T Wöhrmann, B Y Kögel, J Schneider, T Matthiesen
Index: Exp. Toxicol. Pathol. 46(1) , 71-3, (1994)
Full Text: HTML
Beagle dogs were exposed orally to the prostacyclin analogue taprostene for four weeks. Dose levels of 200-3000 micrograms/kg body weight/day were used. Specific activity of taprostene on the digestive system compared to other species is reported. It is characterized by hypermotility of the gastrointestinal tract resulting in intestinal invagination in some animals. Gastrointestinal symptoms occurred also after intravenous administration indicating a systemic stimulating effect on smooth muscles. Concerning reversible gastrointestinal side effects in humans after intravenous infusion of prostacyclin the results of this subacute toxicity study indicated that the dog is an adequate and sensitive species for preclinical testing of prostacyclins.
Structure | Name/CAS No. | Molecular Formula | Articles |
---|---|---|---|
![]() |
TAPROSTENE SODIUM
CAS:87440-45-7 |
C24H29NaO5 |
In vitro analysis of synergistic effects of fibrinolytic age...
1997-01-01 [Haemostasis 27(4) , 184-92, (1997)] |
[Effect of the prostacyclin analog taprostene on ischemic ST...
1994-04-01 [Z. Kardiol. 83(4) , 258-63, (1994)] |
Effects of prostacyclin on hearing recovery after repetitive...
1994-01-01 [ORL J. Otorhinolaryngol. Relat. Spec. 56(6) , 305-9, (1994)] |
Partial agonism of taprostene at prostanoid IP receptors in ...
2004-06-01 [J. Cardiovasc. Pharmacol. 43(6) , 795-807, (2004)] |
Agonists can discriminate between cloned human and mouse pro...
2004-05-01 [Prostaglandins Leukot. Essent. Fatty Acids 70(5) , 423-9, (2004)] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2024 ChemSrc All Rights Reserved