Nucléosides

<p>2',3',5'-Tri-O-acetyl-5-bromouridine is a nucleoside analog of uridine, a basic building block of RNA. It has the addition of a bromine atom and three acetyl groups. 2',3',5'-Tri-O-acetyl-5-bromouridine can be used in research</p>

<p>1-(3,5-Di-o-acetyl-β-D-deoxyribofuranosyl)-4-(1,2,4-triazol-1-yl)-5-methylpyrmidin-2-one is a novel antiviral drug that is synthesized from ribonucleosides and deoxyribonucleosides. It has been shown to be an activator of the enzyme telomerase by binding to the DNA template, which in turn increases the synthesis of telomerase and leads to cell death. The synthesis of this drug includes the use of phosphoramidites and it is CAS No. 80991-41-9. This drug is also anticancerous due to its ability to inhibit the production of RNA.</p>

<p>5’-C-Methylguanosine (5’-GMG) is a nucleoside that is the major product of viral RNA replication. It has been shown to be effective against tobacco mosaic virus and other plant viruses, including strains resistant to other nucleosides. 5’-GMG can be used in combination with other antiviral agents as an inoculant or as a systemic agent for treatment of plants infected with viruses. The sensitivity of cowpea chlorotic mottle virus to 5’-GMG was found to be dependent on the strain of the virus. Incubation of infected leaves with 5’-GMG resulted in a greater number of chlorotic lesions than incubation with water or uninfected leaves.</p>

<p>2'-Deoxy-5'-O-DMT-inosine is a chain congener of uridine and cytidine. It is an analog of guanosine, which is found in DNA. 2'-Deoxy-5'-O-DMT-inosine has shown to have cytotoxic effects on the cardiovascular system, as well as inflammatory properties. This drug can also inhibit nitric oxide production and chloride transport. The nitro group in 2'-deoxy-5'-O-DMT-inosine can be removed by ammonolysis or debenzoylation and glycosylation can be added to the molecule with the addition of glucose.</p>

<p>5'-O-Acetyladenosine is a labile nucleoside that can be converted to adenosine. It is a substrate for the enzyme ribonucleotide reductase, which converts it to adenosine monophosphate. 5'-O-Acetyladenosine has been shown to function as an equilibrating agent in the synthesis of guanosine and other pyrimidine nucleotides. In addition, it is a precursor for the synthesis of purines. 5'-O-Acetyladenosine can be synthesized from trimethyl phosphate and chloride gas yields acetaldehyde, which then reacts with phosphorus oxychloride to form 5'-O-acetyladeninol, which undergoes hydrolysis to yield 5'-O-acetyladenosine. The regioselectivity of this reaction depends on the concentration of reactants and solvents used in the reaction.</p>

<p>4-Thiouridine-5'-triphosphate sodium salt - aqueous solution (4TUTP) is an analog of uridine and can be used as a template for the synthesis of single-stranded DNA. 4TUTP has been shown to have a high affinity for dsDNA, allowing it to form a ternary complex with DNA polymerase and single-stranded DNA template. 4TUTP can also be used to prepare samples for profiling experiments or other molecular studies. It is reactive, so should be handled with caution in order to avoid unwanted crosslinking. 4TUTP may also be used in chloroplast research.</p>

<p>3'-O-Methylinosine is a synthetic nucleoside that inhibits the synthesis of viral DNA and RNA by interacting with the enzyme ribonucleotide reductase. This antiviral agent has been shown to be effective against a wide range of viruses, including human cytomegalovirus, herpes simplex virus type 1, varicella-zoster virus, and influenza A virus. 3'-O-Methylinosine has also been shown to inhibit the growth of cancer cells in vitro and in vivo.</p>

<p>5-Methoxyuridine is a nucleoside that is structurally related to uridine. It is an intermediate in the biosynthesis of pyrimidines and is also used as a precursor for other compounds. 5-Methoxyuridine has been shown to inhibit protein synthesis by binding to purine receptors and inhibiting the function of protein kinases. The x-ray crystal structures of 5-methoxyuridine bound to two different p2y receptors have been determined. The analytical chemistry of 5-methoxyuridine is based on UV absorption measurements, which are able to identify hydrogen bonds between the base and the sugar moiety. This drug has been investigated for its potential use in cancer therapy due to its ability to inhibit RNA synthesis, which can lead to cell death by incomplete replication or transcription. 5-Methoxyuridine inhibits messenger RNA (mRNA) production in bacteria by interfering with sequence recognition and binding sites within the ribosome and preventing</p>

<p>3'-O-Methylcytidine is an acidic guanine nucleoside that is a component of RNA. It is a biochemical building block and a co-substrate in the synthesis of DNA and RNA. 3'-O-Methylcytidine has been shown to be hydroxylated by the enzyme cytidine 5'-monophosphate, which leads to its termination when it reaches the ribosome. This nucleoside also inhibits bacterial growth through inhibition of ribosomal function, leading to reduced protein synthesis. 3'-O-Methylcytidine can act as an environmental pollutant, especially in chloride environments such as seawater. It has been found to be globally distributed in dinucleotides and monomethylated forms, with biosynthetic pathways similar to other nucleic acids.</p>

<p>2'-Deoxy-L-guanosine is a nucleoside that is used as an antibiotic. It inhibits protein synthesis, which leads to cell death. This drug has a high level of resistance against bacteria and is effective in the treatment of gram-positive bacteria. 2'-Deoxy-L-guanosine binds to the ribose phosphate backbone of DNA, phosphorylating it and preventing the base pairing of adenosine with thymine. This inhibits the production of DNA and RNA, leading to cell death. 2'-Deoxy-L-guanosine has been shown to be active against Listeria monocytogenes and Mycobacterium tuberculosis. The enantiomer form is more potent than the racemic mixture, but both forms are effective antibiotics.</p>

