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Señalización PI3K / Akt / mTOR

Señalización PI3K / Akt / mTOR

Los inhibidores de la señalización PI3K/Akt/mTOR son compuestos que se dirigen a las vías de la fosfoinositida 3-cinasa (PI3K), la cinasa Akt y el blanco de la rapamicina en mamíferos (mTOR). Estas vías son reguladores críticos del crecimiento celular, la supervivencia, el metabolismo y la autofagia, lo que las convierte en objetivos clave en la investigación del cáncer y los trastornos metabólicos. Inhibir estas vías puede ayudar a controlar el crecimiento y la proliferación tumoral, ofreciendo potenciales estrategias terapéuticas para varios tipos de cáncer y otras enfermedades caracterizadas por una señalización celular desregulada. En CymitQuimica, ofrecemos una amplia selección de inhibidores de alta calidad de PI3K/Akt/mTOR para apoyar su investigación en oncología, señalización celular y enfermedades metabólicas.

Subcategorías de "Señalización PI3K / Akt / mTOR"

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Se han encontrado 1038 productos de "Señalización PI3K / Akt / mTOR"

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  • O-Desmethyl gefitinib

    CAS:
    <p>O-Desmethyl gefitinib is an active EGFR inhibitor (IC50: 36 nM), a metabolite of Gefitinib, formed by CYP2D6.</p>
    Fórmula:C21H22ClFN4O3
    Pureza:97.17%
    Forma y color:Solid
    Peso molecular:432.88
  • LCH-7749944

    CAS:
    <p>LCH-7749944 suppresses human gastric cancer cell growth, induces apoptosis, and inhibits PAK4 with IC50 of 14.93 μM.</p>
    Fórmula:C20H22N4O2
    Pureza:99.48%
    Forma y color:Solid
    Peso molecular:350.41
  • NSC781406

    CAS:
    <p>NSC781406 is a highly effective inhibitor of PI3K and mTOR (IC50: 2 nM for PI3Kα).</p>
    Fórmula:C29H27F2N5O5S2
    Pureza:99.58%
    Forma y color:Solid
    Peso molecular:627.68
  • Petosemtamab

    CAS:
    <p>Petosemtamab (MCLA 158), a dual-action monoclonal antibody targets EGFR &amp; LGR5, used in solid tumor research like HNSCC &amp; CRC.</p>
    Pureza:> 95% - > 95%
    Forma y color:Liquid
    Peso molecular:145.97 kDa
  • GSK-3 inhibitor 4

    CAS:
    <p>Orally active GSK-3 inhibitor 4 targets GSK-3α/β, CDK2/5 (IC50: 0.45-0.68 μM) and may aid in Alzheimer's research by lowering Tau protein.</p>
    Fórmula:C22H15F2N5O
    Pureza:99.41%
    Forma y color:Soild
    Peso molecular:403.38
  • STL127705

    CAS:
    <p>STL127705 inhibits Ku 70/80 protein &amp; DNA-PKCS kinase, IC50s: 3.5 μM &amp; 2.5 μM.</p>
    Fórmula:C22H20FN5O4
    Pureza:99.53% - 99.81%
    Forma y color:Solid
    Peso molecular:437.42
  • LTURM34

    CAS:
    <p>LTURM34 is an inhibitor of DNA-PK with IC50 of 34 nM.</p>
    Fórmula:C24H18N2O3S
    Pureza:99.34%
    Forma y color:Solid
    Peso molecular:414.48
  • Erlotinib hydrochloride

    CAS:
    <p>Erlotinib hydrochloride (NSC 718781) is an EGFR inhibitor (IC50: 2 nM). It is used for the treatment of non-small cell lung cancer.</p>
    Fórmula:C22H23N3O4·HCl
    Pureza:99.78% - 99.85%
    Forma y color:White Or Off-White Powder
    Peso molecular:429.9
  • Varlitinib Tosylate

    CAS:
    <p>Varlitinib Tosylate is a selective and potent inhibitor of ErbB1(EGFR) and ErbB2(HER2).</p>
    Fórmula:C36H35ClN6O8S3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:811.34
  • Anticancer agent 271


