Synthèse ADN/ARN
Les inhibiteurs de la synthèse de l'ADN et de l'ARN sont des composés qui interfèrent avec les processus de réplication et de transcription dans les cellules, empêchant ainsi la production de matériel génétique essentiel. Ces inhibiteurs peuvent cibler diverses enzymes et protéines impliquées dans la synthèse des acides nucléiques, ce qui en fait des outils précieux pour étudier les mécanismes de réplication, de transcription et de traduction. Ils sont également utilisés dans le développement de traitements contre les infections et le cancer. Chez CymitQuimica, nous offrons une large gamme d'inhibiteurs de la synthèse de l'ADN/ARN pour soutenir vos recherches en biologie moléculaire, virologie et développement thérapeutique.
708 produits trouvés pour "Synthèse ADN/ARN"
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Eriodictyol
CAS :<p>Eriodictyol: anti-inflammatory, antioxidant, may improve diabetes and atopic dermatitis symptoms.</p>Formule :C15H12O6Degré de pureté :98.03% - 99.32%Couleur et forme :SolidMasse moléculaire :288.253-Deazauridine
CAS :<p>3-Deazauridine (NSC-126849), a uridine analog, blocks CTP synthesis by competing with CTP synthetase.</p>Formule :C10H13NO6Degré de pureté :99.86%Couleur et forme :SolidMasse moléculaire :243.21T-5224
CAS :<p>T-5224 is a transcription factor c-Fos/AP-1 inhibitor, which specifically inhibits the DNA binding activity of c-Fos/c-Jun without affecting other transcription</p>Formule :C29H27NO8Degré de pureté :97.88% - 99.29%Couleur et forme :SolidMasse moléculaire :517.53AI-10-49
CAS :<p>AI-10-49 is a selective inhibitor of the binding of CBFβ-SMMHC to RUNX1 with IC50 of 260 nM.</p>Formule :C30H22F6N6O5Degré de pureté :97.14%Couleur et forme :SolidMasse moléculaire :660.52Brr2-IN-3
CAS :<p>Brr2-IN-3 (Brr2 Inhibitor C9) is an allosteric inhibitor of the spliceosomal RNA helicase Brr2. Brr2 is implicated in autosomal-dominant retinitis pigmentosa.</p>Formule :C24H20N4O3SDegré de pureté :99.26%Couleur et forme :SolidMasse moléculaire :444.51Deoxythymidine triphosphate
CAS :<p>Deoxythymidine triphosphate (dTTP) is one of the four nucleoside triphosphates that are used in the in vivo synthesis of DNA.</p>Formule :C10H14N2Na3O14P3Degré de pureté :99.78%Couleur et forme :White Amorphous PowderMasse moléculaire :548.115-BrdU
CAS :<p>5-BrdU (Broxuridine) is a nucleoside analogue, detect proliferating cells and compete with thymidine for incorporation into DNA. High-Quality, Low-Cost!</p>Formule :C9H11BrN2O5Degré de pureté :99.54% - 99.87%Couleur et forme :Crystals From Absolute Ethanol Physical Description White Crystalline Powder (Ntp 1992)Masse moléculaire :307.1Phosphonoformic acid trisodium salt hexa
CAS :<p>Phosphonoformic acid trisodium salt hexa (Sodium phosphonatoformate hexahydrate) is an antiviral drug for the treatment of CMV retinitis.</p>Formule :CH12Na3O11PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :300.03Tipiracil
CAS :<p>Tipiracil inhibits thymidine phosphorylase, enhancing trifluridine bioavailability, and is studied in colorectal and gastric cancer treatment.</p>Formule :C9H11ClN4O2Degré de pureté :99.815%Couleur et forme :SolidMasse moléculaire :242.661,4-Anthraquinone
