
Nucleotides
Subcategories of "Nucleotides"
Found 2637 products of "Nucleotides"
S-(5'-Adenosyl)-L-methionine chloride dihydrochloride
CAS:S-adenosyl-L-methionine chloride dihydrochloride is a form of S-adenosyl-L-methionine. It is used as a nutritional supplement and has been shown to increase the production of antibodies in the body. This drug is also used for the treatment of inflammatory diseases, such as rheumatoid arthritis and osteoarthritis, because it inhibits cyclooxygenase enzymes. S-adenosyl-L-methionine chloride dihydrochloride binds to the response element on DNA that regulates gene expression and inhibits polymerase chain reactions by blocking the binding of nucleic acids to their complementary strands. The mechanism of action of this drug has not been established but may be related to its ability to inhibit nuclear DNA transcription or cell proliferation by affecting camp concentration.Formula:C15H23ClN6O5S·2HClPurity:Min. 75 Area-%Color and Shape:White Off-White PowderMolecular weight:507.82 g/molInosine
CAS:Inosine is a purine nucleoside in which hypoxanthine is attached to ribofuranose via a beta-N(9)-glycosidic bond. Inosine derives from a hypoxanthine and a ribofuranose. Inosine plays a key role as a metabolite in bacteria, fungi, humans, and other animals. There is preliminary evidence that inosine may have neurorestorative, anti-inflammatory, immunomodulatory, and cardioprotective effects.
Formula:C10H12N4O5Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:268.23 g/molb-Nicotinamide adenine dinucleotide phosphate disodium salt
CAS:Coenzyme and regenerating electron donor in catabolic processesFormula:C21H26N7Na2O17P3Purity:Min. 93 Area-%Color and Shape:White PowderMolecular weight:787.4 g/mol3'-Azido-3'-deoxyuridine
CAS:3'-Azido-3'-deoxyuridine is a nucleoside analog that is used as a substrate for DNA synthesis in the cell. 3'-Azido-3'-deoxyuridine is transported across the blood-brain barrier by a sodium-independent transporter and accumulates in the carotid artery, where it is converted to uridine. This drug has been shown to be activated at the site of infection and may have regiospecific activity against bacteria. 3'-Azido-3'-deoxyuridine has an imidazole ring and dinucleoside structure, which are important for its activity as a terminal half-life enhancer and anticancer agent. 3'-Azido-3'-deoxyuridine has also been used in liquid chromatography to purify nucleic acids research products.Formula:C9H11N5O5Purity:Min. 95%Color and Shape:PowderMolecular weight:269.21 g/molUridine-2',3'-cyclic monophosphate sodium salt
CAS:Uridine-2',3'-cyclic monophosphate sodium salt (CAS No. 15718-50-0) is a novel anticancer agent that has been shown to inhibit the growth of cancer cells in vitro and in vivo. It is a nucleoside analog that inhibits the synthesis of DNA by inhibiting ribonucleotide reductase and deoxyribonucleotide reductase, two enzymes involved in the production of DNA. Uridine-2',3'-cyclic monophosphate sodium salt is also an antiviral agent used to treat herpesvirus infections, such as herpes simplex type 1 and 2. This drug binds to viral RNA polymerase, which prevents viral replication by preventing mRNA synthesis.Formula:C9H10N2NaO8PPurity:Min. 98 Area-%Color and Shape:PowderMolecular weight:328.15 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/mol3',5'-Di-O-benzoyl-2'-deoxy-2',2'-difluorouridine
CAS:An intermediate for the preparation of modified oligonucleotides and other uridine derivatives containing a 2',2'-difluoro modification.Formula:C23H18F2N2O7Purity:Min. 95%Color and Shape:White PowderMolecular weight:472.4 g/mol5-Iodouridine
CAS:5-Iodouridine is a pyrimidine nucleoside that is found in the human body. It is used as a starting material for the synthesis of 5-iodo-2'-deoxyuridine, which has been shown to have biological properties. 5-Iodouridine binds to the dna template and prevents radiation from altering it's conformation. This binding has been shown to be specific for ultraviolet (UV) radiation, with little absorption at visible wavelengths. The biological effects of 5-iodouridine are dependent on its acidic pH and hydrogen bonding ability. In vitro assays have demonstrated that this compound can inhibit prostate cancer cells from proliferating and may be useful in treating cervical cancer.Formula:C9H11IN2O6Purity:Min. 95%Color and Shape:White PowderMolecular weight:370.1 g/mol2'-C-Methylguanosine 5'-diphosphate triethylammonium salt
2'-C-Methylguanosine 5'-diphosphate triethylammonium salt is a synthetic nucleotide analog for use in researchFormula:C11H16N5O11P2·C18H45N3Purity:Min. 95%Color and Shape:PowderMolecular weight:759.79 g/molE-5-(2-Carbomethoxyvinyl)-2'-deoxyuridine
CAS:E-5-(2-Carbomethoxyvinyl)-2'-deoxyuridine is a nucleoside that is a modified form of uridine. It is a nucleotide analog that inhibits the synthesis of DNA and RNA and can be used to treat cancer. E-5-(2-Carbomethoxyvinyl)-2'-deoxyuridine is an activator that activates the phosphoramidites in the synthesis of DNA and RNA. This drug can also be used as antiviral therapy for herpes simplex virus type 1, influenza virus, and HIV. E-5-(2-Carbomethoxyvinyl)-2'-deoxyuridine has been shown to have anti-inflammatory properties by inhibiting prostaglandin synthesis.Formula:C13H16N2O7Purity:Min. 95%Color and Shape:White to off-white solid.Molecular weight:312.28 g/mol5-O-[[[(1S)-1-Methyl-2-(1-methylethoxy)-2-oxoethyl]amino]-phenoxyphosphinyl]-cytidine
CAS:5-O-[[[(1S)-1-Methyl-2-(1-methylethoxy)-2-oxoethyl]amino]-phenoxyphosphinyl]-cytidine is a modified nucleoside analog that inhibits the synthesis of DNA and RNA. It has been shown to have antiviral, anticancer, and antiinflammatory activities. 5-O-[[[(1S)-1-Methyl-2-(1-methylethoxy)-2-oxoethyl]amino]-phenoxyphosphinyl]-cytidine is a ribonucleoside that can be used as a building block for the production of deoxyribonucleosides (i.e., as an activator). This product also has high purity and quality, as well as being novel in structure.Formula:C21H29N4O9PPurity:Min. 95%Color and Shape:White to off-white solid.Molecular weight:512.45 g/molN2-Diboc-7/9-(2,3,4,6-tetra-O-acetyl-D-mannopyranosyl)-6-chloro-2-aminopurine
N2-Diboc-7/9-(2,3,4,6-tetra-O-acetyl-D-mannopyranosyl)-6-chloro-2-aminopurine is a nucleoside that is modified with a chlorine group. The modification of the nucleoside may enhance its anticancer activity. N2-Diboc-7/9-(2,3,4,6-tetra-O-acetyl-D-mannopyranosyl)-6-chloro-2 aminopurine has been shown to inhibit the growth of virus and cancer cells by inhibiting DNA synthesis. It has also been shown to induce apoptosis in human leukemia cells.Formula:C21H30ClN5O9Purity:Min. 95%Color and Shape:White to beige solid.Molecular weight:531.94 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/mol5'-O-DMT-2'-O-methyl-N6-phenylacetyladenosine
5'-O-DMT-2'-O-methyl-N6-phenylacetyladenosine is a synthetic nucleoside with anticancer properties. It is modified to be more resistant to phosphodiesterase which blocks the synthesis of DNA and RNA. This drug has been shown to activate the immune system, inhibit tumor growth, and inhibit viral replication. It has been shown to be effective in animal models against leukemia and lymphoma. The high quality pure chemical will be used for use in research purposes only.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/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/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/mol5-Methyluridine
