CymitQuimica logo
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"

Ordenar por

Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
productos por página.
  • NSC305787

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

    CAS:
    <p>Clathrin-IN-25 is the most effective clathrin terminal domain-amphiphysin inhibitor reported to date.</p>
    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
  • HR22C16

    CAS:
    <p>HR22C16 is an effective, selective, and cell-permeable mitotic kinesin Eg5 inhibitor.</p>
    Fórmula:C23H23N3O3
    Forma y color:Solid
    Peso molecular:389.45
  • CGP60474

    CAS:
    <p>CGP60474 is an inhibitor of VEGFR-2 (IC50 = 84 nM) and an inhibitor of ATP-competitive PKC.</p>
    Fórmula:C18H18ClN5O
    Pureza:98.81%
    Forma y color:Solid
    Peso molecular:355.82
  • DAT1

    CAS:
    <p>DAT1 is an antimitotic and antiangiogenic that acts by binding to the colchicine binding site of tubulin.</p>
    Fórmula:C17H15N3O2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:325.38
  • Shz 1

    CAS:
    <p>Shz 1 is a cardiogenic agent that induces phenotypic differentiation and various cardiac-specific genes including sarcomeric tropomyosin.</p>
    Fórmula:C13H11BrN2O3S
    Pureza:99.57% - 99.91%
    Forma y color:Solid
    Peso molecular:355.21
  • GSK-3008348

    CAS:
    <p>GSK-3008348 is an antagonist of integrin alpha(v)beta6.</p>
    Fórmula:C29H37N5O2
    Pureza:99.547%
    Forma y color:Solid
    Peso molecular:487.64
  • BNC105P

    CAS:
    <p>BNC105P, a prodrug VDA, converts to BNC105, blocks tubulin polymerization, disrupts tumor vessels, and evades P-glycoprotein resistance.</p>
    Fórmula:C20H21O10P
    Forma y color:Solid
    Peso molecular:452.3485
  • YM-01 Tosylate

    CAS:
    <p>YM-01 Tosylate, a potent antitumor agent, selectively targets cancer cells and overcoming tamoxifen resistance.</p>
    Fórmula:C27H27N3O4S3
    Forma y color:Solid
    Peso molecular:553.72
  • Displurigen

    CAS:
    <p>Displurigen is an inhibitor of ATPase activity of HSP70.</p>
    Fórmula:C15H10O4S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:286.3
  • NSC47924

    CAS:
    <p>NSC47924 is a laminin receptor (LR) inhibitor.</p>
    Fórmula:C18H17NO2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:279.33
  • ML-243

    CAS:
    <p>inhibitor of cancer stem cells</p>
    Fórmula:C14H16N2OS
    Pureza:98%
    Forma y color:Solid
    Peso molecular:260.35
  • Ro 43-5054

    CAS:
    <p>Ro 43-5054 is a small molecular, noncyclic peptidomimetic inhibitor.</p>
    Fórmula:C24H27N5O7
    Pureza:98%
    Forma y color:Solid
    Peso molecular:497.5
  • AKT-IN-9

    CAS:
    <p>AKT-IN-9, a potent AKT inhibitor, may aid breast/prostate cancer studies. See WO2021185238A1.</p>
    Fórmula:C24H29ClN6O
    Forma y color:Solid
    Peso molecular:452.98
  • D011-2120

    CAS:
    <p>D011-2120: Antiviral that blocks microtubule growth, disrupts Golgi, and hinders viral egress.</p>
    Fórmula:C17H15NO3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:281.31
  • JG-48

    CAS:
    <p>JG-48 is an inhibitor of Hsp70. JG-48 suppresses phosphorylated and total Tau in cells, endogenous Tau in neuroblastoma cells.</p>
    Fórmula:C20H16F3N3OS2
    Forma y color:Solid
    Peso molecular:435.49
  • Mps-BAY2b

    CAS:
    <p>Mps-BAY2b is a novel MPS1 inhibitor.</p>
    Fórmula:C20H23N5O
    Forma y color:Solid
    Peso molecular:349.43
  • PU24FCl

    CAS:
    <p>PU24FCl is a specific inhibitor of tumor Hsp90.</p>
    Fórmula:C20H21ClFN5O3
    Forma y color:Solid
    Peso molecular:433.86
  • LDN-193665

