ChemSpider 2D Image | 5-Nonyloxytryptamine oxalate | C21H32N2O5

5-Nonyloxytryptamine oxalate

  • Molecular FormulaC21H32N2O5
  • Average mass392.489 Da
  • Monoisotopic mass392.231110 Da
  • ChemSpider ID8302112

More details:

Validated by Experts, Validated by Users, Non-Validated, Removed by Users

157798-12-4 [RN]
157798-13-5 [RN]
1H-Indole-3-ethanamine, 5-(nonyloxy)-, ethanedioate (1:1) [ACD/Index Name]
2-(5-(Nonyloxy)-1H-indol-3-yl)ethanamine oxalate
2-[5-(Nonyloxy)-1H-indol-3-yl]ethanamine ethanedioate (1:1) [ACD/IUPAC Name]
2-[5-(Nonyloxy)-1H-indol-3-yl]éthanamine oxalate (1:1) [French] [ACD/IUPAC Name]
5-Nonyloxytryptamine oxalate
Ethandisäure --2-[5-(nonyloxy)-1H-indol-3-yl]ethanamin (1:1) [German] [ACD/IUPAC Name]
Nonyloxytryptamine (oxalate)
[157798-12-4] [RN]
More...

Validated by Experts, Validated by Users, Non-Validated, Removed by Users

CHEBI:64147 [DBID]
UNII-DJ1F4R673N [DBID]
  • Experimental Physico-chemical Properties
  • Miscellaneous

    • Chemical Class:

      An oxalate salt obtained by reaction of 5-nonyloxytryptamine with one equivalent of oxalic acid. 5-HT<smallsub>1B</smallsub> selective agonist, several times more potent than sumatriptan and inactive as a 5-HT<smallsub>1A</smallsub> agonist (Ki at 5-HT<smallsub>1B</smallsub> = 1 nM, selectivity over 5-HT<smallsub>1A</smallsub> <greaterthan/> 300-fold). ChEBI CHEBI:64147
      An oxalate salt obtained by reaction of 5-nonyloxytryptamine with one equivalent of oxalic acid. 5-HT1B selective agonist, several times more potent than sumatriptan and inactive ; as a 5-HT1A agonist (Ki at 5-HT1B = 1 nM, selectivity over 5-HT1A > 300-fold). ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:64147
      An oxalate salt obtained by reaction of 5-nonyloxytryptamine with one equivalent of oxalic acid. 5-HT1B selective agonist, several times more potent than sumatriptan and inactive as a 5-HT1A agonist ( Ki at 5-HT1B = 1 nM, selectivity over 5-HT1A > 300-fold). ChEBI CHEBI:64147

    • Bio Activity:

      5-HT Receptors Tocris Bioscience 901
      5-HT1 Receptors Tocris Bioscience 901
      5-HT1B selective agonist, several times more potent than sumatriptan and inactive as a 5-HT1A agonist (Ki at 5-HT1B = 1 nM, selectivity over 5-HT1A > 300-fold). Mimics polysialic acid activity, stimul ates neuritogenesis, myelination and Schwann cell migration in vitro. Tocris Bioscience 0901
      5-HT1B selective agonist, several times more potent than sumatriptan and inactive as a 5-HT1A agonist (Ki at 5-HT1B = 1 nM, selectivity over 5-HT1A > 300-fold). Mimics polysialic acid activity, stimulates neuritogenesis, myelination and Schwann cell migration in vitro. Tocris Bioscience 901
      7-TM Receptors Tocris Bioscience 901
      Selective 5-HT1B agonist Tocris Bioscience 0901, 901

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

No predicted properties have been calculated for this compound.

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