Examples of 'nucleoside analogues' in a sentence

Meaning of "nucleoside analogues"

nucleoside analogues: This phrase refers to a class of antiviral or anticancer drugs that are structurally similar to nucleosides, the building blocks of DNA and RNA. Nucleoside analogues work by interfering with the replication process of viruses or cancer cells, thus inhibiting their ability to multiply and spread

How to use "nucleoside analogues" in a sentence

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nucleoside analogues
Nucleoside analogues are also used as antiviral agents.
It belongs to a class of medications called nucleoside analogues.
Combinations of nucleoside analogues may also be employed.
Similar effects have been observed with other nucleoside analogues.
Dosage levels for nucleoside analogues are well established.
Nucleoside analogues are any modified versions of a natural nucleoside.
Phosphorylated nucleoside analogues are known.
Nucleoside analogues and derivatives are an important class of therapeutic agents.
The problem is different with regard to the nucleoside analogues.
In medicine several nucleoside analogues are used as antiviral or anticancer agents.
Most of the existing antiviral preparations are the nucleoside analogues.
A great number of nucleoside analogues exhibit several antimetabolic activities.
Certain disease cell cycle targeting ligands are nucleoside analogues.
Nucleotide and nucleoside analogues are well known on the art.
None of the patients had been treated with nucleoside analogues before.

See also

Use of dideoxy nucleoside analogues in the treatment of viral infections.
Modified fluorinated nucleoside analogues.
Many nucleoside analogues have been found to possess anticancer cancer activity.
Synthesis of nucleoside analogues.
Nucleoside analogues and oligonucleotide derivative comprising nucleotide analogue thereof.
The lipids are attached to the nucleoside analogues through phosphate linkages.
This is consistent with the known activity of other nucleoside analogues.
Various derivatives of nucleoside analogues have been found to exhibit antiviral activity.
The latter are sometimes used for the synthesis of nucleoside analogues.
The nucleoside analogues of the present invention can be prepared in different ways.
Therefore a general stereoselective synthesis of cis nucleoside analogues is an important goal.
Nucleoside analogues are a range of antiviral products used to prevent viral replication in infected cells.
It is an object of the present invention to provide a novel class of nucleoside analogues.
Thus for example amino acid esters of nucleoside analogues have been synthesised.
Clinically significant interactions have not been observed between nelfinavir and nucleoside analogues.
The present invention relates to nucleoside analogues and their use in medicine.
Such agents will be particularly useful in long term treatment by nucleoside analogues.
Attention has focussed on nucleoside analogues for the treatment of herpes viral infections.
This invention relates to a process for the preparation of certain nucleoside analogues.
Tenofovir is structurally related to nucleoside analogues hence the risk of lipodystrophy can not be excluded.
Conventional treatment of cancer using chemotherapeutics is largely based on the use of nucleoside analogues.
Such nucleoside analogues have shown interesting activity against pancreatic cancer cell lines.
The invention also concerns nucleic acids comprising said nucleotide and nucleoside analogues.
A first category are real nucleoside analogues since they contain a nucleobase and a sugar moiety.
Thus ribonucleosides and deoxyribonucleosides and dideoxyribonucleosides are envisaged together with other nucleoside analogues.
Prevalence of genotypic resistance to nucleoside analogues and protease inhibitors in Spain.
The resulting agents showed a decreased toxicity and increased stability over the unincorporated nucleoside analogues.
Lamivudine and zidovudine are nucleoside analogues which have activity against HIV.
Nucleoside analogues protect cells by serving as chain breakers in the transcription of viral RNA.
These oligonucleotides may be synthesized exclusively from the nucleoside analogues of the present invention.
The nucleoside analogues of formula I are new compounds.
General outline of the invention A great number of nucleoside analogues exhibit several antimetabolic activities.
These occur particularly when Aptivus or other protease inhibitors are taken together with nucleoside analogues.
These nucleoside analogues inhibit replication of viral DNA by their incorporation into a growing DNA strand.
Other treatment options for chronic hepatitis B include nucleoside analogues.

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