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c-Myc

c-Myc

c-Myc inhibitors target the c-Myc protein, a transcription factor that plays a pivotal role in cell growth, proliferation, and apoptosis. c-Myc regulates the expression of numerous genes involved in the cell cycle and is often overexpressed in various cancers, leading to uncontrolled cell proliferation and tumor growth. Inhibiting c-Myc can disrupt these processes, inducing cell cycle arrest and apoptosis in cancer cells. c-Myc inhibitors are important tools in cancer research and therapeutic development. At CymitQuimica, we offer a wide range of high-quality c-Myc inhibitors to support your research in oncology, cell cycle regulation, and transcriptional control.

Found 69 products of "c-Myc"

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  • EN4
    Targetmol
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    EN4

    CAS:
    <p>EN4 (EN4 MYC inhibitor) MYC inhibitor is a covalent ligand that targets cysteine 171 (C171) of MYC.</p>
    Formula:C25H24N2O4
    Purity:98.51%
    Color and Shape:Solid
    Molecular weight:416.47

    Ref: TM-T9061

  • PARL Protein, Human, Recombinant (Myc)
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    PARL Protein, Human, Recombinant (Myc)

    <p>Required for the control of apoptosis during postnatal growth.</p>
    Color and Shape:Lyophilized Powder
    Molecular weight:37.8 kDa (predicted)

    Ref: TM-TMPH-01898

  • ACOX1 Protein, Mouse, Recombinant (Myc)
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    ACOX1 Protein, Mouse, Recombinant (Myc)

    <p>Catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs.</p>
    Color and Shape:Lyophilized Powder
    Molecular weight:76.2 kDa (predicted)

    Ref: TM-TMPH-02825

  • 2-5A-dependent Rnase Protein, Human, Recombinant (Myc)
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    2-5A-dependent Rnase Protein, Human, Recombinant (Myc)

    <p>2-5A-dependent Rnase Protein, Human, Recombinant (Myc) is expressed in E.</p>
    Purity:85% - 85%
    Color and Shape:Lyophilized Powder
    Molecular weight:85.1 kDa (predicted)

    Ref: TM-TMPH-00847

  • c-Myc inhibitor 9
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    c-Myc inhibitor 9

    CAS:
    <p>c-Myc inhibitor 9 (compound 332) with logEC50 ≥6, suppresses tumors in mice, useful for cancer research.</p>
    Formula:C27H31N5OS
    Color and Shape:Solid
    Molecular weight:473.63

    Ref: TM-T72620

  • RK-9123016
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    RK-9123016

    CAS:
    <p>RK-9123016 is a SIRT2 inhibitor.</p>
    Formula:C16H18N6O3S
    Purity:99.65%
    Color and Shape:Solid
    Molecular weight:374.42

    Ref: TM-T28543

  • FUBP1-IN-2
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    FUBP1-IN-2

    CAS:
    <p>FUBP1-IN-2 hinders FUBP1, affects c-Myc and p21 expression, and depletes polyamines.</p>
    Formula:C26H26ClN3O4
    Color and Shape:Solid
    Molecular weight:479.96

    Ref: TM-T73166

  • KSI-3716
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    KSI-3716

    CAS:
    <p>KSI-3716 is a c-Myc inhibitor, a bladder chemotherapy agent that blocks the formation of complexes between c-MYC/MAX and target gene promoters.</p>
    Formula:C17H11BrCl2N2O2
    Purity:98.94%
    Color and Shape:Solid
    Molecular weight:426.09

    Ref: TM-T11783

  • BI8622
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    BI8622

    CAS:
    <p>BI8622 is a HUWE1 antagonist that restores levels of RP2 mutants in retinal cell lines and inhibits cellular activation of NLRP3 and AIM2 inflammatory vesicles.</p>
    Formula:C25H26N6O
    Purity:98.28%
    Color and Shape:Solid
    Molecular weight:426.51

    Ref: TM-T14568

  • VPC-70619
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    VPC-70619

    CAS:
    <p>VPC-70619: Oral, selective N-Myc inhibitor; blocks cancer growth by hindering N-Myc-Max/DNA binding; well-absorbed.</p>
    Formula:C16H8ClF3N4O
    Color and Shape:Solid
    Molecular weight:364.71

    Ref: TM-T9731

  • c-Myc inhibitor 8
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    c-Myc inhibitor 8