CAS:5-Methyluridine is a nucleoside that is used to inhibit the replication of cells. It is also used for the treatment of cancer, infectious diseases, and other conditions. 5-Methyluridine inhibits cellular replication by binding to ribothymidine and uridine in the nucleus. The inhibition of cellular proliferation is due to a lack of dna synthesis and RNA synthesis. This nucleoside has been shown to have inhibitory properties against mouse tumor cells grown in vitro, as well as the wild-type strain grown in vivo. 5-Methyluridine may be useful for the treatment of cancer tissues because it can suppress the growth of tumors by inhibiting their ability to replicate.Formula:C10H14N2O6Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:258.23 g/molTrifluorothymidine
CAS:Treats herpes-associated keratitis and keratoconjunctivitis; antineoplasticFormula:C10H11F3N2O5Purity:Min. 95%Color and Shape:PowderMolecular weight:296.2 g/molCytidine-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/mol2',3'-Di-O-acetyl-D-uridine
CAS:2',3'-Di-O-acetyl-D-uridine is a nucleoside for use in research applicationsFormula:C13H16N2O8Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:328.27 g/mol2'-Deoxy-6-methylthioguanosine
CAS:2'-Deoxy-6-methylthioguanosine is a novel nucleoside and nucleotide analog with antiviral and anticancer activities. It has been shown to inhibit the replication of DNA by inhibiting the activity of DNA polymerase. The target of this drug is not related to any virus or bacterial species, but it inhibits the growth of cancer cells in vitro. The synthesis of 2'-deoxy-6-methylthioguanosine can be achieved by modifying commercially available phosphoramidites.Formula:C11H15N5O3SPurity:Min. 95%Color and Shape:PowderMolecular weight:297.33 g/mol2'-O-Benzoyl-5'-O-DMT-4-thiouridine
2'-O-Benzoyl-5'-O-DMT-4-thiouridine is a phosphoramidite monophosphate nucleoside analog. It has antiviral and anticancer properties, and has been shown to activate the immune system in mice. 2'-O-Benzoyl-5'-O-DMT-4-thiouridine is also novel because it is structurally different from all other nucleosides that have been studied for antiviral and anticancer activity. This drug can be used as an activator of DNA synthesis in vitro.Formula:C37H34N2O8SPurity:Min. 95%Color and Shape:Yellow SolidMolecular weight:666.76 g/mol3',5'-O-(1,1,3,3-Tetraisopropyldisiloxane-1,3-diyl)-2'-ketouridine
CAS:Used as a protected 2'-ketouridine nucleoside in the synthesis of modified RNA oligonucleotides. The 1,1,3,3-tetraisopropyldisiloxane-1,3-diyl (TIPDS or TBDPSi2) group protects the 3' and 5' hydroxyl groups, while the 2'-keto (or 2'-oxo) modification introduces a specific functional group at the 2' position of the ribose sugar.Formula:C21H36N2O7Si2Purity:Min. 95%Color and Shape:White PowderMolecular weight:484.69 g/mol2'-O-Methyladenosine
CAS:2'-O-Methyladenosine (2'-OMeA) is a nucleoside that is a low-energy analog of adenosine. It has been shown to be an effective inhibitor of protein synthesis in vitro, by inhibiting RNA polymerase in the process of transcription. 2'-OMeA has also been shown to inhibit virus replication in vitro and to have potent inhibitory activity against human immunodeficiency virus type 1 (HIV-1). 2'-OMeA inhibits viral replication by binding to the viral ribonucleotide reductase enzyme and blocking the conversion of ribonucleotides into deoxyribonucleotides. The chemical structures of 2'-OMeA are similar to those found in fatty acids and can be detected using chemical ionization mass spectroscopy. The sequence for 2'-OMeA was determined through sequencing methods including NMR spectroscopy and nuclear magnetic resonance data analysis.Formula:C11H15N5O4Purity:Min. 98 Area-%Color and Shape:White Off-White PowderMolecular weight:281.27 g/molInosine 5'-diphosphate disodium salt
CAS:Inosine-5'-diphosphate disodium salt (IDPS) is a nitro compound that is used in the synthesis of antibacterial drugs. It is also used in the production of polymers and as a precursor to other organic compounds. IDPS has been shown to have antibacterial activity against halogeno bacteria, such as buprestidae, and many Gram-positive bacteria, including encapsulated strains. IDPS has been shown to be effective against both damaged cells and healthy cells in culture. The mechanism of action may involve inhibition of protein synthesis by blocking the ribosomes or by interfering with DNA replication. This drug also inhibits growth rate of japonica rice and heterocycles.Formula:C10H12N4Na2O11P2Purity:Min. 90.0 Area-%Color and Shape:White PowderMolecular weight:472.15 g/molBucladesine calcium salt
CAS:Protein kinase A inhibitor; cAMP agonistFormula:C18H24N5O8PCaPurity:Min. 95%Color and Shape:PowderMolecular weight:489.42 g/mol5-Hydroxymethylcytidine
CAS:5-Hydroxymethylcytidine is a nucleoside that has been shown to inhibit the activity of RNA polymerase by forming hydrogen bonds with the enzyme. It is used in vitro to study the role of messenger RNA in regulating gene expression, and also as a probe for transcriptase activity. 5-Hydroxymethylcytidine has also been shown to have a biological function in solid tumours and may be an analytical method for detecting cancer.Formula:C10H15N3O6Purity:Min. 95 Area-%Color and Shape:White PowderMolecular weight:273.24 g/mol5-Fluorocytidine
CAS:5-Fluorocytidine (5FC) is an antiviral drug that inhibits the synthesis of DNA. 5FC is a prodrug that is converted to cytosine in vivo, and then incorporated into viral DNA by polymerase chain reactions. The incorporation of 5FC into viral DNA prevents replication and transcription, which can lead to the death of cells infected with HIV. In addition, 5FC has been shown to be effective in treating chronic viral hepatitis and bowel diseases such as Crohn's disease. It also has potential use as a drug target for cancer treatments. 5FC has been shown to inhibit transcription activators in murine hepatoma cells and inhibit the growth of tumors in transfection experiments using human colon cancer cells. This antiviral agent has also been shown to have antimicrobial activity against Gram-positive bacteria, including Clostridium difficile, Staphylococcus aureus, Streptococcus pyogenes and Enterococcus faecFormula:C9H12FN3O5Purity:Min. 99 Area-%Color and Shape:White PowderMolecular weight:261.21 g/molOrotidine
CAS:Orotidine is a decarboxylase inhibitor. It inhibits the enzyme that converts orotate to uridine and the enzyme that converts orotate to decarboxylase. Orotidine has been shown to inhibit the growth of opportunistic fungal organisms and may be useful in treating infections caused by these pathogens. Orotidine is an analytical method for measuring the activity of orotidase, which catalyzes conversion of orotate to uridine. The enzyme form of orotidase found in human erythrocytes is very sensitive to inhibition by picolinic acid, which is used as a substrate for this reaction.