<p>N6-Benzoyl-2'-O-tert-butyldimethylsilyl-5'-O-toluoyladenosine 3'-CE phosphoramidite is a novel antiviral nucleoside that has been modified to be more resistant to enzymatic degradation. This nucleoside is synthesized as a high purity, high quality DNA synthon. It is an activator of viral RNA polymerase and inhibits the synthesis of viral DNA, which prevents replication of the virus. N6-Benzoyl-2'-O-tert-butyldimethylsilyl-5'-O-toluoyladenosine 3'-CE phosphoramidite has also shown anticancer activity in preclinical studies.</p>

<p>(E)-5-(2-Carboxyvinyl)-2'-deoxyuridine is a nucleoside for a range of applications</p>

<p>6-Chloro-9-(b-D-ribofuranosyl)purine is a purine analog that inhibits the synthesis of DNA, RNA, and protein. It has been shown to have physiological effects in cells, and it has been used as a positive control for enzyme activity studies. 6-Chloro-9-(b-D-ribofuranosyl)purine binds to an enzyme called hydroxymethylbilane synthase (HMBS), which inhibits the production of a molecule called tetrahydrobiopterin (THB). THB is essential for the synthesis of nitric oxide (NO), an important neurotransmitter that regulates neuronal death. 6-Chloro-9-(b-D-ribofuranosyl)purine also has significant cytotoxicity against melanoma cells in vitro.</p>

<p>3'-Azido-3'-deoxy-N6-methyladenosine is a novel modified nucleoside. It has antiviral activity, as it inhibits DNA and RNA synthesis. 3'-Azido-3'-deoxy-N6-methyladenosine is an effective inhibitor of HIV replication in vitro and in vivo and has been shown to inhibit the growth of cancer cells in mice. The compound binds to the ribonucleotide reductase enzyme, which prevents the conversion of ribonucleotides to deoxynucleotides, inhibiting DNA and RNA synthesis. 3'-Azido-3'-deoxy-N6-methyladenosine is being developed as a potential anticancer agent because it may inhibit tumor growth by blocking the production of ATP and reducing intracellular levels of adenosine triphosphate (ATP).</p>

<p>Deoxynucleoside with an alkyne handle on the base which can be used for conjugation via click chemistry.</p>

<p>3'-O-acetyl-2'-deoxycytidine is an activator that can be used in the synthesis of deoxyribonucleosides and nucleosides. It is a novel, modified, and high purity chemical entity that has shown anticancer and antiviral properties. 3'-O-acetyl-2'-deoxycytidine is a monophosphate nucleotide, which can be used in the synthesis of various pharmaceuticals. This product has been synthesized using high quality reagents in order to provide the best possible product for research purposes.</p>

<p>Cytidine 2',3'-cyclic monophosphate monosodium salt is a nucleotide that is used in the synthesis of DNA and RNA. It has antiviral and anticancer properties. Cytidine 2',3'-cyclic monophosphate monosodium salt is a high purity, high quality nucleotide with strong activator properties. It is also an excellent substrate for DNA polymerases, which may be due to its ability to bind to the phosphate groups on the enzyme's active site. This product can be used as a phosphoramidite during DNA synthesis or as an antiviral agent that inhibits viral replication by inhibiting the formation of viral DNA.</p>

<p>2'-Chloro-2'-deoxyuridine is a thymidine analog for research applications</p>

<p>Second messenger in intracellular signal transduction</p>

<p>Cytokinins are plant hormones involved in developmental processes and in the modulation of plant immune system. Zeatin was identified as the first naturally occurring cytokinin from the endosperm of corn (latin: Zea mays). Water-soluble trans-Zeatin Riboside is a major long-distance signaling molecule in xylem vessels and its action depends on metabolic conversion in proximity to the site of action. Trans-Zeatin Riboside is a powerful agent used in horticulture to improve shoot growth or to induce callus formation (e.g. in tomato). It is used for plant regeneration from leaf explants (e.g. in potato) and for the direct initiation of shoot cultures from bract axils of many plant species.</p>

<p>5'-O-DMT-thymidine 3'-Rp-oxazaphospholidine is a novel nucleoside analogue. It has antiviral activity and can be used to treat infections caused by herpes virus. It also has anticancer activity against some types of cancer cells and can inhibit the growth of tumour cells. 5'-O-DMT-thymidine 3'-Rp-oxazaphospholidine acts as an inhibitor of DNA polymerase, preventing the synthesis of DNA from RNA. It also inhibits ribonucleotide reductase, which is involved in the production of ribonucleotides from diphosphate nucleotides. This drug can be used as a monophosphate or phosphoramidite for the synthesis of oligodeoxyribonucleotides and deoxyribonucleotides.</p>

<p>2'-Deoxy-2'-fluorocytidine-5'-triphosphate sodium, 100mM aqueous solution is a nucleoside analog that is modified at both the 2' position of the sugar (deoxyribose) with a fluoro group and the 5' position with a triphosphate group. This compound is an important tool in biochemistry, molecular biology, and drug development, particularly for studying nucleic acid synthesis and genetic processes.</p>

<p>5-Aminouridine hydrochloride is a novel nucleoside that is an inhibitor of RNA polymerase. It has been shown to be active against cancer cells, and is also effective in the treatment of viral infections such as HIV and hepatitis B. 5-Aminouridine hydrochloride is synthesized by reacting uracil with ammonia and hydrogen chloride. The product can be used as a building block for monophosphate or diphosphate analogs, which are important components in the synthesis of DNA and RNA. This product is available at high purity with low impurity levels.</p>

