Nucleotidi
I nucleotidi sono composti organici che fungono da mattoni per la costruzione degli acidi nucleici, essenziali per la formazione del DNA e dell'RNA. Ogni nucleotide è composto da una base azotata, una molecola di zucchero e uno o più gruppi fosfato. Questi nucleotidi si uniscono per formare lunghe catene, creando il materiale genetico che porta e trasmette informazioni genetiche in tutti gli organismi viventi. In questa sezione, troverai una vasta gamma di nucleotidi cruciali per la ricerca in genetica, biologia molecolare e biochimica. Sono fondamentali per studiare i processi genetici, sintetizzare acidi nucleici e sviluppare strumenti diagnostici e terapeutici. Da CymitQuimica, offriamo nucleotidi di alta qualità per supportare la tua ricerca scientifica e applicazioni, garantendo precisione e affidabilità nei tuoi esperimenti.
Sottocategorie di "Nucleotidi"
Trovati 2634 prodotti di "Nucleotidi"
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5′-O-DMT-LNA N-Bz adenosine
CAS:<p>5′-O-DMT-LNA N-Bz adenosine is a novel nucleoside that has been modified with an aminooxy group. The compound is synthesized by the phosphoramidite method and it is designed for use in antiviral and anticancer research. 5′-O-DMT-LNA N-Bz adenosine can be used as a substrate for DNA polymerases and other enzymes to produce nucleic acid strands. This product is CAS No. 206055-74-5, monophosphate, Phosphoramidites, Synthetic, Deoxyribonucleosides, Anticancer, Ribonuclesides, High purity.</p>Formula:C39H35N5O7Purezza:Min. 95%Peso molecolare:685.73 g/mol5-Methoxyuridine-5'-triphosphate sodium, 100mM aqueous solution
CAS:5-Methoxyuridine-5'-triphosphate is a monophosphate nucleoside that serves as a precursor for the synthesis of 5-methoxyuridine (5MU) and other nucleosides. It has antiviral effects, and is used in the treatment of herpes zoster infection. 5-Methoxyuridine-5'-triphosphate is an analog of uridine and deoxyribonucleosides with antiviral activity, which can be used to treat herpes zoster infection. This drug also has anticancer properties, which may be due to its ability to inhibit DNA synthesis by inhibiting ribonucleotide reductase and DNA polymerase, leading to cell death.Formula:C10H17N2O16P3•NaxPurezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:514.17 g/mol2'-Deoxy-3,4,5,6-tetrahydrouridine
CAS:<p>2'-Deoxy-3,4,5,6-tetrahydrouridine (2DTHR) is a cytidine deaminase inhibitor that is used in vitro to inhibit the production of tumor necrosis factor (TNF). 2DTHR has been shown to be active against hepatocellular carcinoma cells. It is also reactive with tumor tissue and can be eliminated at a rate similar to that of deoxycytidine kinase. This drug binds to the enzyme target and inhibits its activity by increasing enzyme levels, which causes cell death. 2DTHR inhibits TNF production in tumor tissue by binding to cytidine deaminase and preventing conversion of cytidine into uracil. This drug has been shown to cause tumor inhibition in vitro.</p>Formula:C9H16N2O5Purezza:Min. 95%Colore e forma:PowderPeso molecolare:232.23 g/mol3-Acetylpyridine adenine dinucleotide disodium, reduced form
CAS:<p>Reduced synthetic analog of NADH with an acetylpyridine modification. It is used as a reducing substrate to study the mechanisms of NAD(P)+-dependent reductases and to probe the active sites and catalytic processes of these important enzymes through its altered spectroscopic and binding properties. The disodium salt ensures good solubility for biochemical applications.</p>Formula:C22H30N6O14P2•Na2Purezza:Min. 95%Colore e forma:Slightly Yellow PowderPeso molecolare:710.43 g/mol7-Deaza-2'-C-ethynyladenosine
CAS:7-Deaza-2'-C-ethynyladenosine (7DAA) is a research inhibitor that is classified as a polymerase inhibitor. It binds to the active site of the viral NS5B polymerase and inhibits RNA synthesis, which leads to virus replication. 7DAA has shown activity against hepatitis B virus (HBV) and hepatitis C virus (HCV). It also shows multifunctional properties in its inhibition of HBV genotypes A1, A3, and D1. In addition, 7DAA interacts with the RNA binding site on HCV polymerase protein and prevents binding of the viral RNA genome to this site. 7DAA also inhibits HIV replication by preventing assembly of the reverse transcriptase enzyme complex at an early stage.Formula:C13H14N4O4Purezza:Min. 95%Colore e forma:PowderPeso molecolare:290.27 g/mol2'-Deoxy-4'-ethynyl-2-fluoroadenosine
