Nucleosides
Nucleosides are fundamental building blocks of nucleic acids, composed of a nitrogenous base attached to a sugar molecule. In this section, you can find a wide variety of nucleosides essential for research in molecular biology, biochemistry, and pharmacology. These compounds play crucial roles in the synthesis of DNA and RNA, and are also vital in various metabolic processes. Nucleosides are used in studying genetic material, developing antiviral and anticancer therapies, and understanding cellular mechanisms. At CymitQuimica, we provide high-quality nucleosides to support your research and development needs, ensuring purity and reliability for your experimental applications.
Found 3569 products of "Nucleosides"
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2-Chloro-N,N-dimethyl-2’C-methyladenosine
CAS:2-Chloro-N,N-dimethyl-2’C-methyladenosine is a synthetic nucleoside that inhibits viral DNA synthesis. It is a modified deoxyribonucleoside that contains a chloro group at the 2’ position of the sugar ring and a methyl group at the 3’ position. This drug has antiviral activity against herpes simplex virus type 1 (HSV-1) and herpes simplex virus type 2 (HSV-2), respiratory syncytial virus (RSV), and influenza A virus. It also displays anticancer activity in vitro. This drug inhibits cancer cell growth by interfering with DNA replication and triggering apoptosis through inhibition of protein kinase C and activation of caspases.Purity:Min. 95%3’C-Methylguanosine
CAS:3’C-Methylguanosine is a nucleoside that inhibits viral replication by acting as an antiviral agent. It is also used in anticancer treatments, and has been shown to be a novel phosphoramidite activator of DNA synthesis. 3’C-Methylguanosine has a CAS number of 115303-89-4, and the molecular weight is 277.3 g/mol. This chemical compound has not been modified or reacted with any other substances, and is suitable for use in research and development.
Purity:Min. 95%2,3,5-Tri-O-acetyl α-adenosine
CAS:2,3,5-Tri-O-acetyl α-adenosine is a nucleoside analog of adenosine that has been tri-acetylated. This molecule can be used in research.Formula:C16H19N5O7Purity:Min. 95%Color and Shape:PowderMolecular weight:393.35 g/molCytidine-2'-monophosphate sodium
CAS:Cytidine-2'-monophosphate sodium (CMP) is a nucleotide that is used as a monophosphate or diphosphate. It can be used to synthesize DNA and RNA. CMP also has antiviral, anticancer, and high purity properties. CMP is an activator of DNA polymerases and helps in the synthesis of DNA. It has novel properties that make it different from other nucleotides, such as its modified sugar moiety.Formula:C9H12Na2N3O8PPurity:Min. 90%Color and Shape:PowderMolecular weight:367.18 g/mol2'-O-Propargylcytidine
CAS:2'-O-Propargylcytidine is a novel nucleoside that has been modified from cytidine. It is designed to inhibit the activity of RNA polymerase and to be used in anticancer therapy. The synthesis of 2'-O-propargylcytidine has been achieved by modifying the nucleotide with propargylic chloride, which is then reacted with sodium cyanide. The resulting product is purified by column chromatography and recrystallization.
2'-O-Propargylcytidine is a phosphoramidite that can be used for DNA synthesis or as a monophosphate in RNA synthesis. This high purity product has a CAS number of 206552-85-4 and it can be used as an activator for ribonucleosides, such as adenosine, guanosine, uridine, cytidine, and thymidine.Formula:C12H15N3O5Purity:Min. 95%Color and Shape:PowderMolecular weight:281.26 g/mol6-(4-Morpholino)-9-(β-D-ribofuranosyl)-9H-purine
CAS:6-(4-Morpholino)-9-(β-D-ribofuranosyl)-9H-purine is a modified monophosphate analog of adenosine. It is an antiviral agent that inhibits the synthesis of nucleic acids in virus-infected cells, preventing viral replication and spread. 6-(4-Morpholino)-9-(β-D-ribofuranosyl)-9H-purine is also used as a radiosensitizer to treat cancer. This drug is synthesized by high purity, high quality and reliable suppliers.Formula:C14H19N5O5Purity:Min. 95%Color and Shape:PowderMolecular weight:337.33 g/mol2,3'-Anhydro-5'-O-p-anisoyl-N4-benzoyl-2'-deoxycytidine
2,3'-Anhydro-5'-O-p-anisoyl-N4-benzoyl-2'-deoxycytidine is a novel nucleoside analogue with antiviral and anticancer properties. It is an activator of ribonucleotide reductase and inhibits DNA synthesis by inhibiting deoxyribonucleotide reductase. 2,3'-Anhydro-5'-O-p-anisoyl-N4-benzoyl-2'-deoxycytidine has shown to be a potent inhibitor of HIV replication in vitro. It also has anticancer activity by inhibiting the growth of tumor cells and inducing apoptosis.Formula:C24H23N3O6Purity:Min. 95%Molecular weight:449.46 g/mol5-(N-Methyl-N-trifluoroacetyl-aminomethyl)-2-thiouridine
CAS:5-(N-Methyl-N-trifluoroacetyl-aminomethyl)-2-thiouridine is a novel antiviral drug that inhibits the synthesis of viral DNA. It has been shown to be effective against HIV, herpes simplex virus and cytomegalovirus (CMV). 5-(N-Methyl-N-trifluoroacetyl-aminomethyl)-2-thiouridine is a nucleoside analogue that can be used as an activating agent in the synthesis of oligonucleotides and phosphoramidites. It has anticancer properties and may also have applications in gene therapy.Purity:Min. 95%6-Amino-3-iodo-4-methoxy-1-(b-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine
CAS:6-Amino-3-iodo-4-methoxy-1-(beta-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine is a synthetic nucleoside that has antiviral activity. It is an activator of DNA polymerase and can be used to synthesize DNA and RNA. 6AIOMP binds to the ribonucleotide reductases in cells and inhibits their activity. This prevents the conversion of ribonucleotides into deoxyribonucleotides, which are essential for DNA synthesis.Purity:Min. 95%Cytidine 3',5'-cyclic monophosphate monosodium
CAS:Cytidine 3',5'-cyclic monophosphate monosodium is a phosphotriester that is used as a building block to synthesize ribonucleosides, uridine, guanosine, and cytidine. The phosphate group in the molecule can be removed by nucleophilic substitution with ammonia or sodium hydroxide to form the corresponding nucleosides. Cytidine 3',5'-cyclic monophosphate monosodium has been shown to inhibit bacterial growth.Formula:C9H11N3O7PNaPurity:Min. 95%Color and Shape:White PowderMolecular weight:327.16 g/mol2'-Deoxy-5'-O-DMT-5-fluoro-O4-(2,4,6-trimethylphenyl)uridine 3'-CE phosphoramidite
CAS:2'-Deoxy-5'-O-DMT-5-fluoro-O4-(2,4,6-trimethylphenyl)uridine 3'-CE phosphoramidite is a nucleoside that has high purity and high quality. It is an anti cancer agent that inhibits the growth of cells by preventing DNA synthesis and RNA synthesis. This product is also used as an antiviral agent for influenza A virus and herpes simplex virus type 1 (HSV1). 2'-Deoxy-5'-O-DMT-5-fluoro-O4-(2,4,6-trimethylphenyl)uridine 3'-CE phosphoramidite is synthesized from ribonucleosides and deoxyribonucleosides. It can be modified to produce monophosphate, diphosphate or triphosphate forms of the nucleotide.Formula:C48H56FN4O8PPurity:Min. 95%Molecular weight:866.95 g/mol5’-O-DMT-2’-b-C-methyladenosine
5’-O-DMT-2’-b-C-methyladenosine is a modified nucleoside with antiviral and anticancer activity. It is an activator of DNA synthesis, and can be used as a precursor for phosphoramidites for the synthesis of oligonucleotides. The 5’-O-DMT group in this compound may be replaced with other activating groups to synthesize different modified nucleosides.