Formula:C10H12N2O8Purity:Min. 95 Area-%Color and Shape:White PowderMolecular weight:288.21 g/mol2'-Deoxypseudoisocytidine
CAS:2'-Deoxypseudoisocytidine is a synthetic nucleoside that is structurally similar to pseudoisocytidine. It is used as an anti-cancer agent in labeling studies. The compound exhibits cytotoxic activity against tumor cells and inhibits the growth of cultured human cancer cell lines. 2'-Deoxypseudoisocytidine has been shown to be effective in preventing the growth of brain tumors in mice by targeting DNA synthesis, which may be due to its ability to act as an analog of cytosine and bind to DNA. This drug also has potential for use as a chemotherapeutic agent for leukemia and other cancers.Formula:C9H13N3O4Purity:Min. 95%Color and Shape:PowderMolecular weight:227.22 g/mol2'-Chloro-2'-deoxycytidine
CAS:2'-Chloro-2'-deoxycytidine is a synthetic nucleoside analog. It is a modified deoxycytidine with a chlorine atom at the 2'-position of the deoxyribose sugar. This molecule can be used in research applicationsFormula:C9H12ClN3O4Purity:Min. 95%Color and Shape:PowderMolecular weight:261.66 g/mol5'-O-DMT-5-iodo-2'-O-methyluridine
CAS:5'-O-DMT-5-iodo-2'-O-methyluridine is an activator and antitumor agent that is used in the synthesis of 5'-O-DMT-5-iodo-2'-O-(2,4,6-trimethoxybenzoyl)uridine for cancer research. This chemical is a novel synthetic nucleoside with a high purity and quality that can be used to synthesize deoxyribonucleosides, nucleosides, and phosphoramidites. It has a CAS number of 588691-24-1. 5'-O-DMT-5-iodo-2'-O-(2,4,6 trimethoxybenzoyl)uridine can be used as an antiviral agent against HIV and other retroviruses.Formula:C31H31IN2O8Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:686.49 g/mol2',3'-Dideoxy-2',3'-didehydroadenosine
CAS:2′,3′-Dideoxy-2′,3′-didehydroadenosine, abbreviated to d4A, is a synthetic purine nucleoside analog. Possible applications are its use to study antiviral activity.Formula:C10H11N5O2Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:233.23 g/mol3'-Amino-3'-deoxythymidine
CAS:Also known as AMT, this is a catabolite of the nucleoside analog zidovudine (AZT), a drug used to treat HIV infection.Formula:C10H15N3O4Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:241.24 g/molAdenosine-3'-monophosphate
CAS:Adenosine-3'-monophosphate is a nucleotide that is an important precursor in the synthesis of proteins. The ribosome, which is a large macromolecular complex that catalyzes protein synthesis, binds to the 3' end of the mRNA and adds adenosine-3'-monophosphate to the growing polypeptide chain. Adenosine-3'-monophosphate plays an important role in bacterial ribosomal RNA termination and protein synthesis. It also has sequence analysis capabilities and helps determine the sequence of subunits in the ribosome by providing a terminal nucleotide.Formula:C10H14N5O7PPurity:Min. 95%Color and Shape:White PowderMolecular weight:347.22 g/mol5'-(N-Cyclopropyl)carboxamidoadenosine
CAS:5'-(N-Cyclopropyl)carboxamidoadenosine (5' CAPA) is a cyclic nucleotide analog. It has been shown to have photochemical properties and can be used as a fluorescent probe for the detection of DNA. 5' CAPA binds to the α subunit of RNA polymerase and inhibits transcription, which may result in reduced expression of proteins involved in growth control. Structural analysis has revealed that 5' CAPA binds to the catalytic site of the enzyme, sterically interfering with ATP binding. The inhibitory effect is reversible by removal of 5' CAPA from the reaction solution or by addition of cytosolic calcium chelators. 5' CAPA was found to have no effect on phycocyanin production by phytoplankton when added at concentrations up to 1 mM and did not affect transcription-polymerase chain reactions or regulatory processes in bacterial cells. 5'-(N-CyFormula:C13H16N6O4Purity:Min. 95%Molecular weight:320.31 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/molAdenosine 5'-monophosphate
CAS:AMP plays a crucial role in cellular metabolic processes, including the synthesis of RNA and the regulation of enzymes like AMP-activated protein kinase (AMPK)
Formula:C10H14N5O7PPurity:Min. 98 Area-%Color and Shape:White Off-White PowderMolecular weight:347.22 g/mol5-Azidouridine
CAS:5-Azidouridine is used for nucleotide labelling and promptly reacts via a click reaction with a terminal alkyne or cyclooctyne conjugated to a reporter (fluorophore or biotine). The formed labelled nucleotide has a stable triazole linker. 5-Azidouridine has been used in living cell fluorescent imaging of cancer cells.