CAS :<p>1,4-Anthraquinone: anticancer, hinders nucleoside transport, inhibits synthesis, fragments DNA, curbs L1210 cell growth; aids HPLC analysis of NAC, CAP.</p>Formule :C14H8O2Degré de pureté :95.96% - 97.01%Couleur et forme :Orange Brown SolidMasse moléculaire :208.21TH588 hydrochloride
CAS :<p>TH588 hydrochloride is first-in-class inhibitor of nudix hydrolase family that selectively and effectively bind and inhibit the MTH1 with IC50 value of 5 nM.</p>Formule :C13H13Cl3N4Couleur et forme :SolidMasse moléculaire :331.63SCR7 pyrazine
CAS :<p>SCR7 pyrazine (SCR7) enhances CRISPR-Cas9-mediated homology-directed repair (HDR) efficiency in vitro up to 19-fold. Inhibits nonhomologous end-joining (NHEJ).</p>Formule :C18H12N4OSDegré de pureté :98.72% - 99.85%Couleur et forme :SolidMasse moléculaire :332.38Triazavirin
CAS :<p>Triazavirin is a nucleoside analogue of nucleic acid and an antiviral agent.</p>Formule :C5H7N6NaO5SDegré de pureté :99.55%Couleur et forme :SolidMasse moléculaire :286.2CX-5461 dihydrochloride
<p>CX-5461 dihydrochloride: Oral Pol I inhibitor, HCT-116 (IC50: 142 nM), A375 (IC50: 113 nM), MIA PaCa-2 (IC50: 54 nM), weak on Pol II (IC50 ≥ 25 μM).</p>Formule :C27H29Cl2N7O2SCouleur et forme :SolidMasse moléculaire :586.54Simeprevir
CAS :<p>Simeprevir (TMC435) is a potent HCV NS3/4A protease inhibitor, and inhibits HCV replication with EC50 of 8 nM.</p>Formule :C38H47N5O7S2Degré de pureté :99.45% - 99.92%Couleur et forme :SolidMasse moléculaire :749.94Simeprevir sodium
CAS :<p>Simeprevir is a drug for the treatment and cure of hepatitis C.</p>Formule :C38H46N5NaO7S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :771.92Pyridostatin hydrochloride
CAS :<p>Pyridostatin hydrochloride stabilizes G-quadruplex DNA (Kd=490nM), inhibits cancer cell growth, and reduces SRC in breast cancer.</p>Formule :C31H37Cl5N8O5Couleur et forme :SolidMasse moléculaire :778.941-Hydroxyanthraquinone
CAS :<p>1-Hydroxyanthraquinone is an anthraquinone that has been found in Morinda officinalis and has genotoxic and carcinogenic activities.</p>Formule :C14H8O3Degré de pureté :99.56%Couleur et forme :Orange Red Needles Red-Orange To Fine Yellow CrystalsMasse moléculaire :224.21Dasabuvir sodium
CAS :<p>Dasabuvir sodium (ABT-333) inhibits HCV NS5B polymerase, targeting genotypes 1a (EC50: 7.7 nM) and 1b (EC50: 1.8 nM).</p>Formule :C26H26N3NaO5SCouleur et forme :SolidMasse moléculaire :515.56Idarubicin hydrochloride
CAS :<p>Idarubicin hydrochloride (Zavedos), a hydrochloride salt form of Idarubicin, is a DNA topoisomerase II (topo II) inhibitor for MCF-7 cells ( IC50: 3.3 ng/mL).</p>Formule :C26H27NO9·HClDegré de pureté :98.91% - 99.96%Couleur et forme :SolidMasse moléculaire :533.95BRD32048
CAS :<p>BRD32048 is a top candidate ETV1 perturbagen. BRD32048 inhibits p300-dependent acetylation of ETV1, thereby promoting its degradation.</p>Formule :C16H22N6ODegré de pureté :99.87%Couleur et forme :SolidMasse moléculaire :314.39RI-1
CAS :<p>RI-1 (RAD51 inhibitor 1) is a RAD51 inhibitor (IC50: 5-30 μM).</p>Formule :C14H11Cl3N2O3Degré de pureté :99.3% - 99.62%Couleur et forme :SolidMasse moléculaire :361.61Risdiplam
CAS :<p>Risdiplam (RG7916) is a centrally and peripherally distributed and orally administrable small molecule SMN2 pre-mRNA splicing modifier.Cost-effective and quality-assured.</p>Formule :C22H23N7ODegré de pureté :98.68% - 99.64%Couleur et forme :SolidMasse moléculaire :401.46TH5487
