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Merck

PPADS, a novel functionally selective antagonist of P2 purinoceptor-mediated responses.

European journal of pharmacology (1992-07-07)
G Lambrecht, T Friebe, U Grimm, U Windscheif, E Bungardt, C Hildebrandt, H G Bäumert, G Spatz-Kümbel, E Mutschler
RESUMEN

We have characterized PPADS (pyridoxalphosphate-6-azophenyl-2',4'-disulfonic acid) as a novel antagonist which selectively blocks P2 purinoceptor-mediated responses in rabbit vas deferens at pre- and postjunctional sites. PPADS did not interact with alpha 1-adrenoceptors, muscarinic M2 and M3 receptors, histamine H1 and adenosine A1 receptors. Thus, PPADS is a novel and useful pharmacological tool to study co-transmission in tissues where ATP and co-existing neurotransmitters act in concert.

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Sigma-Aldrich
Pyridoxal phosphate-6-azo(benzene-2,4-disulfonic acid) tetrasodium salt hydrate, solid, ≥98% (HPLC)