Formula:C9H11N5O6Purity:Min. 95%Color and Shape:PowderMolecular weight:285.21 g/molThionicotinamide adenine dinucleotide
CAS: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. 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.Formula:C21H27N7O13P2SPurity:Min. 95%Color and Shape:Yellow PowderMolecular weight:679.49 g/mol2'-Deoxy-L-cytidine 3'-O-L-valinyl ester 2HCl
CAS:2'-Deoxy-L-cytidine 3'-O-L-valinyl ester 2HCl is a nucleoside analog that is converted to its active form by intracellular dephosphorylation. It inhibits viral DNA polymerase, thereby preventing the replication of the virus. This drug has been shown to be effective against hepatitis B virus and influenza A virus. The triphosphate form of 2'-deoxy-3'-O-L-valinyl cytidine 2HCl is used as an antiviral agent in the treatment of chronic hepatitis and for prophylaxis against influenza A.Formula:C14H22N4O5·2HClPurity:Min. 95%Color and Shape:Off-White PowderMolecular weight:399.27 g/mol8-Benzyloxy-2'-deoxyguanosine
CAS:8-Benzyloxy-2'-deoxyguanosine is a dinucleoside that is synthesised from uracil and hydrogenated 8-hydroxyquinoline. The synthesis of 8-benzyloxy-2'-deoxyguanosine was achieved by cyclic photocyclization of 2,4,6-trichlorobenzaldehyde with 2,4,6-trimethoxyphenylacetone in the presence of sodium nitrite. This compound has been used for the quantification of DNA damage caused by irradiation or sodium chloride. 8-Benzyloxy-2'-deoxyguanosine has also been shown to inhibit the polymerase chain reaction (PCR) amplification of oligodeoxynucleotides.Formula:C17H19N5O5Purity:Min. 95%Color and Shape:Off-White To Brown SolidMolecular weight:373.36 g/mol8-Chloroadenosine-5'-monophosphate triethylammonium, about 28 mg/ml aqueous solution
CAS:8-Chloroadenosine-5'-monophosphate triethylammonium is a novel phosphoramidite that is used in the synthesis of DNA. 8-Chloroadenosine-5'-monophosphate triethylammonium has been shown to activate antiviral and anticancer drugs with high specificity. It is also used as a reagent for the synthesis of deoxyribonucleosides and nucleosides. 8-Chloroadenosine-5'-monophosphate triethylammonium has high purity and can be used in the synthesis of DNA, RNA, and other nucleosides.Formula:C10H13ClN5O7P•(C6H15N)2Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:584.05 g/mol2'-Deoxy-5'-O-DMT-N2-isobutyryl-a-guanosine
CAS:2'-Deoxy-5'-O-DMT-N2-isobutyryl-a-guanosine is a nucleoside that is synthesized from 2'-deoxyribonucleosides and activated with diphosphate. It is an antiviral and anticancer agent that inhibits viral DNA polymerases, leading to the inhibition of viral replication. 2'-Deoxy-5'-O-DMT-N2-isobutyryl-a-guanosine has also been shown to inhibit cancer cell growth in vitro by inhibiting the synthesis of cellular DNA. This nucleoside has high purity and quality as it is made synthetically and has novel properties because it contains modified groups.Formula:C35H37N5O7Purity:Min. 95%Color and Shape:White to off-white solid.Molecular weight:639.71 g/mol2'-Deoxy-5'-O-DMT-N6-phenoxyacetyladenosine
CAS:2'-Deoxy-5'-O-DMT-N6-phenoxyacetyladenosine is a novel phosphoramidite nucleoside that is an antiviral and anticancer agent. It can be used as a monophosphate or diphosphate. 2'-Deoxy-5'-O-DMT-N6-phenoxyacetyladenosine has been shown to inhibit the replication of DNA, RNA, and protein synthesis. This compound also has an activating effect on the immune system by inducing lymphocyte proliferation and increasing NK activity. It inhibits the growth of viruses such as HIV and influenza A virus. The purity of 2'-Deoxy-5'-O-DMT-N6-phenoxyacetyladenosine is high, with a CAS number of 11052282-2.Formula:C39H37N5O7Purity:Min. 95%Color and Shape:PowderMolecular weight:687.76 g/mol3',5'-Di-O-(tert-butyldimethylsilyl)-2'-deoxyguanosine
CAS:3',5'-Di-O-(tert-butyldimethylsilyl)-2'-deoxyguanosine is a synthetic nucleoside with antiviral properties. It is a monophosphate that can be used to activate other nucleosides. This product has been shown to inhibit human immunodeficiency virus (HIV) reverse transcriptase in vitro and in vivo, as well as the replication of other viruses such as herpes simplex virus (HSV).Formula:C22H41N5O4Si2Purity:Min. 95%Color and Shape:PowderMolecular weight:495.76 g/mol3',5'-Di-O-acetyl-5-bromo-2'-deoxyuridine
CAS:Please enquire for more information about 3',5'-Di-O-acetyl-5-bromo-2'-deoxyuridine including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C13H15BrN2O7Purity:Min. 95%Color and Shape:PowderMolecular weight:391.18 g/mol2,3'-Anhydro-5'-O-tert-butyldiphenylsilylthymidine
2,3'-Anhydro-5'-O-tert-butyldiphenylsilylthymidine is a synthetically modified thymidine analog for use in researchPurity:Min. 95%Color and Shape:White to off-white solid.1-(2'-O-4-C-Methylene-b-D-ribofuranosyl)thymine
CAS:1-(2'-O-4-C-Methylene-b-D-ribofuranosyl)thymine is a nucleoside analog with a modified ribofuranosyl sugar, which includes a 2'-O-4'-C-methylene bridge that constrains the sugar conformation.Formula:C11H14N2O6Purity:Min. 95%Color and Shape:PowderMolecular weight:270.24 g/mol2-Azidoadenosine
CAS:2-Azidoadenosine is a nucleoside analog of adenosine, where the 2'-hydroxyl group of the ribose sugar is replaced with an azido group (–N₃). This substitution imparts unique chemical properties, notably enabling molecules to undergo bioorthogonal reactions, such as click chemistry, which involves the cycloaddition of the azide group with alkynes.
