L-Anserine Nitrate Salt - 10mM in Water , CAS No.10030-52-1

CAS: 10030-52-1 Cat. No.: L420261 Molecular Weight: 303.27 EC Number: 233-079-7 PubChem CID: 112071

GRADE & PURITY 10mM in Water

Synonyms

L-Anserine nitrate salt | L-Anserine nitrate salt, hydroxyl radical scavenger | (S)-2-(3-Aminopropanamido)-3-(1-methyl-1H-imidazol-5-yl)propanoicacidcompoundwithnitricacid(1:x) | AKOS027250723 | OLWOKAYJAHHSNY-QRPNPIFTSA-N | EINECS 233-079-7 | (S)-2-(3-Am

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Overview

An antioxidant dipeptide.

Specifications

Synonyms

L-Anserine nitrate salt | L-Anserine nitrate salt, hydroxyl radical scavenger | (S)-2-(3-Aminopropanamido)-3-(1-methyl-1H-imidazol-5-yl)propanoicacidcompoundwithnitricacid(1:x) | AKOS027250723 | OLWOKAYJAHHSNY-QRPNPIFTSA-N | EINECS 233-079-7 | (S)-2-(3-Am

Specifications & Purity

10mM in Water

Biochemical and Physiological Mechanisms

L-serine is a dipeptide found in most animal tissues. In the model system, it is an effective antioxidant and hydroxyl radical volatiles. Inhibition of aldose and ketosugar-induced nonenzymatic glycosylation. As an inhibitor of protein-protein cross-linki

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

This product requires cold chain shipping. Ground and other economy services are not available.

Names and Identifiers

• Canonical Smiles: CN1C=NC=C1CC(C(=O)O)NC(=O)CCN.[N+](=O)(O)[O-]
• IUPAC Name: (2S)-2-(3-aminopropanoylamino)-3-(3-methylimidazol-4-yl)propanoic acid;nitric acid
• InChIKey: OLWOKAYJAHHSNY-QRPNPIFTSA-N
• INCHI: 1S/C10H16N4O3.HNO3/c1-14-6-12-5-7(14)4-8(10(16)17)13-9(15)2-3-11;2-1(3)4/h5-6,8H,2-4,11H2,1H3,(H,13,15)(H,16,17);(H,2,3,4)/t8-;/m0./s1
• Isomeric SMILES: CN1C=NC=C1C[C@@H](C(=O)O)NC(=O)CCN.[N+](=O)(O)[O-]
• WGK Germany: 3
• PubChem CID: 112071
• Molecular Weight: 303.27

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Peptidomimetics
      • Subclass Hybrid peptides

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Peptidomimetics
• Subclass: Hybrid peptides
• Intermediate Tree Nodes: Not available
• Direct Parent: Hybrid peptides
• Alternative Parents: Histidine and derivatives N-acyl-L-alpha-amino acids Beta amino acids and derivatives Imidazolyl carboxylic acids and derivatives N-substituted imidazoles Organic nitrates Heteroaromatic compounds Secondary carboxylic acid amides Organic nitro compounds Organic nitric acids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organic zwitterions Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Hybrid peptide - Histidine or derivatives - N-acyl-l-alpha-amino acid - N-acyl-alpha amino acid or derivatives - N-acyl-alpha-amino acid - Beta amino acid or derivatives - Alpha-amino acid or derivatives - Imidazolyl carboxylic acid derivative - N-substituted imidazole - Heteroaromatic compound - Organic nitrate - Imidazole - Azole - Amino acid - Organic nitro compound - Secondary carboxylic acid amide - Organic nitric acid or derivatives - Organic nitric acid - Carboxamide group - Amino acid or derivatives - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as hybrid peptides. These are compounds containing at least two different types of amino acids (alpha, beta, gamma, delta) linked to each other through a peptide bond.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Molecular Weight: 303.270 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 6
• Exact Mass: 303.118 Da
• Monoisotopic Mass: 303.118 Da
• Topological Polar Surface Area: 176.000 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 309.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

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