Palmitoyl Tripeptide-1, CAS No.147732-56-7

CAS: 147732-56-7 Cat. No.: P292758 Peso molecular: 578.79 Número EC: 680-607-0

GRADE & PURITY ≥97%

Descripción general

Anti-wrinkle and anti-aging, improve skin quality, facial and phtsical care, facial, neck and hand care products. It can be added to skin care prodicts, such as lotion, morning cream, eye essence, etc.

application：

Palmitoyl Tripeptide-1, has shown to have effects on on collagen, fibronectin, hyaluronic acid synthesis in human dermal fibroblasts, and thus can be used in preparation of antiaging cosmetic creams.

Efficacy and Mechanism of Action

Palmitoyl tripeptide-1, also known as pal-GHK and palmitoyl oligopeptide (sequence: Pal-Gly-His-Lys), is a messenger peptide for collagen renewal. Retinoic acid has the same activity as retinoic acid and does not cause stimulation. Stimulate collagen and glycosaminoglycan synthesis, enhance the epidermis, reduce wrinkles. It is suggested that the peptide acts on TGF to stimulate fibrillary formation. It is used in cosmetics, wrinkle-resistant skin care and cosmetic products.

Specifications

Product Name

Palmitoyl Tripeptide-1, CAS No.147732-56-7

Sinónimos

N2-[N-[N-(1-Oxohexadecyl)glycyl]-L-histidyl]-L-lysine | N-(1-oxohexadecyl)glycyl-L-histidyl-L-lysine | L-Lysine, N-(1-oxohexadecyl)glycyl-L-histidyl- | HY-P0047 | Palmitoyl Tripeptide-1 | PALMITOYL-GHK TRIPEPTIDE | (2S)-6-amino-2-[[(2S)-2-[[2-(hexadecanoy

Especificaciones y pureza

≥97%

Secuencia

Pal-Gly-His-Lys

CAS

147732-56-7

Tipo de molécula

Peptide

Almacenamiento y envío

Condiciones de almacenamiento de almacenamiento

Store at -20°C

Enviado en

Ice chest + Ice pads

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Not available
• Direct Parent: Peptides
• Alternative Parents: Histidine and derivatives N-acyl-L-alpha-amino acids Alpha amino acid amides Medium-chain fatty acids Imidazolyl carboxylic acids and derivatives Amino fatty acids Heterocyclic fatty acids N-acyl amines Heteroaromatic compounds Secondary carboxylic acid amides Amino acids Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Monoalkylamines Organic oxides
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Alpha peptide - Histidine or derivatives - N-acyl-l-alpha-amino acid - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Imidazolyl carboxylic acid derivative - Medium-chain fatty acid - Amino fatty acid - Heterocyclic fatty acid - Fatty amide - N-acyl-amine - Fatty acyl - Fatty acid - Azole - Imidazole - Heteroaromatic compound - Secondary carboxylic acid amide - Amino acid or derivatives - Amino acid - Carboxamide group - Organoheterocyclic compound - Azacycle - Carboxylic acid - Monocarboxylic acid or derivatives - Primary amine - Organic oxygen compound - Carbonyl group - Organooxygen compound - Organic oxide - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Primary aliphatic amine - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as peptides. These are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another.
• 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