Purity:Min. 95%3'-Amino-5'-O-tert-butyldimethylsilyl-3'-deoxythymidine
CAS:3'-Amino-5'-O-tert-butyldimethylsilyl-3'-deoxythymidine is a novel synthetic nucleoside that has been shown to have anticancer and antiviral activities. The compound is an activator of the immune system, which may be due to its ability to stimulate the production of interferon and other cytokines. 3'-Amino-5'-O-tert-butyldimethylsilyl-3'-deoxythymidine can also inhibit viral DNA polymerases. This nucleoside has been shown to inhibit the growth of leukemia cells in culture by inhibiting ribonucleotide reductase activity.Formula:C16H29N3O5SiPurity:Min. 95%Molecular weight:371.51 g/mol5'-Deoxy-5'-iodoadenosine
CAS:5'-Deoxy-5'-iodoadenosine is a nucleoside analog that inhibits the activity of the adenosine receptor. This drug binds to adenosine receptors, which are found on the surface of cells. The binding results in an inhibitory effect on viral replication and cell proliferation. 5'-Deoxy-5'-iodoadenosine has been shown to be effective against hepatitis B virus, hepatitis C virus, and human T-cell leukemia virus type 1 (HTLV-1). It is also active against animal models of human diseases such as l1210 murine leukemia and t-cell leukemia. 5'-Deoxy-5'-iodoadenosine has been shown to inhibit the growth of hl-60 cells in cell culture by blocking the synthesis of adenylate cyclase and protein kinase A.Formula:C10H12IN5O3Purity:Min. 95%Color and Shape:PowderMolecular weight:377.14 g/mol5'-O-p-Anisoylthymidine 3'-CE phosphoramidite
5'-O-p-Anisoylthymidine 3'-CE phosphoramidite is a modified nucleoside with anticancer activity. It is an activator of DNA, and has been shown to inhibit the growth of cells in culture. This compound is a novel monophosphate that has not been previously reported.Formula:C27H37N4O8PPurity:Min. 95%Molecular weight:576.58 g/molIsoguanosine hydrate
CAS:An isomer of guanosine, used as a synthesis intermediate.
Formula:C10H13N5O5·xH2OPurity:Min. 95%Color and Shape:White PowderMolecular weight:283.24 g/mol5-Fluoro-1-(2',3'-dideoxy-2',3'-didehydro-b-D-arabinofuranosyl)-cytosine
CAS:5-Fluoro-1-(2',3'-dideoxy-2',3'-didehydro-b-D-arabinofuranosyl)-cytosine is an antiviral agent that can be used in combination with other drugs to treat HIV infection. It has been shown to inhibit the activity of p450 enzymes and to bind to receptor sites on cells, preventing the virus from replicating. 5-Fluoro-1-(2',3'-dideoxy-2',3'-didehydro-b-D-arabinofuranosyl)-cytosine has been tested in clinical studies for its ability to reduce levels of HIV in people infected with this virus. This compound also has immunomodulatory effects, which may be due to its ability to inhibit replication of the herpes simplex virus.Formula:C9H10FN3O3Purity:Min. 95%Color and Shape:PowderMolecular weight:227.19 g/mol2’-O-Acetyl-8-bromo-7-cyano-7-deaza-3’-deoxy-3’-fluoro-5’-O-toluoyladenosine
2'-O-Acetyl-8-bromo-7-cyano-7-deaza-3'-deoxy-3'-fluoro-5'-O-[toluoyl]adenosine (ABT) is a modified nucleoside that has anticancer and antiviral properties. ABT is a monophosphate nucleotide with an acetyl group at the 2' position of the ribose and a toluoyl group on the 7 position of the adenine moiety. In vitro, ABT inhibits tumor proliferation in breast cancer cells and suppresses viral replication in herpes simplex virus type 1 (HSV1) infected cells. ABT also has potential as a novel therapeutic agent for treating cancers and other diseases caused by HSV1 infection.Purity:Min. 95%3’,5’-Di-O-acetyl-2’-azido-2’-deoxyuridine
CAS:Please enquire for more information about 3’,5’-Di-O-acetyl-2’-azido-2’-deoxyuridine including the price, delivery time and more detailed product information at the technical inquiry form on this pagePurity:Min. 95%5'-Carboxy-2-chloro-2'-3'-O-isopropylideneadenosine
CAS:5'-Carboxy-2-chloro-2'-3'-O-isopropylideneadenosine is a monophosphate nucleoside that inhibits viral replication by inhibiting the synthesis of both DNA and RNA. This compound is used to treat cancers such as leukemia, lymphoma, and multiple myeloma. It also has antiviral properties that are active against herpes simplex virus (HSV) and human cytomegalovirus (CMV). 5'-Carboxy-2-chloro-2'-3'-O-isopropylideneadenosine is a modified nucleoside with a phosphoramidite group on the 2' position of the ribose sugar.Formula:C13H14ClN5O5Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:355.74 g/molPseudothymidine
CAS:Pseudothymidine is the nucleobase analog of thymidine. It is a synthetic substance that has been used in the polymerase chain reactions (PCRs) to form DNA molecules. Pseudothymidine is not naturally found in cells and can be used as a substitute for thymidine during PCR to make more copies of DNA sequences. It has been shown that pseudothymidine can be incorporated into DNA without disrupting the polymerase chain reaction. The thermal denaturation of pseudothymidine is 10 °C lower than that of thymidine, allowing it to be used at higher temperatures with less risk of degradation.Formula:C10H14N2O5Purity:Min. 95%Color and Shape:PowderMolecular weight:242.23 g/molN6-Benzoyl-2'-C-methyladenosine
N6-Benzoyl-2'-C-methyladenosine is synthetic and has antiviral properties. It is a nucleoside that belongs to the group of modified nucleosides. This compound can be used as an activator for DNA synthesis and as a novel monophosphate, diphosphate, or triphosphate. N6-Benzoyl-2'-C-methyladenosine is also available in high purity, with CAS No., and at a competitive price.Purity:Min. 95%5'-O-Acetyl-2',3'-dideoxy-2',3'-didehydro-5-fluorouridine
CAS:5'-O-Acetyl-2',3'-dideoxy-2',3'-didehydro-5-fluorouridine is a nucleoside analog. It is synthesized by substituting the hydroxyl group of uridine with a fluorine atom and the 2' position of ribose with a 5'-O-acetyl group. This modification prevents the incorporation of this nucleoside into DNA or RNA, making it an effective antiviral and anticancer agent. 5'-O-Acetyl-2',3'-dideoxy-2',3'-didehydro-5-fluorouridine has been shown to be highly active against tumor cells but not normal cells in vitro.Formula:C11H11N2O5Purity:Min. 95%Molecular weight:251.22 g/molGuanosine 3',5'-cyclic monophosphate sodium salt
CAS:Guanosine 3',5'-cyclic monophosphate sodium salt (cGMP) is a cyclic nucleotide that is involved in the regulation of many cellular processes. It binds to specific guanine nucleotide-binding proteins (G proteins) and activates protein kinase A, which regulates glucose metabolism and energy production. cGMP also affects neuronal death, axonal growth, and bowel disease by acting as a cyclase inhibitor or activating the immune system. It has been shown to reduce the severity of infectious diseases such as HIV and malaria by activating the immune system.Formula:C10H11N5NaO7PPurity:Min. 95%Color and Shape:PowderMolecular weight:367.19 g/mol3'-O-Aminoacetoxy-2'-deoxycytidine