<p>2'-O-methylpseudouridine is a modified nucleoside that belongs to the group of modified nucleosides. It is found in ribonucleic acid (RNA) and deoxyribonucleic acid (DNA). 2'-O-methylpseudouridine is a derivative of pseudouridine and can be categorized as a modified nucleotide. The chemical structure of this compound has been shown using reversed-phase high-performance liquid chromatography. This technique can help identify modifications in RNA, such as 5-carbamoylmethyluridine. 2'-O-methylpseudouridine is an epigenetic marker that may be used to study tissues or sequences.</p>

<p>N4-Benzyl-2'-deoxy-2'-fluoro-5'-O-tritylcytidine 3'-CE phosphoramidite is a nucleotide analogue that has antiviral and anticancer properties. It inhibits viral replication by inhibiting the synthesis of viral DNA, which leads to the death of cells infected with viruses. N4-Benzyl-2'-deoxy-2'-fluoro-5'-O-tritylcytidine 3'-CE phosphoramidite also has anticancer activity by inhibiting the proliferation of cancer cells. This drug is synthesized in high purity and high quality.</p>

<p>[1',2',3',4',5'-13C5]-Kinetin riboside is an adenine derivative linked to a ribose sugar moiety. It has also been labeled with ¹³C, a stable isotope of carbon.</p>

<p>Carbocyclic inosine is a natural product that has been found to have inhibitory effects on the growth of mammalian cells and soil bacteria. It has been shown to be an analog of guanine, and it binds reversibly to the adenine-binding site of DNA. Carbocyclic inosine inhibits cell nuclei by preventing the formation of RNA and protein, which are essential for cell division. Carbocyclic inosine also inhibits the synthesis of DNA, RNA, and protein in mammalian cells. This agent has allelopathic properties that may be due to its ability to inhibit the growth of other plants.</p>

<p>Thionicotinamide adenine dinucleotide is a cofactor in the production of ATP, and is also used as a reagent for determining the activity of dehydrogenases. It is produced by the oxidation of thionocinamide ribonucleotide, which is synthesized from dihydroxyacetone phosphate and phosphoric acid.<br>Thionicotinamide adenine dinucleotide binds to NADP+, which acts as a hydrogen acceptor, and transfers two electrons to it. The nadph then donates an electron to the dehydrogenase, which converts a substrate into its product in a redox reaction.</p>

<p>5'-Deoxythymidine is a nucleoside analog with low-energy electrons. This drug inhibits the synthesis of DNA by binding to the ribonucleotide reductase enzyme and preventing the conversion of ribonucleotides to deoxyribonucleotides. 5'-Deoxythymidine has been shown to inhibit cell growth in tumor cell lines, which may be due to its ability to interfere with mirna-mediated gene expression. This drug also has a kinetic effect on regulatory proteins, such as cyclin-dependent kinases, that are involved in the regulation of cell cycle progression.</p>

<p>3'-Deoxy-5-methyluridine-5'-triphosphate is a DNA activator that has been synthesized. It is a modified nucleoside and can be used as an antiviral, anti-cancer, and novel drug. 3'-Deoxy-5-methyluridine-5'-triphosphate is a synthetic nucleoside with high purity and high quality. CAS No. 365-08-2</p>

<p>5-Bromouridine is an energy-related metabolite that is a precursor of uridine. It is a nucleotide base that is incorporated into DNA during DNA replication. 5-Bromouridine has been shown to have radiation resistance and high resistance to viral life. It also binds to the nuclear DNA in cells, where it can act as a transcriptional regulator. 5-Bromouridine is used in the treatment of malignant brain tumors, where it can inhibit tumor growth by binding to the dna of cancer cells and preventing the synthesis of proteins required for cell division. 5-Bromouridine binds with high affinity to basic fibroblast, which may be related to its effects on cancer cells.</p>

<p>9-(b-D-Ribofuranosyl)purine (9-BRP) is a purine nucleoside that is used in the synthesis of dyes. It has been shown to be an effective inhibitor of the enzyme phosphodiesterase 3B, which breaks down cyclic adenosine monophosphate (cAMP), and therefore can prevent kidney fibrosis. 9-BRP has also been shown to inhibit the synthesis of collagen by binding to cAMP. In addition, 9-BRP binds to DNA and forms hydrogen bonds with nitrogen atoms on the phosphate groups in DNA. This interaction prevents the formation of hydrogen bonds between water molecules in water vapor and phosphate groups, thus slowing down their rate of dissociation from each other. 9-BRP also has a high affinity for Toll-like receptor 4 (TLR4), which is involved in the inflammatory response, making it an ideal therapeutic candidate for treating inflammation and renal fibrosis.</p>

<p>5'-O-p-Anisoyl-3'-azido-3'-deoxythymidine is a phosphoramidite nucleoside which is an antiviral agent. It is a novel chemical entity with anticancer activity and has been shown to inhibit the synthesis of DNA by blocking ribonucleotide reductase. This product has CAS No. 53907-02-6 and is produced using an improved process to provide high purity and quality.</p>

<p>3'-Amino-5'-O-benzyl-3'-deoxy-D3-thymidine is a novel antiviral agent that inhibits the replication of retroviruses. It is an activator of ribonucleotide reductase, which converts ribonucleotides to deoxyribonucleotides. The drug has been shown to inhibit DNA and RNA synthesis in vitro. 3'-Amino-5'-O-benzyl-3'-deoxy-D3-thymidine is also being studied for its anticancer properties.</p>

<p>2',3'-Dideoxy-2'-fluorouridine (ddFU) is a nucleoside that is used in the treatment of cancer. It inhibits DNA synthesis and cellular proliferation by blocking the activity of DNA polymerase, which is an enzyme required for DNA replication. 2',3'-Dideoxy-2'-fluorouridine has been shown to be an effective agent against leukemias, lymphomas, and solid tumors. In addition, this compound is being studied for its potential use as a radiation sensitizer to enhance the therapeutic effect of radiation therapy in the treatment of cancer.</p>

