ChemSpider 2D Image | MFCD00467639 | C12H12ClN3

MFCD00467639

  • Molecular FormulaC12H12ClN3
  • Average mass233.697 Da
  • Monoisotopic mass233.071976 Da
  • ChemSpider ID10131720

More details:

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

187173-05-3 [RN]
2-(4,5-Dihydro-1H-imidazol-2-yl)chinolinhydrochlorid (1:1) [German] [ACD/IUPAC Name]
2-(4,5-Dihydro-1H-imidazol-2-yl)quinoléine, chlorhydrate (1:1) [French] [ACD/IUPAC Name]
2-(4,5-Dihydro-1H-imidazol-2-yl)quinoline hydrochloride
2-(4,5-Dihydro-1H-imidazol-2-yl)quinoline hydrochloride (1:1) [ACD/IUPAC Name]
2-(4,5-Dihydroimidazol-2-yl)quinoline hydrochloride
205437-64-5 [RN]
BU224 hydrochloride
MFCD00467639
Quinoline, 2-(4,5-dihydro-1H-imidazol-2-yl)-, hydrochloride (1:1) [ACD/Index Name]
More...

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

B154_SIGMA [DBID]
EU-0100167 [DBID]
  • Experimental Physico-chemical Properties
  • Miscellaneous

    • Bio Activity:

      High affinity ligand for the imidazoline I2 binding site (Ki = 2.1 nM). Putative I2 antagonist; antagonizes the effects of imidazoline ligands on morphine antinociception. Produces ipsiversive rotatio nal behavior in rats with a full 6-OHDA lesion of the nigrostriatal tract. Tocris Bioscience 0725
      High affinity ligand for the imidazoline I2 binding site (Ki = 2.1 nM). Putative I2 antagonist; antagonizes the effects of imidazoline ligands on morphine antinociception. Produces ipsiversive rotational behavior in rats with a full 6-OHDA lesion of the nigrostriatal tract. Tocris Bioscience 725
      I2 Receptors Tocris Bioscience 725
      Imidazoline Receptors Tocris Bioscience 725
      Other Pharmacology Tocris Bioscience 725
      Potent, selective I2 ligand. Putative antagonist Tocris Bioscience 0725, 725

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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