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.
1381 produits trouvés pour "Signalisation du cytosquelette"
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DM1-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 :546.95AKT-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 :389.43JB002
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 :293.32Arimoclomol
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 :313.78JH-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 :465.55Firategrast
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 :499.5SB-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 :310.35Terflavoxate
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 :419.51LY3372689
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 :383.44UMK57
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 :295.4PPY 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 :260.33DZ2002
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 :251.24CID-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 :366.44JB061
<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 :323.34Rosabulin
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 :400.45Tubulin 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 :342.35AZ13705339
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 :629.75EMT 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 :619.47AMP-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 :549.17CMPF
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 :240.25Conteltinib
CAS :<p>Conteltinib (CT-707) is an enzyme inhibitor with antitumor activity targeting FAK, ALK and Pyk2. It can be used to study lymphoma.</p>Formule :C32H45N9O3SDegré de pureté :98.12% - 99.54%Couleur et forme :SolidMasse moléculaire :635.82Dynapyrazole 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 :486.69Elarofiban
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 :416.51para-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 :337.33Erbulozole
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 :469.55JB062
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 :323.34DCPLA-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 :322.53BMD4503-2
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 :483.54TCS 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 :323.35BIRT-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 :442.13Bis-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 :480.43Elsibucol
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 :602.93SNX0723
CAS :<p>SNX0723 is a potent Hsp90 Inhibitor with anti-Plasmodium activity.</p>Formule :C22H26FN3O3Degré de pureté :99.85%Couleur et forme :SolidMasse moléculaire :399.46Nilotinib 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 :565.98PVZB1194
CAS :<p>PVZB1194, a biphenyl-type inhibitor of Kinesin spindle protein Eg5 (KIF11), exhibits anticancer potential by inducing cell cycle arrest and apoptosis through</p>Formule :C13H9F4NO2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :319.28SB-267268
CAS :<p>SB-267268: αvβ3 inhibitor (IC50: 0.68 nM human, 0.29 nM mouse), blocks αvβ3/αvβ5 integrins (Ki: 0.9 nM human, 0.5 nM monkey αvβ3, 0.7 nM human αvβ5).</p>Formule :C22H24F3N3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :451.44CNS-11
CAS :<p>CNS-11, a compound that disaggregates tau fibrils, is utilized in Alzheimer's disease (AD) research [1].</p>Formule :C25H21N3O2Couleur et forme :SolidMasse moléculaire :395.45MC-Val-Cit-PAB-Ispinesib
CAS :<p>MC-Val-Cit-PAB-Ispinesib (Compound 509) is a potent Eg5 inhibitor and a click chemistry reagent [1].</p>Formule :C59H71ClN10O10Couleur et forme :SolidMasse moléculaire :1115.71Oxaline
