ChemSpider 2D Image | N,N'-dibenzhydrylethane-1,2-diamine dihydrochloride | C28H30Cl2N2

N,N'-dibenzhydrylethane-1,2-diamine dihydrochloride

  • Molecular FormulaC28H30Cl2N2
  • Average mass465.457 Da
  • Monoisotopic mass464.178589 Da
  • ChemSpider ID9873115

More details:






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

1,2-Ethanediamine, N1,N2-bis(diphenylmethyl)-, hydrochloride (1:2) [ACD/Index Name]
N,N'-Bis(diphenylmethyl)-1,2-ethandiamindihydrochlorid [German] [ACD/IUPAC Name]
N,N'-Bis(diphenylmethyl)-1,2-ethanediamine dihydrochloride [ACD/IUPAC Name]
N,N'-Bis(diphénylméthyl)-1,2-éthanediamine, dichlorhydrate [French] [ACD/IUPAC Name]
N,N'-Bis(diphenylmethyl)ethane-1,2-diamine dihydrochloride
N,N'-dibenzhydrylethane-1,2-diamine dihydrochloride
[97075-46-2]
N,N'-Bis(diphenylmethyl)-1,2-ethanediamine dihydrochloride
83027-13-8 [RN]
97075-46-2 [RN]
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

A6605_SIGMA [DBID]
  • Experimental Physico-chemical Properties
    • Experimental Solubility:

      Soluble to 100 mM in DMSO and to 10 mM in methanol Tocris Bioscience 2385
      Soluble to 100 mM in DMSO and to 2 mM in water with gentle warming Tocris Bioscience 2385
      Soluble to 100 mM in DMSO and to 5 mM in water with gentle warming Tocris Bioscience 2385
  • Miscellaneous
    • Bio Activity:

      7-TM Receptors Tocris Bioscience 2385
      Glutamate (Metabotropic) Group III Receptors Tocris Bioscience 2385
      Glutamate (Metabotropic) Receptors Tocris Bioscience 2385
      The first selective mGlu7 agonist Tocris Bioscience 2385
      The first selective mGlu7 agonist. Potently inhibits cAMP accumulation and stimulates GTP?S binding in recombinant cells and on membranes expressing mGlu7 (EC50 = 64 - 290 nM). Selective over other mG luR subtypes and selected ionotropic glutamate receptors up to 10 ?M. Acts via a novel allosteric site and is orally active and brain penetrant. Reduces haloperidol-induced catalepsy in rats. Tocris Bioscience 2385
      The first selective mGlu7 agonist. Potently inhibits cAMP accumulation and stimulates GTP?S binding in recombinant cells and on membranes expressing mGlu7 (EC50 = 64 - 290 nM). Selective over other mGluR subtypes and selected ionotropic glutamate receptors up to 10 ?M. Acts via a novel allosteric site and is orally active and brain penetrant. Reduces haloperidol-induced catalepsy in rats. Tocris Bioscience 2385

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module

No predicted properties have been calculated for this compound.

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