ChemSpider 2D Image | MFCD11519966 | C21H31ClN2O

MFCD11519966

  • Molecular FormulaC21H31ClN2O
  • Average mass362.937 Da
  • Monoisotopic mass362.212494 Da
  • ChemSpider ID24605989

More details:






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

1013933-37-3 [RN]
2-(Mesityloxy)-3,6-dimethyl-N-(3-pentanyl)-4-pyridinamine hydrochloride (1:1) [ACD/IUPAC Name]
2-(Mésityloxy)-3,6-diméthyl-N-(3-pentanyl)-4-pyridinamine, chlorhydrate (1:1) [French] [ACD/IUPAC Name]
2-(Mesityloxy)-3,6-dimethyl-N-(3-pentanyl)-4-pyridinaminhydrochlorid (1:1) [German] [ACD/IUPAC Name]
2-(Mesityloxy)-3,6-dimethyl-N-(pentan-3-yl)pyridin-4-amine hydrochloride (1:1)
4-Pyridinamine, N-(1-ethylpropyl)-3,6-dimethyl-2-(2,4,6-trimethylphenoxy)-, hydrochloride (1:1) [ACD/Index Name]
CP376395 hydrochloride
CP-376395 hydrochloride
MFCD11519966
N-(1-Ethylpropyl)-3,6-dimethyl-2-(2,4,6-trimethylphenox y)-4-pyridinamine hydrochloride
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

CD 271 | Differin | [DBID]
GR 38032 | [DBID]
  • Experimental Physico-chemical Properties
  • Miscellaneous
    • Bio Activity:

      7-TM Receptors Tocris Bioscience 3212
      CRF Receptors Tocris Bioscience 3212
      Peptide Receptors Tocris Bioscience 3212
      Potent and selective CRF1 antagonist Tocris Bioscience 3212
      Potent and selective CRF1 receptor antagonist (Ki values are 12 and >10000 nM for CRF1 and CRF2 receptors respectively). Attenuates CRF-induced activation of the HPA axis in vivo following i.v. admini stration. Orally active. Tocris Bioscience 3212
      Potent and selective CRF1 receptor antagonist (Ki values are 12 and >10000 nM for CRF1 and CRF2 receptors respectively). Attenuates CRF-induced activation of the HPA axis in vivo following i.v. administration. Orally active. Tocris Bioscience 3212

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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