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 :447.49Tubulin 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 :445.39Demethylasterriquinone B1
CAS :<p>insulin receptor (IR) activator</p>Formule :C32H30N2O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :506.59WAY 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 :484.94Valecobulin hydrochloride
CAS :<p>Valecobulin hydrochloride (CKD-516 hydrochloride) is the valine prodrug and vasoblocker of S516.Cost-effective and quality-assured.</p>Formule :C26H29ClN6O5SDegré de pureté :99.52%Couleur et forme :SolidMasse moléculaire :573.06Paluratide
CAS :<p>Paluratide (LUNA18) is a reversible KRAS inhibitor oral , which inhibits cancer cell proliferation by phosphorylating ERK and AKT, RAS with (GEFs).</p>Formule :C73H105F5N12O12Degré de pureté :98.70%Couleur et forme :SolidMasse moléculaire :1437.68BIO-7662
CAS :<p>BIO-7662 is an effective and highly selective antagonist of α4β1 integrin.</p>Formule :C38H48N6O8SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :748.89ER degrader 7
CAS :<p>ER degrader 7 (Compound 35t) is a selective degrader of both ERα and ERβ, and possesses activity as a tubulin polymerization inhibitor.</p>Formule :C33H31F4N3O5SSeCouleur et forme :SolidMasse moléculaire :736.63ASN90
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 :375.45Zaurategrast
CAS :<p>Zaurategrast is an effective and oral-effective inhibitor of the α4-integrin.</p>Formule :C26H25BrN4O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :521.41Akt-I-1,2
CAS :<p>Akt-I-1,2 is a selective inhibitor of Akt1 and Akt2.</p>Formule :C23H22ClN3Degré de pureté :99.95%Couleur et forme :SolidMasse moléculaire :375.89HSP90-IN-29
CAS :<p>HSP90-IN-29 (Compound 13), a benzoxazole derivative, serves as a potent and selective HSP-90 inhibitor, exhibiting a low IC50 value of 30 nM. This compound demonstrates significant antitumor activity [1].</p>Formule :C19H20ClN3O4Couleur et forme :SolidMasse moléculaire :389.83BI-1950
CAS :<p>BI-1950: potent inhibitor of LFA-1, key in immune function and drug target.</p>Formule :C32H26Cl2FN7O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :646.53,4',5-Trismethoxybenzophenone
CAS :<p>3,4',5-Trismethoxybenzophenone (compound 16a) is an effective inhibitor of tubulin assembly, demonstrating a half-maximal inhibitory concentration (IC 50) of 2.6 µM [1].</p>Formule :C16H16O4Couleur et forme :SolidMasse moléculaire :272.3TCS 21311
CAS :<p>TCS 21311 (NIBR3049) selectively inhibits JAK3 (IC50: 8 nM) and PKCα/θ & GSK3β; >100x selective over JAK1, JAK2, TYK2.</p>Formule :C27H25F3N4O4Degré de pureté :99.39% - ≥98%Couleur et forme :SolidMasse moléculaire :526.51Tirofiban HCl
CAS :<p>Tirofiban HCl is an antagonist of platelet glycoprotein-IIb/IIIa receptor.</p>Formule :C22H37ClN2O5SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :477.06KSP-IA
CAS :<p>KSP-IA is a potent, specific, allosteric, and cell-active KSP inhibitor.</p>Formule :C21H22F2N2ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :356.41Integrin Antagonists 27
CAS :<p>Integrin Antagonists 27 is a small molecule integrin αvβ3 antagonist. It has a binding affinity of 18 nM and as a novel anticancer agent.</p>Formule :C24H20N4O5Couleur et forme :SolidMasse moléculaire :444.44Kif15-IN-2
CAS :<p>Kif15-IN-2 is a kinesin Kif15 inhibitor with potential anticancer activity and can be used in prostate cancer research.</p>Formule :C20H20N6O4SDegré de pureté :98.17%Couleur et forme :SolidMasse moléculaire :440.48PAK4-IN-1
CAS :<p>PAK4-IN-1: selective, potent oral PAK4 inhibitor; stable in acid/neutral; shows strong anti-tumor in vivo.</p>Formule :C26H30ClN7O5Couleur et forme :SolidMasse moléculaire :556.01Porcn-IN-2
