CA2172534C - Analogues de nucleosides structurellement bloques - Google Patents

Analogues de nucleosides structurellement bloques Download PDF

Info

Publication number
CA2172534C
CA2172534C CA002172534A CA2172534A CA2172534C CA 2172534 C CA2172534 C CA 2172534C CA 002172534 A CA002172534 A CA 002172534A CA 2172534 A CA2172534 A CA 2172534A CA 2172534 C CA2172534 C CA 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.)
Expired - Lifetime
Application number
CA002172534A
Other languages
English (en)
Other versions
CA2172534A1 (fr
Inventor
Victor E. Marquez
Juan B. Rodriguez
Marc C. Nicklaus
Joseph J. Barchi, Jr.
Maqbool A. Siddiqui
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 Services filed Critical US Department of Health and Human Services
Priority claimed from PCT/US1994/010794 external-priority patent/WO1995008541A1/fr
Publication of CA2172534A1 publication Critical patent/CA2172534A1/fr
Application granted granted Critical
Publication of CA2172534C publication Critical patent/CA2172534C/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • 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.
CA002172534A 1993-09-24 1994-09-23 Analogues de nucleosides structurellement bloques Expired - Lifetime CA2172534C (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US12679693A 1993-09-24 1993-09-24
US08/126,796 1993-09-24
PCT/US1994/010794 WO1995008541A1 (fr) 1993-09-24 1994-09-23 Analogues de nucleosides de conformation verrouillee

Publications (2)

Publication Number Publication Date
CA2172534A1 CA2172534A1 (fr) 1995-03-30
CA2172534C true CA2172534C (fr) 2005-11-15

Family

ID=35520908

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002172534A Expired - Lifetime CA2172534C (fr) 1993-09-24 1994-09-23 Analogues de nucleosides structurellement bloques

Country Status (1)

Country Link
CA (1) CA2172534C (fr)

Also Published As

Publication number Publication date
CA2172534A1 (fr) 1995-03-30

Similar Documents

Publication Publication Date Title
US6090932A (en) Method of preparation of known and novel 2'-modified nucleosides by intramolecular nucleophilic displacement
US6525191B1 (en) Conformationally constrained L-nucleosides
AU757724B2 (en) Novel nucleosides having bicyclic sugar moiety
EP0720604B1 (fr) Analogues de nucleosides de conformation verrouillee
EP1853616B1 (fr) Intermediaire et procede de preparation de 2' desoxy, 2', 2'-difluoro-d-ribofuranosyl nucleosides enrichis en anomeres beta
IE62227B1 (en) 2', 3'-Dideoxy-2' -fluoronucleosides
WO1991010670A1 (fr) Procede pratique de synthese de 2'-desoxynucleosides et de 2',3'-didesoxy-2'-3'-didehydronucleosides
FI95384C (fi) Menetelmä 3'-deoksi-3'-substituoitujen metyylinukleosidien valmistamiseksi ja menetelmässä käytettäviä välituotteita
KR20030092037A (ko) 2'-할로-β-L-아라비노퓨라노실 뉴클레오사이드의 제조방법
CA2172534C (fr) Analogues de nucleosides structurellement bloques
Chu et al. Nucleosides. 107. Synthesis of 5-(. beta.-D-arabinofuranosyl) isocytosine and related C-nucleosides
BrianáLamont Enantiospecific synthesis of 3′-hetero-dideoxy nucleoside analogues as potential anti-HIV agents
Kotra et al. Synthesis of 2, 3-dideoxy-2, 2-difluoro-L-glycero-pentofuranosyl nucleosides
US20230129710A1 (en) Methods and Reagents for Synthesizing Nucleosides and Analogues Thereof
US5144018A (en) 2',3'-dideoxy-adenosine derivatives
KR102269009B1 (ko) 핵산 내로의 혼입을 위한 5-(n-보호된-트립타미노카복시아미드)-2''-데옥시유리딘 포스포아미다이트의 합성을 위한 화합물 및 방법
Zheng et al. Homologues of Isomeric Dideoxynucleosides as Potential Antiviral Agents: Synthesis of Isodideoxy-Nucleosides with a Furanethanol Sugar Moiety
Yamaguchi et al. 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
Urata et al. Design and racemic synthesis of conformationally restricted carbocyclic pyrimidine nucleoside analogs based on the structure of the L-nucleoside residue in heterochiral DNA
Lim et al. Synthesis and biological study of the cyclopentenyl carbocyclic nucleoside analogue of 5-azacytidine
Cavalcanti et al. Synthesis of 2′, 3′-Dideoxy-2′-Fluoro-l-threo-Pentofuranosyl Nucleosides as Potential Antiviral Agents
WO2003052053A2 (fr) Bibliotheques nucleosidiques et composes obtenus au moyen de strategies combinatoires mcc realisees sur support solide
JPH0296590A (ja) 新規核酸類
Mathé et al. Synthesis and antiviral evaluation of the β-L-enantiomers of some thymine 3′-deoxypentofuranonucleoside derivatives
KR0142110B1 (ko) 2', 3'-디데옥시-2', 3'-디데히드로누클레오시드의 제조방법

Legal Events

Date Code Title Description
EEER Examination request
MKEX Expiry

Effective date: 20140923