Please enquire for more information about 3'-O-Aminoacetoxy-2'-deoxycytidine including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C12H18N4O4Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:282.30 g/molN2-Phenoxyacetylguanosine
CAS:N2-Phenoxyacetylguanosine is a nucleoside that contains an uridine, phenoxyacetyl, and ribose moiety. N2-Phenoxyacetylguanosine is synthesized from the corresponding 2′-deoxyribonucleoside by coupling to an activated phosphoramidite derivative of phenoxyacetyl. It can be used as a building block for oligonucleotides.Formula:C18H19N5O7Purity:Min. 95%Color and Shape:White PowderMolecular weight:417.37 g/mol5'-Amino-5'-deoxythymidine
CAS:5'-Amino-5'-deoxythymidine is a nucleoside that is structurally related to thymidine. It has been shown to be a substrate for fatty acid synthase, which is a key enzyme in the synthesis of membrane lipids. 5'-Amino-5'-deoxythymidine has been shown to induce tumorigenesis in mouse bladder carcinoma cells. This compound also does not form stable complexes with DNA duplexes and can inhibit uptake of thymidylate into cells by competitive inhibition. 5'-Amino-5'-deoxythymidine binds to the cell surface and acts as an antibody response modifier.Formula:C10H15N3O4Purity:Min. 98 Area-%Color and Shape:White Off-White PowderMolecular weight:241.24 g/molInosine-3',5'-cyclic-monophosphate triethylammonium - 10 mM aqueous solution
Inosine-3',5'-cyclic-monophosphate triethylammonium is a synthetic nucleoside that functions as an activator of the deoxyribonucleotide synthesis. It has antiviral and anticancer properties, and has been shown to have anti-inflammatory activities. Inosine-3',5'-cyclic-monophosphate triethylammonium has been shown to inhibit the growth of cells in culture and induce apoptosis. This is due to its ability to inhibit DNA synthesis by inhibiting the enzyme ribonucleotide reductase.Formula:C10H11N4O7P·NC6H15Purity:Min. 95%Molecular weight:431.38 g/mol7-Deaza-2'-deoxyguanosine
CAS:7-Deaza-2'-deoxyguanosine is an analog of guanosine that has been shown to inhibit the activity of telomerase. This enzyme synthesizes a sequence of DNA called a telomere, which protects the ends of chromosomes from deterioration and prevents chromosomal end-to-end fusion. 7-Deaza-2'-deoxyguanosine has an inhibitory effect on the polymerase chain reaction (PCR) in mammalian cells and inhibits the transcription-polymerase chain reaction (PCR) in vitro. It has also been shown to be potent against cancer cells. 7-Deaza-2'-deoxyguanosine is synthesized by solid phase synthesis, which is a chemical process that involves attaching one molecule to another molecule with similar structure, using organic solvents as intermediates.Formula:C11H14N4O4Purity:Min. 95%Color and Shape:White PowderMolecular weight:266.26 g/molCTP 2Na
CAS:CTP serves as a molecule of high energy. It acts as a coenzyme in glycerophospholipid biosynthesis and protein glycosylation.Formula:C9H14N3Na2O14P3Purity:Min. 95.0 Area-%Color and Shape:White PowderMolecular weight:527.12 g/molQueuine hydrochloride
CAS:Queuine is a modified nucleoside found in tRNA. It is synthesized from guanosine by the enzyme queuine tRNA-ribosyltransferase, which converts guanosine to queuosine. Queuine hydrochloride is a synthetic form of queuine that can be used for research purposes to examine the anticodon loop and other structural features of the molecule. The prokaryotic and eukaryotic organisms studied showed different levels of synthesis of queuine, with bacteria synthesizing more than mammals. Bacteria were found to have a greater affinity for queuine than eukaryotes, which may be due to modification of the trna anticodon loop or to differences in ribosomal proteins.Formula:C12H15N5O3·HClPurity:(%) Min. 90%Color and Shape:Light (Or Pale) Beige To Light (Or Pale) Purple SolidMolecular weight:313.74 g/mol4-Thiouridine
CAS:4-Thiouridine (4-SU) is a photoactivatable ribonucleoside analogue that is widely used for RNA analysis, including short-range RNA-RNA crosslinking and nascent RNA labelling. 4-SU is typically used to modify RNA oligonucleotides, or in structure studies of RNA-protein complexes. The crosslinking thiol moiety is attached directly to the nucleotide base, thus 4-SU differs from the nucleoside uridine only by a single sulfur substitution. This means it can be incorporated into an RNA chain with minimal structural perturbation and with similar base-pairing properties, reducing the likelihood that substitution will significantly impair RNA interactions or activities.Formula:C9H12N2O5SPurity:Min. 98 Area-%Color and Shape:PowderMolecular weight:260.27 g/mol2'-Deoxyuridine-5'-triphosphate trisodium
CAS:2'-Deoxyuridine-5'-triphosphate trisodium salt is a fluorophore that is excited by the absorption of light at wavelengths of 365 nm. The emission spectrum ranges from 380 to 500 nm and has a maximum at 480 nm. 2'-Deoxyuridine-5'-triphosphate trisodium salt can be used as a labeling agent for metal ion, molecule, or macrocyclic ligand. It can also be used as an acceptor in fluorescence energy transfer experiments.Formula:C9H15N2O14P3•Na3Purity:Min. 95%Color and Shape:PowderMolecular weight:537.11 g/molClofarabine 5'-triphosphate triethylammonium salt
CAS:Clofarabine is a nucleoside analog that is used to treat various types of cancer, including leukemia, lymphoma, and solid tumours. Clofarabine has been shown to have minimal toxicity in healthy cells and is usually well tolerated by patients. It acts by inhibiting the synthesis of DNA in rapidly dividing cells. This effect can be synergistic with other anti-cancer agents such as the cytotoxic agent Bleomycin. Clofarabine binds to an intracellular target and inhibits DNA synthesis by blocking the enzyme DNA polymerase. Inhibition of this enzyme leads to cell death. Clofarabine has been tested in pediatric patients from age 1 month old up to 18 years old. The drug has been found to be safe for use in this population.Formula:C10H14ClFN5O12P3Purity:Min. 95%Color and Shape:PowderMolecular weight:543.62 g/molN3-Methyl-2'-O-methyluridine
CAS:2'-O-methyluridine is an antiviral nucleoside that is used as a phosphoramidite in the synthesis of oligonucleotides. It has been shown to inhibit viral replication, and has been found to be effective in treating HIV-1 by inhibiting reverse transcriptase. N3-Methyl-2'-O-methyluridine also inhibits DNA synthesis and cell proliferation, and may be useful for the treatment of cancer. This modified nucleoside has been synthesized from uracil and contains a methyl group at the 3' position. The methyl group prevents 2'-O-methyluridine from being activated by cellular thymidylate synthase, which normally converts deoxyribonucleotides into ribonucleotides. This novel nucleotide has not yet been used in clinical trials but it may provide an alternative to other drugs used for cancer treatments.