<p>2'-Deoxy-2',2'-difluoro-5-methyluridine is a synthetic nucleoside analog for use in research</p>

<p>Adenosine 5′-phosphosulfate sodium salt has been used quantify pyrophosphate and in enzyme-linked bioluminescence assay for adenosine triphosphate (ATP)</p>

<p>1-(2'-Deoxy-5'-O-DMT-b-D-xylofuranosyl) cytosine is a modified nucleoside that is phosphoramidite activated by the addition of a diphosphate. The diphosphate group on the sugar moiety may be hydrolyzed to form 1-(2'-deoxy-5'-O-DMT-b-D-xylofuranosyl)cytosine monophosphate. Cytidine is an antiviral and antifungal agent that is used in the treatment of herpes zoster, chronic myeloid leukemia, and other cancers. It has been shown to inhibit DNA synthesis and viral replication in vitro. <br>!--More--&gt;<br>Cytidine is an antiviral and antifungal agent that is used in the treatment of herpes zoster, chronic myeloid leukemia, and other cancers. It has been shown to inhibit DNA</p>

<p>5'-Deoxy-5'-methyluridine is an activator of DNA polymerases and a monophosphate analog of thymidine. It has been shown to inhibit the synthesis of viral DNA and is also active against some tumor cells. 5'-Deoxy-5'-methyluridine has been synthesized with high purity and yields, making it a novel candidate for use in antiviral therapy.</p>

<p>N6-Benzoyl-5'-O-DMT-3'-O-methyladenosine 3'-CE-phosphoramidite is the monophosphate ester of N6-benzoyl-5'-O-dimethoxytrityloxyadenosine 3'-Ce phosphoramidite. It is a novel nucleoside analog that has antiviral and anticancer activities. N6BMT3'OMeA inhibits replication of HIV by inhibiting reverse transcriptase and DNA polymerases, which prevents the production of viral DNA. N6BMT3'OMeA also inhibits the proliferation of cancer cells by binding to DNA, preventing the normal synthesis of RNA and protein molecules.</p>

<p>L-Adenosine is a nucleoside that is naturally synthesized in the body and is also found in certain foods. It has a variety of functions, including as an adenosine receptor agonist, a transport agent, and a substrate for metabolic pathways. In addition to its function as an adenosine receptor agonist, L-adenosine can be transported into mammalian cells by facilitated diffusion. The uptake of L-adenosine into cells is dependent on the concentration of extracellular adenosine and its concentration-response curve has been determined experimentally. L-Adenosine also acts as an inhibitor of phosphodiesterase enzyme which increases cAMP levels in cells. This increase in cAMP leads to increased calcium ion influx into the cell, which may lead to activation of protein kinase A (PKA) and protein kinase C (PKC). L-Adenosine has been shown to have cardiac effects at high concentrations. These effects may be</p>

<p>Inhibitor of uridine monophosphate synthase</p>

<p>1-(a-D-Mannopyranosyl)thymine is a phosphoramidite nucleoside with antiviral activity. It is an analog of thymine, in which the oxygen atom at the 5-position has been replaced by a mannose group and the hydroxyl group at the 4-position has been replaced by a methyl group. This compound has shown to have anticancer properties as well as inhibitory effects on HIV replication. Studies have also shown that 1-(a-D-mannopyranosyl)thymine inhibits proliferation and induces apoptosis in human cancer cell lines.</p>

<p>2,4-Diamino-6-hydroxy-5-nitrosopyrimidine is a nucleoside for use in research applications</p>

<p>5-(Trifluoromethyl)cytidine is a reactive chemical that can be detected by transcription, translation, and react probes. It has been shown to react with acid halides and carboxylic groups, which can shift the equilibrium in favor of the reaction product. This chemical is also an antitumor agent that exerts its antitumor activity through inhibition of DNA synthesis at the G1 phase of the cell cycle. 5-(Trifluoromethyl)cytidine was used as a probe for detection of RNA polymerase II in calf thymus DNA.</p>

<p>9-(2'-Deoxy-b-D-xylofuranosyl)adenine is a nucleoside that is used in the treatment of bowel disease, cancer, and other diseases. It is also a potential drug target for antimicrobial agents and pharmacological agents. 9-(2'-Deoxy-b-D-xylofuranosyl)adenine has been shown to inhibit DNA synthesis and cause cell death in mouse tumor cells. It also inhibits adenosine uptake by binding to the A3 receptor, which may be due to its similarity to adenosine. This drug has been shown to have anticancer properties in various carcinoma cell lines. 9-(2'-Deoxy-b-D-xylofuranosyl)adenine is metabolized into deoxyadenosine, which can be converted back into adenosinergic acid or deoxyadenosinergic acid, which are potent inhibitors of DNA polymerase alpha activity.</p>

<p>N4-Benzoyl-1-(2'-deoxy-5'-O-DMT-2'-fluoro-b-D-arabinofuranosyl)cytosine 3'-CE phosphoramidite is a nucleoside analog of cytosine, an important component of DNA. N4-Benzoyl-1-(2'-deoxy-5'-O-DMT-2'-fluoro-b-D arabinofuranosyl)cytosine 3'-CE phosphoramidite is a monophosphate derivative that is synthesized from 2',5' fluoro b -D arabinofuranosyl cytidine and benzoyl chloride in the presence of tetrazole. It has been shown to inhibit the growth of cancer cells in vitro and in vivo by inhibiting RNA synthesis. This compound has also been shown to be active against HIV and other viruses, as well as being potentially useful in</p>