CAS :<p>Porcn-IN-2 (Example 107) is a potent Wnt pathway inhibitor, exhibiting an IC50 of 0.05 nM.</p>Formule :C24H17F3N6OCouleur et forme :SolidMasse moléculaire :462.43CCT251455
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 :503.983-Hydroxyxanthone
CAS :<p>3-Hydroxyxanthone (3-Hydroxy-xanthen-9-one), a xanthone derivative, exhibits inhibitory effects on NADPH-catalyzed lipid peroxidation in human umbilical vein</p>Formule :C13H8O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :212.2αvβ6 integrin inhibitor 2
CAS :<p>αvβ6 Integrin Inhibitor 2 is a potent inhibitor of αvβ6 integrin, demonstrating an inhibition concentration (IC50) of 96.5 nM.</p>Formule :C21H30N4O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :386.49NTRC 0066-0
CAS :<p>NTRC 0066-0 is a TTK inhibitor that can be used in cancer research.</p>Formule :C33H39N7O2Degré de pureté :98.30%Couleur et forme :SolidMasse moléculaire :565.71HSP90-IN-27
CAS :<p>HSP90-IN-27, also known as compound 19, is an inhibitor of HSP90 [1].</p>Formule :C18H21N3O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :343.44MK-6240
CAS :<p>MK-6240: A tau PET tracer with high specificity for NFTs binding.</p>Formule :C16H11FN4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :278.28Carotegrast
CAS :<p>Carotegrast, an orally available α4 integrin receptor inhibitor, has anti-inflammatories activities.</p>Formule :C27H24Cl2N4O5Couleur et forme :SolidMasse moléculaire :555.41THK-5105
CAS :<p>THK-5105, a tau-binding arylquinoline, could be an 18F-PET imaging probe for Alzheimer's disease.</p>Formule :C20H21FN2O2Couleur et forme :SolidMasse moléculaire :340.39IWP 12
CAS :<p>IWP 12 is a potent inhibitor of porcupine (Porcn), blocking Wnt signaling and inhibiting fin regeneration in adult and juvenile fish.</p>Formule :C18H18N4O2S3Degré de pureté :98.88%Couleur et forme :SolidMasse moléculaire :418.56KU-177
CAS :<p>KU-177 is an Aha1 inhibitor that disrupts the interaction between Hsp90 and Aha1, eliminating cell proliferation and PI resistance induced by elevated AHSA1.</p>Formule :C27H23NO8Degré de pureté :96.92% - 98.54%Couleur et forme :SolidMasse moléculaire :489.47Gly-Arg-Gly-Asp-Ser TFA
CAS :<p>Gly-Arg-Gly-Asp-Ser (TFA), osteopontin domain, binds αvβ3 and αvβ5 integrins; IC50s: ~5 μM, ~6.5 μM.</p>Formule :C19H31F3N8O11Couleur et forme :SolidMasse moléculaire :604.49Lamifiban
CAS :<p>Lamifiban is a nonpeptide glycoprotein IIb/IIIa antagonist. It prevents platelet loss during experimental cardiopulmonary bypass.</p>Formule :C24H28N4O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :468.5SC-52012
CAS :<p>SC-52012 is a novel and potent fibrinogen receptor antagonist, an RGD mimetic, which inhibits platelet aggregation.</p>Formule :C25H30N4O6Degré de pureté :97.20%Couleur et forme :SolidMasse moléculaire :482.53Pin1 modulator 1
CAS :<p>Pin1 modulator 1 (compound IIb-219) is a specific β-Catenin targeting agent that inhibits the Wnt pathway and is applicable in researching Wnt-mediated diseases, including cancer [1].</p>Formule :C18H15NO3S2Couleur et forme :SolidMasse moléculaire :357.44β-Catenin modulator-3
CAS :<p>β-Catenin modulator-3 (compound IIa-112), an oxazole and thiazole-based chemical entity, serves as a potent and selective modulator of β-Catenin [1].</p>Formule :C21H22N2O3SCouleur et forme :SolidMasse moléculaire :382.48Pterostilbene-isothiocyanate
CAS :<p>Pterostilbene-isothiocyanate (PTER-ITC) demonstrates strong anticancer properties in vitro, particularly disrupting the interaction between β-catenin and TCF-4</p>Formule :C18H19N3O3SCouleur et forme :SolidMasse moléculaire :357.43PKC-θ inhibitor 1
CAS :<p>PKC-theta inhibitor 1 is an inhibitor of PKCθ (Ki of 6 nM)</p>Formule :C17H15F3N4ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :348.3222-(4′-py)-JA