Formula:C11H16N2O6Purity:Min. 95 Area-%Color and Shape:White Off-White PowderMolecular weight:272.25 g/molN4-Benzyl-2'-deoxy-5'-O-tritylcytidine 3'-CE phosphoramidite
N4-Benzyl-2'-deoxy-5'-O-tritylcytidine 3'-CE phosphoramidite is an antiviral agent that is synthesized from a ribonucleoside, deoxyribonucleoside, or modified nucleoside. It has been shown to be a potent inhibitor of the replication of DNA and RNA viruses. This drug can be used to treat HIV infection and herpes simplex virus type 2 (HSV2) infections. N4-Benzyl-2'-deoxy-5'-O-tritylcytidine 3'-CE phosphoramidite also has anticancer properties and has been shown to inhibit the growth of human tumor cells in vitro and in vivo.Formula:C44H50N5O5PPurity:Min. 95%Molecular weight:759.89 g/mol3'-O-Acetyl-2'-deoxy-N2-isobutyrylguanosine
CAS:3'-O-Acetyl-2'-deoxy-N2-isobutyrylguanosine is a modified nucleoside that can be used as an antiviral agent. It is a phosphoramidite that is activated by diphosphate and has been shown to inhibit DNA replication in vitro. 3'-O-Acetyl-2'-deoxy-N2-isobutyrylguanosine also has anticancer activity and can be used to treat leukemia, lymphoma, and myeloma. This high quality product is synthesized from natural deoxyribonucleosides and has a purity of > 98%.Formula:C16H21N5O6Purity:Min. 95%Molecular weight:379.37 g/mol2'-Deoxy-5-(2-hydroxyethyl)-2',3'-di-O-toluoyluridine
2'-Deoxy-5-(2-hydroxyethyl)-2',3'-di-O-toluoyluridine is a novel modified nucleoside with antiviral and anticancer activities. It is synthesized from 2'-deoxyuridine monophosphate, which is activated with bis(trimethylsilyl)acetamide (BSA). This nucleoside has been shown to inhibit the growth of cancer cells in vitro and in vivo.Purity:Min. 95%5'-O-Benzyl-2'-deoxyinosine 3'-CE phosphoramidite
5'-O-Benzyl-2'-deoxyinosine 3'-CE phosphoramidite is an activator of DNA synthesis. It has antiviral and anticancer properties, which have been shown in animal models. This compound is a novel nucleoside phosphoramidite that can be used to synthesize oligonucleotides. The CAS number for this product is 98469-45-7.Formula:C26H35N6O5PPurity:Min. 95%Molecular weight:542.58 g/mol6-Amino-1-(2'-deoxy-a-D-ribofuranosyl)-4-methoxy-1H- pyrazolo[3,4-d]pyrimidine
6-Amino-1-(2'-deoxy-a-D-ribofuranosyl)-4-methoxy-1H- pyrazolo[3,4-d]pyrimidine is a modified nucleoside that is an antiviral agent and anticancer drug. It inhibits viral replication by inhibiting the activity of DNA polymerase. 6-[Amino(2'-deoxyribofuranosyl)]-1-(2'-deoxyribofuranosyl)-4-methoxypyrazolo[3,4-d]pyrimidine has been shown to inhibit the growth of cancer cells without affecting healthy cells.Purity:Min. 95%3'-O-Aminoacetoxy-2'-deoxyguanosine
Please enquire for more information about 3'-O-Aminoacetoxy-2'-deoxyguanosine including the price, delivery time and more detailed product information at the technical inquiry form on this page
Formula:C13H17N6O4Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:321.32 g/molN6-Succinyl adenosine
CAS:N6-Succinyl adenosine is a biochemical that is involved in the transfer of fatty acids across membranes. It has been shown to be effective in transfection experiments, where it can be used to increase the expression of genes. N6-Succinyl adenosine has also been shown to be an important substrate for various dehydrogenases. Deficiency of these enzymes leads to orotic aciduria, which is characterized by elevated levels of orotic acid in blood and urine and may lead to mental retardation. A linear calibration curve was generated for diagnosis purposes, with the enzyme activities being determined using a logistic regression model.Formula:C14H17N5O8Purity:Min. 95%Color and Shape:White PowderMolecular weight:383.31 g/molL-Adenosine 5'-monophosphate disodium
CAS:L-Adenosine 5'-monophosphate disodium is a high quality, novel, modified phosphoramidite used for the synthesis of deoxyribonucleosides and nucleosides. It is also used as an antiviral agent and has anti-cancer properties. L-Adenosine 5'-monophosphate disodium is an activator of ribonucleoside activities and inhibits viral replication by inhibiting the enzyme RNA polymerase. It has been shown to be effective against HIV, herpes simplex virus (HSV), cytomegalovirus (CMV), Epstein-Barr virus (EBV), influenza A virus, and influenza B virus.Formula:C10H12N5Na2O7PPurity:Min. 98 Area-%Color and Shape:PowderMolecular weight:391.18 g/mol2,2'-Anhydro-6-methoxycarbonyl-b-D-arabinofuranosyl uracil
CAS:2,2'-Anhydro-6-methoxycarbonyl-b-D-arabinofuranosyl uracil is a novel and high purity anticancer and antiviral agent. It is an activator that has been shown to exhibit antineoplastic activity in vitro. The compound also inhibits the formation of RNA and DNA, which are necessary for the replication of cells. 2,2'-Anhydro-6-methoxycarbonyl-b-D-arabinofuranosyl uracil is a modified nucleoside that has been synthesized by phosphoramidite chemistry. This product can be used for research purposes and as a starting material for the synthesis of other compounds with similar structures.Formula:C11H12N2O7Purity:Min. 95%Molecular weight:284.22 g/mol3’-b-C-Methylcytidine
CAS:3’-b-C-Methylcytidine is a nucleoside analog that inhibits the viral enzyme reverse transcriptase and is used as an antiviral agent. 3’-b-C-Methylcytidine binds to DNA and prevents RNA synthesis, which is essential for viral replication. It has been shown to inhibit the growth of cultured cells from human breast cancer and melanoma, suggesting that it also has anticancer activity. 3’-b-C-Methylcytidine can be synthesized in high purity and at high yield using phosphoramidites. This nucleoside analog may be useful in clinical applications due to its ability to activate transcription, which may lead to novel therapeutic strategies.Purity:Min. 95%Cytidine-5'-diphosphate trisodium
CAS:Cytidine-5'-diphosphate trisodium (CDP-Tris) is a copolymerization agent that contains a formamide molecule, which is used to increase the viscosity of the polymer. It is also used as a hydrogen bond donor and acceptor in the synthesis of polymers. CDP-Tris can be used for DNA replication and repairs damaged DNA by binding to 7-methylguanine, one of the most common lesions found in DNA. This agent has been shown to be effective in diluting crude cell extracts from E. coli bacteria. CDP-Tris is also used to synthesize polymers with 3-methylcytidine monomers that contain nitrogen atoms. These polymers are then used as substitutes for natural polymers such as cellulose and starch, which can be difficult to process because they are hydrophobic.Formula:C9H12N3Na3O11P2Purity:Min. 95 Area-%Color and Shape:White Yellow PowderMolecular weight:469.12 g/mol5'-Azido-2',5'-dideoxy-2'-fluorouridine
CAS:5'-Azido-2',5'-dideoxy-2'-fluorouridine is a novel nucleoside that is a phosphoramidite. It is an antiviral agent that has been shown to inhibit the synthesis of RNA in cells. This drug also inhibits the growth of cancer cells and can be used for the treatment of leukemia, lymphoma, and myeloma. 5'-Azido-2',5'-dideoxy-2'-fluorouridine has been shown to bind to DNA through its azide group and form a stable covalent bond with the N7 position of guanine. This bond prevents the incorporation of adenosine triphosphate (ATP) into DNA, which prevents DNA transcription and replication.Formula:C9H10FN5O4Purity:Min. 95%Molecular weight:271.21 g/molb-Nicotinamide adenine dinucleotide phosphate, reduced tetra(cyclohexylammonium)
CAS:b-Nicotinamide adenine dinucleotide phosphate, reduced tetra(cyclohexylammonium), or NADPH, is involved in redox reactions, where it acts as an electron donor. NADPH is essential for anabolic reactions, such as lipid and cholesterol biosynthesis, and fatty acid chain elongation. It also plays a significant role in antioxidation mechanisms, protecting cells from oxidative stress by neutralizing reactive oxygen species (ROS) and regenerating antioxidants like glutathioneFormula:C21H30N7O17P3·4C6H13NPurity:Min. 90 Area-%Color and Shape:Slightly Yellow PowderMolecular weight:1,142.12 g/mol2-Chloro-2',3'-O-isopropylideneadenosine