<p>3’-O-Levulinyl-2’-deoxyadenosine is a nucleoside and a prodrug for the anticancer drug 2’,3’-dideoxyadenosine. 3’-O-Levulinyl-2’-deoxyadenosine is an activator of deoxyribonucleic acid (DNA) synthesis and also inhibits DNA repair. In mammals, 3’-O-levulinyl-2’deoxyadenosine is converted to 2’,3′ dideoxyadenosine monophosphate (ddAMP), which can be phosphorylated to ddATP in cells. 3′ -O -levulinyl -2′ -deoxyadenosine has been shown to inhibit the growth of cancer cells in vitro and in vivo.</p>

<p>Adenosine-2-carboxamide (ACA) is a potent and selective adenosine A2A receptor ligand with high affinity and selectivity. This drug has been shown to be a competitive antagonist of the adenosine A2A receptor with an IC50 of 0.8 nM and was highly selective for this receptor over the other adenosine receptors. ACA has also been shown to inhibit binding of radioligands to the adenosine A2A receptor in functional assays, as well as improve binding activity in cell-based assays. These results were confirmed by in silico studies that showed ACA to have high binding affinity, low off-target activity, and good pharmacokinetic properties.</p>

<p>8-Aminoadenosine can be used to study the mitochondrial membrane potential, a critical cellular function in which ATP levels are maintained by oxidative phosphorylation. 8-Aminoadenosine is one of the few drugs that have been shown to increase ATP levels in cells. It does this by increasing the permeability of mitochondria membranes and the rate of electron transport from complex I to complex II. The reaction mechanism is thought to involve an intramolecular hydrogen transfer from NADH to 8-aminoadenosine, forming an unstable intermediate that undergoes a conformational change that enables it to react with oxygen. 8-Aminoadenosine has been shown as an effective treatment for certain autoimmune diseases and resistant breast cancer. It also has anti-inflammatory effects, as well as receptor activity against HIV infection and Toll-like receptors.</p>

<p>2’-Deoxy-2’-fluoroguanosine 5’-monophosphate triethyl ammonium is a modified nucleotide that inhibits the replication of DNA by blocking the activity of the enzyme ribonuclease (RNase). It has been shown to inhibit the growth of cancer cells and is currently being studied as an anticancer agent. 2'-Deoxy-2'-fluoroguanosine 5'-monophosphate triethyl ammonium has also been shown to have antiviral properties against herpes simplex virus type 1. The compound is a synthetic nucleoside phosphoramidite with high purity and quality, which can be used for synthesis of oligonucleotides and ribonucleosides.</p>

<p>3'-Deoxycytidine is a nucleoside analog used to treat hepatitis. It is an inhibitor of the viral enzyme reverse transcriptase and prevents the synthesis of viral DNA by blocking the formation of low-energy hydrogen bonds between the 3'-hydroxyl group and the 5'-phosphate group of deoxyribonucleotide triphosphates. 3'-Deoxycytidine can be synthesized using solid-phase methods, and has been shown to inhibit human immunodeficiency virus (HIV) in control experiments. This drug also has been shown to have anti-inflammatory effects in experimental bladder inflammation models.</p>

<p>5'-O-Benzoylthymidine is an oxidative, single-stranded DNA (ssDNA) stabilizing agent. It has been shown to stabilize ssDNA by preventing the formation of intrastrand and interstrand disulfide bonds. This agent also destabilizes ssDNA by forming covalent adducts with the 5' ends of oligodeoxyribonucleotides. The stability and destabilization of ssDNA can be used in research on nucleic acid sequences, such as antigene sequences or oligonucleotide sequences.</p>

<p>o-Topolin riboside is a hydroxy derivative that can be found in Helleborus niger. It has been shown to have hormone-like effects on the body, and is an endogenous compound that can be found in human blood plasma. The dry weight of H. niger leaves was increased by o-topolin riboside, and it also increased the photosynthetic activity of isolated chloroplasts from wheat leaves. The enzyme immunoassays showed that o-topolin riboside binds to both apical and basal surfaces of excised chloroplasts. This binding inhibits the decomposition of pyridine nucleotides, which are necessary for photosynthesis. The binding also inhibits the degradation of starch and glycogen, leading to an increase in carbon dioxide fixation rates.</p>

<p>6-Thioguanosine is a purine analog that is used in the treatment of skin cancer and bowel disease. It has been shown to be an inhibitor of leukemia cells and also inhibits the growth of colon cancer cells. 6-Thioguanosine binds to the rate constant for uridine phosphorylation, which prevents the production of DNA. This drug also has an anti-inflammatory effect on bowel disease, which may be due to its ability to inhibit bcl-2 protein expression.<br>6-Thioguanosine is a fluorescent derivative that can be used as a substrate for x-ray diffraction data or as a biological sample in biological studies.</p>

<p>5,6-Dihydro-2'-deoxyuridine (dUrd) is a pyrimidine nucleoside that is an important component of DNA. It is phosphorylated by deoxyribonucleoside kinase to form dUrd monophosphate. This compound has been shown to inhibit the activity of catalase and other enzymes that hydrolyze hydrogen peroxide, indicating it may have antiviral properties. The enzyme activities of 5,6-dihydro-2'-deoxyuridine on simplex virus type 1 have been studied in vitro using lymphoblastoid cells. In these studies, the compounds was found to inhibit viral growth and terminate replication. 5,6-Dihydro-2'-deoxyuridine also inhibits the synthesis of DNA by inhibiting oxidative deamination reactions and termini formation in herpes simplex virus type 1. This drug has also been shown to inhibit amine oxidases in hep</p>

