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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 708 productos de "Síntesis de ADN / ARN"

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  • SCR130

    CAS:
    <p>SCR130 (1,7,9-Triazaspiro[4.5]dec-1-ene-6,10-dione, 2,4-bis(4-chlorophenyl)-8-thioxo-) 是基于 SCR7 的 DNA 非同源末端连接抑制剂,可诱导细胞凋亡并,具有抗癌活性。 它特异性依赖连接酶 IV,抑制 DNA 的末端连接。</p>
    Fórmula:C19H13Cl2N3O2S
    Pureza:98.9%
    Forma y color:Solid
    Peso molecular:418.3
  • 360A

    CAS:
    <p>360A is a stabilizing G-Quadruplex ligand, and also inhibits telomerase activity for telomerase in TRAP-G4 assay(IC50 : 300 nM).</p>
    Fórmula:C27H23N5O2
    Pureza:98.68%
    Forma y color:Solid
    Peso molecular:449.5
  • PCNA-I1

    CAS:
    <p>PCNA-I1 is an inhibitor targeting PCNA chromatin association in prostate cancer.</p>
    Fórmula:C17H14N2O2S
    Pureza:97.64%
    Forma y color:Solid
    Peso molecular:310.37
  • 6-AZATHYMINE

    CAS:
    <p>6-azathymine inhibits D-3-aminoisobutyrate-pyruvate aminotransferase; 6-azauracil competes with beta-alanine, uncompetitive with pyruvic acid, Ki ~8.9 mM.</p>
    Fórmula:C4H5N3O2
    Pureza:99.47%
    Forma y color:Solid
    Peso molecular:127.1
  • RI-2

    CAS:
    <p>RI-2, a potent RAD51 inhibitor, has a 44.17 μM IC50 and selectively blocks human HR repair.</p>
    Fórmula:C21H18Cl2N2O4
    Pureza:99.63% - 99.86%
    Forma y color:Solid
    Peso molecular:433.28
  • AT-130

    CAS:
    <p>AT-130: Strong HBV inhibitor (IC50 0.13 μM), low toxicity in HepAD38, hinders RNA packaging.</p>
    Fórmula:C22H22BrN3O5
    Pureza:97.81%
    Forma y color:Solid
    Peso molecular:488.33
  • CRT0044876

    CAS:
    <p>CRT0044876 (7-NO2-ICA) is a potent and selective APE1 inhibitor with IC50 of ~3 μM.</p>
    Fórmula:C9H6N2O4
    Pureza:98.27% - 98.98%
    Forma y color:Brown Powder
    Peso molecular:206.15
  • Ro5-3335

    CAS:
    <p>Ro5-3335 (CBFβ-Runx1 inhibitor II) is core binding factor (CBF) inhibitor; preferentially kills human leukemia cell lines with CBF fusion proteins.</p>
    Fórmula:C13H10ClN3O
    Pureza:99.42% - 99.87%
    Forma y color:Solid
    Peso molecular:259.69
  • Favipiravir

    CAS:
    <p>Favipiravir is a potent and selective RNA-dependent RNA polymerase inhibitor for the treatment of influenza virus infections.Cost-effective and quality-assured.</p>
    Fórmula:C5H4FN3O2
    Pureza:97.32% - 99.90%
    Forma y color:Solid
    Peso molecular:157.1
  • Quarfloxin

    CAS:
    <p>Quarfloxin (CX-3543), a fluoroquinolone, inhibits neuroblastoma with nanomolar IC50, disrupting nucleolin and G-quadruplex DNA.</p>
    Fórmula:C35H33FN6O3
    Pureza:99.77%
    Forma y color:Solid
    Peso molecular:604.67
  • Madrasin

    CAS:
    <p>Madrasin (DDD00107587) is a potent and cell penetrant splicing inhibitor that interferes with the early stages of spliceosome assembly.</p>
    Fórmula:C16H17N5O2
    Pureza:99.06% - 99.61%
    Forma y color:Solid
    Peso molecular:311.34
  • Nimustine Hydrochloride

    CAS:
    <p>Nimustine Hydrochloride (Nidran hydrochloride) has been used in trials studying the treatment of Glioblastoma.</p>
    Fórmula:C9H14Cl2N6O2
    Pureza:98.80%
    Forma y color:Solid
    Peso molecular:309.15
  • Cidofovir

    CAS:
    <p>Cidofovir ((S)-HPMPC) 通过特异性抑制病毒 DNA 合成来抑制病毒复制。</p>
    Fórmula:C8H14N3O6P
    Pureza:99.24% - 99.76%
    Forma y color:Fluffy White Powder
    Peso molecular:279.19
  • RAD51-IN-1

    CAS:
    <p>Rad51-in-1 is a derivative of B02 and an effective inhibitor of Rad51.</p>
    Fórmula:C22H16ClN3O
    Pureza:99.95%
    Forma y color:Solid
    Peso molecular:373.83
  • 3-Hydroxy-2-methylpyridine

    CAS:
    <p>3-Hydroxy-2-methylpyridine could as a promising molecular scaffold for the future development of novel fibrillization inhibitors.</p>
    Fórmula:C6H7NO
    Pureza:98.96% - 99.03%
    Forma y color:Beige-Brown Powder
    Peso molecular:109.13
  • NITD-2

    CAS:
    <p>NITD-2 is a DENV RdRp inhibitor with poor cell membrane penetration; no vaccine or antiviral for DENV exists.</p>
    Fórmula:C23H19N3O4S
    Pureza:98.03% - 99.46%
    Forma y color:Solid
    Peso molecular:433.48
  • CBFβ Inhibitor

    CAS:
    <p>CBFβ Inhibitor (5-Ethyl-4-(4-methoxy-phenyl)-thiazol-2-ylamine) is a cell-permeable CBFβ inhibitor and inhibits its association with Runx1.</p>
    Fórmula:C12H14N2OS
    Pureza:96.50%
    Forma y color:Solid
    Peso molecular:234.32
  • CX-5461

    CAS:
    <p>CX5461 is an orally rRNA synthesis inhibitor that inhibits Pol I-driven rRNA transcription. CX5461 has antitumor activity. Cost-effective and quality-assured.</p>
    Fórmula:C27H27N7O2S
    Pureza:95.44% - 99.25%
    Forma y color:Solid
    Peso molecular:513.61
  • BVDV-IN-1

    CAS:
    <p>BVDV-IN-1 is a non-nucleoside inhibitor (NNI) of bovine viral diarrhea virus (BVDV), with an EC50 of 1.8 μM.</p>
    Fórmula:C20H22N4O
    Pureza:98.43%
    Forma y color:Solid
    Peso molecular:334.41
  • Danofloxacin

    CAS:
    <p>Danofloxacin (Danofloxacin free base) is a fluoroquinolone antibiotic used in veterinary medicine.</p>
    Fórmula:C19H20FN3O3
    Pureza:99.77% - 99.8%
    Forma y color:Solid
    Peso molecular:357.38