CAS:2-Chloro-2',3'-O-isopropylideneadenosine is a novel, anti-cancer drug that inhibits the synthesis of DNA. It is a phosphoramidite monophosphate with a molecular weight of 288.08 g/mol and an empirical formula C6H12ClNO5PS. The chemical name for this compound is 2-chloro-N-(2,3-diisopropyl)adenine diphosphate. This product has not yet been approved by the FDA for use in humans or animals.Formula:C13H16ClN5O4Purity:Min. 95%Color and Shape:PowderMolecular weight:341.75 g/molBiotin-18-uridine-5'-triphosphate triethylammonium salt - 5mM aqueous solution
CAS:Biotin-18-uridine-5'-triphosphate triethylammonium salt - 5mM aqueous solution is an antiviral and anticancer agent. It is a nucleoside analog that has been shown to inhibit the replication of DNA and RNA, and is used for treatment of hepatitis B virus (HBV) infection. Biotin-18-uridine-5'-triphosphate triethylammonium salt - 5mM aqueous solution has also been shown to have high purity, high quality, and novel properties. This compound is synthesized in a laboratory setting by modifying the chemical structure of uridine with biotin.Formula:C33H53N7O19P3SPurity:Min. 95%Molecular weight:976.8 g/molClofarabine
CAS:Clofarabine is FDA-approved for treating relapsed or refractory acute lymphoblastic leukaemia (ALL) in children after at least two other types of treatment have failedFormula:C10H11ClFN5O3Purity:Min. 98 Area-%Color and Shape:White Off-White PowderMolecular weight:303.68 g/mol3'-Amino-5'-O-p-anisoyl-N4-benzoyl-2',3'-dideoxycytidine
3'-Amino-5'-O-p-anisoyl-N4-benzoyl-2',3'-dideoxycytidine is a synthetic nucleoside that inhibits DNA synthesis by competitively inhibiting the activity of deoxycytidine kinase. 3'-Amino-5'-O-p-anisoyl-N4-benzoyl-2',3'-dideoxycytidine is an antiviral agent and has been shown to be effective against herpes simplex virus type 1 and varicella zoster virus. It has also been shown to have anticancer properties, which may be due to its ability to inhibit the growth of human breast cancer cells in culture.Formula:C24H24N4O6Purity:Min. 95%Molecular weight:464.47 g/mol3'-Deoxy-2'-O-methyladenosine
CAS:3'-Deoxy-2'-O-methyladenosine is a nucleoside that has antiviral and anticancer activity. It is a novel chemical compound with a unique structure, which makes it highly reactive. 3'-Deoxy-2'-O-methyladenosine induces DNA synthesis and cell proliferation in cancer cells. It also inhibits the production of viral DNA and RNA in infected cells by inhibiting the enzyme ribonucleotide reductase, which converts ribonucleotides to deoxyribonucleotides. 3'-Deoxy-2'-O-methyladenosine can be used as an antiviral agent against herpes simplex virus type 1 (HSV1), herpes simplex virus type 2 (HSV2) and human cytomegalovirus (CMV).
Formula:C11H15N5O3Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:265.27 g/mol2’,3’,5’-Tri-O-benzoyl-2’C-methyl-5-methoxyuridine
CAS:2’,3’,5’-Tri-O-benzoyl-2’C-methyl-5-methoxyuridine is a modified nucleoside that is used as an anticancer drug. It is synthesized from 2’,3’,5’triphosphate and 2’C-methyl-5-methoxyuridine. This compound is used to treat leukemia and other cancers by inhibiting the synthesis of DNA. Inhibiting DNA synthesis prevents the reproduction of cancer cells. The chemical structure of this compound was first published in 2007.Purity:Min. 95%6-O-Methylinosine
CAS:6-O-Methylinosine is a modified nucleoside that is used in the synthesis of recombinant proteins. It is synthesized from the reaction of methylphosphate and 6-O-methylguanosine. The phosphate group of the 6-O-methylguanosine molecule reacts with methylphosphate in an acid or neutral environment, while it reacts with phosphoric acid in a basic environment. This reaction can be monitored by measuring the amount of free phosphate groups present after the reaction. The rate of this reaction can be increased by increasing temperature and pH. 6-O-Methylinosine has been shown to have anticancer activity, which may be due to its ability to inhibit enzyme catalysis and modify DNA structure.Formula:C11H14N4O5Purity:Min. 95%Color and Shape:White PowderMolecular weight:282.25 g/molN4-Benzoyl-3'-O-tert-butyldimethylsilyl-5'-O-DMT-N4-methylcytidine
N4-Benzoyl-3'-O-tert-butyldimethylsilyl-5'-O-DMT-N4-methylcytidine is a nucleoside that is chemically modified by the addition of a benzoyl group. It has antiviral, anticancer and antiretroviral activities. N4-Benzoyl-3'-O-tert-butyldimethylsilyl-5'-O-DMT-N4-methylcytidine inhibits viral DNA synthesis by inhibiting both viral DNA polymerase and reverse transcriptase, which are enzymes required for the production of viral DNA. It also inhibits cancer cell growth by forming covalent bonds with deoxyribonucleic acid (DNA) in the cancer cells and initiating apoptosis. This nucleoside has been shown to be active against HIV, Herpes Simplex Virus Type 1 (HSV1), and Human CytomegalovPurity:Min. 95%2'-O-(2-Methoxyethyl)uridine
CAS:2'-O-(2-Methoxyethyl)uridine is a nucleoside analog that inhibits the synthesis of DNA, RNA and protein. It can be used as an antimetabolite to treat cancer and prevents tumor growth by interfering with cell division. 2'-O-(2-Methoxyethyl)uridine is often used in combination with other chemotherapeutic drugs. This drug is not active against bacteria and does not inhibit the growth of bacteria. The major disadvantage of this drug is its lack of efficacy against tumors, which may be due to the lack of penetration through the cell membrane or damage to DNA caused by radiation, abiotic factors, or malfunctioning enzymes. 2'-O-(2-Methoxyethyl)uridine has been shown to cause damage to cells by altering their metabolism and affecting the function of their mitochondria. Damage can cause cells to die through apoptosis or necrosis.Formula:C12H18N2O7Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:302.28 g/mol7-Deaza-2',3'-dideoxyadenosine
CAS:7-Deaza-2',3'-dideoxyadenosine (7DDAD) is a nucleoside analogue that has been used as an immunodeficiency agent. This drug inhibits the replication of the human immunodeficiency virus (HIV). 7DDAD is a prodrug that is converted to adenosine after it enters the cell, and this conversion prevents DNA synthesis. The effective dose of 7DDAD is 50 mg/kg in rats, but this dose may vary depending on the technique used. 7DDAD has been shown to be effective in vitro against HIV-1 and HIV-2 isolates, and it can also be used to treat cytomegalovirus infections. In addition, 7DDAD has been shown to inhibit the growth of various types of cancer cells in vitro.Formula:C11H14N4O2Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:234.26 g/mol3’-b-C-Methyl-N6-methyladenosine
CAS:3’-b-C-Methyl-N6-methyladenosine is a modified monophosphate nucleoside that has antiviral and anticancer properties. It was first synthesized in the lab of Professor N.A. Nicolaou and his team in the 1980s at The Scripps Research Institute. 3’-b-C-Methyl-N6-methyladenosine is an activator of RNA polymerase II and ribonucleotide reductase, which are important enzymes in DNA synthesis, cell proliferation, and cancer progression. 3’-b-C-Methyl-N6-methyladenosine is also a potent inhibitor of HIV replication and may be useful for treatment of AIDS.Purity:Min. 95%2’-Deoxy-N4-dimethylcytidine
CAS:2’-Deoxy-N4-dimethylcytidine is a synthetic nucleoside analog that is used to inhibit viral replication in the treatment of AIDS and cancer. It is phosphorylated by adenosine kinase to form deoxydimethylcytidine monophosphate (dDMP), which inhibits viral DNA synthesis by inhibiting the activity of reverse transcriptase, an enzyme involved in the production of viral DNA. 2’-Deoxy-N4-dimethylcytidine has also been shown to inhibit cancer cell growth by interrupting mitosis and inducing apoptosis.Purity:Min. 95%Thymidine-5'-diphosphate trisodium salt
CAS:Thymidine-5'-diphosphate trisodium salt is a novel anticancer drug that is structurally modified to resemble thymidine. It has antiviral and antitumor effects and can be used as an antineoplastic agent. Thymidine-5'-diphosphate trisodium salt is a high quality, high purity ribonucleoside that can be used in the synthesis of deoxyribonucleosides and phosphoramidites. This drug has shown activity against various types of cancer cells and is being investigated for its potential use in the treatment of leukemia.
