ChemSpider 2D Image | ZK 93423 hydrochloride | C23H23ClN2O4

ZK 93423 hydrochloride

  • Molecular FormulaC23H23ClN2O4
  • Average mass426.893 Da
  • Monoisotopic mass426.134644 Da
  • ChemSpider ID21475085

More details:

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

6-(Benzyloxy)-4-(méthoxyméthyl)-9H-β-carboline-3-carboxylate d'éthyle, chlorhydrate (1:1) [French] [ACD/IUPAC Name]
9H-Pyrido[3,4-b]indole-3-carboxylic acid, 4-(methoxymethyl)-6-(phenylmethoxy)-, ethyl ester, hydrochloride (1:1) [ACD/Index Name]
Ethyl 6-(benzyloxy)-4-(methoxymethyl)-9H-β-carboline-3-carboxylate hydrochloride (1:1) [ACD/IUPAC Name]
Ethyl-6-(benzyloxy)-4-(methoxymethyl)-9H-β-carbolin-3-carboxylathydrochlorid (1:1) [German] [ACD/IUPAC Name]
ZK 93423 hydrochloride
[1216574-52-5] [RN]
1216574-52-5 [RN]
4-(methoxymethyl)-6-(phenylmethoxy)-9H-Pyrido[3,4-b]indole-3-carboxylic acid ethyl ester
4-(Methoxymethyl)-6-(phenylmethoxy)-9H-pyrido[3,4-b]indole-3-carboxylic acid ethyl ester hydrochloride
83910-44-5 [RN]

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

ZK 93423 [DBID]
  • Experimental Physico-chemical Properties
  • Miscellaneous

    • Bio Activity:

      GABAA and A-rho Receptors Tocris Bioscience 1994
      Ion Channels Tocris Bioscience 1994
      Ligand-gated Ion Channels Tocris Bioscience 1994
      Potent benzodiazepine agonist Tocris Bioscience 1994
      Potent benzodiazepine receptor agonist (IC50 = 1 nM). Non-selective between ?1-, ?2-, ?3- and ?5-subunit containing GABAA receptors (Ki values are 4.1, 4.2, 6 and 4.5 nM for inhibition of [3H]Ro15-178 8 binding to human recombinant ?1?3?2, ?2?3?2, ?3?3?2 and ?5?3?2 receptors respectively). Anxiolytic following systemic administration in vivo. Tocris Bioscience 1994
      Potent benzodiazepine receptor agonist (IC50 = 1 nM). Non-selective between ?1-, ?2-, ?3- and ?5-subunit containing GABAA receptors (Ki values are 4.1, 4.2, 6 and 4.5 nM for inhibition of [3H]Ro15-1788 binding to human recombinant ?1?3?2, ?2?3?2, ?3?3?2 and ?5?3?2 receptors respectively). Anxiolytic following systemic administration in vivo. Tocris Bioscience 1994
      Potent benzodiazepine receptor agonist (IC50 = 1 nM). Non-selective between alpha1-, alpha2-, alpha3- and alpha5-subunit containing GABAA receptors (Ki values are 4.1, 4.2, 6 and 4.5 nM for inhibition of [3H]Ro15-1788 binding to human recombinant alpha1beta3gamma2, alpha2beta3gamma2, alpha3beta3gamma2 and alpha5beta3gamma2 receptors respectively). Anxiolytic following systemic administration in vivo. Tocris Bioscience 1994

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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