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Señalización citoesquelética

Señalización citoesquelética

Los inhibidores de la señalización del citoesqueleto son compuestos que interrumpen las vías de señalización que regulan el citoesqueleto, crucial para la forma celular, la motilidad, la división y el transporte intracelular. Estos inhibidores se utilizan para estudiar la dinámica de las proteínas del citoesqueleto, como la actina y la tubulina, y su papel en procesos como la migración celular, la adhesión y la metástasis del cáncer. Los inhibidores de la señalización del citoesqueleto son valiosos en la investigación sobre biología celular, cáncer y neurobiología. En CymitQuimica, ofrecemos una amplia gama de inhibidores de la señalización del citoesqueleto de alta calidad para apoyar su investigación en estas áreas.

Se han encontrado 1460 productos de "Señalización citoesquelética"

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  • DHNQ

    CAS:
    <p>DHNQ is a novel inhibitor of the PI3K enzyme activity and transcriptional as well as translational expression levels in colorectal cancer (CRC).</p>
    Fórmula:C18H14N2O
    Forma y color:Solid
    Peso molecular:274.32
  • NSC305787

    CAS:
    NSC305787 is an ezrin inhibitor with antitumor activity, inhibits ezrin phosphorylation caused by PKCΙ, and can be used in the study of pancreatic cancer.
    Fórmula:C25H30Cl2N2O
    Pureza:99.40%
    Forma y color:Solid
    Peso molecular:445.42
  • Clathrin-IN-25

    CAS:
    Clathrin-IN-25 is the most effective clathrin terminal domain-amphiphysin inhibitor reported to date.
    Fórmula:C19H13KNO5S
    Forma y color:Solid
    Peso molecular:406.47
  • BGB659

    CAS:
    <p>BGB659 is effective inhibitor of RAF.</p>
    Fórmula:C29H29F3N4O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:538.56
  • Retaspimycin Hydrochloride

    CAS:
    Retaspimycin Hydrochloride is a potent and water-soluble Hsp90 inhibitor(Hsp90 and Grp9 with EC50s of 119 nM).
    Fórmula:C31H46ClN3O8
    Pureza:98%
    Forma y color:Solid
    Peso molecular:624.17
  • Anticancer agent 48

    CAS:
    <p>Compound 48: broad-spectrum, anti-proliferative, inhibits microtubules, active in vivo, with potential for tumor research.</p>
    Fórmula:C26H25N3O4
    Forma y color:Solid
    Peso molecular:443.49
  • CAY10701

    CAS:
    CAY10701, a 7-deazahypoxanthine, impedes cell growth (GI50: 9-38 nM) while sparing normal fibroblasts (>1,500-fold), and shrinks mouse colorectal tumors.
    Fórmula:C24H19N3O2
    Forma y color:Solid
    Peso molecular:381.43
  • ME-143

    CAS:
    ME-143, a 2nd-gen NADH oxidase inhibitor, blocks WNT/β-catenin pathway, active against various cancers in vitro/vivo.
    Fórmula:C21H18O4
    Forma y color:Solid
    Peso molecular:334.37
  • GR 144053 trihydrochloride

    CAS:
    <p>platelet fibrinogen receptor glycoprotein IIb/IIIa (GpIIb/IIIa) antagonist</p>
    Fórmula:C18H30Cl3N5O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:454.82
  • EMD534085

    CAS:
    <p>EMD534085 is an effective and selective mitotic kinesin-5 inhibitor (IC50: 8 nM).</p>
    Fórmula:C25H31F3N4O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:476.53
  • 6BrCaQ

    CAS:
    <p>6BrCaQ inhibits TRAP1, has antiproliferative effects, and is used in 6BrCaQ-TPP synthesis.</p>
    Fórmula:C18H15BrN2O3
    Forma y color:Solid
    Peso molecular:387.23
  • MPC-3100

    CAS:
    <p>MPC-3100 is an orally bioavailable, synthetic, second-generation small-molecule inhibitor of Hsp90 with significant antitumor activity [1].</p>
    Fórmula:C22H25BrN6O4S
    Forma y color:Solid
    Peso molecular:549.44
  • Tau-aggregation-IN-1

    CAS:
    Tau-aggregation-IN-1 is a dopamine D2 and D3 receptor agonist and an inhibitor of tau441 protein aggregation (IC50: 21 μM).
    Fórmula:C28H37N5O2S
    Forma y color:Solid
    Peso molecular:507.69
  • Hydromethylthionine HBr

    CAS:
    <p>Hydromethylthionine (LMTM/Leucomethylene Blue) inhibits tau in Alzheimer's/frontotemporal dementia and improves brain function.</p>
    Fórmula:C16H21Br2N3S
    Forma y color:Solid
    Peso molecular:447.233
  • Ellipticine quinone

    CAS:
    Ellipticine quinone (NSC-383230) outperforms mdivi-1 in inhibiting Drp1, reduces lung cancer growth, and lessens IR injury by curbing mitochondrial issues.
    Fórmula:C15H8N2O2
    Forma y color:Solid
    Peso molecular:248.24
  • MK-0668 Mesylate

    CAS:
    MK-0668 Mesylate is the mesylate form of MK-0668 that is a very potent and orally active very late antigen-4 antagonist.
    Fórmula:C32H34Cl2N6O9S2
    Forma y color:Solid
    Peso molecular:781.68
  • Tubulin polymerization-IN-7

    CAS:
    <p>Tubulin aggregation-IN-7 is a potent tubulin aggregation inhibitor that has shown research potential for cancer diseases.</p>
    Fórmula:C28H24N4O6S
    Forma y color:Solid
    Peso molecular:544.58
  • NC043

    CAS:
    NC043 is an inhibitor of Wnt/β-catenin signaling, it forms a covalent bond with the Cys-516 residue of CARF.
    Fórmula:C20H26O4
    Pureza:98%
    Forma y color:Solid
    Peso molecular:330.42
  • S-methyl DM1

    CAS:
    S-methyl DM1 is a thiomethyl derivative of Maytansine. S-methyl DM1 binds to tubulin(Kd of 0.93 μM) and inhibts microtubule polymerization.
    Fórmula:C36H50ClN3O10S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:752.31
  • Tubulin polymerization-IN-39


    <p>Tubulin-IN-39 inhibits polymerization (IC50: 4.9 μM), blocks colchicine site, stops cancer growth.</p>
    Fórmula:C21H21N5O5
    Forma y color:Solid
    Peso molecular:423.42