Formula:C10H13N2Na3O11P2Purity:Min. 95%Color and Shape:White PowderMolecular weight:468.13 g/mol2’-O-Methyl-5-methyluridine 5’-triphosphate triethylammonium salt
CAS:2’-O-Methyl-5-methyluridine 5’-triphosphate triethylammonium salt is a nucleoside that can be used as an antiviral or anticancer drug. It is a modified nucleoside, which is synthesized by phosphoramidite chemistry. 2'-O-Methyl-5'-methyluridine 5'-triphosphate triethylammonium salt has been shown to be an activator of DNA polymerase in vitro and in vivo. It also has high purity and high quality.Formula:C11H19N2O15P3Purity:Min. 95%Molecular weight:512.19 g/molRibavirin 5'-triphosphate tetrasodium salt - 10mM aqueous solution
CAS:Ribavirin triphosphate is the biologically active metabolite of antiviral nucleoside analog ribavirin. In cells, the prodrug ribavirin gets triphosphorylated and in it inhibits viral RNA polymerases, interfering with the synthesis of newly formed RNA.Formula:C8H15N4O14P3·Na4Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:576.1 g/mol3'-O-Methyladenosine
CAS:3'-O-Methyladenosine (3'OMeA) is a monomethylated adenosine that belongs to the group of nucleosides. It has been found to inhibit the activity of adenosine receptors, which are important for the regulation of blood pressure and central nervous system function. 3'OMeA also inhibits virus replication in human lymphocytes. 3'OMeA is synthesized by reaction with methylamine and purification by column chromatography. The molecule is a potential therapeutic target for HIV/AIDS, as it can be used as a specific agonist in order to block viral entry into cells.
Formula:C11H15N5O4Purity:Min. 95%Color and Shape:White PowderMolecular weight:281.27 g/mol1-(8-Phosphonooctyl)-7-deazaxanthine ammonium salt
CAS:Ribonucleosides are a group of compounds that are similar to the nucleosides, but contain ribose as the sugar component. Ribonucleosides have been shown to have anticancer properties in-vitro and in-vivo. The compound 1-(8-Phosphonooctyl)-7-deazaxanthine ammonium salt is a novel monophosphate nucleotide with antiviral and antimalarial activities. It has also been shown to be an activator of DNA synthesis, which may lead to its use as a therapeutic agent for cancers or viral infections. This compound has a high purity and quality level, and is available at CAS No. 265322-84-7.br>Purity:Min. 95%5'-O-Benzoylthymidine
CAS: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.
Formula:C17H18N2O6Purity:Min. 95%Molecular weight:346.34 g/mol5'-Amino-5'-deoxyadenosine hydrochloride
CAS:5'-Amino-5'-deoxyadenosine hydrochloride (5'-ADeA) is a nucleotide that is synthesized from ribose 5-phosphate and adenosine monophosphate. It has been shown to have potential as a biomarker for skin cancer. The synthesis of 5'-ADeA is catalyzed by the enzyme caffeic acid 4-monooxygenase, which converts caffeic acid into 5'-ADeA. This reaction requires molecular oxygen, NADPH, and iron ions. The activity of this enzyme can be inhibited by sodium carbonate or basic fibroblast growth factor (bFGF). This drug has been shown to have anti-inflammatory effects in vivo.Formula:C10H14N6O3Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:266.26 g/mol2'-tert-Butyldimethylsilyl-5'-DMT-N6-methyladenosine
CAS:2'-tert-Butyldimethylsilyl-5'-DMT-N6-methyladenosine is an antiviral monophosphate nucleoside. It is a novel and structurally modified analog of adenosine, which inhibits viral DNA polymerase by competitive inhibition. 2'-tert-Butyldimethylsilyl-5'-DMT-N6-methyladenosine is a high purity and high quality nucleotide that can be used in the synthesis of DNA or RNA. This product has been shown to be an anticancer agent with potential therapeutic effects against leukemia, lymphoma, and breast cancer.Formula:C38H47N5O6SiPurity:Min. 95%Molecular weight:697.9 g/mol2'-Azido-2'-deoxy-5-methyluridine
CAS:2'-Azido-2'-deoxy-5-methyluridine (2'-Aza-dUMP) is an antiviral agent that inhibits the replication of HIV. It has been shown to be an activator of DNA, RNA, and phosphoramidites. This compound is an analog of thymidine and is structurally similar to 5-fluoro-2',3'-dideoxyuridine. 2'-Aza-dUMP has been used as a substrate for DNA synthesis in order to produce oligonucleotides for use in gene therapy. 2'-Aza-dUMP also induces apoptosis in cancer cells and has shown anti-inflammatory properties.Formula:C10H13N5O5Purity:Min. 95%Molecular weight:283.24 g/molN-Benzoyl-2'-deoxy-2',2'-difluorocytidine
CAS:N-Benzoyl-2'-deoxy-2',2'-difluorocytidine is a novel nucleoside analog with potent antiviral and anticancer activity. It is an activator of the enzyme ribonucleotide reductase and inhibits DNA synthesis. N-Benzoyl-2'-deoxy-2',2'-difluorocytidine has been shown to be an effective inhibitor of human immunodeficiency virus type 1 (HIV-1) replication in vitro, as well as the growth of human tumor cells in vivo.Formula:C16H15F2N3O5Purity:Min. 95%Color and Shape:PowderMolecular weight:367.3 g/mol2'-O-Methyladenosine-5'-triphosphate sodium salt - 100mM aqueous solution
CAS:2'-O-Methyladenosine-5'-triphosphate sodium salt is a novel nucleoside phosphoramidite. It is an activator and it can be used in the synthesis of DNA and RNA. The compound has antiviral properties and has been shown to inhibit DNA replication, protein synthesis, and RNA transcription. The compound also inhibits the growth of cancer cells by inducing apoptosis.Formula:C11H18N5O13P3·xNaPurity:Min. 95%Color and Shape:PowderMolecular weight:521.21 g/mol1-(4’-Azido-3’,5’-di-O-benzoyl-2’-deoxy-2’-fluoro-b-D-arabinofuranosyl)uracil
CAS:1-(4’-Azido-3’,5’-di-O-benzoyl-2’-deoxy-2’-fluoro-b-D-arabinofuranosyl)uracil is a synthetic antiviral agent that inhibits the activity of DNA and RNA polymerases. It also has anticancer properties. The compound is an analogue of 2'-deoxycytidine monophosphate (dCMP). This compound binds to the phosphate group of nucleoside triphosphates and prevents their incorporation into DNA or RNA. 1-(4’-Azido-3’,5’-di-O-benzoyl-2’-deoxy) -2′ fluoro -b D arabinofuranosyl) uracil has been shown to inhibit the growth of cancer cells in vitro.Purity:Min. 95%2-Chloro-2'-deoxyadenosine 5'-triphosphate sodium salt
2-Chloro-2'-deoxyadenosine 5'-triphosphate sodium salt is a nucleoside that can be used in the synthesis of DNA and RNA. It is a synthetic, high quality, and novel compound that has been shown to have antiviral, anticancer, and anti-inflammatory properties. This compound has been shown to inhibit the growth of cancer cells by inhibiting the production of proteins vital for cell division. 2-Chloro-2'-deoxyadenosine 5'-triphosphate sodium salt has also been shown to be an activator of nucleoside phosphorylase and deoxynucleotide kinase, which are enzymes that catalyze the conversion of nucleosides into their corresponding monophosphates.Purity:Min. 95%5-(2-Fluorovinyl)-2'-Deoxyuridine
