Results 201 to 210 of about 651,747 (238)
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EFFICIENT SYNTHESIS OF OLIGONUCLEOTIDE-PEPTIDE CONJUGATES ON LARGE SCALE
Nucleosides, Nucleotides and Nucleic Acids, 2001The conjugation of oligonucleotide phosphorothioates with antennapedia peptide was studied in detail to allow efficient preparation of the conjugates on up to 15 mumol scale. Under optimized conditions, the use of oligonucleotides and the peptide in an equimolecular ratio gave the desired conjugates in more than 60% isolated yield.
S O, Doronina, A P, Guzaev, M, Manoharan
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Facile preparation of 3′oligonucleotide-peptide conjugates
Tetrahedron Letters, 1991Abstract The solid phase synthesis of 3′ deoxyoligonucleotide (17 mer)-peptide conjugates is described. The oligonucleotide is complementary to the template strand of the measles virus in the region of the nucleocapsid protein on the 60 nucleotide leader RNA.
Carl D. Juby +2 more
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Thermodynamic Melting Studies on Oligonucleotide-Peptide Conjugates
Nucleosides and Nucleotides, 1999Abstract A small library of oligonucleotide-peptide conjugates has been prepared and studied to explore the influence of the various peptide side chain (cationic, anionic or hydrophobic) on the hybridation properties of the DNA.
C. Frier +2 more
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Sequence-specific RNA cleavage by oligonucleotide-peptide conjugates
Russian Chemical Bulletin, 2002This paper considers the site-directed cleavage of the in vitro transcript of human tRNALys3 by the conjugate CNH2Gly(ArgLeu)3ArgLeuN—p-DAG—5"CCCTGGACCCTCAGAT3" (conjugate pep-1A) of the oligodeoxyribonucleotide 1A (CCCTGGACCCTCAGAT) with a peptide [LeuArg]4Gly attached at the 5" terminus of the oligonucleotide through diethylene glycol as a linker ...
N. L. Mironova +6 more
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RNA-Cleaving Oligonucleotide-Peptide Conjugates
2004The most widely described artificial ribonucleases are designed on the basis of RNA-binding domains and low molecular weight constructs bearing functional groups of amino acid residues from catalytic centers of natural RNases: conjugates containing imidazole and carboxylate ions, guanidinium groups (see review Silnikov and Vlassov 200l).
N. L. Mironova +2 more
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Bioorganic & Medicinal Chemistry Letters, 2007
Phosphorothioate oligonucleotide-peptide conjugates were synthesized by solid phase fragment condensation (SPFC). Arginine rich peptides could be successfully conjugated in 2.8-13.4% isolated yields. All the products were fully characterized by reversed phase HPLC and MALDI-TOF-MS to give satisfactory results.
Irmina, Diala +7 more
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Phosphorothioate oligonucleotide-peptide conjugates were synthesized by solid phase fragment condensation (SPFC). Arginine rich peptides could be successfully conjugated in 2.8-13.4% isolated yields. All the products were fully characterized by reversed phase HPLC and MALDI-TOF-MS to give satisfactory results.
Irmina, Diala +7 more
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Synthesis of Oligonucleotide—Peptide and Oligonucleotide—Protein Conjugates
ChemInform, 2004AbstractFor Abstract see ChemInform Abstract in Full Text.
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Native chemical ligation in the synthesis of internally modified oligonucleotide–peptide conjugates
Peptide Science, 2010AbstractPeptide–oligonucleotide conjugates have frequently been synthesized to improve cellular delivery of antisense or antigene compounds, to allow the immobilization of peptide and protein conjugates on DNA arrays, or to decorate nucleic acid architectures with peptide functions. In such applications, the site of conjugation is of little importance,
Franziska, Diezmann +2 more
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Synthesis of oligonucleotide–peptide conjugates using hydrazone chemical ligation
Tetrahedron Letters, 2002Oligonucleotides constitute a class of potential therapeutic agents. Improvement of certain properties, such as cell-specific delivery, cellular uptake efficiency, intracellular distribution, and target specificity can be accomplished by covalent association to peptides [1], Rather than forming ionic oligonucleotide-peptide complexes, covalent ...
Nathalie Ollivier +5 more
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Synthesis of Oligonucleotide—Peptide Conjugates and Nucleopeptides
ChemInform, 2001AbstractFor Abstract see ChemInform Abstract in Full Text.
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