<p>7-Deaza-2',3'-dideoxyguanosine is a nucleoside analogue that is silylated on the 2' and 3' hydroxyl groups. It is also substituted with a deoxygenated 7-deaza-2',3'-dideoxyribose moiety. The substitution of the ribose sugar with deoxygenated 7-deaza-2',3'-dideoxyribose prevents the formation of hydrogen bonds between the sugar and phosphate backbones, which inhibits the enzyme ribonucleotide reductase from catalyzing the conversion of ribonucleotides to deoxynucleotides. This in turn blocks DNA synthesis, leading to cell death.br&gt;<br>7-Deaza-2',3'-dideoxyguanosine has been shown to be effective against Mycobacterium tuberculosis and Mycobacterium avium complex.</p>

<p>2'-Deoxy-5-ethynylcytidine is a cytosine analog that inhibits the synthesis of viral DNA and the production of new virus particles. It has been shown to inhibit herpes simplex virus type-1 (HSV-1) in cell cultures, as well as other viruses such as vaccinia and adenovirus. 2'-Deoxy-5-ethynylcytidine has also been shown to have anti-cancer properties in animal studies. This drug binds to the cellular nucleic acid, preventing transcription of viral genes into messenger RNA and preventing protein synthesis, thereby inhibiting replication of the virus. 2'-Deoxy-5-ethynylcytidine also inhibits the synthesis of cellular DNA by binding to nuclear DNA.<br>2'-Deoxy-5-ethynylcytidine is an analog of cytosine that binds to dna polymerase and prevents it from adding on new nucleotides, which blocks viral reproduction.</p>

<p>3'-Amino-2',3'-dideoxyadenosine's lack of a 3'-hydroxyl group makes it a chain terminator for DNA polymerase, a key application in Sanger sequencing. Additionally, the 3'-amino group serves as a functional handle for modifying the 3' end of oligonucleotides with various labels or conjugates, expanding their utility in research and diagnostics.</p>

<p>3’-Deoxy-5-methoxyuridine is a modified nucleoside that has antiviral and anticancer properties. It is an activator of DNA synthesis, which is the first step in the process of DNA replication. It also inhibits DNA gyrase and topoisomerase II, enzymes that maintain the integrity of bacterial DNA. 3’-Deoxy-5-methoxyuridine phosphoramidites are used in anticancer drugs.</p>

<p>2'-Deoxy-5-formyluridine (2DFO) is a nucleobase analogue that inhibits the enzymatic activity of DNA glycosylases, which are enzymes that remove sugar residues from damaged DNA. 2DFO has been shown to induce apoptosis in cancer cells by inhibiting DNA synthesis and promoting oxidative damage to the cell's DNA. 2DFO has also been shown to inhibit the growth of DU-145 cells in vitro and in vivo models. This drug was found to be more effective at preventing metastasis of colorectal cancer when it was administered with a platinum-based chemotherapy drug.</p>

<p>2'-Bromo-2'-deoxyuridine is a synthetic nucleoside analog of deoxyuridine, in which the 2'-hydroxyl group of the ribose sugar is replaced with a bromine atom (Br) at the 2' position. This modification allows it to be incorporated into DNA during DNA synthesis, where it can replace the normal thymidine. This molecule can potentially be used in molecular biology and cell biology as a thymidine analog to study DNA replication, cell proliferation, and DNA repair.</p>

<p>5'-O-Acetyl-2',3'-dideoxy-3'-fluoro-cytidine is an anticancer agent that has been shown to cause DNA chain termination. This drug is a modified nucleoside with the 3' hydroxyl group replaced by a 2',3'-dideoxy group. It inhibits cell division, and is active against various types of cancer cells. 5'-O-Acetyl-2',3'-dideoxy-3'-fluoro-cytidine may be used as a radiosensitizer for cancer therapy, in addition to its use as an antiviral agent.</p>

<p>The 4-Amino-6-hydroxy-2-mercapto-5-nitrosopyrimidine ammonium salt is a solvent that has been used in the synthesis of various organic and inorganic compounds. It is a five membered ring compound with solvents, such as chlorides, and it can be found in diffraction patterns. 4-Amino-6-hydroxy-2-mercapto-5 nitrosopyrimidine ammonium salt can also act as a ligand in metal complexes. The molecule has carbonyl groups which chelate to the metal atom and form a ring with chlorine atoms.</p>

<p>N2-Benzoyl-2'-O-tert-butyldimethylsilyl-5'-O-DMT-guanosine 3'-CE phosphoramidite is a novel, modified ribonucleoside that is used for the synthesis of oligodeoxyribonucleotides. It has been shown to have antiviral and anticancer properties. N2-Benzoyl-2'-O-tert-butyldimethylsilyl-5'-O-DMT-guanosine 3'-CE phosphoramidite is an analog of guanosine and has been shown to be an activator of RNA polymerase II. The compound is synthesized through a high quality, high purity process that produces a monophosphate product with an excellent yield.</p>

<p>2'-Deoxy-8-oxo-adenosine is a nucleoside that is a hydrogen bond donor. It is an analogue of adenosine, and has been shown to inhibit the growth of breast cancer cells. 2'-Deoxy-8-oxo-adenosine reacts with the enzyme dATP pyrophosphohydrolase to form 8-oxo-2'-deoxyadenosine, which inhibits mitochondrial DNA synthesis by preventing the incorporation of inorganic phosphate into mitochondrial DNA. This process leads to reduced ATP production, leading to cell death. The reactive properties of 2'-Deoxy-8-oxo-adenosine make it suitable for use as a probe molecule in chemical biology, as well as in biochemical studies on human serum.</p>

<p>Also known as AMT, this is a catabolite of the nucleoside analog zidovudine (AZT), a drug used to treat HIV infection.</p>

<p>2'-Amino-2'-deoxyinosine is a modified nucleoside, based on inosine. This compound has a 2'-amino substitution instead of a 2'-hydroxyl group, which has the potential to make the nucleoside more resistant to enzymatic degradation and<br> enhance or alter base-pairing properties.</p>

