117693-24-0Relevant academic research and scientific papers
Inhibition of tumor necrosis factor alpha (TNFα) expression and function in vitro by modified antisense oligonucleotides
Ojwang, Joshua O.,Sudhakar Rao,Marshall, Helene B.,Mustain, Shawn D.,Chaudhary, Nilabh,Walker, David A.,Peyman, Anusch,Uhlmann, Eugen,Revankar, Ganapathi R.,Rando, Robert F.
, p. 1703 - 1707 (1997)
Antisense oligonucleotides containing C-5 hexynyl/propynyl modified pyrimidines were synthesized using solid phase phosphoramidite chemistry. These modified oligonucleotides were found to have significant inhibitory activity against TNFα production in vit
Oligodeoxynucleotides Containing C-5 Propyne Analogs of 2'-Deoxyuridine and 2'-Deoxycytidine
Froehler, Brian C.,Wadwani, Shalini,Terhorst, Terry J.,Gerrard, Sonja R.
, p. 5307 - 5310 (1992)
Oligodeoxynucleotides (ODN) containing 5-(1-propynyl)-2'-deoxyuridine and 5-(1-propynyl)-2'-deoxycytidine significantly enhance double-helix formation with single strand RNA and 5-(1-propynyl)-2'-deoxyuridine significantly enhances triple-helix formation with double stranded DNA.
NANOPARTICLE NUCLEIC ACID BINDING COMPOUND CONJUGATES FORMING I-MOTIFS
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Page/Page column 68; sheet 16, (2008/06/13)
The present invention concerns the field of nanoparticle bioconjugates which form an i-motif or an i-motif related structure (compositions) (i) without or (ii) with at least one further nucleic acid binding compound (Figure 1). The i-motif base pairs can
Oligonucleotides forming an i-motif: The pH-dependent assembly of individual strands and branched structures containing 2′-deoxy-5- propynylcytidine
Seela, Frank,Budow, Simone,Leonard, Peter
, p. 1858 - 1872 (2008/02/10)
Non-branched and branched oligonucleotides incorporating consecutive runs of 2′-deoxy-5-propynylcytidine residues (2) instead of 2′-deoxycytidine (1) were synthesized. For this, phosphoramidite building blocks of 2′-deoxy-5-propynylcytidine (3a-c) were pr
Antiviral compounds
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, (2008/06/13)
The present invention relates to certain novel 5-substituted pyrimidine nucleosides and pharmaceutically acceptable derivatives thereof and their use in the treatment of varicella zoster virus, cytomegalovirus and Epstein Barr virus infections. Also provided are pharmaceutical formulations and processes for the preparation of the compounds according to the invention.