Formula:C10H12H8O4Purity:Min. 95%Color and Shape:PowderMolecular weight:308.25 g/mol6-Methylmercapto-9-(b-D-ribofuranosyl)purine
CAS:6-Methylmercapto-9-(b-D-ribofuranosyl)purine (6MMPR) is a nucleotide analog that is synthesized through the process of ribosylation. It has been shown to be reactive and inflammatory in the colon, which may be due to its role as an enzyme inhibitor. 6MMPR inhibits target enzymes such as 2-methylthio-6-chloropurine riboside, which are involved in DNA synthesis and repair. This drug also has anti-inflammatory properties, which may be due to its ability to inhibit the production of inflammatory cytokines by activated immune cells. 6MMPR is used for the treatment of bowel diseases such as Crohn's disease and ulcerative colitis.Formula:C11H14N4O4SPurity:Min. 95%Color and Shape:White PowderMolecular weight:298.32 g/mol6-Aza-2-thiouridine
CAS:6-Aza-2-thiouridine is a molecule that has been shown to inhibit human immunodeficiency virus (HIV). The compound is cytotoxic to leukemia cells and selectively inhibits the function of cytidine deaminase, which is an enzyme required for DNA synthesis. 6-Aza-2-thiouridine also inhibits the production of viruses by interfering with the activity of their nucleic acid polymerases. This inhibition may be due to its ability to hydrolyze extracellular hydroxyl groups on the viral nucleotide. 6-Aza-2-thiouridine has also been shown to have anti-cancer properties in mammalian cells.
Formula:C8H11N3O5SPurity:Min. 95%Color and Shape:White PowderMolecular weight:261.26 g/mol7-Deaza-2'-C-methyladenosine
CAS:7-Deaza-2'-C-methyladenosine (7DMA) is an antiviral agent that has shown anti-Hepatitis C virus activity in vitro. 7DMA inhibits the binding of a number of compounds to the viral RNA polymerase and blocks mRNA synthesis, leading to inhibition of viral replication. This drug also binds to the Toll-like receptor 3, which is involved in the immune response against hepatitis. 7DMA has been shown to have a pharmacokinetic profile suitable for use as an antiviral agent. However, it does not show any significant pharmacokinetic properties in vivo and needs further study.Formula:C12H16N4O4Purity:Min. 97.0 Area-%Molecular weight:280.28 g/molRef: 3D-W-202771
1gTo inquire50mgTo inquire100mgTo inquire250mgTo inquire500mgTo inquire-Unit-ggTo inquire6-(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/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/molN2-Methylguanosine
CAS:N2-Methylguanosine is an antiviral agent that has been modified from the natural form of guanosine. It has been shown to inhibit the replication of a number of viruses, including herpes simplex virus type 1 and type 2, cytomegalovirus, and others. N2-Methylguanosine also inhibits the growth of tumor cells in vitro and in vivo. In addition to its antiviral activity, it has been found to have anticancer effects in preclinical studies. N2-Methylguanosine has also been shown to inhibit diphosphate kinase (DPK) and phosphoramidite synthase (PAS), enzymes that are involved in DNA replication. N2-Methylguanosine is synthesized by reacting 5'-monophosphate nucleosides with 2-methyl-4-(4-nitrophenyl)thiourea followed by purification by ion exchange chromatography.Formula:C11H15N5O5Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:297.27 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/mol2'-Deoxy-2'-fluoro-5-iodouridine
CAS:2'-Deoxy-2'-fluoro-5-iodouridine is a nucleoside analog that is a modified version of uridine, where the 2'-fluoro modification is added to the sugar (deoxyribose), and an iodine atom is attached at the 5' position of the uracil base. This combination of modifications provides unique properties that may be useful for research and therapeutic applications.
Formula:C9H10FIN2O5Purity:Min. 95%Color and Shape:White PowderMolecular weight:372.09 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/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-Chloropurine
CAS:2-Chloropurine is a halogenated derivative of purine, a bicyclic nitrogen-containing heterocycle that forms the core of many biologically important molecules like DNA, RNA, ATP, and GTP. This molecule has applications in researchFormula:C5H3ClN4Purity:Min. 95%Color and Shape:PowderMolecular weight:154.56 g/mol7-Deaza-4-Cl-2'-deoxyguanosine
CAS:7-Deaza-4-Cl-2'-deoxyguanosine is a novel antiviral drug that has been synthesized in the laboratory. It is an analogue of deoxyguanosine, a nucleoside that is found in DNA and RNA. 7-Deaza-4-Cl-2'-deoxyguanosine has anti cancer properties because it inhibits the synthesis of DNA by inhibiting the activity of ribonucleoside reductase, an enzyme that converts ribonucleosides to deoxyribonucleosides. This drug has been shown to have potent anticancer activity against human lung cancer cells and mouse leukemia cells.Formula:C11H13ClN4O3Purity:Min. 95%Color and Shape:PowderMolecular weight:284.7 g/molXanthosine 5'-triphosphate disodium salt
CAS:Xanthosine 5'-triphosphate disodium salt is a nucleotide that is an intermediate in the synthesis of DNA and RNA. It has a hydroxyl group at the 5' carbon atom and two carboxylic acid groups on the 3' carbon atom. Xanthosine 5'-triphosphate disodium salt can be found in many compounds, such as d-glucose, which contains six hydroxyl groups. Xanthosine 5'-triphosphate disodium salt is also used as a building block for other molecules, such as ATP, which contains adenosine with one hydroxyl group on the 2' carbon atom and three phosphate groups.Formula:C10H13N4O15P3·2NaPurity:Min. 95%Color and Shape:PowderMolecular weight:568.13 g/molDeoxyribonucleic acid sodium salt - (Salmon)
CAS:Deoxyribonucleic acid sodium salt (DNA) is a linear polymer made up of nucleotide subunits. It is the genetic material of most living organisms and plays a role in the storage, retrieval, and transmission of information. DNA is susceptible to attack by electrophilic agents such as aldehydes and nitroaldol, which can lead to the formation of DNA strand breaks. DNA from salmon testes can be used in commercial production of veterinary vaccines.Color and Shape:Powder1-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/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/mol9-(2'-Deoxy-2'-fluoro-b-D-ribofuranosyl)-isoguanine
9-(2'-Deoxy-2'-fluoro-b-D-ribofuranosyl)-isoguanine is an oligonucleotide with a fluorinated nucleobase that is used to stabilize DNA duplexes. It is synthesized from 5'-deoxy-5'-fluorocytidine, which is a phosphoramidite, and 2',3',5'-triacetylpyrimidine, which is a substituent. The deprotection of the fluorinated oligonucleotide can be achieved by treatment with sodium hydroxide in ethanol or hydrochloric acid in acetic acid. 9-(2'-Deoxy-2'-fluoro-b-D-ribofuranosyl)-isoguanine has been shown to be stable and antiparallel when incorporated into double stranded DNA molecules.Formula:C10H12FN5O4Purity:Min. 95%Color and Shape:White PowderMolecular weight:285.24 g/molN6-Carbamoylthreonyladenosine sodium salt
CAS:N6-Carbamoylthreonyladenosine sodium salt is a fatty acid that is found in the bacterial cell wall. It has been shown to be an essential component of the cell wall for Gram-positive and Gram-negative bacteria. N6-Carbamoylthreonyladenosine sodium salt has been used to study the mechanism of protein synthesis in bacteria, especially how enzymes are involved in this process. Chemical biology studies have shown that this molecule can bind to DNA and inhibit bacterial growth. The crystal structure of N6-Carbamoylthreonyladenosine sodium salt has also been determined using x-ray diffraction data. This molecule inhibits the binding of proteins to DNA, which prevents transcription and replication. The reaction mechanism involves hydrogen bonding between the oxygen atoms on N6-Carbamoylthreonyladenosine sodium salt and divalent metal ions such as magnesium or zinc, which are required for protein synthesis.Formula:C15H19N6O8·NaPurity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:434.34 g/mol3'-O-Propargylcytidine
3'-O-Propargylcytidine is a monophosphate nucleoside that belongs to the group of synthetic, novel nucleosides and deoxyribonucleosides. It is a modified form of cytidine with an extra methyl group attached to the 3' position of the ribose sugar. 3'-O-Propargylcytidine has been shown to inhibit cancer cells by binding to DNA and preventing transcription and replication. This compound also inhibits virus replication and has antiviral properties. 3'-O-Propargylcytidine is highly pure and high quality, which makes it a good candidate for use in pharmaceuticals or other applications requiring high purity.
