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PI3K/Akt/mTOR Signaling

PI3K/Akt/mTOR Signaling

PI3K/Akt/mTOR signaling inhibitors are compounds that target the phosphoinositide 3-kinase (PI3K), Akt kinase, and mammalian target of rapamycin (mTOR) pathways. These pathways are critical regulators of cell growth, survival, metabolism, and autophagy, making them key targets in cancer research and metabolic disorders. Inhibiting these pathways can help to control tumor growth and proliferation, offering potential therapeutic strategies for various cancers and other diseases characterized by dysregulated cell signaling. At CymitQuimica, we offer a comprehensive selection of high-quality PI3K/Akt/mTOR inhibitors to support your research in oncology, cellular signaling, and metabolic diseases.

Subcategories of "PI3K/Akt/mTOR Signaling"

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Found 1037 products of "PI3K/Akt/mTOR Signaling"

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  • OTSSP167

    CAS:
    <p>OTSSP167 (OTS167) is an orally available inhibitor of maternal embryonic leucine zipper kinase (MELK) with potential antineoplastic activity.</p>
    Formula:C25H28Cl2N4O2
    Purity:98.22% - 99.47%
    Color and Shape:Solid
    Molecular weight:487.42
  • AS-041164

    CAS:
    <p>AS-041164: Oral PI3Kγ inhibitor, IC50 70 nM; weaker on PI3Kα/β/δ; anti-inflammatory.</p>
    Formula:C11H7NO4S
    Purity:99.45%
    Color and Shape:Solid
    Molecular weight:249.24
  • Desmethyl Erlotinib

    CAS:
    <p>Desmethyl Erlotinib (CP-473420) is the active metabolite of Erlotinib (EGFR inhibitor with IC50 of 2 nM).</p>
    Formula:C21H21N3O4
    Purity:97.92% - 98.62%
    Color and Shape:Solid
    Molecular weight:379.41
  • WHI-P258

    CAS:
    <p>WHI-P258, a weak JAK3 inhibitor, is used as a negative control in drug development.</p>
    Formula:C16H15N3O2
    Purity:99.66% - 99.92%
    Color and Shape:Solid
    Molecular weight:281.31
  • IC-87114

    CAS:
    <p>IC-87114 is a specific PI3Kδ inhibitor(IC50=0.5 μM).</p>
    Formula:C22H19N7O
    Purity:99.30% - >99.99%
    Color and Shape:Solid
    Molecular weight:397.43
  • PQR620

    CAS:
    <p>PQR620 is a novel potent and selective, brain penetrant inhibitor of mTORC1/2.</p>
    Formula:C21H25F2N7O2
    Purity:97.61%
    Color and Shape:Solid
    Molecular weight:445.47
  • CC-115

    CAS:
    <p>CC-115 is a inhibitor of mTOR/DNA-PK (IC50= 21/ 13 nM).</p>
    Formula:C16H16N8O
    Purity:86.79% - 99.01%
    Color and Shape:Solid
    Molecular weight:336.35
  • PQR530

    CAS:
    <p>PQR530, a potent dual PI3K/mTORC1/2 inhibitor, blocks PKB and pS6 phosphorylation (IC50: 0.07 μM) and has antitumor properties.</p>
    Formula:C18H23F2N7O2
    Purity:99.5%
    Color and Shape:Solid
    Molecular weight:407.42
  • EX229

    CAS:
    <p>EX229 (C991) is an allosteric activator of AMPK, with Kds of 0.06 μM, 0.06 μM and 0.51 μM for α1β1γ1, α2β1γ1, and α1β2γ1, respectively.</p>
    Formula:C24H18ClN3O3
    Purity:99.20% - 99.36%
    Color and Shape:Solid
    Molecular weight:431.87
  • Olmutinib

    CAS:
    <p>Olmutinib is an oral mutant-specific EGFR inhibitor for cancer treatment with potential lower toxicity.</p>
    Formula:C26H26N6O2S
    Purity:99.63%
    Color and Shape:Solid
    Molecular weight:486.59
  • A-769662

    CAS:
    <p>A-769662 is an effective, reversible AMPK activator(EC50=0.8 μM).</p>
    Formula:C20H12N2O3S
    Purity:97.52% - 99.58%
    Color and Shape:Solid
    Molecular weight:360.39
  • EBE-A22

    CAS:
    <p>EBE-A22 (PD153035 Analog 63) is a derivative of PD 153035 which can inhibit ErbB-1-phosphorylation, whereas EBE-A22 is inactive.</p>
    Formula:C17H16BrN3O2
    Purity:99.087% - 99.88%
    Color and Shape:Solid
    Molecular weight:374.23
  • Tesevatinib

    CAS:
    <p>Tesevatinib (XL-647) is an oral, multi-targeted tyrosine kinase inhibitor.Cost-effective and quality-assured.</p>
    Formula:C24H25Cl2FN4O2
    Purity:97.89% - 98.66%
    Color and Shape:Solid
    Molecular weight:491.39
  • YU238259

    CAS:
    <p>YU238259 is a novel inhibitor of homology-dependent DNA repair(HDR), but does not inhibit non-homologous end-joining (NHEJ), in cell-based GFP reporter assays.</p>
    Formula:C22H22ClN3O4S
    Purity:99.28% - 99.56%
    Color and Shape:Solid
    Molecular weight:459.95
  • Cyasterone

    CAS:
    <p>Cyasterone (Cyasteron), a natural EGFR inhibitor, can inhibit the growth of A549 and MGC823 cells, via regulating EGFR signaling pathway, it may be a promising</p>
    Formula:C29H44O8
    Purity:99.32% - 99.70%
    Color and Shape:Solid
    Molecular weight:520.65
  • KU-0060648

    CAS:
    <p>KU-0060648 is a dual inhibitor of DNA-PK and PI3Kα, PI3Kβ, PI3Kδ with IC50 of 8.6 nM and 4 nM, 0.5 nM, 0.1 nM respectively, less inhibition of PI3Kγ.</p>
    Formula:C33H34N4O4S
    Purity:98.75%
    Color and Shape:Solid
    Molecular weight:582.71
  • Genistein

    CAS:
    <p>Genistein (NPI 031L) is a natural soy isoflavone, a multi-targeted tyrosine kinase inhibitor. Genistein has antitumor effects. Cost effective and quality assured.</p>
    Formula:C15H10O5
    Purity:98.22% - 99.64%
    Color and Shape:Rectangular Or Six-Sided Rods From 60% Alcohol Dendritic Needles From Ether Solid
    Molecular weight:270.24
  • Rostafuroxin

    CAS:
    <p>Rostafuroxin (PST 2238) has been used in trials studying the treatment of Essential Hypertension.</p>
    Formula:C23H34O4
    Purity:99.08% - >99.99%
    Color and Shape:Solid
    Molecular weight:374.51
  • WZ-3146

    CAS:
    <p>WZ3146: EGFR(L858R/E746_A750) inhibitor, IC50=2 nM, selective, doesn't block ERBB2(T798I).</p>
    Formula:C24H25ClN6O2
    Purity:97.15%
    Color and Shape:Solid
    Molecular weight:464.95
  • Almonertinib mesylate

    CAS:
    <p>Almonertinib mesylate: EGFR tyrosine kinase inhibitor, targets EGFR-mutant non-small cell lung cancer.</p>
    Formula:C31H39N7O5S
    Purity:99.92%
    Color and Shape:Solid
    Molecular weight:621.75