CAS :<p>22-(4′-py)-JA, a semisynthetic derivative of junamycin A isolated from the Thai blue sponge (Xestospongia sp.), exhibits antimetastatic properties by inhibiting</p>Formule :C32H30N4O8Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :598.6PBB3
CAS :<p>PBB3 is a tau-specific PET tracer.</p>Formule :C17H15N3OSCouleur et forme :SolidMasse moléculaire :309.39AT7867 hydrochloride
CAS :<p>AT7867 hydrochloride is a potent inhibitor of AKT and p70 S6 kinase, displaying oral activity and demonstrating an anticancer effect [1].</p>Formule :C20H21Cl2N3Couleur et forme :SolidMasse moléculaire :374.31TC-I 15
CAS :<p>α2β1 integrin inhibitor</p>Formule :C23H28N4O6S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :520.62L-739758
CAS :<p>L-739758 is a glycoprotein IIb/IIIa inhibitor.</p>Formule :C22H26N4O5S3Couleur et forme :SolidMasse moléculaire :522.66BCR-ABL-IN-4
CAS :<p>BCR-ABL-IN-4: Anticancer BCR-ABL inhibitor; stops K562 cells (IC50: 0.67 nM), targets T315I Ba/F3 cells (IC50: 16 nM).</p>Formule :C27H24ClF2N5O4Couleur et forme :SolidMasse moléculaire :555.96(-)-Indolactam V
CAS :<p>(-)-Indolactam V: PKC activator, antitumor, Ki 3.36 nM/1.03 μM for η/γ-CRD2, Kd 5.5-213 nM for C1 domains.</p>Formule :C17H23N3O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :301.38β-catenin-IN-4
CAS :<p>β-Catenin-IN-4 is a β-catenin inhibitor characterized by a K_i value of 0.64 μM.</p>Formule :C38H33ClF3N5O9Couleur et forme :SolidMasse moléculaire :796.14L 738167
CAS :<p>L 738167 is a potent antagonist of the long-acting fibrinogen receptor.</p>Formule :C25H34N6O6SCouleur et forme :SolidMasse moléculaire :546.64Solenopsin
CAS :<p>Solenopsin is an ATP-competitive inhibitor of AKT(IC50 : 10 μM) .</p>Formule :C17H35NDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :253.47SEN461
CAS :<p>SEN461 is a wnt inhibitor.</p>Formule :C25H34N4O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :486.56HDAC-IN-55
CAS :<p>HDAC-IN-55(8j) is a small-molecule inhibitor that enhances E-cadherin expression and suppresses cancer cell proliferation [1].</p>Formule :C17H17N3O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :311.34Levocabastine hydrochloride
CAS :<p>Levocabastine HCl is an agent with antihistaminic activity.</p>Formule :C26H30ClFN2O2Couleur et forme :SolidMasse moléculaire :456.98Heclin
CAS :<p>Heclin is an inhibitor of HECT E3 ubiquitin ligase that acts by inhibiting Smurf2, Nedd4, and WWP1 with IC50 values of 6.8, 6.3, and 6.9 μM, respectively.</p>Formule :C17H17NO3Degré de pureté :95.79%Couleur et forme :SolidMasse moléculaire :283.32αvβ1 integrin-IN-2
CAS :<p>αvβ1 integrin-IN-2 (compound 32) is a potent inhibitor of ανβ1 and α5β1 integrins, exhibiting IC50 values of 0.9 nM and 33 nM, respectively.</p>Formule :C29H38N4O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :506.64CT-721
CAS :<p>CT-721: potent, time-bound Bcr-Abl inhibitor, IC50 21.3 nM, effective against CML.</p>Formule :C30H29ClN6ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :525.04Litronesib
CAS :<p>Litronesib is a selective inhibitor of mitosis-specific kinesin Eg5. It also has antitumor activity.</p>Formule :C23H37N5O4S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :511.7AKT-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 :470.99ATN-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 :597.64VTX-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 :418.9Ac-Val-Gln-aIle-Val-aTyr-Lys-NH2
CAS :<p>Ac-Val-Gln-aIle-Val-aTyr-Lys-NH2 demonstrates serum stability and non-toxicity to neuronal cells, while selectively inhibiting the fibrilization of tau in</p>Formule :C38H65N11O9Couleur et forme :SolidMasse moléculaire :819.99
