)-arginine, a novel posttranslational protein modification of arginine formed at high hydrostatic pressure.

  Annals of the New York Academy of Sciences 20050601

• Chemistry and biological effects of melanoidins and glyceraldehyde-derived pyridinium as advanced glycation end products.

  Annals of the New York Academy of Sciences 20050601

• Characterization of bis(levuglandinyl) urea derivatives as products of the reaction between prostaglandin H2 and arginine.

  Biochemistry 20040511

• In vitro effects of L-arginine and guanidino compounds on NTPDase1 and 5'-nucleotidase activities from rat brain synaptosomes.

  International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 20030401

• A role for guanidino compounds in the brain.

  Molecular and cellular biochemistry 20030201

• Oligomeric structure of proclavaminic acid amidino hydrolase: evolution of a hydrolytic enzyme in clavulanic acid biosynthesis.

  The Biochemical journal 20020901

• Antioxidant activity of coffee model systems.

  Journal of agricultural and food chemistry 20020619

• Ligand-selective modulation of the permeability transition pore by arginine modification. Opposing effects of p-hydroxyphenylglyoxal and phenylglyoxal.

  The Journal of biological chemistry 20020111

• In vitro stimulation of oxidative stress in cerebral cortex of rats by the guanidino compounds accumulating in hyperargininemia.

  Brain research 20011227

• Influence of 72% injury in one kidney on several organs involved in guanidino compound metabolism: a time course study.

  Pflugers Archiv : European journal of physiology 20010701

• Early glycation products produce pentosidine cross-links on native proteins. novel mechanism of pentosidine formation and propagation of glycation.

  The Journal of biological chemistry 20010209

• The alpha-amino group of L-arginine mediates its antioxidant effect.

  European journal of clinical investigation 20010201