<p>2'-O-tert-Butyldimethylsilyl-N2-DMF-5'-O-tritylguanosine 3'-CE phosphoramidite (BTS) is a novel, modified nucleoside that has been synthesized to be used in the synthesis of DNA and RNA. This compound is an activator of ribonucleotide reductase and can be used to produce deoxyribonucleosides. BTS has shown anticancer activity in some studies and can also be used as antiviral agents. BTS also has high purity and quality, which makes it suitable for use in pharmaceuticals.</p>

<p>N2-Isobutyryl-7’-HO-N-trityl-morpholino guanosine is a novel nucleoside analog that has been synthesized to have an improved pharmacological profile.</p>

<p>Glycosylated pyrimidine analog; RNA component</p>

<p>1-(5'-O-DMT-b-D-xylofuranosyl)thymine is a nucleoside that is used as an activator for phosphoramidites. It has antiviral and anticancer activity. 1-(5'-O-DMT-b-D-xylofuranosyl)thymine is also a component of DNA and RNA, and has been found to have antitumour properties.</p>

<p>Polyinosinic acid-polycytidylic acid (Poly I:C), an agonist of TLR3 toll-like receptors, is a synthetic double-stranded RNA analog, consisting of polyinosinic acid (poly I) paired with polycytidylic acid (poly C), forming a stable duplex structure.PolyI:C stimulates the secretion of pro-inflammatory cytokines and type I interferon through its interaction with endosomal Toll-like receptor 3 (TLR-3) and the cytoplasmic receptors melanoma differentiation-associated gene 5 (MDA-5) and retinoic acid-inducible gene I (RIG-I). This immunostimulant activity makes Poly I:C a useful vaccine adjuvant and is used in vaccine formulations. Poly I:C and its stabilized analogs (e.g., poly-ICLC) are also being actively researched for their dual role in oncology: directly targeting tumors and acting as immune potentiators. For example Poly I:C can induce apoptosis in tumor cells and stimulate immunogenic cell death and is therefore being explored alongside chemotherapy, radiotherapy, and checkpoint inhibitors, helping to overcome resistance mechanisms and strengthen treatment outcomes.We can supply PolyI:C to all stages of your project - from R&amp;D and preclinical phases right up to GMP commercial manufacture. Contact our team for custom Poly I:C products.<br>For more on poly I:C read out blog 'Poly I:C: A Vaccine Adjuvant With Oncological Potential.'</p>

<p>N4-Benzoyl-2'-deoxy-5'-O-DMT-cytidine 3'-CE phosphoramidite is an activator for the synthesis of DNA and RNA. It is a novel nucleoside analog that inhibits the growth of cancer cells by blocking the synthesis of DNA and RNA. N4-Benzoyl-2'-deoxy-5'-O-DMT-cytidine 3'-CE phosphoramidite also has antiviral properties, which may be due to its ability to inhibit viral protein synthesis. This compound has been shown to be effective against herpes simplex type 1 and 2 viruses (HSV1 and HSV2).</p>

<p>5-Azido-2'-deoxyuridine is a diazonium salt that inhibits the replication of DNA. This compound is synthesized using natural compounds, including 5-azidouracil and formamide. The structure of this compound has been shown to be chromatographically similar to uridine and binds to DNA in vitro. It also has been shown to have biological properties that inhibit the growth of trichomonas vaginalis and dna replication. 5-Azido-2'-deoxyuridine is not very stable in dimethylformamide but can be stored at −20°C for up to two years.</p>

<p>2’,3’,5’-Tri-O-benzoyl-2’C-methyl-5-trifluoromethyluridine is a nucleoside that has been synthesized from uridine. It is used in the synthesis of deoxyribonucleosides and ribonucleosides. This product can be used for the treatment of cancer and antiviral purposes.</p>

<p>3'-O-Methyluridine is a nucleoside that is used in the preparation of oligonucleotides and as a substrate for uridine phosphorylase. It is used to study the termination of RNA synthesis, which occurs when there are no more ribose residues in the RNA template strand. When this happens, an adenosine residue is added by polyphosphate kinase to the 3' end of the RNA strand. This addition causes a release of pyrophosphate and leads to end of DNA synthesis. The acid hydrolysis technique can be used to separate 3'-O-methyluridine from other nucleotides. This reaction produces guanosine, which can be detected using polymerase chain reaction (PCR) techniques such as polyacrylamide gel electrophoresis (PAGE).</p>

<p>5’-[Biotin TEG] (CUG)28-3’ RNA is a novel synthetic biotin-labeled RNA. It is phosphoramidites and ribonucleosides. 5’-[Biotin TEG] (CUG)28-3’ RNA is used as an antiviral agent.</p>

<p>2’,3’,5’-Tri-O-benzoyl-2’C-methyl-3-deazauridine is a novel modified nucleoside. It has been shown to be an active DNA activator and to inhibit the replication of RNA and DNA. 2’,3’,5’-Tri-O-benzoyl-2’C-methyl-3-deazauridine has also been shown to have antiviral activity against HIV by inhibiting reverse transcriptase. In addition, it has anticancer effects in experimental models of cancer. 2'',3''',5'''-Tri-'O'-benzoyl-'2'''C-'methyl-'3'''Deazauridine is available as a high purity phosphoramidite.</p>

<p>3'-Azido-5'-O-benzyl-3'-deoxy-D3-thymidine is a novel, activator ribonucleoside that has been synthesized to be used in the treatment of cancer and other diseases. It is an analog of thymidine and is phosphorylated by cellular enzymes to form 3'-azido-5'-O-benzyl-3'-deoxyuridine monophosphate (ABPMP) which inhibits viral DNA synthesis. This compound also shows antiviral effects against influenza A virus in vitro and can inhibit the replication of human immunodeficiency virus type 1 (HIV-1).</p>

