Nucleosides

<p>2-Benzylthio-6-chloropurine is a synthetic nucleoside analogue that is an antiviral agent. It inhibits the synthesis of viral DNA by competitive inhibition of thymidine kinase, which is an enzyme necessary for the conversion of deoxyribonucleotides to their monophosphate form. 2-Benzylthio-6-chloropurine has been found to be effective against herpes simplex virus 1 and 2 (HSV1 and HSV2). The drug is also active against HIV, influenza A virus, and cytomegalovirus.</p>

<p>N6-Propargyladenosine is an alkyne functionalised nucleoside.</p>

<p>4-(2-Methoxyethylamino)-2-(methylthio)pyrimidine-5-carboxylic acid (4MEAP) is a novel phosphoramidite that can be used in the synthesis of ribonucleosides and deoxyribonucleosides. 4MEAP has antiviral activity, cytotoxicity, and anticancer properties. It may also have potential as an anti-inflammatory agent due to its ability to inhibit prostaglandin production.</p>

<p>1-(2'-Deoxy-3',5'-di-O-toluoyl-D-ribofuranosyl)-4-amino-1,3-dihydro-2-oxo-1,3,5-triazine is a nucleoside that is used as an anticancer drug. It is a modified nucleotide with a 2'-deoxyribofuranosyl group attached to the 3' carbon of the sugar moiety. It has been shown to be active against viruses and cancer cells. 1-(2'-Deoxy-3',5'-di-O-toluoyl-D-ribofuranosyl)-4-amino -1,3 -dihydro -2 -oxo -1,3,5 -triazine inhibits the replication of DNA by inhibiting DNA polymerase. This in turn prevents RNA synthesis and protein synthesis.</p>

<p>N2-Isobutyl-2'-deoxyguanosine is a novel, synthetic nucleoside analogue that has been shown to inhibit cancer cells and also to be an antiviral and anticancer agent. It has been shown to induce dsDNA breaks in DNA strands of human leukemia cells and also inhibits the replication of the Influenza A virus. N2-Isobutyl-2'-deoxyguanosine is a high purity, deoxyribonucleoside with a CAS number of 142554-22-1.</p>

<p>1,5-Anhydro-3-O-benzoyl-4,6-O-benzylidene-2-deoxy-2-(N6-benzoyladenin-1)-yl)-D-altrohexitol is a novel anticancer and antiviral agent. It is a phosphoramidate nucleotide analog that inhibits viral replication by blocking the synthesis of viral DNA. It also has an inhibitory effect on cancer cells, which may be due to its ability to activate natural killer cells or cytotoxic T lymphocytes.</p>

<p>3'-O-tert-Butyldimethylsilyl-2'-deoxy-5'-O-DMT-adenosine is a nucleoside with a novel chemical structure. It is a deoxyribonucleoside monophosphate, which has antiviral and anticancer properties. 3'-O-tert-Butyldimethylsilyl-2'-deoxy-5'-O-DMT-adenosine inhibits the formation of diphosphate from ATP, which prevents DNA and RNA synthesis in cells. This drug also binds to the enzyme ribonuclease, preventing the breakdown of RNA. The phosphoramidites used for synthesizing 3'-O-tert-Butyldimethylsilyl-2'-deoxy-5'-O-DMT adenosine are of high quality and can be used for making other nucleosides.</p>

<p>Adenosine-5'-O-diphospho-(1''-(4-nitrophenoxy)-ribose) sodium is a nucleic acid analog that is used in antiviral, anticancer, and gene therapy. It is a modified nucleotide with a phosphoramidite group at the 5' position. The phosphoramidite group is used for the synthesis of DNA or RNA. It has been shown to activate cellular processes such as transcription, translation, and replication in vitro. This compound also inhibits cancer cell growth in vivo and has been shown to be effective against bacterial infections caused by Mycobacterium tuberculosis and Mycobacterium avium complex.</p>

<p>2'-O-tert-Butyldimethylsilyl-5-O-DMT-nebularine 3'-CE phosphoramidite is a monophosphate nucleoside analog. It has been shown to have anticancer and antiviral activity. This compound is synthesized by reacting 5'-O-DMT-nebularine with 2'-deoxyribonucleosides with an activator, such as pyridine. The resulting product can be used as a building block in the synthesis of DNA or RNA.</p>

<p>4-Chloro-6-imidazol-1-yl-pyrimidine is a quaternary ammonium compound that can be used to make antireflection coatings. It has been shown to have a high degree of compatibility with polymers, such as allyl carbonate, which are used in functional groups. 4-Chloro-6-imidazol-1-yl-pyrimidine has also been shown to react with stannous octoate, and the reaction time is dependent on the concentration of both compounds. This molecule has been found to be biodegradable and liquid crystal compositions can be made from it by changing the ratio of molecules to liquid crystals. 4-Chloro-6-imidazol-1-yl pyrimidine reacts with hydroxyl groups in epoxy resins and diolefinic hydrocarbons, forming crosslinks in sealants or coatings. The sealant</p>

