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CAS 128549-96-2

:

N-(20-Amino-4-hydroxy-4,8,12,17-tetraazaeicos-1-yl)-1H-indole-3-acetamide

Description:
N-(20-Amino-4-hydroxy-4,8,12,17-tetraazaeicos-1-yl)-1H-indole-3-acetamide, with the CAS number 128549-96-2, is a complex organic compound characterized by its unique structure that includes an indole moiety and a long tetraaza side chain. The presence of multiple amino and hydroxy groups suggests that this compound may exhibit significant hydrophilicity, potentially influencing its solubility and reactivity in biological systems. The indole structure is known for its role in various biological activities, including its involvement in neurotransmitter function and as a precursor to several important biomolecules. The tetraaza component indicates that the molecule contains multiple nitrogen atoms, which may contribute to its potential as a ligand in coordination chemistry or as a pharmacophore in medicinal chemistry. Overall, this compound's intricate structure suggests potential applications in pharmaceuticals, particularly in areas related to neurochemistry or as a therapeutic agent targeting specific biological pathways. Further studies would be necessary to elucidate its specific properties and biological activities.
Formula:C26H47N7O2
InChI:InChI=1S/C26H47N7O2/c27-11-5-14-28-12-3-4-13-29-15-6-16-30-17-7-19-33(35)20-8-18-31-26(34)21-23-22-32-25-10-2-1-9-24(23)25/h1-2,9-10,22,28-30,32,35H,3-8,11-21,27H2,(H,31,34)
InChI key:InChIKey=LIURIBSBVUMOJS-UHFFFAOYSA-N
SMILES:C(C(NCCCN(CCCNCCCNCCCCNCCCN)O)=O)C=1C=2C(NC1)=CC=CC2
Synonyms:
  • Agelenotoxin 489
  • N-(20-Amino-4-hydroxy-4,8,12,17-tetraazaeicos-1-yl)-1H-indole-3-acetamide
  • 1H-Indole-3-acetamide, N-(20-amino-4-hydroxy-4,8,12,17-tetraazaeicos-1-yl)-
  • Agel 489
  • AG 489
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