Formula:C12H15N3O5Purity:(%) Min. 97%Color and Shape:PowderMolecular weight:281.26 g/molL-Uridine
CAS:L-Uridine is a nucleoside that is the major precursor of RNA and DNA. It is also an equilibrative nucleoside, which means that it can act as either an acid or a base. L-Uridine has been shown to have anti-tumor activity in squamous cell carcinoma and human malignancies. It has also been shown to be an active inhibitor of arabinoside, which is a drug used for the treatment of acute myeloid leukemia (AML). L-Uridine may also have antitumor immunity effects by activating natural killer cells.Formula:C9H12N2O6Purity:Min. 95%Color and Shape:PowderMolecular weight:244.2 g/molb-Nicotinamide adenine dinucleotide phosphate sodium salt
CAS:Coenzyme and regenerating electron donor in catabolic processesFormula:C21H27N7NaO17P3Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:765.39 g/mol3',5'-O-(1,1,3,3-Tetraisopropyl-1,3-disiloxanediyl)cytidine
CAS:Used as a protected cytidine nucleoside in RNA synthesis. Similar to its adenosine counterpart, the 1,1,3,3-tetraisopropyl-1,3-disiloxanediyl (TIPDS or TBDPSi2) group serves as a bulky and selectively acid-labile protecting group for the 3' and 5' hydroxyl groups of the cytidine ribonucleoside during RNA oligonucleotide synthesis.Formula:C21H39N3O6Si2Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:485.72 g/molGuanosine 5'-triphosphate sodium salt hydrate
CAS:Guanosine 5'-triphosphate sodium salt hydrate (GTP) is an energy-rich nucleotide that is synthesized from guanosine and inorganic phosphate. GTP acts as a coenzyme in the synthesis of proteins, lipids, and other biological molecules. It also has been shown to inhibit the growth of murine sarcoma virus by regulating intracellular calcium levels. GTP's binding to a receptor on the surface of cells leads to a cascade of reactions that ultimately lead to the production of proteins. This process can be inhibited by pharmacological agents such as thiostrepton, which blocks GTP's incorporation into proteins.Formula:C10H16N5O14P3•Nax•(H2O)xPurity:Min. 95%Color and Shape:White PowderMolecular weight:523.18 g/mol3'-Azido-5'-O-benzoyl-3'-deoxythymidine
CAS:3'-Azido-5'-O-benzoyl-3'-deoxythymidine is a novel antiviral agent that is synthesized by modifying the structure of thymidine. It has been shown to have high antiviral activity against HIV and other viruses in vitro. 3'-Azido-5'-O-benzoyl-3'-deoxythymidine also inhibits tumor growth in animal models and may be useful as an anticancer drug. This compound is found to be active against a number of cancers, including leukemia, colon cancer, and prostate cancer. 3'-Azido-5'-O-benzoyl-3'-deoxythymidine is phosphoramidites for DNA synthesis, which can be used in the production of ribonucleosides or deoxyribonucleosides.Formula:C17H19N5O4Purity:Min. 95%Molecular weight:357.36 g/molCytidine 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/moltrans-Zeatin riboside-5'-monophosphate sodium salt
CAS:Trans-zeatin riboside-5'-monophosphate sodium salt is a growth rate inhibitor that inhibits protein synthesis by binding to the 30S subunit of the ribosome. This compound has been shown to inhibit cell growth and proliferation in vitro when applied to tissue cultures of tabacum l. and other plants. Trans-zeatin riboside-5'-monophosphate sodium salt is not active against plant tissues grown in vivo, which may be due to its inability to cross the plasma membrane or cell wall.Formula:C15H20N5O8PNa2Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:475.3 g/mol5-Cyanouridine
CAS:5-Cyanouridine is a pyrimidine nucleoside that is synthesized from uracil. It is a potent inhibitor of the enzyme decarboxylase, which catalyzes the conversion of 5-cytosine to 5-uracil, and has been used for the treatment of malignant lymphoma. 5-Cyanouridine is also a substrate for DNA replication and can be used as a target for antiviral drugs. The drug inhibits viral RNA synthesis by acting on the vesicular stomatitis virus (VSV) in two different ways: first, by inhibiting viral RNA polymerase activity; second, by incorporation into viral DNA. This incorporation can lead to chain termination or to translesion synthesis. 5-Cyanouridine has been shown to inhibit VSV replication in cell culture at concentrations as low as 1 μM.Formula:C10H11N3O6Purity:Min. 95%Color and Shape:PowderMolecular weight:269.21 g/mol5,6-Dihydro-5-methyluridine
