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Ras

Ras

Ras proteins are small GTPases that act as molecular switches in the MAPK signaling pathway, controlling cell growth, differentiation, and survival. Activated Ras initiates a signaling cascade that includes Raf, MEK, and ERK, leading to various cellular responses. Mutations in Ras genes are common in cancers, making Ras an important focus of cancer research. At CymitQuimica, we offer a range of Ras modulators to support your research in cancer biology, signal transduction, and therapeutic development.

Found 175 products for "Ras".

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  • K-Ras G12C-IN-4

    CAS:
    K-Ras G12C-IN-4 是一种 KRAS G12C 共价抑制剂。
    Formula:C31H33ClN4O4
    Purity:99.41%
    Color and Shape:White Solid
    Molecular weight:561.071
  • Ketoconazole

    CAS:
    Ketoconazole (R-41400), a CYP3A4 inhibitor, is an imidazole anti-fungal agent.
    Formula:C26H28Cl2N4O4
    Purity:99.53% - 99.95%
    Color and Shape:White Solid
    Molecular weight:531.43
  • ARS-1630

    CAS:
    ARS-1630 is a mutant K-ras G12C inhibitor. It is a less active enantiomer of ARS-1620.
    Formula:C21H17ClF2N4O2
    Purity:97.78%
    Color and Shape:Solid
    Molecular weight:430.84
  • BI-3406

    CAS:
    BI-3406 is an orally active, highly potent and selective between KRAS and Son of Sevenless 1 (SOS1) interaction inhibitor(IC50 : 6 nM),with anticancer activity.
    Formula:C23H25F3N4O3
    Purity:99.2% - 99.66%
    Color and Shape:Solid
    Molecular weight:462.4648
  • MRTX-1257

    CAS:
    MRTX-1257: selective, irreversible KRAS G12C inhibitor; IC50 of 900 pM; 31% bioavailable in mice; 77% target engagement.
    Formula:C33H39N7O2
    Purity:96.76% - 97.3%
    Color and Shape:Yellow Solid
    Molecular weight:565.7085
  • HJC0197

    CAS:
    HJC0197 is a selective Epac antagonist; blocks cAMP-induced activation with IC50=5.9 μM for Epac2.
    Formula:C19H21N3OS
    Purity:98.05%
    Color and Shape:Solid
    Molecular weight:339.455
  • MBQ-167

    CAS:
    MBQ-167 is a dual inhibitor of Rac/Cdc42 (IC50s: 103 nM for Rac 1/2/3 and 78 nM for Cdc42 in MDA-MB-231 cells, respectively).
    Formula:C22H18N4
    Purity:98.07% - 99.52%
    Color and Shape:Solid
    Molecular weight:338.4051
  • MAPK Inhibitor Library


    A unique collection of xnum cancer cell differentiation inducing compounds for high throughput and high content screening;
    Color and Shape:Odour Solid
  • Sotorasib-D7


    Sotorasib-D7 is a deuterium-labeled version of Sotorasib. Sotorasib (T8684) (AMG-510) is a potent, orally bioavailable, selective covalent inhibitor of KRAS G12C. It locks KRAS G12C in the inactive GDP-bound state and causes regression of locally advanced or metastatic non-small cell lung cancer (NSCLC) with KRAS G12C mutation.
  • MC 976

    CAS:
    MC 976 is a derivative of Vitamin D3.
    Formula:C27H42O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:414.63
  • pan-KRAS-IN-8


    pan-KRAS-IN-8 (Compound 38) is an inhibitor of the human tumor mutated gene KRAS. It effectively suppresses the proliferation of KRAS mutant cells AsPC-1 (G12D mutant) and SW480 (G12V mutant), with IC50 values of 0.07 nM and 0.18 nM, respectively.
    Formula:C48H61N7O7S
    Molecular weight:879.43532
  • GGDPS-IN-1


    GGDPS-IN-1 (Compound 37) is an inhibitor of geranylgeranyl diphosphate synthase (GGDPS) with an IC50 of 49.4 nM, disrupting protein geranylgeranylation in myeloma cells.
    Formula:C15H28N4O6P2
    Color and Shape:Solid
    Molecular weight:422.14841
  • RAS GTPase inhibitor 1

    CAS:
    RAS GTPase inhibitor 1 Free Base is a highly potent RAS GTPase inhibitor with antitumor activity.
    Formula:C25H27ClFN5
    Color and Shape:White Solid
    Molecular weight:451.97
  • ADT-007

    CAS:
    ADT-007 is a pan-RAS inhibitor with potent anticancer activity.
    Formula:C26H24FNO5
    Purity:98.82%
    Color and Shape:Yellow Solid
    Molecular weight:449.47
  • KRAS-IN-47

    CAS:
    KRAS-IN-47 (Example 28) is a KRAS inhibitor with an IC50 value of less than 50 nM for KRAS G12V. It is applicable in cancer research.
    Formula:C33H29F5N6O2
    Molecular weight:638.64
  • KRASG12C IN-14


    KRASG12C IN-14 (compound 15), a potent inhibitor specifically designed for the KRAS G12C mutation, exhibits impressive efficacy in impeding CYPA-dependent KRAS-BRAF interaction and ERK phosphorylation in NCI-H358 cells, both with an IC 50 of 0.002 μM.
    Formula:C51H65F4N9O9S2
    Color and Shape:Solid
    Molecular weight:1088.24
  • TAT-PAK18 R192A


    TAT-PAK18 R192A is an inactive Tat-Pak peptide. It does not influence Rac1 translocation triggered by any tested proteins.
    Formula:C143H247N55O37
    Molecular weight:3326.91369
  • (RS)-G12Di-1


    (RS)-G12Di-1 is a selective covalent inhibitor of K-Ras-G12D.
    Formula:C37H35FN6O4
    Color and Shape:Solid
    Molecular weight:646.27038
  • ASP6918


    ASP6918 is a potent, orally active KRAS G12C inhibitor with an IC50 of 0.028 µM. It inhibits cell growth and demonstrates antitumor activity.
    Formula:C36H43N7O3
    Color and Shape:Solid
    Molecular weight:621.34274
  • KRAS-IN-43


    KRAS-IN-43 (Compound 9) is a broad-spectrum KRAS inhibitor with IC50 values of 0.15 μM for KRASG12V, 0.14 μM for KRASG12C, and 0.47 μM for wild-type KRAS. It disrupts the interaction between KRAS and cRAF and suppresses ERK phosphorylation. KRAS-IN-43 shows potential for research in KRAS mutation-associated cancers, including pancreatic, colorectal, and lung cancers.
    Color and Shape:Odour Solid