CA2172534C - Analogues de nucleosides structurellement bloques
- Google Patents
Analogues de nucleosides structurellement bloques
Download PDF
Info
Publication number
CA2172534C
CA2172534CCA002172534ACA2172534ACA2172534CCA 2172534 CCA2172534 CCA 2172534CCA 002172534 ACA002172534 ACA 002172534ACA 2172534 ACA2172534 ACA 2172534ACA 2172534 CCA2172534 CCA 2172534C
Authority
CA
Canada
Prior art keywords
carbocyclic
compound
cyclopropyl
group
ribonucleoside
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
US Department of Health and Human Services
Original Assignee
US Department of Health and Human Services
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by US Department of Health and Human ServicesfiledCriticalUS Department of Health and Human Services
Priority claimed from PCT/US1994/010794external-prioritypatent/WO1995008541A1/fr
Publication of CA2172534A1publicationCriticalpatent/CA2172534A1/fr
Application grantedgrantedCritical
Publication of CA2172534CpublicationCriticalpatent/CA2172534C/fr
Pharmaceuticals Containing Other Organic And Inorganic Compounds
(AREA)
Saccharide Compounds
(AREA)
Abstract
L'invention concerne des analogues de nucléosides carbocycliques fusionnés à 4',6'-cyclopropane, de conformation verrouillée. Les composés sont préparés en condensant un alcool allylique carbocyclique fusionné à cyclopropane avec des bases à substitution purine ou pyrimidine. Les produits de condensation sont ensuite modifiés afin d'obtenir adénosine, guanosine, cytidine, thymidine et des analogues de nucléoside uracil. Les composés sont utiles en thérapie comme antimétabolites, ou dans la préparation d'agents antimétaboliques.
CA002172534A1993-09-241994-09-23Analogues de nucleosides structurellement bloques
Expired - LifetimeCA2172534C
(fr)
Synthetic Nucleosides and Nucleotides. XXX. 1 Synthesis and Antiviral Activity of 3′-Azido, 2′, 3′-Unsaturated and 2′, 3′-Dideoxy Derivatives of E-5-Styryl-2′-Deoxyuridine on Human Immunodeficiency Virus
Design and racemic synthesis of conformationally restricted carbocyclic pyrimidine nucleoside analogs based on the structure of the L-nucleoside residue in heterochiral DNA