CAS:5,6-Dihydro-5-methyluridine is a nucleoside that is found in the human genome. It is a precursor of uridine and can be used to synthesize 5-methylcytosine, which is an epigenetic modification that occurs in DNA. This modification can affect the expression of genes by changing the structure of chromatin. This drug has been identified as a potential drug target for cancer treatment and other diseases. Structural analysis has shown that this compound has a number of hydrogen bonds with oxygen atoms and hydroxyl groups, which may make it more effective than other drugs currently being studied. 5,6-Dihydro-5-methyluridine forms a phylogenetic tree with other compounds that are also found in the human genome, suggesting that it may have evolved through natural selection.Formula:C10H16N2O6Purity:Min. 95%Color and Shape:White Off-White PowderMolecular weight:260.24 g/molAdenosine 5'-phosphosulfate sodium salt, 10 mM in water
CAS:Adenosine 5′-phosphosulfate sodium salt has been used quantify pyrophosphate and in enzyme-linked bioluminescence assay for adenosine triphosphate (ATP).Product provided as 10 mM solution in water.Formula:C10H14N5O10PSPurity:Min. 90.0 Area-%Molecular weight:427.28 g/mol5-Carboxyhydroxymethyluridine
CAS:5-Carboxyhydroxymethyluridine is a hydroxylated nucleoside that is used to study DNA repair. It is a nucleotide analogue that has been modified at the hydroxyl group by methylation. 5-Carboxyhydroxymethyluridine can be converted back to uridine by escherichia coli hydroxylases, but this conversion does not occur in vivo. 5-Carboxyhydroxymethyluridine can be used as a substrate for methyltransferase enzymes, which are involved in DNA repair. The enzyme 5'-methylthioadenosine phosphorylase converts 5-carboxyhydroxymethyluridine into S-adenosylhomocysteine and adenine. This conversion can be reversed by the enzyme methionine synthase. Some homologues of 5-carboxyhydroxymethyluridine have been found in nature and other modifications have been made on theFormula:C11H14N2O9Purity:Min. 95%Color and Shape:PowderMolecular weight:318.24 g/mol5'-O-DMT-2'-O-methylcytidine
CAS:5'-O-DMT-2'-O-methylcytidine is a monophosphate nucleoside of cytidine. It is used as an antiviral agent and has been shown to have anticancer effects in vitro. 5'-O-DMT-2'-O-methylcytidine is synthesized by modification of the natural deoxyribonucleosides, which are then phosphoramidited to form a 5'-O-DMT-2'-O-methylcytidine monophosphate. The synthesis process also produces diphosphate and triphosphate forms of the nucleoside, which can be used for other purposes.
Formula:C31H33N3O7Purity:Min. 95%Molecular weight:559.61 g/molGlycinamide ribonucleotide
CAS:Glycinamide ribonucleotide (GAR) is a reactive metabolite that is formed from glycinamide, which is an intermediate in the synthesis of purines. GAR has been shown to bind to intracellular targets and inhibit their enzyme activities. GAR has been shown to inhibit the activity of enzymes that are involved in the synthesis of purines, such as ribonucleotides and nucleoside phosphates. These enzymes have been found in human tissues. GAR also inhibits the polymerase chain reaction (PCR) by binding to DNA and inhibiting its replication. This drug has also been shown to be effective against bowel disease by binding to bacterial dna gyrase, dna topoisomerase, and rna synthesis.
Formula:C7H15N2O8PPurity:Min. 80 Area-%Color and Shape:PowderMolecular weight:286.18 g/molN1-Methyladenosine
CAS:N1-Methyladenosine is a nucleoside that has been shown to inhibit the synthesis of proteins in the ribosome, which are essential for all cellular functions. N1-Methyladenosine has been shown to be effective against HIV infection, and has also been used as a chemotherapeutic agent in cancer cells. The optimum concentration of this drug is unknown, but it is known that at high concentrations, it can cause cellular death. N1-Methyladenosine has also been shown to be effective in treating metabolic disorders and autoimmune diseases.Formula:C11H15N5O4Purity:Min. 95%Color and Shape:White PowderMolecular weight:281.27 g/molC2-Methyladenosine
CAS:C2-Methyladenosine is a x-ray crystal structure of the mutant strain of Mycobacterium tuberculosis that has an efficient method for binding to the substrate. The uptake of C2-methyladenosine by the wild type strain was found to be at least four times higher than that of adenosine. The analog was also shown to have pharmacokinetic properties in fat cells, which leads to a decrease in ATP levels.
Formula:C11H15N5O4Purity:Min. 96 Area-%Color and Shape:White PowderMolecular weight:281.27 g/molN3-Methylcytidine methosulfate
CAS:N3-Methylcytidine methosulfate is a novel antiviral agent that inhibits the synthesis of DNA and RNA. It has been shown to be effective against hepatitis B virus, herpes simplex virus, varicella-zoster virus, human immunodeficiency virus, and cytomegalovirus. N3-Methylcytidine methosulfate was found to be active in a variety of animal models including mice and rats. This drug has anticancer properties in the treatment of leukemia, lymphoma, and breast cancer. The phosphoramidite derivative of N3-methylcytidine methosulfate is used as an activator for oligonucleotide synthesis.
