
DNA/RNA Synthesis
Inhibitors of DNA and RNA synthesis are compounds that interfere with the replication and transcription processes in cells, thereby preventing the production of essential genetic material. These inhibitors can target various enzymes and proteins involved in nucleic acid synthesis, making them valuable tools for studying the mechanisms of replication, transcription, and translation. They are also used in developing treatments for infections and cancer. At CymitQuimica, we offer a broad spectrum of DNA/RNA synthesis inhibitors to support your research in molecular biology, virology, and therapeutic development.
Found 708 products of "DNA/RNA Synthesis"
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Apricitabine
CAS:<p>Apricitabine (SPD754) is a highly selective and orally active HIV-1 reverse transcriptase inhibitor (Ki=0.08 μM), the (-) enantiomer of 2′-deoxy-3′-oxy-4′-</p>Formula:C8H11N3O3SPurity:99.45%Color and Shape:SolidMolecular weight:229.26ST7612AA1
CAS:<p>ST7612AA1: potent, oral HDAC inhibitor; reactivates HIV-1 latency; shows antitumor effects; may study malaria.</p>Formula:C20H27N3O4SPurity:99.71%Color and Shape:SolidMolecular weight:405.51Zelpolib
CAS:<p>Zelpolib is a specific inhibitor of DNA polymerase δ (Pol δ), inhibiting DNA replication. antiproliferative.</p>Formula:C22H21N3O5S2Purity:98.79%Color and Shape:SolidMolecular weight:471.55Homocarbonyltopsentin
CAS:<p>Homocarbonyltopsentin: Small molecule, binds TSL2 pentaloops, enhances SMN2 E7 splicing, EC50 16 μM.</p>Formula:C21H14N4O3Purity:98%Color and Shape:SolidMolecular weight:370.363'-Deoxyuridine-5'-triphosphate
CAS:<p>3'-dUTP, a nucleotide analogue, competitively inhibits RNA polymerases I & II, with a Ki of 2.0 µM.</p>Formula:C9H15N2O14P3Color and Shape:SolidMolecular weight:468.14Phelorphan
CAS:<p>Phelorphan is an inhibitor of enkephalinase.</p>Formula:C20H22N2O4SPurity:98%Color and Shape:SolidMolecular weight:386.46Beaucage reagent
CAS:<p>Beaucage reagent, which is found to be effective in causing DNA cleavage.</p>Formula:C7H4O3S2Purity:98.50%Color and Shape:White To Off-White PowderMolecular weight:200.23JFN05510
CAS:<p>Compound: 3'-O-tert-BDMS-5'-O-DMT-N2-IBG 2'-CE phosphoramidite; has anticancer properties and activates enzymes.</p>Formula:C50H68N7O9PSiColor and Shape:SolidMolecular weight:970.18Triaziquone
CAS:<p>Triaziquone is an alkylating agent that can react with DNA to form intrastrand crosslinks.</p>Formula:C12H13N3O2Color and Shape:SolidMolecular weight:231.25AS-136A
CAS:<p>AS-136A is an orally active MV RdRp inhibitor with antiviral activity that inhibits measles virus and blocks viral RNA synthesis.</p>Formula:C17H19F3N4O3SPurity:98.52%Color and Shape:SolidMolecular weight:416.42HIPP
CAS:<p>HIPP is a highly selective inhibitor of antineoplastic CtBP.</p>Formula:C9H9NO3Color and Shape:SolidMolecular weight:179.17BMH-22
CAS:<p>BMH-22 is an RNA polymerase I inhibitor that acts by causing nucleolar stress and showing potent anticancer activity across many tumor types.</p>Formula:C16H17N3Color and Shape:SolidMolecular weight:251.33Phen-DC3
CAS:<p>Phen-DC3 is a G-quadruplex (G4) specific ligand which can inhibit FANCJ and DinG helicases (IC50s of 65±6 and 50±10 nM, respectively).</p>Formula:C34H26N6O2Purity:98%Color and Shape:SolidMolecular weight:550.61NPD9948
CAS:<p>NPD9948 is a competitive inhibitor of MTH1.</p>Formula:C13H14N6Color and Shape:SolidMolecular weight:254.29MLAF50
CAS:<p>MLAF50 is an inhibitor of the REV1 UBM2-Ubiquitin interaction.</p>Formula:C15H12I2O4Color and Shape:SolidMolecular weight:510.06HIV-1 inhibitor-43
CAS:<p>HIV-1 Inhibitor-43 suppresses HIV-1, with EC50: 21.3 nM (Y188L), 6.2 nM (K103N-Y181C), <0.7 nM (K103N/Y181C), and lowers HIV RNA/p24 protein.</p>Formula:C24H21ClN2O4SColor and Shape:SolidMolecular weight:468.95HBV-IN-4
CAS:<p>HBV-IN-4, a phthalazinone, inhibits HBV DNA replication orally (IC50: 14 nM), encouraging genome-free capsids with strong anti-HBV effects.</p>Formula:C24H19ClFN5O3Color and Shape:SolidMolecular weight:479.89Cylindrospermopsin
CAS:<p>Cylindrospermopsin: a toxic cyanobacterial uracil derivative, disrupts protein/glutathione synthesis in hepatocytes, and is genotoxic.</p>Formula:C15H21N5O7SColor and Shape:SolidMolecular weight:415.42EGFR/HER2/TS-IN-2
CAS:<p>EGFR/HER2/TS-IN-2: Strong EGFR, HER2 & TS inhibitor; EGFR IC50=0.173μM, HER2 IC50=0.125μM, TS IC50=1.12μM; kills MDA-MB-231 cells (IC50=1.69μM).</p>Formula:C26H21N7OS2Color and Shape:SolidMolecular weight:511.62BAY-707
CAS:<p>BAY-707: tolerable in mice, no anticancer efficacy; potent, selective MTH1 inhibitor, IC50 = 2.3 nM; good PK profile.</p>Formula:C15H20N4O2Purity:98%Color and Shape:SolidMolecular weight:288.34
