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Síntesis de ADN / ARN

Síntesis de ADN / ARN

Los inhibidores de la síntesis de ADN y ARN son compuestos que interfieren con los procesos de replicación y transcripción en las células, impidiendo así la producción de material genético esencial. Estos inhibidores pueden dirigirse a diversas enzimas y proteínas involucradas en la síntesis de ácidos nucleicos, lo que los convierte en herramientas valiosas para estudiar los mecanismos de replicación, transcripción y traducción. También se utilizan en el desarrollo de tratamientos para infecciones y cáncer. En CymitQuimica, ofrecemos un amplio espectro de inhibidores de la síntesis de ADN/ARN para apoyar su investigación en biología molecular, virología y desarrollo terapéutico.

Se han encontrado 793 productos de "Síntesis de ADN / ARN"

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  • Photoregulin3

    CAS:
    Photoregulin3 is a inhibitor of rod photoreceptor gene expression, potentially though Nr2e3 modulation.
    Fórmula:C22H23N3O3
    Forma y color:Solid
    Peso molecular:377.44
  • 3'-Deoxyuridine-5'-triphosphate

    CAS:
    3'-dUTP, a nucleotide analogue, competitively inhibits RNA polymerases I & II, with a Ki of 2.0 µM.
    Fórmula:C9H15N2O14P3
    Forma y color:Solid
    Peso molecular:468.14
  • JFN05510

    CAS:
    Compound: 3'-O-tert-BDMS-5'-O-DMT-N2-IBG 2'-CE phosphoramidite; has anticancer properties and activates enzymes.
    Fórmula:C50H68N7O9PSi
    Forma y color:Solid
    Peso molecular:970.18
  • Cylindrospermopsin

    CAS:
    Cylindrospermopsin: a toxic cyanobacterial uracil derivative, disrupts protein/glutathione synthesis in hepatocytes, and is genotoxic.
    Fórmula:C15H21N5O7S
    Forma y color:Solid
    Peso molecular:415.42
  • Beaucage reagent

    CAS:
    Beaucage reagent, which is found to be effective in causing DNA cleavage.
    Fórmula:C7H4O3S2
    Pureza:98.50%
    Forma y color:White To Off-White Powder
    Peso molecular:200.23
  • BAY-707

    CAS:
    BAY-707: tolerable in mice, no anticancer efficacy; potent, selective MTH1 inhibitor, IC50 = 2.3 nM; good PK profile.
    Fórmula:C15H20N4O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:288.34
  • TDRL-X80

    CAS:
    TDRL-X80 inhibits XPA DNA binding; effective on single, double, and cisplatin-damaged DNA; IC50: 18-29 μM (FP), 21-39 μM (ELISA).
    Fórmula:C23H15ClN2O6
    Forma y color:Solid
    Peso molecular:450.83
  • Valomaciclovir

    CAS:
    Valomaciclovir is a DNA polymerase inhibitor potentially for treatment of acute herpes zoster and EB virus infection.
    Fórmula:C15H24N6O4
    Forma y color:Solid
    Peso molecular:352.39
  • MLAF50

    CAS:
    MLAF50 is an inhibitor of the REV1 UBM2-Ubiquitin interaction.
    Fórmula:C15H12I2O4
    Forma y color:Solid
    Peso molecular:510.06
  • 2-Fluoroadenine

    CAS:
    <p>2-Fluoroadenine (NSC-27364) has toxicity in nonproliferating and proliferating tumor cells. 2-Fluoroadenine can be used for anticancer studies.</p>
    Fórmula:C5H4FN5
    Pureza:98.84% - 99.62%
    Forma y color:White To Light Yellow Crystal Powder
    Peso molecular:153.12
  • ATB107

    CAS:
    ATB107 is a potent and novel inhibitor of indole-3-glycerol phosphate synthase (IGPS, KD: 3 μM).
    Fórmula:C21H28N8
    Pureza:98%
    Forma y color:Solid
    Peso molecular:392.5
  • Antibacterial agent 124

    CAS:
    Antibacterial agent 124 inhibits Sa ProRS with an IC50 of 0.18 μM.
    Fórmula:C16H17ClFN3O2
    Forma y color:Solid
    Peso molecular:337.78
  • NSC666715

    CAS:
    NSC666715 is the strand-displacement activity of DNA polymerase inhibitor.
    Fórmula:C15H13Cl2N5O2S2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:430.33
  • HBV-IN-4

    CAS:
    HBV-IN-4, a phthalazinone, inhibits HBV DNA replication orally (IC50: 14 nM), encouraging genome-free capsids with strong anti-HBV effects.
    Fórmula:C24H19ClFN5O3
    Forma y color:Solid
    Peso molecular:479.89
  • HBV-IN-16

    CAS:
    HBV-IN-16, a quinoline derivative, inhibits HBV cccDNA, key for viral replication (from patent WO2019121357A1).
    Fórmula:C22H20ClNO4
    Forma y color:Solid
    Peso molecular:397.85
  • Laromustine

    CAS:
    Laromustine (VNP40101M) is a sulfonyl hydrolysis alkylation prodrug for cancer treatment with significant anticancer activity, inhibiting thioredoxin reductase.
    Fórmula:C6H14ClN3O5S2
    Pureza:≥98%
    Forma y color:Solid
    Peso molecular:307.78
  • BPIC

    CAS:
    BPIC is an agent of anti-tumor that acts by inhibiting inflammation and scavenging free radicals.
    Fórmula:C27H20N2O5
    Forma y color:Solid
    Peso molecular:452.46
  • BMH-22

    CAS:
    BMH-22 is an RNA polymerase I inhibitor that acts by causing nucleolar stress and showing potent anticancer activity across many tumor types.
    Fórmula:C16H17N3
    Forma y color:Solid
    Peso molecular:251.33
  • Triaziquone

    CAS:
    Triaziquone is an alkylating agent that can react with DNA to form intrastrand crosslinks.
    Fórmula:C12H13N3O2
    Forma y color:Solid
    Peso molecular:231.25
  • EGFR/HER2/TS-IN-2

    CAS:
    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).
    Fórmula:C26H21N7OS2
    Forma y color:Solid
    Peso molecular:511.62