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Carbohydr Res ; 338(12): 1271-82, 2003 Jun 16.
Article in English | MEDLINE | ID: mdl-12791280

ABSTRACT

In the search for new orally active antithrombotic drugs that are metabolically stable, we explored the synthesis of 1-C-(5-thio-D-xylosyl) derivatives, examining radical and nucleophilic methods. Thus synthesized were aryl, benzyl, alkylcarboxymethylenyl, arylsulfonylmethylenyl and alkylaminocarboxymethylenyl C-linked analogues of 5-thio-D-xylopyranosides.


Subject(s)
Thioglycosides/chemical synthesis , Thioglycosides/therapeutic use , Xylose/chemistry , Administration, Oral , Animals , Disease Models, Animal , Fibrinolytic Agents/chemical synthesis , Fibrinolytic Agents/chemistry , Fibrinolytic Agents/therapeutic use , Models, Chemical , Molecular Structure , Rats , Structure-Activity Relationship , Thioglycosides/chemistry , Thrombosis/drug therapy
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