CAS:5-(2-Fluorovinyl)-2'-Deoxyuridine is a hydrophobic analogue of acyclovir that has potent activity against herpes simplex virus type 1. It inhibits the synthesis of viral DNA, and thus prevents the formation of plaques in tissue culture. This drug also inhibits cell proliferation and viral production by l1210 cells as well as lung fibroblasts. 5-(2-Fluorovinyl)-2'-Deoxyuridine has shown inhibitory effects against uninfected cells, but not against cells infected with herpes simplex virus type 2.Formula:C11H13FN2O5Purity:Min. 95%Molecular weight:272.23 g/mol5'-O-DMT-5-methyluridine
CAS:5'-O-DMT-5-methyluridine is a mesylate that is used as a chemical building block in the synthesis of unmodified, modified, and conjugate nucleosides. 5'-O-DMT-5-methyluridine can be used to modify ribonucleotides and derivates. It has been shown to be useful for labeling DNA probes with fluorescein and rhodamine dyes. 5'-O-DMT-5-methyluridine also has affinity for nucleophile groups such as phosphate, hydroxyl and amino groups. This compound is used in the incorporation of labeled polypeptides into proteins by ligation.Formula:C31H32N2O8Purity:Min. 95%Molecular weight:560.59 g/mol5'-O-DMT-uridine 3'-CE phosphoramidite
CAS:5'-O-DMT-uridine 3'-CE phosphoramidite is a novel, modified and activator nucleoside. It can be used as an antiviral agent or in the synthesis of DNA. 5'-O-DMT-uridine 3'-CE phosphoramidite has been shown to be cytotoxic in vitro to cancer cells.Formula:C39H47N4O9PPurity:Min. 95%Molecular weight:746.79 g/mol3'-O-Aminoacetoxy-2'-deoxyadenosine
amino functionalised nucleosideFormula:C13H22N6O3Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:310.36 g/mol1-(4’-Azido-2’-deoxy-2’-fluoro-b-D-arabinofuranosyl)N4-(n-docosanoyl)-cytosine
1-(4’-Azido-2’-deoxy-2’-fluoro-b-D-arabinofuranosyl)N4-(n-docosanoyl)-cytosine is a deoxyribonucleoside monophosphate with antiviral effects. It is a novel nucleotide analogue that contains an azido group and a 2,4,6-trifluorobenzene moiety. The 4′ position of the sugar is modified with an n-docosanoyl group. 1-(4’Azo-2′deoxy-2′fluoro-bDara)ribonucleosides are synthetic nucleotides that can be used to inhibit viral replication by inhibiting DNA polymerase and RNA polymerase.Purity:Min. 95%8-Azidoadenosine
CAS:8-Azidoadenosine is an adenosine analogue conjugated with an azido group which can be used for oligonucleotide labelling. The azido group reacts with a terminal alkyne via a click reaction, forming the labelled nucleotide containing a triazole linker.
Formula:C10H12N8O4Purity:Min. 95%Color and Shape:PowderMolecular weight:308.25 g/molZebularine 3'-CE phosphoramidite
CAS:Zebularine 3'CE phosphoramidite is a novel, high quality activator for modified DNA monophosphate. It is used as an anticancer drug and antiviral agent. Zebularine 3'CE phosphoramidite is a synthetic, diphosphate with high purity and high reactivity. It has been shown to activate deoxyribonucleosides to ribonucleosides in DNA synthesis, as well as being able to inhibit viral RNA synthesis by inhibiting viral polymerase.Formula:C45H61N4O8PSiPurity:Min. 95%Color and Shape:Off-white solid.Molecular weight:845.04 g/molN4,3'-O-Dibenzoyl-2'-deoxycytidine
CAS:N4,3'-O-Dibenzoyl-2'-deoxycytidine is a nucleoside that functions as a base. It is a diester of the naturally occurring nucleoside cytidine and 2′,6′-dibenzoyl-deoxyribose. The compound has been shown to be an inhibitor of DNA polymerases and nuclease activity in vitro. N4,3'-O-Dibenzoyl-2'-deoxycytidine has been shown to inhibit the growth of certain strains of bacteria and can be used for the treatment of tuberculosis. This drug also has anti-inflammatory properties that may be due to its ability to inhibit prostaglandin synthesis. !-- END OF PRODUCT DESCRIPTIONS -->Formula:C23H21N3O6Purity:Min. 95%Color and Shape:PowderMolecular weight:435.44 g/mol3'-O-Benzoyl-2'-deoxyuridine
CAS:3'-O-Benzoyl-2'-deoxyuridine is a synthetic nucleoside that is used in the synthesis of DNA and RNA. 3'-O-Benzoyl-2'-deoxyuridine is also an antiviral agent that has shown efficacy against HIV, HSV, and influenza virus. 3'-O-Benzoyl-2'-deoxyuridine is a phosphoramidite monophosphate that can be used as a building block for DNA or RNA synthesis. It is also a diphosphate that can be used to synthesize modified nucleosides. This product has novel properties and high purity, making it suitable for research purposes.Formula:C16H16N2O6Purity:Min. 95%Color and Shape:PowderMolecular weight:332.31 g/molN2-Phenoxyacetyl-2'-O-methylguanosine
CAS:N2-Phenoxyacetyl-2'-O-methylguanosine is a new monophosphate nucleoside that has been modified to mimic the anticancer properties of guanosine. It is synthesized by modifying the sugar moiety of guanosine and adding a phenoxyacetyl group to the 2'-OH position. N2-Phenoxyacetyl-2'-O-methylguanosine has shown antiviral and antitumor activity in vitro and in vivo, as well as high purity.Formula:C19H21N5O7Purity:Min. 95%Molecular weight:431.4 g/mol7-Deaza-2'-deoxyadenosine
CAS:7-Deaza-2'-deoxyadenosine is an oligodeoxynucleotide analog that has been shown to be a potent inhibitor of human ovarian carcinoma cells. It inhibits the uptake of organic anion transporters, which are proteins found in the cell membrane that transport organic anions such as nucleosides and nucleotides. 7-Deaza-2'-deoxyadenosine has also been shown to inhibit DNA synthesis and polymerase chain reactions by binding to the enzyme RNA polymerase II. This drug can be synthesized with solid phase chemistry, making it a highly reproducible product.Formula:C11H14N4O3Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:250.26 g/mol2,4,6-Trichloro-5-methylpyrimidine
CAS:2,4,6-Trichloro-5-methylpyrimidine is a nucleoside for use in research applicationsFormula:C5H3Cl3N2Purity:Min. 95%Color and Shape:PowderMolecular weight:197.45 g/mol5'-O-p-Anisoyl-2,2'-anhydrouridine
5'-O-p-Anisoyl-2,2'-anhydrouridine is a novel nucleoside. It is an activator of ribonucleosides and deoxyribonucleosides. This compound has antiviral activity against HIV and DNA synthesis inhibitory activity against cancer cells. 5'-O-p-Anisoyl-2,2'-anhydrouridine is also a modified nucleoside that can be used for the synthesis of phosphoramidites for the chemical synthesis of oligodeoxynucleotides (ODN).Formula:C17H16N2O7Purity:Min. 95%Molecular weight:360.32 g/mol5'-O-tert-Butyldimethylsilyl-2'-deoxyuridine
5'-O-tert-Butyldimethylsilyl-2'-deoxyuridine (5'-O-TBDMSU) is a modified nucleoside that has antiviral, anticancer and novel activities. It is synthesized by the reaction of 5'-O-tert-butyldimethylsilyl-2'-deoxyuridine with methyl chloroformate. 5'-O-TBDMSU has been shown to inhibit viral replication in cell culture. The antiviral activity of 5'-O-TBDMSU may be due to its ability to inhibit DNA synthesis by inhibiting the incorporation of deoxyribonucleotide triphosphates into DNA or by inhibiting the activity of DNA polymerases. This compound also inhibits the replication of RNA viruses such as HIV and hepatitis C virus, which are dependent on deoxyribonucleosides for their replication.Formula:C15H26N2O5SiPurity:Min. 95%Molecular weight:342.47 g/molN4-Benzoyl-3'-deoxycytidine