    <p>Anticanceragent 271 (compound 5C) exhibits antiproliferative activity against lung cancer (A549), colon cancer (Caco-2) cell lines, and human lung fibroblasts (WI38), with an IC50 value of 9.18 μM for A549 cells. This compound can downregulate PI3K and mTOR gene expression and is applicable in cancer research.</p>
    Forma y color:Odour Solid
  • RMC-4529

    CAS:
    <p>RMC-4529 is a chemical compound that demonstrates potent inhibition, with an IC50 value of 1.0 nM, against p-4E-BP1-(T37/46) in mTOR kinase cellular assays.</p>
    Fórmula:C90H139N13O23
    Forma y color:Solid
    Peso molecular:1771.17
  • IBI-334


    <p>IBI-334 is a bispecific antibody targeting both B7-H3 and EGFR. It features an EGFR arm responsible for signal blocking, connected to a modified B7-H3 arm that ensures optimal affinity and binding. The antibody is afucosylated to enhance its antibody-dependent cellular cytotoxicity (ADCC) effects. IBI-334 is widely applicable in EGFR-driven solid tumors.</p>
    Forma y color:Odour Liquid
  • Duligotuzumab

    CAS:
    <p>Duligotuzumab is a dual-targeting anti-EGFR/HER3 mAb that blocks signaling and induces ADCC for tumors with poor prognosis.</p>
    Pureza:95% - 95%
    Forma y color:Liquid
  • Cetuximab MMAE


    <p>Cetuximab-MMAE, an antibody-drug conjugate (ADC), combines an EGFR-targeting antibody with Monomethyl auristatin E (MMAE) to investigate colorectal and head and neck cancers.</p>
    Forma y color:Liquid
    Peso molecular:150 kDa
  • YH32367


    <p>YH32367 (ABL105) is a bispecific antibody targeting HER2 and 4-1BB. It induces the secretion of IFN-γ, resulting in the death of tumor cells when co-cultured with hPBMC and HER2-expressing tumor cells. YH32367 demonstrates notable antitumor activity.</p>
    Forma y color:Odour Liquid
  • Lyso-Monosialoganglioside GM3

    CAS:
    <p>Lyso-Monosialoganglioside GM3 (Lyso-GM3) is an analog of Ganglioside GM3 with antitumor properties. It inhibits the increase in EGFR kinase activity induced by EGF in A431 epithelial cancer cells.</p>
    Fórmula:C41H74N2O20
    Forma y color:Solid
    Peso molecular:915.028
  • HER2/neu (654-662) GP2

    CAS:
    <p>Phage display selected Affibody ligands for HER2/neu from a protein library based on a 58-residue Staphylococcal protein A Z domain.</p>
    Fórmula:C42H77N9O11
    Pureza:98%
    Forma y color:Solid
    Peso molecular:884.11
  • Tephrosin

    CAS:
    <p>Tephrosin induces degradation of of EGFR and ErbB2 by inducing internalization of the receptors, has potent antitumor activities.</p>
    Fórmula:C23H22O7
    Pureza:98%
    Forma y color:Solid
    Peso molecular:410.42
  • Multi-target kinase inhibitor 4


    <p>Multi-target kinase inhibitor 4 (Compound 2) is a PI3K/DNA-PK inhibitor and a potent chemosensitizer that enhances the number of DNA double-strand breaks induced by Doxorubicin. It serves as an effective multidrug resistance (MDR) inhibitor, demonstrating inhibitory activity against P-glycoprotein (P-gp) mediated drug efflux. Multi-target kinase inhibitor 4 can be encapsulated in PEG-coated lipid nanoparticles.</p>
    Forma y color:Odour Solid
  • Duvelisib (R enantiomer) hydrochloride


    <p>Duvelisib (R enantiomer) hydrochloride (INK1197 R enantiomer HCl) is a PI3K inhibitor.</p>
    Fórmula:C22H18Cl2N6O
    Pureza:99.88% - >99.99%
    Forma y color:Soild
    Peso molecular:453.32