New antithrombotic aryl-sulfonylthiosemicarbazide derivatives synthesized from natural safrole

Citation
Lm. Lima et al., New antithrombotic aryl-sulfonylthiosemicarbazide derivatives synthesized from natural safrole, J BRAZ CHEM, 10(5), 1999, pp. 421-428
Citations number
25
Categorie Soggetti
Chemistry
Journal title
JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY
ISSN journal
01035053 → ACNP
Volume
10
Issue
5
Year of publication
1999
Pages
421 - 428
Database
ISI
SICI code
0103-5053(199909/10)10:5<421:NAADSF>2.0.ZU;2-F
Abstract
As part of a research program aiming at the synthesis and pharmacological e valuation of novel lead-compounds exploring Brazilian abundant natural prod ucts, we describe herein the synthesis and the antithrombotic profile of ne w aryl-sulfonylsemicarbazides and aryl-sulfonylthiosemicar-bazides (10a-d). The new derivatives, designed with basis on the molecular hybridization co ncept, were prepared in good yields from natural safrole ((9) under bar), i solated from sassafras oil. The anti-aggregating activity of these new derivatives (<(10a-d)under bar>) on platelet aggregation induced by ADP, collagen, arachidonic acid and U-4 6619, indicates an important antithrombotic profile for the 6-methyl-3,4-me thylenedioxyphenyl-sulfonyl-N-phenylthiosemicarbazide derivative(<(10d)unde r bar>), acting at the arachidonic acid cascade and representing a new lead -compound with antithrombotic activity.