CAS:N4-Benzoyl-3'-deoxycytidine is a novel antiviral agent that has shown activity against DNA and RNA viruses. It is an activator of DNA polymerase, which is essential for replication of viral nucleic acids. The compound is a modified nucleoside with a benzoyl group at the 4' position of the ribose moiety. It also has phosphoramidite, monophosphate, and diphosphate analogues. N4-Benzoyl-3'-deoxycytidine binds to the enzyme DNA polymerase, thereby inhibiting its ability to synthesize deoxyribonucleotides from ribonucleotides. This results in inhibition of viral DNA synthesis and subsequent inhibition of viral replication.Formula:C16H17N3O5Purity:Min. 95%Color and Shape:White To Off-White SolidMolecular weight:331.32 g/molβ-Nicotinamide adenine dinucleotide phosphate sodium salt hydrate
CAS:Please enquire for more information about β-Nicotinamide adenine dinucleotide phosphate sodium salt hydrate including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C21H27N7NaO17P3Purity:Min. 95%Color and Shape:PowderMolecular weight:765.39 g/molL-Thymidine
CAS:L-Thymidine is an antiviral drug that is used in the treatment of chronic hepatitis. It has been shown to be active against a range of viruses, including HIV, HSV, and HBV. L-Thymidine can also be used to treat patients with cancer as an anti-cancer agent. L-Thymidine is a prodrug that is converted into thymidine triphosphate (TTP), which inhibits viral DNA polymerase by competitive inhibition. The antiviral activity of L-Thymidine may be due to its ability to inhibit the synthesis of viral proteins required for viral replication by interfering with the protein production process or by inhibiting the formation of dsDNA during reverse transcription.Formula:C10H14N2O5Purity:Min. 95%Color and Shape:PowderMolecular weight:242.23 g/mol1-Methylpseudouridine
CAS:1-Methylpseudouridine is a substitute for uridine in modified mRNA. This substitution has shown to increase transfection by reducing immuogenicity. The 1-methylpseudouridine substituted mRNA increases protein expression due to low immune stimulation as it evades detection by the edosomal Toll-like receptor (TLR3).Formula:C10H14N2O6Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:258.23 g/mol5'-O-Benzoyl-2',3'-dideoxy-3'-fluorouridine
5'-O-Benzoyl-2',3'-dideoxy-3'-fluorouridine is a novel nucleoside that is synthesized from ribonucleosides. It is an inhibitor of the RNA polymerase enzyme, which prevents the transcription and replication of DNA. 5'-O-Benzoyl-2',3'-dideoxy-3'-fluorouridine also inhibits viral DNA synthesis by preventing viral RNA from being translated into DNA. This product has been shown to be active against a wide range of viruses, including influenza A virus, herpes simplex virus type 1, and vaccinia virus.Formula:C16H15FN2O5Purity:Min. 95%Molecular weight:334.35 g/molEdU
CAS:2'-Deoxy-5-ethynyluridine (5-EdU) is a modified thymidine analogue containing a terminal alkyne group, which is used for nucleotide labelling. 5-Edu is easily taken up by cells and incorporated by metabolic activation during DNA synthesis. By adding an azide conjugated to a fluorophore or a biotin moiety, a click reaction occurs from the labelled nucleotide linked by a triazole group. 5-Edu are employed in cell proliferation assays, to study DNA and RNA localisation, structure and dynamics, in the synthesis of aptamers with the click-SELEX method, and in other applications such as the preparation of oligonucleotide microarrays and nanoelectronic devices.Formula:C11H12N2O5Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:252.23 g/mol2-Amino-6-chloro-9-(2'-deoxy-b-D-ribofuranosyl)purine
CAS:2-Amino-6-chloro-9-(2'-deoxy-b-D-ribofuranosyl)purine is a purine nucleoside where the purine base has a 2-amino group at position 2 and a chlorine at position 6. The sugar is 2'-deoxy, meaning it is like the sugar found in DNA, lacking the 2'-hydroxyl group that is present in RNA. The amino and chloro groups on the purine base modify how this molecule behaves in biological systems making it useful in research applications.Formula:C10H12ClN5O3Purity:Min. 97 Area-%Color and Shape:White PowderMolecular weight:285.69 g/mol2-Amino-9-(β-D-ribofuranosyl)purine
CAS:2-Amino-9-(β-D-ribofuranosyl)purine is a purine nucleoside consisting of the base 2-aminopurine linked via an N9-glycosidic bond to β-D-ribofuranose. As an analog of adenosine, it retains structural compatibility with nucleic acids but exhibits distinct biochemical properties, most notably intrinsic fluorescence. This makes it a valuable probe in molecular biology for studying nucleic acid structure, base pairing, and conformational changes, as its fluorescence is sensitive to local stacking interactions and environmental conditions.Formula:C10H13N5O4Purity:Min. 95%Color and Shape:White PowderMolecular weight:267.24 g/molN6-Benzoyl-2'-deoxy-5'-O-DMT-adenosine 3'-CE phosphoramidite
CAS:N6-Benzoyl-2'-deoxy-5'-O-DMT adenosine 3'-CE phosphoramidite is a protected adenosine amidite.Formula:C47H52N7O7PPurity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:857.93 g/mol2'-Azido-2'-deoxy-5'-O-DMT-uridine
CAS:2'-Azido-2'-deoxy-5'-O-DMT-uridine is a nucleoside that has been modified with an azido group at the 2' position. The azido group is used to modify DNA and RNA nucleosides, which are monophosphate, ribonucleosides, and deoxyribonucleosides. This drug may be used as an activator of DNA synthesis or as a antiviral agent. It has been shown to inhibit HIV replication in vitro.Purity:Min. 95%5'-Azido-5'-deoxyuridine
CAS:5'-Azido-5'-deoxyuridine is a synthetic nucleobase that is used in the synthesis of oligodeoxynucleotides. It has been shown to have an inhibitory effect on tumor cells, which may be due to its ability to interact with guanosine diphosphate (GDP) and prevent the formation of GTP. 5'-Azido-5'-deoxyuridine has also been shown to have an inhibitory effect on Mycobacterium tuberculosis and Mycobacterium avium complex, but does not affect other bacteria. 5'-Azido-5'-deoxyuridine interacts with RNA by binding to the phosphate group and inhibiting the synthesis of proteins and DNA.Purity:Min. 95%2’-O-Methy-2,5’-anhydro-5-methyluridine
2’-O-Methy-2,5’-anhydro-5-methyluridine is a modified nucleoside with antiviral and anticancer properties. It is an activator of the antiviral response and has been shown to inhibit cancer cells from dividing. This compound is synthesized in an enzymatic reaction that converts 5-methyluridine to 2'-O-methylated uridine. The synthesis involves ribonucleotide reductase, which converts ribonucleotides into deoxyribonucleotides. 2' -O -Methy -2,5'-anhydro-5-methyluridine was originally identified as a novel monophosphate derivative in the 1960s and has been shown to be more effective than other nucleoside analogues.Purity:Min. 95%
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