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DNA/RNA Synthesis

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:C8H11N3O3S
    Purity:99.45%
    Color and Shape:Solid
    Molecular weight:229.26
  • ST7612AA1

    CAS:
    <p>ST7612AA1: potent, oral HDAC inhibitor; reactivates HIV-1 latency; shows antitumor effects; may study malaria.</p>
    Formula:C20H27N3O4S
    Purity:99.71%
    Color and Shape:Solid
    Molecular weight:405.51
  • Zelpolib

    CAS:
    <p>Zelpolib is a specific inhibitor of DNA polymerase δ (Pol δ), inhibiting DNA replication. antiproliferative.</p>
    Formula:C22H21N3O5S2
    Purity:98.79%
    Color and Shape:Solid
    Molecular weight:471.55
  • Homocarbonyltopsentin

    CAS:
    <p>Homocarbonyltopsentin: Small molecule, binds TSL2 pentaloops, enhances SMN2 E7 splicing, EC50 16 μM.</p>
    Formula:C21H14N4O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:370.36
  • 3'-Deoxyuridine-5'-triphosphate

    CAS:
    <p>3'-dUTP, a nucleotide analogue, competitively inhibits RNA polymerases I &amp; II, with a Ki of 2.0 µM.</p>
    Formula:C9H15N2O14P3
    Color and Shape:Solid
    Molecular weight:468.14
  • Phelorphan

    CAS:
    <p>Phelorphan is an inhibitor of enkephalinase.</p>
    Formula:C20H22N2O4S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:386.46
  • Beaucage reagent

    CAS:
    <p>Beaucage reagent, which is found to be effective in causing DNA cleavage.</p>
    Formula:C7H4O3S2
    Purity:98.50%
    Color and Shape:White To Off-White Powder
    Molecular weight:200.23
  • JFN05510

    CAS:
    <p>Compound: 3'-O-tert-BDMS-5'-O-DMT-N2-IBG 2'-CE phosphoramidite; has anticancer properties and activates enzymes.</p>
    Formula:C50H68N7O9PSi
    Color and Shape:Solid
    Molecular weight:970.18
  • Triaziquone

    CAS:
    <p>Triaziquone is an alkylating agent that can react with DNA to form intrastrand crosslinks.</p>
    Formula:C12H13N3O2
    Color and Shape:Solid
    Molecular weight:231.25
  • AS-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:C17H19F3N4O3S
    Purity:98.52%
    Color and Shape:Solid
    Molecular weight:416.42
  • HIPP

    CAS:
    <p>HIPP is a highly selective inhibitor of antineoplastic CtBP.</p>
    Formula:C9H9NO3
    Color and Shape:Solid
    Molecular weight:179.17
  • BMH-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:C16H17N3
    Color and Shape:Solid
    Molecular weight:251.33
  • Phen-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:C34H26N6O2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:550.61
  • NPD9948

    CAS:
    <p>NPD9948 is a competitive inhibitor of MTH1.</p>
    Formula:C13H14N6
    Color and Shape:Solid
    Molecular weight:254.29
  • MLAF50

    CAS:
    <p>MLAF50 is an inhibitor of the REV1 UBM2-Ubiquitin interaction.</p>
    Formula:C15H12I2O4
    Color and Shape:Solid
    Molecular weight:510.06
  • HIV-1 inhibitor-43

    CAS:
    <p>HIV-1 Inhibitor-43 suppresses HIV-1, with EC50: 21.3 nM (Y188L), 6.2 nM (K103N-Y181C), &lt;0.7 nM (K103N/Y181C), and lowers HIV RNA/p24 protein.</p>
    Formula:C24H21ClN2O4S
    Color and Shape:Solid
    Molecular weight:468.95
  • HBV-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:C24H19ClFN5O3
    Color and Shape:Solid
    Molecular weight:479.89
  • Cylindrospermopsin

    CAS:
    <p>Cylindrospermopsin: a toxic cyanobacterial uracil derivative, disrupts protein/glutathione synthesis in hepatocytes, and is genotoxic.</p>
    Formula:C15H21N5O7S
    Color and Shape:Solid
    Molecular weight:415.42
  • EGFR/HER2/TS-IN-2

    CAS:
    <p>EGFR/HER2/TS-IN-2: Strong EGFR, HER2 &amp; TS inhibitor; EGFR IC50=0.173μM, HER2 IC50=0.125μM, TS IC50=1.12μM; kills MDA-MB-231 cells (IC50=1.69μM).</p>
    Formula:C26H21N7OS2
    Color and Shape:Solid
    Molecular weight:511.62
  • BAY-707

    CAS:
    <p>BAY-707: tolerable in mice, no anticancer efficacy; potent, selective MTH1 inhibitor, IC50 = 2.3 nM; good PK profile.</p>
    Formula:C15H20N4O2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:288.34