CAS:<p>2'-Deoxy-4'-ethynyl-2-fluoroadenosine (EFdA) is an analog of adenosine. EFdA is a potent inhibitor of HIV replication, and has been shown to be effective against other viruses such as influenza virus, herpes simplex virus, and vesicular stomatitis virus. EFdA was the first nucleoside analog to show antiviral activity in tissue culture against these viruses. This drug also inhibits the synthesis of mitochondrial rRNA and reduces the formation of mitochondrial DNA in human cells by inhibiting mitochondrial DNA polymerase γ. EFdA also prevents the binding of monoclonal antibodies to human B lymphocytes, which may be due to its steric interactions with plasma RNA. This drug is metabolized by cytochrome P450 2C8 and 2C9 into a variety of metabolites that are excreted in urine as glucuronides or sulfates. EFdA has a long</p>Formula:C12H12FN5O3Purezza:Min. 95%Peso molecolare:293.25 g/mol5'-O-DMT-thymidine-3'-succinyl CPG 2000 Å
5'-O-DMT-thymidine-3'-succinyl CPG 2000 Å is a synthetic nucleoside that contains an acetyl group at the 5' position. The succinyl group has been added to the 3' position of the nucleoside and is bonded to a carrier molecule (2000 Å). This product is used as an activator in DNA synthesis, it also has antiviral and anticancer activities.Colore e forma:PowderRibavirin 5'-triphosphate triethylammonium salt - 10 mM aqueous solution
CAS:<p>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.</p>Formula:C8H15N4O14P3•(C6H15N)xPurezza:Min. 95 Area-%Colore e forma:Clear LiquidPeso molecolare:789.73Citicoline sodium
CAS:<p>Citicoline is a complex organic molecule, a form of B-vitamin choline that acts as an intermediate in many biosynthetic pathways, for example, in the biosynthesis of cell membrane phospholipids. As a dietary supplement, citicoline is a source of choline and cytidine, two components that are quickly absorbed in the intestine and across the blood-brain barrier. The neuroprotective properties of citicoline improves mental performance increasing the levels of other brain-related chemicals like dopamine and norepinephrine, helping with recovery in stroke patients, reducing memory loss due to aging and improving vision in patients with glaucoma.</p>Formula:C14H26N4O11P2•NaPurezza:Min. 98.0 Area-%Colore e forma:White To Off-White SolidPeso molecolare:511.31 g/molGuanylyl-3',5'-guanosine ammonium salt
CAS:<p>Guanylyl-3',5'-guanosine ammonium salt is a novel antiviral agent that has high antiviral activity against influenza A virus. It is a guanine derivative which has been modified to include an aminopropyl group and an ammonium cation. This compound also acts as an activator for deoxyribonucleosides, nucleotides, and ribonucleosides. Guanylyl-3',5'-guanosine ammonium salt may be used in the manufacture of DNA, RNA, and phosphoramidites. This compound also has anticancer effects by inhibiting the proliferation of tumor cells and inducing apoptosis.</p>Formula:C20H25N10O12P·H3NPurezza:Min. 95%Peso molecolare:645.48 g/mol4-Chloro-5-iodo-pyrrolo[2,3-d]pyriMidine-7-carboxylic acid tert-butyl ester
CAS:Focuses is a chemical compound that does not have any known commercial or industrial uses.Purezza:Min. 95%ent-abacavir
CAS:Ent-abacavir is a drug that belongs to the group of antiretroviral drugs. It has minimal toxicity and has been shown to be effective in long-term treatment of HIV/AIDS. Ent-abacavir is also used as part of active antiretroviral therapy, which includes at least three or four different drugs. It inhibits the activity of reverse transcriptase, an enzyme involved in the replication process of HIV and other retroviruses. This drug has been shown to have few drug interactions with other medications, although caution should be taken when using ent-abacavir with drugs that are metabolized by cytochrome P450 enzymes. Ent-abacavir is not recommended for use in patients who have chronic viral hepatitis or who have a body mass index greater than 30 kg/m2 because its pharmacokinetic properties may be altered in these individuals.Formula:C14H18N6OPurezza:Min. 95%Peso molecolare:286.33 g/molAbacavir 5'-phosphate
