CymitQuimica logo
GTPasa

GTPasa

Las GTPasas son una familia de enzimas que hidrolizan el guanosín trifosfato (GTP) a guanosín difosfato (GDP), desempeñando un papel crucial en las vías de transducción de señales, incluidas las mediadas por GPCR. Las GTPasas actúan como interruptores moleculares en varios procesos celulares, como la división, el crecimiento y la diferenciación celular. La desregulación de la actividad de las GTPasas está implicada en numerosas enfermedades, incluido el cáncer y los trastornos genéticos. En CymitQuimica, ofrecemos una selección de moduladores de GTPasa de alta calidad para apoyar su investigación en señalización celular, biología del cáncer y vías relacionadas con GPCR.

Se han encontrado 28 productos para "GTPasa".

productos por página.
  • PT-129


    PT-129 is a PROTAC degrader targeting the NTF2 domain of G3BP1/2, degrading stress granules in stressed cells, suppressing proliferation.
    Fórmula:C46H48N8O12S
    Forma y color:Yellow Solid
    Peso molecular:936.98
  • RGS2-Galpha-q interaction-IN-1


    RGS2–Galpha-q interaction-IN-1 (Compound AJ-3) is an inhibitor of the RGS2-Galpha-q interaction. It inhibits the growth of cancer cell lines that express RGS2 and has anti-cell migration properties.
    Fórmula:C30H30ClN7O3
    Forma y color:Solid
    Peso molecular:572.06
  • Myristoylated ARF6 (2-13)


    Myristoylated ARF6 (2-13) inhibits the MyD88–ARNO–ARF6 signaling axis by inactivating ARF6.
    Fórmula:C74H128N16O18
    Forma y color:Solid
    Peso molecular:1528.95925
  • ART5537


    ART5537 is a selective EXO1 inhibitor with an EC50 of 55 nM, an IC50 of 3.4 nM, and a Kd of 6.8 nM. It inhibits the homologous recombination (HR) process in HAP1 parental cells with an EC50 of 7.2 nM. The selectivity of ART5537 for the broad-spectrum nuclease superfamily members is over 200-fold higher. Its biological effects are entirely driven by EXO1 inhibition. ART5537 enhances sensitivity to ionizing radiation and exhibits synergism with Olaparib. It is applicable in research on breast and colon cancers.
  • ARF6 (2-13)

    CAS:
    ARF6 (2-13), a peptide with the sequence GKVLSKIFGNKE, acts as an inhibitor of ARF6 and can be utilized in endotoxemia research [1].
    Fórmula:C60H102N16O17
    Peso molecular:1319.55
  • CID-1067700

    CAS:
    CID-1067700 is one of the first identified competitive inhibitors of nucleotide binding by Ras-related GTPases(Rab7 with a Ki of 13 nM).
    Fórmula:C18H18N2O4S2
    Pureza:99.46%
    Forma y color:Solid
    Peso molecular:390.477
  • Exo-1

    CAS:
    Exo-1 (Methyl 3-(4-fluorobenzoyl)-6-methyl-2-pyridinecarboxylate) is a synthetic compound that has been shown to affect the metabolism of various nutrients, as
    Fórmula:C15H12FNO3
    Pureza:99.45%
    Forma y color:White Solid
    Peso molecular:273.2591
  • BQU57

    CAS:
    BQU57 shows selective inhibition for Ral relative to Ras or Rho and inhibit xenograft tumor growth.
    Fórmula:C16H13F3N4O
    Pureza:97.45% - 98.72%
    Forma y color:Solid
    Peso molecular:334.2958
  • CCG-50014

    CAS:
    CCG-50014 is a potent and selective inhibitor of RGS4 with IC50 of 30 nM.
    Fórmula:C16H13FN2O2S
    Pureza:98.53%
    Forma y color:White Solid
    Peso molecular:316.35
  • Exo1

    CAS:
    Exo1 is an inhibitor of the exocytic pathway
    Fórmula:C15H12FNO3
    Pureza:98.75%
    Forma y color:Solid
    Peso molecular:273.26
  • MLS-573151

    CAS:
    MLS-573151 is a selective inhibitor of GTPase Cdc42(EC50 of 2 μM).
    Fórmula:C21H19N3O2S
    Pureza:98.80%
    Forma y color:White Solid
    Peso molecular:377.459
  • NAV-2729

    CAS:
    NAV-2729 inhibits six ArfGEFs (human ARNO, EFA6, BIG1, and BRAG2 and Legionella and Rickettsia RalF), the strongest effects being against BRAG2, Arf1 and Arf6.
    Fórmula:C25H17ClN4O3
    Pureza:98.91% - 99.57%
    Forma y color:Yellow Solid
    Peso molecular:456.88
  • RBC8

    CAS:
    RBC8 is a specific GTPases RalA/RalB inhibitor by inhibiting the binding of Ral to its effector RALBP1, no inhibition on the GTPases RhoA and Ras.
    Fórmula:C25H20N4O3
    Pureza:98.44% - 99.81%
    Forma y color:White Solid
    Peso molecular:424.4513
  • ML-097

    CAS:
    ML-097 (CID-2160985) is a pan activator of Ras-related GTPases
    Fórmula:C14H11BrO3
    Pureza:99.12%
    Forma y color:Solid
    Peso molecular:307.139
  • Dynamin inhibitory peptide Acetate


    Dynamin inhibitory peptide Acetate is a peptide with the sequence Gln-Val-Pro-Ser-Arg-Pro-Asn-Arg-Ala-Pro that inhibit the GTPase dynamin.
    Fórmula:C49H84N18O16
    Pureza:97.28%
    Forma y color:Solid
    Peso molecular:1181.3
  • Arf1-GEFs-IN-1

    CAS:
    Arf1-GEFs-IN-1 is a potent and orally active inhibitor of ADP-ribosylation factor 1-guanine nucleotide exchange factors (Arf1-GEFs), exhibiting an IC50 value of 40 μM in CT26 cells. Primarily, Arf1-GEFs-IN-1 induces tumor regression by triggering anti-tumor immune responses rather than direct cytotoxicity. It effectively enhances CCL5 expression and demonstrates excellent in vivo efficacy. Arf1-GEFs-IN-1 is applicable in colon cancer research.
    Fórmula:C19H18N6S
    Peso molecular:362.45
  • QS11

    CAS:
    QS11, a GTPase ARFGAP1, modulates ARF-GTP levels and synergizes with the Wnt/β-catenin signaling pathway to upregulate β-catenin nuclear translocation.
    Fórmula:C36H33N5O2
    Pureza:98.59%
    Forma y color:Solid
    Peso molecular:567.68
  • Bragsin1

    CAS:
    Bragsin1 is a potent and selective and noncompetitive ArfGEF BRAG2 inhibitor, inhibits Arf GTPase activation(IC50 : 3 μM),and with anti-cancer activity.
    Fórmula:C11H6F3NO4
    Forma y color:Solid
    Peso molecular:273.1648
  • CCG-2046

    CAS:
    CCG-2046 is a chemical inhibitor targeting RGS4, demonstrating an inhibition concentration (IC50) of 4.3 μM for the interaction between RGS4 and Gαo signal.
    Fórmula:C11H10N4
    Forma y color:Solid
    Peso molecular:198.2239
  • CCG-4986

    CAS:
    CCG-4986 is the first small molecule RGS inhibitor reported that directly bound to an RGS protein.
    Fórmula:C13H11ClN2O5S2
    Forma y color:Solid
    Peso molecular:374.82