Discovery of novel pyrrolopyridazine scaffolds as transient receptor potential vanilloid (TRPV1) antagonists.

Ismet Dorange, Rickard Forsblom, Istvan Macsari, Mats Svensson, Johan Bylund, Yevgeni Besidski, Jan Blid, Daniel Sohn, Ylva Gravenfors
Author Information
  1. Ismet Dorange: Medicinal Chemistry, CNSP iMed Science, AstraZeneca R&D, Innovative Medicines, SE-15185 Södertälje, Sweden. i.dorange@hotmail.com

Abstract

A novel indolizine class of compounds was identified as TRPV1 antagonist from an HTS campaign. However, this indolizine class proved to be unstable and reacted readily with glutathione when exposed to light and oxygen. Reactivity was reduced by the introduction of a nitrogen atom alpha to the indolizine nitrogen. The pyrrolopyridazine core obtained proved to be inert to the action of light and oxygen. The synthesis route followed the one used for the indolizine compounds, and the potency and ADMET profile proved to be similar.

MeSH Term

Animals
Caco-2 Cells
Cell Membrane Permeability
Drug Evaluation, Preclinical
Humans
Indolizidines
Microsomes, Liver
Pyridazines
Pyrroles
Rats
Structure-Activity Relationship
TRPV Cation Channels

Chemicals

Indolizidines
Pyridazines
Pyrroles
Pyrrolopyridazine
TRPV Cation Channels
TRPV1 protein, human

Word Cloud

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