Polaprezinc - ≥97% , CAS No.107667-60-7

CAS: 107667-60-7 Cat. No.: P413473 Formula: C₉H₁₂N₄O₃Zn Peso molecolare: 289.61 PubChem CID: 51051629

GRADE & PURITY ≥97%

Synonyms

Polaprezinc|107667-60-7|Zinc L-carnosine|DTXSID7048615|beta-alanyl-L-histidinato zinc|NCGC00181764-01|CHEMBL3184454|DTXCID4028541|Tox21_112950|AKOS037515832|DB09221|CAS-107667-60-7|E76520

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

Information

Polaprezinc (Aprozinate, Carnosine zinc complex, Zinc L-carnosine) is an orally bioavailable chelate composed of zinc and L-carnosine, with potential gastroprotective, anti-oxidant, anti-ulcer and anti-inflammatory activities.

Specifications

Sinonimi

Polaprezinc | 107667-60-7 | Zinc L-carnosine | DTXSID7048615 | beta-alanyl-L-histidinato zinc | NCGC00181764-01 | CHEMBL3184454 | DTXCID4028541 | Tox21_112950 | AKOS037515832 | DB09221 | CAS-107667-60-7 | E76520

Specifiche e purezza

≥97%

Meccanismi biochimici e fisiologici

Polaprezinc is a available Zinc L-carnosine complex. It is a mucosal protective agent that exhibits ROS-quenching activities, which promotes the repair of damaged tissues. Polaprezinc exerts cytoprotection through stimulation of Hsp70 expression that prev

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥97%

Nomi e identificatori

• Pubchem Sid: 508810668
• Sorrisi canonici: C1=C(NC=N1)CC(C(=O)O)[N-]C(=O)CCN.[Zn]
• IUPAC Name: 3-aminopropanoyl-[(1S)-1-carboxy-2-(1H-imidazol-5-yl)ethyl]azanide;zinc
• InChIKey: GFWBKUDRXMQSFD-FJXQXJEOSA-M
• INCHI: 1S/C9H14N4O3.Zn/c10-2-1-8(14)13-7(9(15)16)3-6-4-11-5-12-6;/h4-5,7H,1-3,10H2,(H3,11,12,13,14,15,16);/p-1/t7-;/m0./s1
• Isomeri SMILES: C1=C(NC=N1)C[C@@H](C(=O)O)[N-]C(=O)CCN.[Zn]
• PubChem CID: 51051629
• Peso molecolare: 289.61

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Peptidomimetics
• Subclass: Hybrid peptides
• Intermediate Tree Nodes: Not available
• Direct Parent: Hybrid peptides
• Alternative Parents: N-acyl-L-alpha-amino acids Beta amino acids and derivatives Imidazoles Heteroaromatic compounds Organic transition metal salts Monocarboxylic acids and derivatives Formamidines Carboxylic acids Carboximidamides Carbene-type 1,3-dipolar compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Organic anions
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Hybrid peptide - 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 - Heteroaromatic compound - Imidazole - Azole - Formamidine - Azacycle - Organic transition metal salt - Organoheterocyclic compound - Carbene-type 1,3-dipolar compound - Carboximidamide - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Amidine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic anion - Aromatic heteromonocyclic compound
• Descrizione: 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

Proprietà chimiche e fisiche

• Punto di fusione (°C): >300° C