Nucleoside dimers analogues with a 1,2,3-triazole linkage: conjugation of floxuridine and thymidine provides novel tools for cancer treatment. Part II
Published 2019 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Nucleoside dimers analogues with a 1,2,3-triazole linkage: conjugation of floxuridine and thymidine provides novel tools for cancer treatment. Part II
Authors
Keywords
-
Journal
NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS
Volume -, Issue -, Pages 1-29
Publisher
Informa UK Limited
Online
2019-06-08
DOI
10.1080/15257770.2019.1610891
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Synthesis and biological assay of new 2’-deoxyuridine dimers containing a 1,2,3-triazole linker. Part I
- (2018) Lucyna Michalska et al. NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS
- 3′-O- and 5′-O-Propargyl Derivatives of 5-Fluoro-2′-Deoxyuridine: Synthesis, Cytotoxic Evaluation and Conformational Analysis
- (2016) Dagmara Baraniak et al. NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS
- Bioactive nucleoside analogues possessing selected five-membered azaheterocyclic bases
- (2015) Joanna Zeidler et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- Are 1,4- and 1,5-Disubstituted 1,2,3-Triazoles Good Pharmacophoric Groups?
- (2014) Alberto Massarotti et al. ChemMedChem
- Synthesis of 3′-azido-2′,3′-dideoxy-5-fluorouridine phosphoramidates and evaluation of their anticancer activity
- (2013) Marta Lewandowska et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- 15N NMR spectroscopic and theoretical GIAO-DFT studies for the unambiguous characterization of disubstituted 1,2,3-triazoles
- (2013) Miriam Corredor et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Cytotoxicity of new duplex drugs linking 3′-C-ethynylcytidine and 5-fluor-2′-deoxyuridine against human melanoma cells
- (2012) Sarah Schott et al. INTERNATIONAL JOURNAL OF CANCER
- Method for Assigning Structure of 1,2,3-Triazoles
- (2012) Xavier Creary et al. JOURNAL OF ORGANIC CHEMISTRY
- The cytostatic activity of NUC-3073, a phosphoramidate prodrug of 5-fluoro-2′-deoxyuridine, is independent of activation by thymidine kinase and insensitive to degradation by phosphorolytic enzymes
- (2011) Johan Vande Voorde et al. BIOCHEMICAL PHARMACOLOGY
- Novel Anticancer Polymeric Conjugates of Activated Nucleoside Analogues
- (2011) Thulani H. Senanayake et al. BIOCONJUGATE CHEMISTRY
- Click Chemistry: 1,2,3-Triazoles as Pharmacophores
- (2011) Sandip G. Agalave et al. Chemistry-An Asian Journal
- Phosphoramidate ProTides of the Anticancer Agent FUDR Successfully Deliver the Preformed Bioactive Monophosphate in Cells and Confer Advantage over the Parent Nucleoside
- (2011) Christopher McGuigan et al. JOURNAL OF MEDICINAL CHEMISTRY
- Novel effects of glycyrrhetinic acid on the central nervous system tumorigenic progenitor cells: Induction of actin disruption and tumor cell-selective toxicity
- (2010) Hideaki Yamaguchi et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- Synthesis and in vitro activities of new anticancer duplex drugs linking 2′-deoxy-5-fluorouridine (5-FdU) with 3′-C-ethynylcytidine (ECyd) via a phosphodiester bonding
- (2009) Herbert Schott et al. BIOORGANIC & MEDICINAL CHEMISTRY
- Efficient construction of therapeutics, bioconjugates, biomaterials and bioactive surfaces using azide–alkyne “click” chemistry☆
- (2008) J LUTZ et al. ADVANCED DRUG DELIVERY REVIEWS
- Cu-Catalyzed Azide−Alkyne Cycloaddition
- (2008) Morten Meldal et al. CHEMICAL REVIEWS
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started