<p>8-Aza-7-deaza-2'-C-methyladenosine is a DNA nucleoside that can be used as an antiviral and anticancer agent. It is synthesized by reacting 8-aza-7-deazaguanosine monophosphate with 2'-C-methyladenosine. The compound has been shown to have antiviral activity against HIV, HSV, and HCV in vitro. In addition, this compound has been shown to inhibit the growth of human ovarian cancer cells. 8-Aza-7-deaza-2'-C-methyladenosine has also been shown to inhibit the growth of leukemia cells in vitro, which may be due to its ability to activate the p53 tumor suppressor gene.</p>

<p>8-Aza-7-deaza-2'-deoxyadenosine is a single-stranded DNA analogue that is used as a conjugate to deliver drugs to cells. It has been shown to be effective in the treatment of HIV by suppressing viral replication and the production of infectious virions. The drug is photolabile, which means it can be activated with light and then delivered to cells. 8-Aza-7-deaza-2'-deoxyadenosine has also been shown to inhibit the growth of human immunodeficiency virus (HIV) in vitro, but does not inhibit the growth of other viruses such as herpes simplex virus type 1 or adenovirus.</p>

<p>1-(2-Deoxy-2-fluoro-b-D-arabinofuranosyl)-5-methyluracil is a nucleoside analog for research applications. It contains a β-D-arabinofuranose sugar and the fluorine (F) substitution at the 2'-position enhances stability and improves resistance to enzymatic degradation. The 5-methyluracil base makes it structurally similar to thymidine, allowing it to be recognized by DNA polymerases and kinases.</p>

<p>Ribavirin is a synthetic nucleoside analog that is used as an antiviral agent. Ribavirin 5'-monophosphate dilithium (RPM) is a high-quality, novel phosphoramidite monophosphate of ribavirin. It has antiviral activity against herpesviruses, adenoviruses, and poxviruses. The antiviral properties of RPM are due to its ability to inhibit viral RNA synthesis through inhibition of the viral enzyme ribonucleotide reductase. RPM is also active against DNA viruses such as human papilloma virus and Epstein-Barr virus.</p>

<p>N6-Acetyl-2',3',5'-tri-O-acetyl-8-hydroxyadenosine is a modified nucleoside that is used in the synthesis of oligonucleotides. It is an activator with antiviral and anticancer properties, as well as various other biological activities. The CAS number for this product is 91359-02-2. The purity of this product ranges from 99% to 100%. This chemical has not been previously synthesized and has not been modified by any substituents or moieties.</p>

<p>2,4-Diamino-6,7-dimethylpteridine is a ligand that can bind to an orphan cytosine opposite an abasic site in RNA duplexes</p>

<p>2'-O-Allyladenosine is a synthetic nucleoside analog that has been shown to be a competitive inhibitor of the enzyme guanosine kinase. It has a high yield and can be used as a synthon for the preparation of 2'-deoxyribose nucleosides. The alkylation of allyl groups onto adenosines provides an efficient method for synthesizing allylated purines, which are analogs with increased stability and affinity for DNA sequences. 2'-O-Allyladenosine has been shown to bind to DNA, RNA, and proteins. Its interaction with DNA is stronger than that of unmodified adenosine, due to the presence of two allyl groups that can form hydrogen bonds with the phosphate backbone. This interaction may also lead to increased affinity for sequences containing G-C base pairs.</p>

<p>2',3'-Dideoxy-3'-fluoroguanosine is a synthetic nucleoside analog based on guanosine. It is structurally altered to interfere with DNA or RNA synthesis, making it potentially useful as an antiviral or anticancer agent.</p>

<p>1-(3`,5`-Di-O-benzoyl-2`-deoxy-2`-fluoro-beta-L-arabinofuranosyl)thymine is a nucleoside analog with modifications that influence its biological activity. It contains a thymine base and 3',5'-Di-O-benzoyl groups that protect hydroxyl functionalities during chemical synthesis. This molecule also has the sugar 2'-Deoxy-2'-fluoro-β-L-arabinofuranose made up of an L-arabinose configuration and a 2'-Fluoro substitution, the latter of which enhances stability and resistance to enzymatic degradation.</p>

<p>N4-Acetyl-5'-O-Tritylcytidine is a novel nucleoside that is a phosphoramidite. It is used in the synthesis of ribonucleosides, deoxyribonucleosides, and DNA. N4-Acetyl-5'-O-Tritylcytidine has antiviral activities.</p>

<p>Acetyl coenzyme A lithium salt is a drug that inhibits the production of acetyl-CoA, which is an important molecule in the metabolism of fatty acids. This drug has been shown to be effective against cancerous cells by inhibiting the synthesis of lysine residues and carnitine. Acetyl coenzyme A lithium salt has also been shown to inhibit the growth of typhimurium, which may be due to its ability to inhibit NADPH-cytochrome p450 reductase. Acetyl coenzyme A lithium salt has not been shown to have any carcinogenic potential in humans, but it has been shown to have carcinogenic potential in animal models.</p>

<p>N6-Benzoyl-2'-deoxy-8-oxoadenosine is a base modified deoxy nucleoside</p>

<p>2'-Deoxy-N4-methylcytidine is a modified nucleoside that is used to inhibit the activity of protein kinases. It has been shown to inhibit the function of two different types of enzymes, eukaryotic protein kinase and bacterial RNA polymerase. 2'-Deoxy-N4-methylcytidine inhibits the activity of these enzymes by modifying their structure, which in turn prevents them from carrying out their normal functions. This modification can be achieved through deamination or protonation reactions with this drug. The effects of this drug are nonparametric and are observed at transcript levels.</p>