Signalisation du cytosquelette
Les inhibiteurs de la signalisation du cytosquelette sont des composés qui perturbent les voies de signalisation régulant le cytosquelette, essentiel pour la forme, la motilité, la division des cellules et le transport intracellulaire. Ces inhibiteurs sont utilisés pour étudier la dynamique des protéines du cytosquelette, telles que l'actine et la tubuline, et leur rôle dans des processus comme la migration cellulaire, l'adhésion et la métastase du cancer. Les inhibiteurs de la signalisation du cytosquelette sont précieux dans la recherche en biologie cellulaire, en cancérologie et en neurobiologie. Chez CymitQuimica, nous offrons une gamme complète d'inhibiteurs de la signalisation du cytosquelette de haute qualité pour soutenir vos recherches dans ces domaines.
1382 produits trouvés pour "Signalisation du cytosquelette"
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para-Nitroblebbistatin
CAS :<p>para-Nitroblebbistatin is a non-cytotoxic, non-fluorescent, photostable, and specific inhibitor of myosin II.Cost-effective and quality-assured.</p>Formule :C18H15N3O4Degré de pureté :99.09% - 99.84%Couleur et forme :SolidMasse moléculaire :337.33Rosabulin
CAS :<p>v Rosabulin (STA 5312) is an orally active microtubule inhibitor with potency.</p>Formule :C22H16N4O2SDegré de pureté :98.06%Couleur et forme :SolidMasse moléculaire :400.45JB062
CAS :<p>JB062 is a chemical compound acting as a nonmuscle myosin inhibitor, exhibiting IC50 values of 1.6, 5.4, and >100 μM against skeletal muscle myosin, cardiac</p>Formule :C19H17NO4Degré de pureté :99.89%Couleur et forme :SolidMasse moléculaire :323.34Elarofiban
CAS :<p>Elarofiban(RWJ-53308) is a novel and orally active GPIIb/IIIa antagonist.</p>Formule :C22H32N4O4Degré de pureté :98.76%Couleur et forme :SolidMasse moléculaire :416.51JB002
CAS :<p>JB002, a myosin II inhibitor, exhibits potent activity with an IC50 of ≤10 μM.</p>Formule :C18H15NO3Degré de pureté :99.74%Couleur et forme :SoildMasse moléculaire :293.32LY3372689
CAS :<p>LY3372689 (Formulaic Ia) is an orally active O-GlcNAcase (OGA) enzyme inhibitor for tau protein-based disorders including Alzheimer's disease.</p>Formule :C16H22FN5O3SDegré de pureté :99.43% - 99.53%Couleur et forme :SolidMasse moléculaire :383.44DCPLA-ME
CAS :<p>DCPLA-ME (2-[(2-Pentylcyclopropyl)methyl]cyclopropaneoctanoic acid methyl ester) is the methyl ester form of DCPLA and can be used to treat neurodegenerative</p>Formule :C21H38O2Degré de pureté :99.80%Couleur et forme :SolidMasse moléculaire :322.53CID-663143
CAS :<p>CID-663143 inhibits cancer cell growth and shows microtubule-binding activity.</p>Formule :C19H18N4O2SDegré de pureté :99.68% - 99.77%Couleur et forme :SolidMasse moléculaire :366.44BIRT-377
CAS :<p>BIRT-377: orally active, hinders ICAM-1/LFA-1, blocks IL-2, useful for immune research. (Ki=25.8 nM).</p>Formule :C18H15BrCl2N2O2Degré de pureté :99.93%Couleur et forme :SolidMasse moléculaire :442.13Nilotinib hydrochloride
CAS :<p>Nilotinib HCl (AMN-107 HCl), an oral Bcr-Abl inhibitor, targets neuroinflammation, cognitive issues, and chronic myelogenous leukemia.</p>Formule :C28H23ClF3N7ODegré de pureté :>99.99%Couleur et forme :SolidMasse moléculaire :565.98TCS 2210
