2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine

2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine

Catalog Number:
L002373180APE
Mfr. No.:
APE-C5246
Price:
$244
  • Size:
    Quantity:
    Add to Cart:
      • Overview
        • Please contact us at for specific academic pricing.

          Background

          2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine is a nonpeptidic angiotensin II receptor antagonist.Angiotensin II is the critical pressor substance of the renin-angiotensin system (RAS). The angiotensin II system, a proteolytic cascade regulating hemodynamics and water and electrolyte balance, is able to contribute to hypertensive states in human. The effects of the octapeptide angiotensin I1 includs cardiac stimulation, vasoconstriction, stimulation of aldosterone synthesis and release, as well as renal reabsorption of sodium. In vitro: In a previous study, 2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine was synthezed by reduction of 2-amino-3-nitropyridine derivatives to the corresponding diaminopyridine which was then condensed with an appropriate carboxylic acid in polyphosphoric acid. In vitro activity study showed that 2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine was a nonpeptidic angiotensin II receptor antagonist whose imidazo[4,5-b]pyridine scaffold had been used to examine plenty of positional substitutions in the development of orally active, long duration antihypertensive agents [1].In vivo: Up to now, there is no animal in vivo data reported.Clinical trial: So far, no clinical study has been conducted.

      • Properties
        • Categories
          nonpeptidic angiotensin II receptor antagonist
          Alternative Name
          2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine
          CAS Number
          133240-06-9
          Molecular Formula
          C10H13N3
          Molecular Weight
          175.2
          Purity
          98.00%
          Solubility
          insoluble in H2O; ≥45.7 mg/mL in EtOH; ≥5.3 mg/mL in DMSO
          Storage
          Store at -20°C
          SMILES
          CC1=CC(C)=C2C(N1)=NC(CC)=N2

          * For Research Use Only

    We Also Recommend

    AL 34662

    $262

    LT175

    $266

    Note: If you don't receive our verification email, do the following:

    Copyright © Amerigo Scientific. All rights reserved.