CAS :<p>TH5487 is an potent inhibitor of 8-oxoguanine DNA glycosylase 1 (OGG1)( IC50 of 342 nM)</p>Formule :C19H18BrIN4O2Degré de pureté :98.38% - 98.73%Couleur et forme :SolidMasse moléculaire :541.18HAMNO
CAS :<p>HAMNO (NSC-111847) is a protein interaction inhibitor of replication protein A (RPA).</p>Formule :C17H13NO2Degré de pureté :99.96%Couleur et forme :SolidMasse moléculaire :263.29BMH-21
CAS :<p>BMH-21, a small molecule DNA intercalator, binds ribosomal DNA and inhibits RNA polymerase I (Pol I) transcription and not affects phosphorylation of H2AX.</p>Formule :C21H20N4O2Degré de pureté :99.47% - 99.84%Couleur et forme :SolidMasse moléculaire :360.41TH287
CAS :<p>TH287 is a potent inhibitor of MTH1 (NUDT1), less potent for MTH2, NUDT5, NUDT12, NUDT14, and NUDT16.</p>Formule :C11H10Cl2N4Degré de pureté :97.73% - 99%Couleur et forme :SolidMasse moléculaire :269.13Adenine hydrochloride
CAS :<p>Adenine hydrochloride (6-Aminopurine hydrochloride) is a hydrochloride salt form of adenine which is a nucleobase with a variety of roles in biochemistry.</p>Formule :C5H5N5·HClDegré de pureté :98.86%Couleur et forme :White To Light Yellow Crystal PowderMasse moléculaire :171.59Lurbinectedin
CAS :<p>Lurbinectedin (PM01183) is a DNA minor groove covalent binder. Lurbinectedin also shows effective anti-tumor activity.</p>Formule :C41H44N4O10SDegré de pureté :98.11%Couleur et forme :SolidMasse moléculaire :784.87FIT-039
CAS :<p>FIT-039 is a selective and ATP-competitive, orally active inhibitor of CDK9( IC50 : 5.8 μM;CDK9/cyclin T1).</p>Formule :C17H18FN3SDegré de pureté :98.61%Couleur et forme :SolidMasse moléculaire :315.41Fosifloxuridine nafalbenamide
CAS :<p>Fosifloxuridine nafalbenamide (NUC 3373), a pyrimidine nucleotide analogue, is a Thymidylate synthase inhibitor.</p>Formule :C29H29FN3O9PDegré de pureté :95.87%Couleur et forme :SolidMasse moléculaire :613.53Brequinar
CAS :<p>Brequinar (NSC-368390) is a potent inhibitor of dihydroorotate dehydrogenase, with potent activities against a broad spectrum of viruses.</p>Formule :C23H15F2NO2Degré de pureté :99.1% - 99.57%Couleur et forme :SolidMasse moléculaire :375.37L-Asparaginase
CAS :<p>L-Asparaginase, an enzyme for acute lymphoblastic leukemia treatment, is administered via injection.</p>Formule :NADegré de pureté :97%Couleur et forme :SolidMasse moléculaire :N/ARCM-1
CAS :<p>RCM-1 is an inhibitor of FOXM1.</p>Formule :C20H12N2OS4Degré de pureté :98.08%Couleur et forme :SolidMasse moléculaire :424.58EG1
CAS :<p>EG1, a novel specific inhibitor of Pax2 transcription activation, targets the DNA binding domain and inhibits embryonic kidney development.</p>Formule :C22H18N2O5Degré de pureté :97.48%Couleur et forme :SolidMasse moléculaire :390.39CB-6644
CAS :<p>CB-6644 is a small molecule inhibitor of the ATPase activity of the RUVBL1/2 complex.Cost-effective and quality-assured.</p>Formule :C29H34ClFN4O5Degré de pureté :96.33% - 99.85%Couleur et forme :SolidMasse moléculaire :573.06FUBP1-IN-1
CAS :<p>FUBP1-in-1: Potent FUBP1 inhibitor with 11.0 M IC50, disrupts FUBP1-DNA binding.</p>Formule :C19H14F3N3O2SDegré de pureté :99.7%Couleur et forme :SolidMasse moléculaire :405.392′-O-Methylcytidine