    CAS:
    LDN-193665 is a potent inhibitor of tau kinase. It acts by targeting CDK5/p25 and GSK3β.
    Fórmula:C15H11FN4OS
    Pureza:98%
    Forma y color:Solid
    Peso molecular:314.34
  • BOP sodium

    CAS:
    <p>BOP sodium salt is an inhibitor of alpha9beta1 and alpha4beta1 integrin.</p>
    Fórmula:C25H29N3NaO7S
    Forma y color:Solid
    Peso molecular:538.57
  • Mivobulin

    CAS:
    <p>Mivobulin is an inhibitor of tubulin .</p>
    Fórmula:C17H19N5O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:325.37
  • 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
  • ZW4864 free base

    CAS:
    <p>ZW4864 (free base) is an orally active and selective β catenin/B-Cell lymphoma 9 protein protein interaction ( β catenin/BCL9 PPI ) inhibitor.</p>
    Fórmula:C33H42N6O3
    Pureza:99.81%
    Forma y color:Solid
    Peso molecular:570.72
  • Diazobenzenesulfonic acid

    CAS:
    <p>Diazobenzenesulfonic acid, white/red crystal, inhibits myosin ATPase 13 as an allosteric desensitizer.</p>
    Fórmula:C6H5N2O3S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:185.18
  • Box5

    CAS:
    <p>Box5 blocks Wnt5a, reducing Ca2+ release and cell migration; promising for melanoma studies.</p>
    Fórmula:C30H50N6O13S2
    Forma y color:Solid
    Peso molecular:766.88
  • CCT036477

    CAS:
    <p>CCT036477 selectively inhibits Wnt/β-catenin signaling, reducing TCF/LEF transcriptional activity.</p>
    Fórmula:C21H18ClN3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:347.84
  • Acodazole hydrochloride

    CAS:
    <p>Acodazole hydrochloride: synthetic imidazoquinoline with antineoplastic activity; disrupts DNA replication by intercalation.</p>
    Fórmula:C20H20ClN5O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:381.86
  • Tubulin polymerization-IN-37

    CAS:
    <p>Tubulin polymerization-IN-37 inhibits tubulin polymerization at the colchicine site (IC50: 2.3 μΜ), potentially aiding lymphoma research.</p>
    Fórmula:C19H20N2O4
    Forma y color:Solid
    Peso molecular:340.37
  • αvβ1 integrin-IN-1 TFA (1689540-62-2 free base)


    <p>αvβ1 integrin-IN-1 TFA is an effective and selective αvβ1 integrin inhibitor (IC50: 0.63 nM).</p>
    Fórmula:C28H35F3N6O8S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:672.67
  • Cevipabulin

    CAS:
    <p>Cevipabulin (TTI-237) is a microtubule-active antitumor compound and inhibits the binding of [3H] vinblastine to tubulin (IC50: 18-40 nM in the human tumor cell</p>
    Fórmula:C18H18ClF5N6O
    Pureza:99.53%
    Forma y color:Solid
    Peso molecular:464.82
  • Anticancer agent 60

    CAS:
    <p>Anticancer agent 60 hinders HepG2 cell growth with IC50 of 4.13 μM and suppresses tumors in HepG2 mouse model.</p>
    Fórmula:C27H33N5O4S
    Forma y color:Solid
    Peso molecular:523.65
  • ABH Hydrochloride

    CAS:
    <p>ABH Hydrochloride is an arginase inhibitor, it enhances both male and female sexual arousal responses.</p>
    Fórmula:C6H15BClNO4
    Forma y color:Solid
    Peso molecular:211.45
  • Malonganenone A

    CAS:
    <p>Malonganenone A is a selective plasmodial Hsp70s modulator. It also has antimalarial activity.</p>
    Fórmula:C26H38N4O2
    Forma y color:Solid
    Peso molecular:438.61
  • BMS-587101

    CAS:
    <p>BMS-587101 is a small molecule antagonist of LFA-1, which can reduce inflammation and joint destruction in the mouse model of arthritis.</p>
    Fórmula:C26H20Cl2N4O4S
    Forma y color:Solid
    Peso molecular:555.43
  • BMS-358233