CAS:<p>Abacavir 5'-phosphate is a nucleoside analog that inhibits the replication of the herpes virus by covalently binding to the viral DNA polymerase and blocking its ability to polymerize dNTPs. Abacavir 5'-phosphate's anti-viral potency has been shown in vivo using a model with herpes simplex virus, and it has been shown to inhibit viral replication in cell culture. The drug also reacts with cellular components such as proteins, lipids, and nucleic acids, which may lead to drug reactions. Abacavir 5'-phosphate is chemically stable, so it can be subjected to analytical methods without degradation. It is an analog of zidovudine (AZT).</p>Formula:C14H19N6O4PPurezza:Min. 95%Peso molecolare:366.31 g/mol2'-O-(2-Methoxyethyl)guanosine 5'-monophosphate
CAS:<p>10umol is approx 5mg.2'-O-(2-Methoxyethyl)guanosine 5'-monophosphate is a novel nucleoside phosphorylated on the 5' position</p>Purezza:Min. 95%2',3'-Di-O-benzoyl-N6-benzoyl-L-adenosine
CAS:<p>2',3'-Di-O-benzoyl-N6-benzoyl-L-adenosine (DBBA) is a modified nucleoside with anticancer, antiviral, and synthetic properties. It can be used as a building block for the synthesis of DNA, RNA, or other nucleotide analogues. DBBA has shown activity against certain cancer cells and has been found to inhibit the replication of HIV and herpes simplex virus type 1 in cell culture. DBBA is also known as 2',3'-Dibenzoyl-N6-benzoyladenosine.</p>Formula:C31H25N5O7Purezza:Min. 95%Peso molecolare:579.56 g/mol2'-Deoxyinosine-5'-triphosphate sodium
CAS:2'-Deoxyinosine-5'-triphosphate sodium is a nucleoside that is used as an antiviral, anticancer and novel drug. It inhibits viral replication by inhibiting DNA synthesis in the cell. 2'-Deoxyinosine-5'-triphosphate sodium binds to viral RNA polymerase, preventing the enzyme from creating new DNA strands. This prevents the virus from replicating and spreading to other cells in the body. 2'-Deoxyinosine-5'-triphosphate sodium has been shown to inhibit cancer growth by binding to DNA, which prevents it from dividing and creating new cells. This drug also has antiviral activity against HIV and Herpes Simplex Virus Type 1 (HSV1). 2'-Deoxyinosine-5'-triphosphate sodium is typically used as a buffer solution for peptide synthesis or as a chemical intermediate for various organic syntheses.Formula:C10H15N4O13P3·xNaPurezza:Min. 95%Colore e forma:White PowderPeso molecolare:492.17 g/mol2-Chloroadenosine 5'-monophosphate triethylamine salt
CAS:<p>2-Chloroadenosine 5'-monophosphate triethylamine salt is a phosphoramidite that has anticancer and antiviral activities. It is synthesized by reacting 2-chloroadenosine with triethylamine. This product has a novel chemical structure and it can be used as an activator for the synthesis of modified DNA, RNA, and other nucleosides. It is also used in the manufacture of deoxyribonucleosides, ribonucleosides, and other nucleotides.</p>Formula:C10H13ClN5O7P·C12H30N2Purezza:Min. 95%Peso molecolare:584.05 g/molN6-Acetyl-2'-deoxyadenosine
CAS:N6-Acetyl-2'-deoxyadenosine is an antiviral and anticancer nucleoside. It is a novel modified nucleoside that has been synthesized with a high degree of purity. N6-Acetyl-2'-deoxyadenosine is active against HIV, Hepatitis C, and other viruses, as well as cancer cells. It also inhibits the activity of bacterial DNA gyrase and topoisomerase IV, which are enzymes that maintain the integrity of bacterial DNA. N6-Acetyl-2'-deoxyadenosine has a phosphoramidite structure and is synthesized from 2'-deoxyribonucleosides.Formula:C12H15N5O4Purezza:Min. 95%Peso molecolare:293.28 g/mol1-(2-Deoxy-β-D-erythro-pentofuranosyl)-4-nitro-1H-indole
CAS:Please enquire for more information about 1-(2-Deoxy-β-D-erythro-pentofuranosyl)-4-nitro-1H-indole including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C13H14N2O5Purezza:Min. 95%Peso molecolare:278.26 g/mol2'-O-Methyluridine-5'-monophosphate triethylammonium
CAS:<p>2'-O-Methyluridine-5'-monophosphate triethylammonium salt is a modified nucleoside analogue that is an antiviral agent. It inhibits viral replication by acting as an inhibitor of RNA synthesis and DNA polymerase, which are necessary for the virus to replicate. This compound also has anticancer activity and can be used as a chemotherapeutic agent. 2'-O-Methyluridine-5'-monophosphate triethylammonium salt is synthesized from uracil, phosphoramidite, and triethylamine. It has high purity and high quality with a CAS number of 67624-43-5.</p>Formula:C10H15N2O9P•(C6H15N)2Purezza:Min. 95%Colore e forma:PowderPeso molecolare:439.21 g/mol
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