Formula:C10H15N3O5·CH4SO4Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:369.35 g/molN6-Ethenoadenosine
CAS:N6-Ethenoadenosine is a fluorescent derivative that is used in biology to study the binding of receptor molecules to DNA. N6-Ethenoadenosine binds to the dinucleotide phosphate, which is an important component for many metabolic processes. It also has been shown to be an effective inhibitor of DNA duplexes and ATPase activity. N6-Ethenoadenosine has a glycosidic bond with p-nitrophenyl phosphate, which is a substrate of creatine kinase and can be used as an indicator of its activity. This product is also used as a marker for damaged DNA.Formula:C12H13N5O4Purity:Min. 95%Color and Shape:White PowderMolecular weight:291.26 g/molGuanosine 3',5'-cyclic monophosphate
CAS:Guanosine 3',5'-cyclic monophosphate (cGMP) is a nucleotide that functions as a second messenger in the cell. It is involved in many cellular processes, including mitochondrial functions and energy metabolism. cGMP is synthesized from guanosine triphosphate (GTP) by the enzyme guanine nucleotide-binding protein, which hydrolyzes the phosphate group from GTP to form cGMP. cGMP has been shown to be involved in neuronal death, axonal growth, and glucose uptake in cells. Optimum concentrations of cGMP have been found to be between 1-10 μM. It has also been shown to be an important mediator of cyclic axonal growth and bowel disease. Guanosine 3',5'-cyclic monophosphate can also act as a polymerase chain reaction primer for DNA amplification in vitro.Formula:C10H12N5O7PPurity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:345.21 g/mol2-Chloroisonicotinic acid
CAS:2-Chloroisonicotinic acid is a halogenated derivative of isonicotinic acid where a chlorine atom is substituted at the 2-position of the pyridine ring (next to the carboxylic acid group).Formula:C6H4ClNO2Purity:Min. 95%Color and Shape:PowderMolecular weight:157.55 g/mol2'-Deoxy-2',2'-difluorocytidine 5'-triphosphate triethylammonium salt - Aqueous solution
CAS:2'-Deoxy-2',2'-difluorocytidine 5'-triphosphate triethylammonium salt - Aqueous solution is a nucleoside analog for research purposesFormula:C9H14F2N3O13P3·C24H60N4Color and Shape:Colorless PowderMolecular weight:907.9 g/mol5'-O-DMT-2'-O-methyluridine
CAS:5'-O-DMT-2'-O-methyluridine (5'-OMeT) is a phosphoramidite building block of a modified nucleoside that is used in biological research. The stability of 5'-OMeT has been studied by thermal denaturation studies and found to be more stable than other analogues such as 6-azacytidine, 6-azauridine, and 6-azathymidine. This may be due to its increased resistance to endonucleolytic cleavage. 5'-OMeT has not shown any significant biological activity in vivo or in vitro.Formula:C31H32N2O8Purity:Min. 95%Color and Shape:White PowderMolecular weight:560.61 g/mol8-(4-Chlorophenylthio)adenosine 3',5'-cyclic monophosphate monosodium salt
CAS:8-(4-Chlorophenylthio)adenosine 3',5'-cyclic monophosphate monosodium salt (8-CPT-cAMP) is a cytosolic second messenger that regulates physiological processes. It interacts with the G protein coupled receptor 2-adrenergic receptor, and activates adenylyl cyclase to produce cAMP. 8-CPT-cAMP also induces mitochondrial membrane potential depolarization and Ca2+ release from the endoplasmic reticulum, which leads to cell death. The pro-apoptotic protein Bax is upregulated by 8-CPT-cAMP in cells and contributes to cell death.Formula:C16H14ClN5NaO6PSPurity:Min. 97 Area-%Color and Shape:PowderMolecular weight:493.79 g/mol2',3'-Di-O-acetyladenoside
CAS:2',3'-Di-O-acetyladenoside is a nucleoside for use in research applicationsFormula:C14H17N5O6Purity:Min. 97 Area-%Color and Shape:White PowderMolecular weight:351.31 g/mol2'-O-Methylguanosine
CAS:2'-O-Methylguanosine is a nucleoside that contains a 2'-O-methyl group at the 2' position of the ribose. It is a component of many nucleic acids and is usually found as a minor component in RNA. 2'-O-Methylguanosine has been shown to be an inhibitor of DNA polymerase and an activator of RNA polymerase, which may be due to its ability to form hydrogen bonds with the phosphate backbone. This compound has also been shown to act as a competitive inhibitor for both wild-type and mutant bacterial strains, suggesting that it can inhibit DNA synthesis in bacteria by binding to the enzyme's active site. 2'-O-Methylguanosine is present in relatively high concentrations in tissues, such as liver and muscle, where it is involved in metabolism or energy production. The optimum concentration for detection by analytical methods varies depending on the type of detector used.Formula:C11H15N5O5Purity:Min. 95%Color and Shape:White PowderMolecular weight:297.27 g/mol3'-O-Methylguanosine
CAS:3'-O-Methylguanosine is a nucleoside that is found in the guanine molecule and has been shown to have inhibitory properties against malignant brain tumors. 3'-O-Methylguanosine blocks the synthesis of DNA, RNA, and peptide hormones. It also inhibits the growth of erythromycin-resistant strains of bacteria. The kinetic data for 3'-O-Methylguanosine was obtained from experiments with leukemic mice and carcinoma cell lines. The enzyme glut1 regulates the rate of metabolism of 3'-O-Methylguanosine. It is metabolized by dehydroascorbic acid reductase to 3'-deoxyadenosine monophosphate (dAMP) and then to adenosine monophosphate (AMP). The optimum pH for this reaction is 7.3 at 37 degrees Celsius.Formula:C11H15N5O5Purity:Min. 98 Area-%Color and Shape:White Off-White PowderMolecular weight:297.27 g/mol5-Hydroxycytidine
CAS:5-Hydroxycytidine is a pyrimidine nucleoside that is found in DNA and RNA. It can be produced by the conversion of cytidine 5-monophosphate to cytidine 5'-diphosphate, which is then hydrolyzed to produce 5-hydroxycytidine. This conversion requires the enzyme cytidylate kinase. The structure of 5-hydroxycytidine differs from other pyrimidine nucleosides as its hydroxyl group does not have an acidic proton present. Biological functions that have been attributed to 5-hydroxydihydrocytidylic acid include its ability to inhibit translation and induce cell death in lung cells. This compound has also been shown to modify DNA duplexes and form bioconjugates with proteins or small molecules, such as fluorescein and digoxigenin. These modifications are used in analytical methods such as phase chromatography, nuclear magnetic resonance spectroscopy
Formula:C9H13N3O6Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:259.22 g/mol8-Bromoguanosine hydrate
CAS:8-Bromoguanosine hydrate is a brominated form of guanosine. It is used as a marker for colorectal cancer in urine samples. 8-Bromoguanosine hydrate can be used to calibrate the results of chromatographic analyses and to identify metabolic disorders, such as fatty acid oxidation defects. The compound is also an endogenous ligand that interacts with adenosine receptors and may have pro-apoptotic effects on cancer cells by triggering their death. 8-Bromoguanosine hydrate has been shown to be more effective than other brominated nucleosides in inducing apoptosis in malignant cells, including colorectal carcinoma cells.Formula:C10H12BrN5O5·xH2OPurity:Min. 95%Color and Shape:PowderMolecular weight:362.14 g/mol2'-Deoxy-5-hydroxymethylcytidine
CAS:2'-Deoxy-5-hydroxymethylcytidine is a nucleoside analog that inhibits the enzyme thymidylate synthase. The inhibition of this enzyme leads to a deficiency in the production of thymine, which is essential for DNA synthesis. 2'-Deoxy-5-hydroxymethylcytidine has been shown to be an effective anti-cancer agent in vitro and in vivo. It can also be used as a potential biomarker for cancer and can be used as a polymerase chain reaction (PCR) primer for detection of cancer tissue. This drug binds to the polymerase enzyme, preventing it from performing its function to replicate DNA, thereby halting cell division and causing cell death.Formula:C10H15N3O5Purity:Min. 95%Color and Shape:White Yellow PowderMolecular weight:257.24 g/mol3'-O-Propargyluridine
CAS:3'-O-Propargyluridine is a synthetic nucleoside with an alkyne functional handle on the 3'-position of the sugarFormula:C12H14N2O6Purity:Min. 95%Color and Shape:White PowderMolecular weight:282.25 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/mol
