Abstract |
The antimetabolite 6-azauridine blocks the de novo synthesis of pyrimidines and causes increased serum levels of several amino acids including homocystine. 6-Azauridine was was withdrawn from clinical use for the treatment of psoriasis because of the occurence of arterial and venous thromboembolic episodes in some psoriatic patients. Utilizing a standard animal model for the recognition of venous and arterial thrombosis, 6-azauridine was demonstrated in this study to cause thrombosis without producing homocystinemia when administered orally or intravenously.
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Authors | S N Gitel, A J Grieco, S Wessler, S E Snyderman |
Journal | Haemostasis
(Haemostasis)
Vol. 8
Issue 1
Pg. 54-7
( 1979)
ISSN: 0301-0147 [Print] Switzerland |
PMID | 456945
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
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Topics |
- Administration, Oral
- Animals
- Azauridine
(administration & dosage, pharmacology)
- Blood Coagulation
(drug effects)
- Dose-Response Relationship, Drug
- Injections, Intravenous
- Male
- Rabbits
- Thrombosis
(etiology)
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