CAS :<p>2′-O-Methylcytidine inhibits NS5B-catalyzed RNA synthesis in vitro, in a manner that is competitive with substrate nucleoside triphosphate.</p>Formule :C10H15N3O5Degré de pureté :99.72%Couleur et forme :SolidMasse moléculaire :257.24Gadodiamide
CAS :<p>Gadodiamide is an MRI contrast agent, used in MR imaging procedures to assist in the visualization of blood vessels.</p>Formule :C16H26GdN5O8Degré de pureté :99.86%Couleur et forme :SolidMasse moléculaire :573.66Antitumor agent-152
CAS :<p>Organic compound, potential dCK inhibitor, with 2-ethyl-3-methoxyphenyl-1,3-thiazole and pyrimidine units.</p>Formule :C17H19N5O2S2Degré de pureté :95.00%Couleur et forme :SolidMasse moléculaire :389.5C/EBPα inducer 1
CAS :<p>C/EBPα inducer 1 (4(3H)-Quinazolinone, 6-fluoro-2-[(1E)-2-(5-nitro-2-furanyl)ethenyl]-3-phenyl-) is a potential inducer of myeloid differentiation via</p>Formule :C20H12FN3O4Degré de pureté :98.99%Couleur et forme :SolidMasse moléculaire :377.33Myoseverin
CAS :<p>Myoseverin triggers myotube fission into single cells, influencing genes for growth, immunity, matrix remodeling, and stress, aiding healing and regeneration.</p>Formule :C24H28N6O2Degré de pureté :99.25%Couleur et forme :SolidMasse moléculaire :432.52VPC-80051 racemate
CAS :<p>VPC-80051 is the first small molecule inhibitor of hnRNP A1 splicing activity by using a computer-aided drug discovery approach.</p>Formule :C16H13F2N3ODegré de pureté :97.36%Couleur et forme :SolidMasse moléculaire :301.295'-Deoxy-5-fluorocytidine
CAS :<p>5'-Deoxy-5-fluorocytidine is an intermediate metabolite of the DNA synthesis inhibitor capecitabine.</p>Formule :C9H12FN3O4Degré de pureté :99.67%Couleur et forme :White SolidMasse moléculaire :245.21TC-E 5003
CAS :<p>TC-E 5003 (NSC-30176) is a selective inhibitor of PRMT1 with IC50 of 1.5 μM.</p>Formule :C16H14Cl2N2O4SDegré de pureté :97.01%Couleur et forme :SolidMasse moléculaire :401.26HALOFUGINONE LACTATE
CAS :<p>HALOFUGINONE LACTATE is a halogenated derivative of febrifugine, a natural quinazolinone-containing compound found in the Chinese herb D.</p>Formule :C19H23BrClN3O6Degré de pureté :99.70% - 99.96%Couleur et forme :SolidMasse moléculaire :504.8Euscaphic acid
CAS :<p>Euscaphic acid has anti-diabetic and anti-inflammatory effects, blocking IKK/MAPKs and NF-κB activation by disrupting TRAF6/IRAK1/TAK1 clustering.</p>Formule :C30H48O5Degré de pureté :98.93%Couleur et forme :SolidMasse moléculaire :488.7Rg3039
CAS :Rg3039 (PF-06687859) is a potent DcpS inhibitor. DcpS is a therapeutic target for spinal muscular atrophy (SMA). RG3039 improves motor function in SMA mice.Formule :C21H23Cl2N5ODegré de pureté :98.24% - 99.58%Couleur et forme :SolidMasse moléculaire :432.35Clevudine
CAS :<p>Clevudine (Levovir) fights HBV, blocks viral DNA synthesis, and has a long half-life reducing relapse risk after treatment.</p>Formule :C10H13FN2O5Degré de pureté :99.88% - 99.97%Couleur et forme :SolidMasse moléculaire :260.22dGTP
CAS :<p>dGTP (2'-Deoxyguanosine-5'-triphosphate) is one of the guanosine nucleotides which is highly susceptible to oxidative damage to 8-O-GDP, 8-O-dGTP, 8-O-GTP, and</p>Formule :C10H16N5O13P3Degré de pureté :99.64%Couleur et forme :SolidMasse moléculaire :507.18
