Investigation into the mast cell stabilizing activity of nature-identical and synthetic indanones

Author:

Frankish Neil1,Farrell Ronan1,Sheridan Helen1

Affiliation:

1. School of Pharmacy, Panoz Institute, Trinity College, Dublin 2, Ireland

Abstract

Abstract As part of an ongoing search for novel molecules with therapeutic potential we examined the mediator release inhibition activity of a number of indanones and their derivatives. The aldol condensation product 18 was approximately twice as potent as disodium cromoglycate as an inhibitor of compound 48/80-stimulated histamine release from rat peritoneal mast cells. The activity of this class of dimeric indanone compound is significantly higher than controls and may represent a new class of mast cell stabilizing agents. Compound 18 has been selected for further biological evaluation of its mast cell stabilization profile.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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