CAS :<p>TCS 2210 promotes neuronal differentiation in stem cells, boosting β-III tubulin and enolase markers.</p>Formule :C18H17N3O3Degré de pureté :98.62%Couleur et forme :SolidMasse moléculaire :323.35SB-216
CAS :<p>SB-216, a potent anti-cancer compound, inhibits tubulin polymerization and curbs growth in various cancer cells.</p>Formule :C17H18N4O2Degré de pureté :99.70%Couleur et forme :SolidMasse moléculaire :310.35AMP-PCP disodium
CAS :<p>AMP-PCP disodium is an ATP analogue with binding affinity to the N-terminal domain of Hsp90, with a Kd value of 3.8 μM.</p>Formule :C11H16N5Na2O12P3Degré de pureté :99.32%Couleur et forme :SolidMasse moléculaire :549.17BMD4503-2
CAS :<p>BMD4503-2 is a competitive inhibitor of the LRP5/6-sclerostin complex that restores the activity of the Wnt/β-catenin signaling pathway cancer.</p>Formule :C26H21N5O3SDegré de pureté :99.18%Couleur et forme :SolidMasse moléculaire :483.54JB061
<p>JB061 is a nonmuscle myosin inhibitor, demonstrating selective inhibitory activity with IC50 values of 4.4 μM (Cardiac muscle myosin), 9.1 μM (Skeletal muscle</p>Formule :C19H17NO4Degré de pureté :99.67%Couleur et forme :SoildMasse moléculaire :323.34NSC668394
CAS :<p>NSC668394 is an ezrin phosphorylation inhibitor.NSC668394 has antitumor activity and increases ezrin cleavage.NSC668394 can be used to study tumor metastasis.</p>Formule :C17H12Br2N2O3Degré de pureté :99.29% - 99.29%Couleur et forme :SolidMasse moléculaire :452.1CMPF
CAS :<p>CMPF is a microtubule protein inhibitor that can be used to study tumors.</p>Formule :C12H16O5Degré de pureté :99.88%Couleur et forme :SolidMasse moléculaire :240.25AZ13705339
CAS :<p>AZ13705339 is an effective inhibitor of PAK1 with an IC50 of 0.33 nM and a Kd of 0.28 nM.</p>Formule :C33H36FN7O3SDegré de pureté :99.77%Couleur et forme :SolidMasse moléculaire :629.75DZ2002
CAS :<p>DZ2002: Oral, reversible SAHH inhibitor (Ki=17.9 nM), low-toxicity, immunosuppressive, counters dermal fibrosis, used in autoimmune research.</p>Formule :C10H13N5O3Degré de pureté :99.91%Couleur et forme :SolidMasse moléculaire :251.24JH-VIII-157-02
CAS :<p>JH-VIII-157-02 inhibits ALK, specifically EML4-ALK variants, with IC50s of 2 nM.</p>Formule :C28H27N5O2Degré de pureté :99.58%Couleur et forme :SolidMasse moléculaire :465.55Arimoclomol
CAS :<p>Arimoclomol (BRX-220 free base) is a co-inducer of heat shock proteins (HSP) and can be used in studies about the treatment of amyotrophic lateral sclerosis (</p>Formule :C14H20ClN3O3Degré de pureté :99.15%Couleur et forme :SolidMasse moléculaire :313.78ZINC00640089
CAS :<p>ZINC00640089: Selective LCN2 inhibitor; curbs SUM149 cell growth and AKT activity; useful for IBC research.</p>Formule :C20H13F3N2O2Degré de pureté :98.41% - 99.80%Couleur et forme :SolidMasse moléculaire :370.32DM1-SMe
CAS :<p>DM1-SMe (DM1-SSMe) potently inhibits microtubules, 3-10x stronger than Maytansine with IC50s of 0.003-0.01 nM in human cancer cells.</p>Formule :C36H50ClN3O10S2Degré de pureté :99.61%Couleur et forme :SolidMasse moléculaire :784.38Defactinib hydrochloride