    CAS:
    <p>BMS-358233 is an effective LCK inhibitor with excellent cell activity against T cell proliferation.</p>
    Fórmula:C25H25ClN6O2S
    Forma y color:Solid
    Peso molecular:509.02
  • Acodazole

    CAS:
    <p>Acodazole is a synthetic imidazoquinoline. It has antimicrobial and antineoplastic properties. It also has been shown to treat arrhythmias.</p>
    Fórmula:C20H19N5O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:345.4
  • L 703014

    CAS:
    <p>L 703014 is an antagonist of the fibrinogen receptor.</p>
    Fórmula:C24H34N4O4
    Pureza:98%
    Forma y color:Solid
    Peso molecular:442.55
  • TCS 2314

    CAS:
    <p>TCS 2314 is an orally active and selective very late antigen-4 antagonist (IC50: 4.4 nM).</p>
    Fórmula:C28H34N4O6
    Pureza:98%
    Forma y color:Solid
    Peso molecular:522.59
  • KIF18A-IN-3

    CAS:
    <p>KIF18A-IN-3 is a KIF18A inhibitor (IC50=61 nM) that causes significant mitotic arrest and increases the number of mitotic cells in tumor tissues.</p>
    Fórmula:C28H38N4O5S2
    Pureza:98.45%
    Forma y color:Solid
    Peso molecular:574.76
  • Hsp90-IN-17

    CAS:
    <p>Hsp90-IN-17 (Example 5) is an inhibitor of HSP90, applicable in researching proliferative diseases, including cancer and neurodegenerative conditions.</p>
    Fórmula:C21H20N4O7
    Forma y color:Solid
    Peso molecular:440.41
  • β-glycosidase-IN-1

    CAS:
    <p>β-glycosidase-IN-1 is a piperidine derivative, and is an inhibitor of β-glycosidase. It has hypoglycemic activity.</p>
    Fórmula:C13H23NO5
    Pureza:98%
    Forma y color:Solid
    Peso molecular:273.33
  • O-GlcNAcase-IN-4

    CAS:
    <p>O-GlcNAcase-IN-4, an inhibitor from patent WO2018140299A1, may aid in neurodegenerative disease research.</p>
    Fórmula:C16H22FN5O3S
    Forma y color:Solid
    Peso molecular:383.44
  • OXi8007

    CAS:
    <p>OXi8007, a water-soluble prodrug for OXi8006, disrupts vasculature and exhibits strong cytotoxicity against DU-145 cancer cells.</p>
    Fórmula:C26H24NNa2O10P
    Forma y color:Solid
    Peso molecular:587.428
  • Tubulin inhibitor 7

    CAS:
    <p>Tubulin inhibitor 7 is an inhibitor of tubulin and a potent inhibitor of multiple cancer cell lines (tubulin polymerization (IC50: 0.52 μM), K562 cell growth (</p>
    Fórmula:C21H14N2O4
    Pureza:98%
    Forma y color:Solid
    Peso molecular:358.35
  • 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
  • K-80003

    CAS:
    <p>K-80003(TX-803) is a potent retinol-like X-receptor-alpha regulator that inhibits TRxrα-dependent Akt activation and tumor cell growth.</p>
    Fórmula:C22H21FO2
    Pureza:99.76%
    Forma y color:Solid
    Peso molecular:336.4
  • PF-2771

    CAS:
    <p>PF-2771: potent CENP-E inhibitor, IC50 of 16.1 nM, used in cancer treatment.</p>
    Fórmula:C29H36ClN5O4
    Pureza:98%
    Forma y color:Solid
    Peso molecular:554.08
  • NC043

    CAS:
    <p>NC043 is an inhibitor of Wnt/β-catenin signaling, it forms a covalent bond with the Cys-516 residue of CARF.</p>
    Fórmula:C20H26O4
    Pureza:98%
    Forma y color:Solid
    Peso molecular:330.42
  • PP2A Cancerous-IN-1

    CAS:
    <p>PP2A Cancerous-IN-1 is a potent inhibitor of CIP2A (Cancerous inhibitor of PP2A) and p-Akt that exhibits potent anti-proliferative effects.</p>
    Fórmula:C30H24N4O3
    Forma y color:Solid
    Peso molecular:488.54