Nonapeptide-1, CAS No.158563-45-2

CAS: 158563-45-2 Cat. No.: N292755 Peso molecular: 1206.50 PubChem CID: 10418849

GRADE & PURITY ≥98%

Descripción general

Efficacy and Mechanism of Action

Whitening and freckle removing, inhibiting excessive melanin production and reducing melanin deposition. It can be added to skin care products, such as skin lightening cream, skin foundation, powdery cake, freckle cream (sunburn, freckles).

By inhibiting MSH (melanotropic hormone), melanin production is reduced and excessive melanin production is prevented.

Specifications

Product Name

Nonapeptide-1, CAS No.158563-45-2

Sinónimos

HY-P0097 | Met-pro-phe-arg-trp-phe-lys-pro-val | (Met5, Pro6, D-Phe7, D-Trp9, Phe10)-a-MSH (5-13) | Met-Pro-D-Phe-Arg-D-Trp-Phe-Lys-Pro-Val-NH2 | Nonapeptide-1 | H-Met-Pro-D-Phe-Arg-D-Trp-Phe-Lys-Pro-Val-NH2 | UNII-64W45420K5 | C72990 | Melanostatine 5 | Nona

Especificaciones y pureza

≥98%

Secuencia

Met-Pro-D-Phe-Arg-D-Trp-Phe- Lys-Pro-Val-NH2

CAS

158563-45-2

Tipo de molécula

Peptide

Almacenamiento y envío

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Peptides
          • Level6 Oligopeptides

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Peptides
• Direct Parent: Oligopeptides
• Alternative Parents: Phenylalanine and derivatives Methionine and derivatives Valine and derivatives N-acyl-alpha amino acids and derivatives Proline and derivatives Alpha amino acid amides Tryptamines and derivatives Amphetamines and derivatives 3-alkylindoles Pyrrolidinecarboxamides N-acylpyrrolidines N-acyl amines Substituted pyrroles Heteroaromatic compounds Tertiary carboxylic acid amides Secondary carboxylic acid amides Guanidines Primary carboxylic acid amides Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Carboximidamides Dialkylthioethers Organic oxides Carbonyl compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Alpha-oligopeptide - Phenylalanine or derivatives - Methionine or derivatives - N-acyl-alpha amino acid or derivatives - Valine or derivatives - Proline or derivatives - Alpha-amino acid amide - Triptan - N-substituted-alpha-amino acid - 3-alkylindole - Alpha-amino acid or derivatives - Amphetamine or derivatives - Indole - Indole or derivatives - Pyrrolidine-2-carboxamide - N-acylpyrrolidine - Pyrrolidine carboxylic acid or derivatives - N-acyl-amine - Substituted pyrrole - Benzenoid - Fatty acyl - Fatty amide - Monocyclic benzene moiety - Heteroaromatic compound - Pyrrole - Pyrrolidine - Tertiary carboxylic acid amide - Secondary carboxylic acid amide - Primary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Guanidine - Carboximidamide - Thioether - Azacycle - Sulfenyl compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Dialkylthioether - Organoheterocyclic compound - Amine - Primary aliphatic amine - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organosulfur compound - Primary amine - Organic oxide - Organic oxygen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.
• 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