TT 232, CAS No.147159-51-1

CAS: 147159-51-1 Cat. No.: T287833 Summenformel: C₄₅H₅₈N₁₀O₉S₂ Molekulargewicht: 947.13 PubChem CID: 6918265

Specifications

Product Name

TT 232, CAS No.147159-51-1

Synonyme

NCGC00249606-01 | CAP 232 | L-Threoninamide, D-phenylalanyl-L-cysteinyl-L-tyrosyl-D-tryptophyl-L-lysyl-L-cysteinyl-, cyclic (2-->6)-disulfide | TT-232 | TT2-32 | D-phenylalanyl-cysteinyl-tyrosyl-tryptophyl-lysyl-cysteinyl-threoninamide | Phe-cys-tyr-trp-l

Biochemische und physiologische Mechanismen

Peptide agonist for sst1/sst4somatostatin receptors. Somatostatin analog; inhibits tyrosine kinase activity in human colon tumor cell lines. Demonstrates an antiproliferative effect bothin vitroandin vivoand induces apoptosis in a pancreatic tumor cell li

Sequenz

fCYwKCT(Modifications: Disulfide bridge between 2 - 6; Thr-7 = C-terminal amide)

CAS

147159-51-1

Molekültyp

Protein

Lagerung und Versand

Storage

Store at -20°C

Verschickt in

Ice chest + Ice pads

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Ebene5 Peptides
          • Ebene6 Oligopeptides

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Peptides
• Direct Parent: Oligopeptides
• Alternative Parents: Cyclic peptides Phenylalanine and derivatives Macrolactams N-acyl-alpha amino acids and derivatives Alpha amino acid amides Amphetamines and derivatives 3-alkylindoles Aralkylamines 1-hydroxy-2-unsubstituted benzenoids Fatty amides Substituted pyrroles Heteroaromatic compounds Primary carboxylic acid amides Secondary alcohols Lactams Secondary carboxylic acid amides Organic disulfides Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Monoalkylamines Organic oxides
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Alpha-oligopeptide - Cyclic alpha peptide - Phenylalanine or derivatives - Macrolactam - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Amphetamine or derivatives - 3-alkylindole - Indole or derivatives - Indole - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Phenol - Fatty acyl - Monocyclic benzene moiety - Fatty amide - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Lactam - Amino acid or derivatives - Organic disulfide - Carboxamide group - Primary carboxylic acid amide - Secondary alcohol - Secondary carboxylic acid amide - Azacycle - Organoheterocyclic compound - Organooxygen compound - Primary amine - Carbonyl group - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Amine - Organic oxide - Organic oxygen compound - Organonitrogen compound - Primary aliphatic amine - Aromatic heteropolycyclic compound
• Beschreibung: 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

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