Cytoskeletal Signaling
Cytoskeletal signaling inhibitors are compounds that disrupt the signaling pathways regulating the cytoskeleton, which is crucial for cell shape, motility, division, and intracellular transport. These inhibitors are used to study the dynamics of cytoskeletal proteins, such as actin and tubulin, and their role in processes like cell migration, adhesion, and cancer metastasis. Cytoskeletal signaling inhibitors are valuable in research on cell biology, cancer, and neurobiology. At CymitQuimica, we offer a comprehensive range of high-quality cytoskeletal signaling inhibitors to support your research in these areas.
Products of "Cytoskeletal Signaling"
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PKCθ pseudosubstrate peptide inhibitor,myristoylated
Myristoylated PKCθ pseudosubstrate peptide inhibitor is a synthetic peptide utilized to investigate the mechanism of action of protein kinase C theta (PKCθ) [1Formula:C105H184N36O21SPurity:98%Color and Shape:SolidMolecular weight:2318.88Miransertib
CAS:Miransertib (ARQ-092) is an orally bioavailable, selective, and potent allosteric Akt inhibitor.Formula:C27H24N6Purity:98.83% - ≥95%Color and Shape:SolidMolecular weight:432.52Ref: TM-T3467
1mg52.00€5mg97.00€10mg169.00€25mg344.00€50mg567.00€100mg908.00€500mg1,795.00€1mL*10mM (DMSO)114.00€Defactinib hydrochloride
CAS:Defactinib hydrochloride (PF 04554878 hydrochloride) is a novel inhibitor of FAK.Formula:C20H22ClF3N8O3SPurity:98.06% - 98.78%Color and Shape:SolidMolecular weight:546.95Midostaurin
CAS:PKC412(Midostaurin (PKC412); CGP41231; CGP41251) is a broad spectrum protein kinase inhibitor.Formula:C35H30N4O4Purity:100% - 99.47%Color and Shape:SolidMolecular weight:570.64Ref: TM-T3211
1mg51.00€5mg88.00€10mg126.00€25mg216.00€50mg328.00€100mg487.00€500mg1,093.00€1mL*10mM (DMSO)96.00€LY3372689
CAS:LY3372689 (Formulaic Ia) is an orally active O-GlcNAcase (OGA) enzyme inhibitor for tau protein-based disorders including Alzheimer's disease.Formula:C16H22FN5O3SPurity:99.27% - 99.45%Color and Shape:SolidMolecular weight:383.44Ref: TM-T61661
1mg99.00€5mg235.00€10mg354.00€25mg635.00€50mg935.00€100mg1,415.00€1mL*10mM (DMSO)259.00€Multi-kinase inhibitor 1
CAS:Multi-kinase inhibitor 1 (Multi-kinase inhibitor I) is a Multi-kinase inhibitor.Formula:C20H17F3N4O3Purity:99.34%Color and Shape:SolidMolecular weight:418.37FRAX597
CAS:FRAX597 is an effective, ATP-competitive inhibitor of group I PAKs, and for PAK1(IC50=8 nM), PAK2(IC50=13 nM), and PAK3 (IC50=19 nM).Formula:C29H28ClN7OSPurity:97.34% - 99.85%Color and Shape:SolidMolecular weight:558.1Ansamitocin P 3'
CAS:Ansamitocin P 3' (Maytansinol butyrate) is an antibody-drug conjugate cytotoxin with antitumor activity.Formula:C32H43ClN2O9Purity:98.16% - 99.16%Color and Shape:SolidMolecular weight:635.14Ref: TM-T1910
2mg34.00€5mg50.00€10mg84.00€25mg145.00€50mg229.00€100mg340.00€200mg472.00€1mL*10mM (DMSO)70.00€Ifebemtinib
CAS:Ifebemtinib (BI-853520) is an adhesion plaque kinase inhibitor with anti-tumour activity for the study of breast cancer.Formula:C28H28F4N6O4Purity:98.07% - 99.82%Color and Shape:SolidMolecular weight:588.55Ionomycin calcium
CAS:Ionomycin calcium (SQ23377 calcium) is an effective and selective calcium ionophore, exhibiting high specificity for calcium ions. Cost-effective and quality-assured.Formula:C41H70CaO9Purity:98% - 98.11%Color and Shape:SolidMolecular weight:747.07NAMI-A
