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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 1381 productos de "Señalización citoesquelética"

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  • MS98

    CAS:
    <p>MS98, a specific PROTAC AKT degrader, depletes T-AKT with DC50 of 78 nM; binds AKT1, AKT2, AKT3 with Kds of 4, 140, 8.1 nM.</p>
    Fórmula:C58H81ClN10O7S
    Forma y color:Solid
    Peso molecular:1097.86
  • gp96-II


    <p>Gp96-II is a gp96-blocking peptide that antagonizes cytokine production induced by gp96-mediated LPS. This compound is useful for research into inflammatory diseases.</p>
    Fórmula:C200H353N59O53S
    Forma y color:Solid
    Peso molecular:4464.37
  • β-catenin-IN-7


    <p>β-Catenin-IN-7 (Compound 9) is an inhibitor of β-catenin that disrupts its interaction with Tcf-4, consequently impeding Wnt-dependent gene expression, and</p>
    Fórmula:C17H13BrN2O2S
    Forma y color:Solid
    Peso molecular:389.27
  • hCA/Wnt/β-catenin-IN-1


    <p>hCA/Wnt/β-catenin-IN-1 (Compd 15) serves as an inhibitor with selective affinity for hCA isoforms II, IX, and XII, exhibiting K i values of 33.6, 24.1, and 6.8</p>
    Forma y color:Odour Solid
  • LY 379196


    <p>LY 379196, a potent PKC-β inhibitor (IC 50: 50 nM for PKC βI and 30 nM for PKC βII), effectively suppresses the proliferation of bovine retinal microvascular endothelial cells (BREC) induced by VEGF, IGF-1, and bFGF. This compound serves as an antiproliferative agent for proliferative retinopathy.</p>
    Fórmula:C30H34N4O5S
    Forma y color:Solid
    Peso molecular:562.68
  • 6BrCaQ-C10-TPP


    <p>6BrCaQ-C10-TPP inhibits TRAP1, halts cancer cell growth (IC50=0.008-0.30µM), disrupts mitochondrial membrane.</p>
    Fórmula:C45H47Br2N2O3P
    Forma y color:Solid
    Peso molecular:854.65
  • αVβ8-IN-1

    CAS:
    <p>αVβ8-IN-1 is an αVβ8 integrin inhibitor that suppresses the growth of multiple tumour cell lines (EMT6, CT26, KPC, TKCC-10).</p>
    Fórmula:C25H32ClN5O4
    Forma y color:Solid
    Peso molecular:502.01
  • JG-258

    CAS:
    <p>JG-258 is an inactive negative control for Hsp70 inhibitors [1] .</p>
    Fórmula:C20H22ClN3OS3
    Forma y color:Solid
    Peso molecular:452.06
  • SNIPER(ABL)-015


    <p>SNIPER(ABL)-015, a compound that conjugates GNF5 (ABL inhibitor) to MV-1 (IAP ligand) via a linker, effectively reduces BCR-ABL protein levels with a DC50 of 5</p>
    Fórmula:C58H70F3N9O9
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1094.23
  • TAT-Gap19

    CAS:
    <p>Cx43 blocker, IC50 ~7μM; doesn't affect gap junctions/Panx1. TAT motif enhances effect; works in vivo, brain-penetrant.</p>
    Fórmula:C119H212N46O26
    Pureza:98%
    Forma y color:Solid
    Peso molecular:2703.28
  • Tubulin inhibitor 36


    <p>Tubulin Inhibitor 36 (Compound 10) serves as a potent novel inhibitor of tubulin polymerization, which consequently induces apoptosis in glioblastoma cells,</p>
    Fórmula:C16H13ClN6S
    Forma y color:Solid
    Peso molecular:356.83
  • Bisindolylmaleimide III

    CAS:
    <p>Bisindolylmaleimide III is a potent and selective inhibitor of protein kinase C (PKC).Bisindolylmaleimide III selectively interacts with PKCα or ribosomal S6</p>
    Fórmula:C23H20N4O2
    Pureza:98.6%
    Forma y color:Solid
    Peso molecular:384.43
  • Zolbetuximab MMAE


    <p>Zolbetuximab MMAE (IMAB362 MMAE) is a compound targeting Claudin 18.2 (CLDN18.2) with anti-cancer activity, used in the study of gastric and pancreatic cancers.</p>
    Pureza:95% - 95%
    Forma y color:Liquid
    Peso molecular:150 kDa
  • Mps1-IN-6


    <p>Mps1-IN-6 is a potent Mps1 inhibitor that demonstrates antiproliferative and antitumor activities, exhibiting an IC50 of 2.596 nM [1].</p>
    Fórmula:C35H39N9O3
    Forma y color:Solid
    Peso molecular:633.74
  • Coronaridine

    CAS:
    <p>Coronaridine is a useful organic compound for research related to life sciences. The catalog number is T124824 and the CAS number is 467-77-6.</p>
    Fórmula:C21H26N2O2
    Forma y color:Solid
    Peso molecular:338.451
  • Tubulin polymerization-IN-46


    <p>Tubulin polymerization-IN-46 (compound 9q) is a microtubule/tubulin inhibitor that impedes tubulin polymerization, induces apoptosis, and arrests MCF-7 breast</p>
    Fórmula:C22H25NO6
    Forma y color:Solid
    Peso molecular:399.44
  • Ceratamine A

    CAS:
    <p>Ceratamine A, from Pseudoceratina sponge, is a cytotoxic, microtubule-stabilizing antimitotic alkaloid.</p>
    Fórmula:C17H16Br2N4O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:468.14
  • SNIPER(ABL)-058

    CAS:
    <p>SNIPER(ABL)-058, a compound that links Imatinib (ABL inhibitor) with a derivative of LCL161 (IAP ligand) through a linker, effectively decreases BCR-ABL protein</p>
    Fórmula:C62H75N11O9S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1150.39
  • KT D606

    CAS:
    <p>KT D606 is a PAK kinase family inhibitor with an IC50 of 4 μM. It selectively inhibits the proliferation of cancer cells transformed by oncogenic RAS mutants, making it useful for studying RAS/PAK1-induced cancers.</p>
    Fórmula:C59H50N6O10
    Forma y color:Solid
    Peso molecular:1003.06
  • Foxy-5

    CAS:
    <p>Foxy-5 is a wnt5a peptide mimetic</p>
    Fórmula:C26H42N6O12S2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:694.77