CAS :<p>Defactinib hydrochloride (PF 04554878 hydrochloride) is a novel inhibitor of FAK.</p>Formule :C20H22ClF3N8O3SDegré de pureté :98.06% - 98.78%Couleur et forme :SolidMasse moléculaire :546.95PPY A
CAS :<p>PPY A is a potent inhibitor of T315l mutant and wild-type Abl kinase and inhibits the growth of Bcr-Abl T315l mutant or wild-type Bcr-Abl gene-transformed cells</p>Formule :C22H20N4O2Degré de pureté :98.77%Couleur et forme :SolidMasse moléculaire :372.42Iroxanadine
CAS :<p>Iroxanadine (BRX-005) is a Novel small molecule MAPK p38 inhibitor that induces phosphorylation of p38 SAPK and induces concentration-dependent relaxation in</p>Formule :C14H20N4ODegré de pureté :98.04% - 99.04%Couleur et forme :SolidMasse moléculaire :260.33Tubulin inhibitor 8
CAS :<p>Tubulin inhibitor 8 blocks tubulin polymerization, stunts K562 cancer cell growth; IC50: 0.73 μM, 14 nM.</p>Formule :C21H14N2O3Degré de pureté :98.51% - 99.87%Couleur et forme :SolidMasse moléculaire :342.35Elsibucol
CAS :<p>Elsibucol (AGI 1096) is a VCAM1 inhibitor for the study of organ transplant rejection.Elsibucol is a metabolically stable propanol derivative with antioxidant,</p>Formule :C35H54O4S2Degré de pureté :99.73%Couleur et forme :SolidMasse moléculaire :602.93AKT-IN-6
CAS :<p>AKT-IN-6 (INCB-047775) inhibits Akt, a key signaling protein linked to type 2 diabetes and cancer.</p>Formule :C22H20FN5ODegré de pureté :98.68%Couleur et forme :SolidMasse moléculaire :389.43Terflavoxate
CAS :<p>Terflavoxate is a novel, orally active, semisynthetic statin microtubule inhibitor commonly used in combination with capecitabine.</p>Formule :C26H29NO4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :419.51Firategrast
CAS :<p>Firategrast (SB 683699) is an orally active and specific α4β1/α4β7 integrin antagonist.Firategrast reduces the transport of lymphocytes into the central nervous</p>Formule :C27H27F2NO6Degré de pureté :99.16%Couleur et forme :SolidMasse moléculaire :499.5SNX0723
CAS :<p>SNX0723 is a potent Hsp90 Inhibitor with anti-Plasmodium activity.</p>Formule :C22H26FN3O3Degré de pureté :99.85%Couleur et forme :SolidMasse moléculaire :399.46Erbulozole
CAS :<p>Erbulozole (R 55104) is a synthetic microtubule inhibitor with anti-invasive activity that induces Wernicke's encephalopathy-like neurotoxicity.</p>Formule :C24H27N3O5SDegré de pureté :99.88%Couleur et forme :SolidMasse moléculaire :469.55Bis-T-23
CAS :<p>Bis-T-23 is a promoter of actin-dependent dynamin oligomerization, an HIV-I integrase inhibitor, and a Telstar derivative.</p>Formule :C23H20N4O8Degré de pureté :96.81% - 98.13%Couleur et forme :SolidMasse moléculaire :480.43Dynapyrazole A
CAS :<p>Dynapyrazole A inhibits dynein 1 and 2 (IC50s: 2.3, 2.6 μM) and Hedgehog signaling (IC50: 1.9 μM).</p>Formule :C20H12ClIN4ODegré de pureté :98.01%Couleur et forme :SolidMasse moléculaire :486.69UMK57
CAS :<p>UMK57 is a CENP-Ei and MCAK enhancer, selectively promoting k-MT attachment error correction to inhibit chromosome missegregation of small molecule compounds,</p>Formule :C17H17N3SDegré de pureté :99.81%Couleur et forme :SolidMasse moléculaire :295.4EMT inhibitor-1