CAS:NAMI-A is a ruthenium-based compound with selective activity against tumor metastasis.NAMI-A inhibits cancer cell adhesion and migration.Formula:C8H15Cl4N4ORuSPurity:98%Color and Shape:SolidMolecular weight:458.18Ipfencarbazone
CAS:Ipfencarbazone herbicide agent, is a substance being developed for the control of weeds such as watergrass in rice.Formula:C18H14Cl2F2N4O2Color and Shape:SolidMolecular weight:427.23Dynapyrazole A
CAS:Dynapyrazole A inhibits dynein 1 and 2 (IC50s: 2.3, 2.6 μM) and Hedgehog signaling (IC50: 1.9 μM).Formula:C20H12ClIN4OPurity:98.01%Color and Shape:SolidMolecular weight:486.69RWJ 50271
CAS:RWJ 50271 inhibits LFA-1/ICAM-1 interaction with IC50 5.0 μM in HL60 cells.Formula:C18H17F3N4O2SPurity:99.09%Color and Shape:SolidMolecular weight:410.41Ref: TM-T12783
1mg127.00€5mg311.00€10mg472.00€25mg747.00€50mg1,017.00€100mg1,311.00€200mg1,786.00€1mL*10mM (DMSO)344.00€AMP-945
CAS:AMP-945 is a proprietary focal adhesion kinase (FAK) inhibitor.Formula:C28H32F3N5O2Purity:99.60%Color and Shape:SolidMolecular weight:527.58Ref: TM-T9576
1mg97.00€5mg188.00€10mg311.00€25mg533.00€50mg755.00€100mg1,035.00€1mL*10mM (DMSO)254.00€Etrolizumab
CAS:MEDI-578 is a CHO-expressed humanized monoclonal antibody targeting NGF/bNGF for the study of neurological and immune system disorders.Purity:95% - 95%Color and Shape:LiquidAdhesamine diTFA
CAS:Adhesamine diTFA, a dumbbell-shaped molecule, activates the MAPK/FAK pathway. It promotes adhesion and growth in mammalian cells and accelerates differentiation and enhances the survival rate of primary cultured mouse hippocampal neurons.Formula:C28H32Cl2F6N8O6S2Color and Shape:SolidMolecular weight:825.63BX-2819
CAS:BX-2819 is an Hsp90 inhibitor that exhibits potent antiproliferative activity with an IC50 of 41 nM .Formula:C21H24N4O4SPurity:98%Color and Shape:SolidMolecular weight:428.51αvβ1 integrin-IN-1 TFA (1689540-62-2 free base)
αvβ1 integrin-IN-1 TFA is an effective and selective αvβ1 integrin inhibitor (IC50: 0.63 nM).Formula:C28H35F3N6O8SPurity:98%Color and Shape:SolidMolecular weight:672.67Hydroxy-Dynasore
CAS:Hydroxy-Dynasore (Dyngo-4a) , a effective dynamin inhibitor, inhibits withDynI (brain), DynI (rec), and DynII (rec) of IC50 of 0.38 μM, 1.1 μM, and 2.3 μM,Formula:C18H14N2O5Purity:100% - 97.60%Color and Shape:SolidMolecular weight:338.31Ref: TM-T6822
5mg50.00€10mg84.00€25mg137.00€50mg221.00€100mg329.00€200mg490.00€500mg783.00€1mL*10mM (DMSO)55.00€αvβ6-IN-1
αvβ6-IN-1 (compound 28) is an effective orally active inhibitor of αvβ6 integrin (αvβ6integrin), with a pIC50 value of 8.1. This compound shows potential for research in idiopathic pulmonary fibrosis.Formula:C25H32F2N4O3Color and Shape:SolidMolecular weight:474.5416-38-Thymosin β4 (cattle) (TFA)
Thymosin β4 (cattle) TFA is a high-affinity activator of MLCK that operates independently of Ca2+ [1].Formula:C120H205F3N32O43Purity:98%Color and Shape:SolidMolecular weight:2841.1K858 (Racemic)
CAS:K858 Racemic (K858) is a selective mitotic kinesin Eg5 inhibitor which acts in an ATP-noncompetitive manner.Formula:C13H15N3O2SPurity:100%Color and Shape:SolidMolecular weight:277.34AZ13705339
CAS:AZ13705339 is an effective inhibitor of PAK1 with an IC50 of 0.33 nM and a Kd of 0.28 nM.Formula:C33H36FN7O3SPurity:98.57%Color and Shape:SolidMolecular weight:629.75FAK-IN-7
CAS:FAK-IN-7 has potential antiproliferative activity and is a FAK inhibitor.Formula:C16H13N3OSPurity:98.2%Color and Shape:SolidMolecular weight:295.36AJH-836
