Abstract
Herein, we report optically pure modified acyclic nucleosides as ideal probes for aptamer modification. These new monomers offer unique advantages in exploring the role played in thrombin inhibition by a single residue modification at key positions of the TBA structure.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antithrombins / chemical synthesis*
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Antithrombins / chemistry
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Aptamers, Nucleotide / chemical synthesis*
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Aptamers, Nucleotide / chemistry
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Circular Dichroism
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G-Quadruplexes
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Models, Molecular
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Molecular Mimicry
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Nucleosides / chemistry*
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Optical Rotation
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Stereoisomerism
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Thermodynamics
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Thrombin / antagonists & inhibitors*
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Thrombin / chemistry
Substances
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Antithrombins
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Aptamers, Nucleotide
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Nucleosides
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thrombin aptamer
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Thrombin