    CAS:
    <p>c-Myc inhibitor 8 suppresses cell growth in various cancers and is used in research.</p>
    Formula:C19H12BrClF3NO3S2
    Color and Shape:Solid
    Molecular weight:538.79

    Ref: TM-T72619

  • m-Se3
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    m-Se3

    CAS:
    <p>m-Se3 is a potent, selective inhibitor of c-MYC transcription with demonstrated capability to inhibit tumor growth and exhibit anti-cancer activity [1].</p>
    Formula:C29H23IN2Se
    Purity:98%
    Color and Shape:Solid
    Molecular weight:605.37

    Ref: TM-T79872

  • SYHA1815
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    SYHA1815

    CAS:
    <p>SYHA1815, an orally active RET inhibitor (IC50=0.9 nmol/L), demonstrates antitumor activity. It exhibits greater selectivity for RET over KDR (IC50=15.9 nmol/L). SYHA1815 operates by downregulating c-Myc, arresting the G1 cell cycle, and inhibiting RET-driven cell proliferation.</p>
    Formula:C27H26ClF4N5O
    Color and Shape:Solid
    Molecular weight:547.98

    Ref: TM-T200124

  • KI-CDK9d-32
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    KI-CDK9d-32

    CAS:
    <p>KI-CDK9d-32 is a CDK9 PROTAC degrader with a DC50 of 0.89 nM. It facilitates the ubiquitination and degradation of CDK9, inhibits the MYC pathway, and disrupts nucleolar homeostasis. KI-CDK9d-32 demonstrates anticancer activity.</p>
    Formula:C39H45N9O4
    Color and Shape:Solid
    Molecular weight:703.83

    Ref: TM-T207184

  • CymitQuimica logo
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    c-Myc inhibitor 4

    <p>Potent oral c-Myc inhibitor 4 reduces the proto-oncogene linked to tumor development.</p>
    Formula:C26H33FN6O3
    Color and Shape:Solid
    Molecular weight:496.58

    Ref: TM-T63359

  • BRD4 Inhibitor-40
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    BRD4 Inhibitor-40

    CAS:
    <p>BRD4 Inhibitor-40 (Compound 23) functions as an inhibitor of BRD, effectively targeting BRD4-BD1, BRD4-BD2, BRD2-BD1, and BRD2-BD2, with IC50 values of 16.1, 142.18, 29.35, and 302.35 nM, respectively. It modulates the expression of c-Myc and p21, induces cell cycle arrest in the G1 phase, and inhibits Pkd1-deficient (PN) renal cystic epithelial cells. Additionally, it prevents renal cyst formation in both Madin-Darby canine kidney and embryonic kidney cyst models, and demonstrates renal cyst inhibition activity in mouse models.</p>
    Formula:C27H32N8O
    Color and Shape:Solid
    Molecular weight:484.596

    Ref: TM-T205510

  • MY05
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    MY05

    CAS:
    <p>MY05 selectively targets c-MYC within cells and disrupts the interaction between MYC and MAX. It binds to intracellular c-MYC, modulating its thermal stability, reducing the transcriptional targets of c-MYC, and exhibiting anticancer activity (TNBC, triple-negative breast cancer).</p>
    Formula:C19H11ClN4O
    Color and Shape:Solid
    Molecular weight:346.77

    Ref: TM-T206537

  • JY-3-094
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    JY-3-094

    CAS:
    <p>JY-3-094 is a selective Myc inhibitor that targets the hydrophobic domain of Myc and inhibits the formation of the Myc-Max heterodimer, with an IC50 of 33 μM, and can be used for cancer research.</p>
    Formula:C13H8N4O5
    Purity:98.72%
    Color and Shape:Solid
    Molecular weight:300.23

    Ref: TM-T86777

  • β-catenin-IN-8
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    β-catenin-IN-8

    CAS:
    <p>β-catenin-IN-8 (Compound 25) is an inhibitor of β-catenin. It effectively lowers the levels of both β-catenin and c-Myc proteins and suppresses Wnt target genes (Fgf20 and Sall4). Additionally, β-catenin-IN-8 exhibits anticancer activity against colorectal cancer and possesses metabolic stability.</p>
    Formula:C15H12ClN3O2S
    Color and Shape:Solid
    Molecular weight:333.79

    Ref: TM-T201581