CAS:AJH-836 is a compound that activates Munc13-1 and PKC ε/α, demonstrating a dissociation constant (Kd) of 4.5 nM for PKCα, and facilitates the translocation ofFormula:C22H38O5Purity:98%Color and Shape:SolidMolecular weight:382.5310-Deacetyltaxol
CAS:10-Deacetyltaxol (10-DAT) is extracted from Taxus brevifolia barks.Formula:C45H49NO13Purity:94.63% - 99.93%Color and Shape:SolidMolecular weight:811.87Tadocizumab
CAS:Tadocizumab (C4G1) is a humanized monoclonal antibody targeting integrin αIIbβ3 with antiplatelet and antithrombotic effects.Color and Shape:LiquidKNK437
CAS:KNK437 (Heat Shock Protein Inhibitor I), a pan-HSP inhibitor, suppresses the synthesis of inducible HSPs(HSP105, HSP72, and HSP40).Formula:C13H11NO4Purity:98.90%Color and Shape:SolidMolecular weight:245.23PKC-IN-1
CAS:PKC-IN-1 is an ATP-competitive and reversible conventional PKC enzymes inhibitor (PKCα, PKCβI, PKCβII, PKCθ, PKCγ, PKC mu and PKCε with IC50s of 2.3, 8.1, 7.6,Formula:C25H37FN8O2Purity:98% - 98.79%Color and Shape:SolidMolecular weight:500.61Gamitrinib TPP
CAS:Gamitrinib TPP targets mitochondrial HSP90, inhibiting cancer, and blocks mitochondrial matrix.Formula:C52H65N3O8PPurity:98%Color and Shape:SolidMolecular weight:891.078API-1
CAS:API-1 (NSC-177223) is a potent inhibitor of Akt. It induces GSK3-dependent, β-TrCP- and FBXW7-mediated Mcl-1 degradation, resulting in induction of apoptosis .Formula:C13H15N5O6Purity:99.07%Color and Shape:SolidMolecular weight:337.29Ref: TM-T8969
1mg59.00€5mg125.00€10mg207.00€25mg376.00€50mg562.00€100mg787.00€200mg1,035.00€1mL*10mM (DMSO)133.00€AKT-IN-1
CAS:AKT-IN-1 (AZD-26) is an allosteric AKT inhibitor (IC50: 1.04 μM).Formula:C22H21N3OPurity:98.63%Color and Shape:SolidMolecular weight:343.42Ref: TM-T4489
1mg113.00€2mg158.00€5mg235.00€10mg400.00€25mg652.00€50mg909.00€100mg1,225.00€1mL*10mM (DMSO)188.00€HSP70/SIRT2-IN-2
CAS:HSP70/SIRT2-IN-2 (Compounds 1a), a dual inhibitor of SIRT2 and HSP70, exhibits an IC50 of 45.1±5.0 μM against SIRT2 and demonstrates antitumor activity [1].Formula:C17H13N3S3Purity:98%Color and Shape:SolidMolecular weight:355.5LXH254
CAS:LXH254 is a B/C RAF inhibitor with IC50 values of 0.2 nM and 0.07 nM for inhibiting BRAF and CRAF.Cost-effective and quality-assured.Formula:C25H25F3N4O4Purity:98.3% - 99.92%Color and Shape:SolidMolecular weight:502.49Ref: TM-T11898
1mg52.00€5mg122.00€10mg185.00€25mg363.00€50mg567.00€100mg690.00€200mg948.00€500mg1,444.00€1mL*10mM (DMSO)135.00€Debio 0932
CAS:Debio 0932 (CUDC-305) is a Hsp9 inhibitor, apoptosis, and has the advantage of being orally available and cross the BBB for cancers NSCLC and neuroblastoma.Formula:C22H30N6O2SPurity:98.98%Color and Shape:SolidMolecular weight:442.58AT9283
CAS:AT9283 (J-504568) is an effective multi-targeted inhibitor of JAK2(IC50=1.2 nM) and JAK3(IC50=1.1 nM), Aurora A, Aurora B and Abl(T315I).Formula:C19H23N7O2Purity:99.83% - 99.98%Color and Shape:SolidMolecular weight:381.43Ref: TM-T3068
1mg47.00€2mg60.00€5mg95.00€10mg170.00€25mg299.00€50mg499.00€100mg723.00€1mL*10mM (DMSO)97.00€Bisindolylmaleimide III
CAS:Bisindolylmaleimide III is a potent and selective inhibitor of protein kinase C (PKC).Bisindolylmaleimide III selectively interacts with PKCα or ribosomal S6Formula:C23H20N4O2Purity:98.6%Color and Shape:SolidMolecular weight:384.43Pifithrin-μ