CAS :<p>EMT inhibitor-1 is an inhibitor of Hippo, Wnt signaling and TGF- macrophages (TGF-) with antitumor activity.</p>Formule :C12H12Cl2N2O2SDegré de pureté :99.53%Couleur et forme :SolidMasse moléculaire :319.21JG-231
CAS :<p>JG-231, a JG-98 analog, shows anticancer properties by blocking Hsp70-BAG3 interaction and hindering TNBC in MDA-MB-231 models.</p>Formule :C22H18BrCl2N3OS4Degré de pureté :99.79%Couleur et forme :SolidMasse moléculaire :619.47ASN90
CAS :<p>ASN90 is a specific, orally active inhibitor of the O-GlcNAcase (OGA) enzyme, demonstrating an IC50 of 10.2 nM.</p>Formule :C17H21N5O3SCouleur et forme :SolidMasse moléculaire :375.45AKT-IN-13
CAS :<p>AKT-IN-13 inhibits Akt1, Akt2, Akt3 (IC50: 1.6, 2.4, 0.3 nM); used in cancer research.</p>Formule :C24H31ClN6O2Couleur et forme :SolidMasse moléculaire :470.99ICAM-1-IN-1
CAS :<p>ICAM-1-IN-1 is a potent and selective E-selectin(IC50 = 7 nM) and ICAM-1(IC50 = 5 nM) inhibitor.</p>Formule :C15H11BrN2O2SDegré de pureté :99.67%Couleur et forme :SolidMasse moléculaire :363.23ATN-161
CAS :<p>ATN-161 is an integrin α5β1 binding peptide and antagonist that inhibits VEGF-induced hCECs migration and angiogenesis.</p>Formule :C23H35N9O8SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :597.64MAO A/HSP90-IN-2
CAS :<p>MAO A/HSP90-IN-2 (compound 4-C), a dual inhibitor of HSP90 and MAO A, exhibits IC50 values of 0.016 μM for MAO A and 4.58 μM for HSP90.</p>Formule :C25H31ClN2O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :458.98VTX-27
CAS :<p>VTX-27 is a selective inhibitor of protein kinase C θ (PKC θ) (Kis: 0.08 nM and 16 nM for PKC θ and PKC δ).</p>Formule :C20H24ClFN6ODegré de pureté :99.84%Couleur et forme :SolidMasse moléculaire :418.9WAY 316606 hydrochloride
CAS :<p>WAY 316606 hydrochloride is a chemical compound that serves as an inhibitor of sFRP-1 (secreted protein), which functions as an endogenous antagonist of the Wnt (secreted glycoprotein). Its affinity for sFRP-1 is measured through the FP (fluorescence polarization) binding assay, revealing an IC50 (half maximal inhibitory concentration) of 0.5 μM [1].</p>Formule :C18H20ClF3N2O4S2Couleur et forme :SolidMasse moléculaire :484.94CCT251455
CAS :<p>CCT251455, the mitotic kinase monopolar spindle 1 (MPS1/TTK) inhibitor, is a potent (IC50=3 nM) and specific chemical tool.</p>Formule :C26H26ClN7O2Degré de pureté :99.1% - 99.1%Couleur et forme :SolidMasse moléculaire :503.98TAK 029
CAS :<p>TAK 029 is a local glycoprotein IIb/IIIa receptor inhibitor.</p>Formule :C19H23N5O7Couleur et forme :SolidMasse moléculaire :433.42JG-23
CAS :<p>JG-23, a 4-chloro-modified analog, effectively induces t-tau degradation and demonstrates robust metabolic stability, exhibiting an extended half-life (T1/2) of</p>Formule :C19H16ClN3OS2Couleur et forme :SolidMasse moléculaire :401.93Tubulin polymerization-IN-52
CAS :<p>Tubulin polymerization-IN-52 (compound SC23) effectively inhibits tubulin polymerization, exhibiting an IC50 value of 2.9 μM [1].</p>Formule :C21H18F3N5O3Couleur et forme :SolidMasse moléculaire :445.39Oxaline
CAS :<p>Oxaline, a fungal alkaloid derived from Penicillium oxalicum, impedes tubulin polymerization, leading to cell cycle arrest at the M phase [1] [2].</p>Formule :C24H25N5O4Couleur et forme :SolidMasse moléculaire :447.49