<p>Lamivudine is a monophosphate antiviral drug that inhibits the synthesis of DNA. It has been shown to inhibit the replication of human immunodeficiency virus-1 (HIV-1) in vitro, and to protect monkeys from simian acquired immune deficiency syndrome (SAIDS). Lamivudine 5'-diphosphate ammonium salt is an antiviral agent that belongs to the group of deoxyribonucleosides. It has been shown to be effective against HIV-1 and SAIDS in animals. The mechanism of action is not fully understood, but it may work by inhibiting viral RNA synthesis or by preventing viral DNA integration into host cell DNA.</p>

<p>N4-Benzoyl-2'-deoxy-5'-O-DMT-cytidine-3'-lcaa-CPG is an antiviral agent that inhibits the RNA polymerase of the virus. It is a phosphoramidite, which is a nucleoside with a phosphate group at the 5' position. N4-Benzoyl-2'-deoxy-5'-O-DMT-cytidine has been shown to be cytotoxic against cancer cells, and have less side effects than other nucleosides. It has been shown to selectively bind to ribonucleosides and deoxyribonucleosides and inhibit their synthesis by binding to the enzyme DNA polymerase. This stops DNA replication and causes cell death.</p>

<p>A cap analog that can incorporated into mRNA</p>

<p>2-Amino-4-(4-methoxyphenyl)pyrimidine (AMP) is a synthetic nucleoside analog. It has antiviral activity and is used for the treatment of hepatitis B virus infection. AMP inhibits viral DNA polymerase and prevents the synthesis of viral DNA and RNA. It has been modified to include a methoxy group at the 4 position, which provides additional stability against the enzyme ribonuclease. AMP is also an activator of ribonucleotide reductase and can be used as a substrate to synthesize deoxyribonucleosides, phosphoramidites, diphosphate, or monophosphate nucleotides for DNA synthesis.<br>AMP has CAS number 99844-02-7 and is available in high purity.</p>

<p>Biotin-11-deoxycytidine-5'-triphosphate, lithium salt - 1 mM aqueous solution is an antiviral nucleoside that has been shown to inhibit HIV and HCV replication in vitro. It also inhibits the proliferation of cancer cells in vitro and induces apoptosis in vivo.<br>Biotin-11-deoxycytidine-5'-triphosphate, lithium salt - 1 mM aqueous solution is a novel nucleoside that was designed for use as an anticancer agent. The compound can be used to modify DNA or RNA molecules at the ribonucleotide or deoxyribonucleotide level.</p>

<p>N6-Benzoyl-7-deaza-2'-deoxyadenosine is a novel synthetic monophosphate activator that can be used to induce cell death in cancer cells. It is structurally similar to the natural nucleotide adenosine, and it binds to the same receptors on cells as adenosine. N6-Benzoyl-7-deaza-2'-deoxyadenosine has been shown to inhibit viral replication by interfering with DNA synthesis and RNA transcription, which are essential for viral reproduction.</p>

<p>3',5'-Di-O-benzoyl-2'-deoxy-2'-fluorouridine is a novel nucleoside analog that has been shown to have anticancer activity in vitro. The compound is a monophosphate, which is synthesized from 2'-deoxyuridine and benzoyl chloride. 3',5'-Di-O-benzoyl-2'-deoxy-2'-fluorouridine was found to have antiviral activity against herpes simplex virus type 1 (HSV1) and cytomegalovirus (CMV). It also inhibited the production of HIV in human lymphocytes. This nucleoside analog can be activated by phosphorylation at the 5' position to form a diphosphate, which inhibits DNA synthesis by incorporating into the growing DNA chain and preventing the movement of RNA polymerase along the template strand.</p>

<p>2'-Deoxy-5'-O-DMT-uridine succinyl 3'-CPG is a novel, synthetic, high purity, and high quality activator for oligonucleotide synthesis. It is a modified nucleoside with a 2' -deoxy-5'-O-dimethoxytrityl group attached to the sugar moiety. This product is used in monophosphate form and can be used as an anticancer agent. This product has antiviral activity, which may be due to its ability to inhibit viral DNA and RNA synthesis.</p>

<p>2’-O,4’-C-Methylenecytidine is a nucleoside that has been used to synthesize oligonucleotides. It has been shown to form duplexes with complementary DNA and RNA strands. 2’-O,4’-C-Methylenecytidine forms bicyclic analogues with high efficiency and can be used as an n-type structural probe.</p>

<p>5'-O-DMT-N4-isobutyryl-2'-O-methyl-5-methylcytidine, also known as 5'-O-(4,4'-dimethoxytrityl)-N4-isobutyryl-2'-O-methyl-5-methylcytidine, is a nucleoside and nucleotide analog. It is an antiviral agent with anticancer activity. This compound has been shown to be highly active against herpes simplex virus type 1 (HSV1) in vitro. The mechanism of action is not yet fully understood but may involve modification of the viral DNA polymerase.</p>