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Bronchodilator Activity of Theophylline Derivatives Substituted at the 7‐Position
Author(s) -
Corsano Stefano,
Scapicchi Rossana,
Strappaghetti Giovannella
Publication year - 1994
Publication title -
archiv der pharmazie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.468
H-Index - 61
eISSN - 1521-4184
pISSN - 0365-6233
DOI - 10.1002/ardp.19943271006
Subject(s) - theophylline , bronchodilator , chemistry , piperazine , pharmacology , stereochemistry , ring (chemistry) , medicine , organic chemistry , asthma
Theophylline derivatives with several groups linked at the 7‐position were synthesized and their pharmacological activities were studied on guinea pig. Relaxant action in the tracheal muscle was increased in comparison with that of theophylline when the 3(2 H )‐pyridazinone system was linked to 7‐(2‐ethyl)‐theophylline through the piperazine ring, but decreased when the 7‐(2‐ethyl)‐theophylline was linked to 3(2 H )‐pyridazinone ring through an amino group.

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