CAS:Pifithrin-μ (NSC-303580) is an inhibitor of p53 and HSP70, with neuroprotective and antitumor activity.Formula:C8H7NO2SPurity:99.33% - 99.79%Color and Shape:SolidMolecular weight:181.21KP-23172
CAS:KP-23172 is a inhibitor of PI3-K/Akt pathway.Formula:C10H4N6OPurity:98%Color and Shape:SolidMolecular weight:224.18ML346
CAS:ML346 is a novel activator of Hsp70.Formula:C14H12N2O4Purity:99.25% - 99.29%Color and Shape:SolidMolecular weight:272.26Ref: TM-T3594
1mg40.00€2mg52.00€5mg85.00€10mg115.00€25mg172.00€50mg274.00€100mg427.00€500mg938.00€1mL*10mM (DMSO)85.00€Degrasyn
CAS:Degrasyn (WP1130) inhibits DUBs (USP5, UCH-L1, USP9x, USP14, UCH37) and Bcr/Abl without affecting the 20S proteasome.Formula:C19H18BrN3OPurity:98.32% - 99.98%Color and Shape:SolidMolecular weight:384.27Ref: TM-T6300
2mg44.00€5mg64.00€10mg97.00€25mg198.00€50mg340.00€100mg532.00€200mg747.00€1mL*10mM (DMSO)69.00€Phorbol 12,13-dibutyrate
CAS:Phorbol 12,13-dibutyrate (Phorbol dibutyrate) is a PKC activator that induces contraction of isolated rabbit vascular smooth muscle.Formula:C28H40O8Purity:100% - 99.32%Color and Shape:SolidMolecular weight:504.61Ref: TM-T16526
1mg62.00€5mg169.00€10mg283.00€25mg557.00€50mg795.00€100mg1,074.00€1mL*10mM (DMSO)180.00€Akt3 degrader 1
CAS:Akt3 degrader 1 counters Osimertinib resistance in NSCLC, inhibits cell growth, and reduces mouse tumors.Formula:C53H72N8O4Purity:98.18% - 99.14%Color and Shape:SolidMolecular weight:885.19VTX-27
CAS: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).Formula:C20H24ClFN6OPurity:99.49%Color and Shape:SolidMolecular weight:418.9Ref: TM-T13314
1mg93.00€2mg125.00€5mg244.00€10mg364.00€25mg562.00€50mg780.00€100mg1,035.00€1mL*10mM (DMSO)225.00€Ruboxistaurin hydrochloride
CAS:Ruboxistaurin HCl (LY 333531) selectively inhibits PKCβI/II with IC50 of 4.7/5.9 nM; much less effective on other PKC types and ATP-kinases.Formula:C28H28N4O3·HClPurity:98.44% - 99.22%Color and Shape:SolidMolecular weight:505.01Ref: TM-T3689
1mg71.00€2mg93.00€5mg157.00€10mg256.00€25mg513.00€50mg740.00€100mg1,035.00€500mg2,072.00€1mL*10mM (DMSO)202.00€Imatinib
CAS:Imatinib (STI571) is a multi-targeted receptor tyrosine kinase inhibitor that selectively inhibits the kinase activities of BCR/ABL, v-Abl, PDGFR, and c-kitFormula:C29H31N7OPurity:100% - 99.94%Color and Shape:Off White PowderMolecular weight:493.6Tetradecyltrimethylammonium bromide
CAS:Tetradecyltrimethylammonium bromide (MitMAB) is a Dynamin GTPase activity inhibitor and a cationic surfactant with asymmetrical structure.Formula:C17H38BrNPurity:100%Color and Shape:SolidMolecular weight:336.39K-252b
CAS:K-252b, an indolocarbazole derived from the actinomycete Nocardiopsis, functions as a protein kinase C (PKC) inhibitor.Formula:C26H19N3O5Purity:98%Color and Shape:Ready-To-Use SolutionMolecular weight:453.45Larazotide acetate
CAS:Larazotide acetate is a synthetic peptide. It functions as a tight junction regulator and reverses leaky junctions to their normally closed state.Formula:C34H59N9O12Purity:95.53%Color and Shape:SolidMolecular weight:785.89para-Nitroblebbistatin
CAS:para-Nitroblebbistatin is a non-cytotoxic, non-fluorescent, photostable, and specific inhibitor of myosin II.Cost-effective and quality-assured.Formula:C18H15N3O4Purity:100% - 99.92%Color and Shape:SolidMolecular weight:337.33Ref: TM-T12360
1mg87.00€5mg212.00€10mg316.00€25mg512.00€50mg695.00€100mg940.00€200mg1,264.00€1mL*10mM (DMSO)215.00€Chromeceptin
CAS:Chromeceptin is an inhibitor of the IGF signaling pathway, decreases the numbers of tumorsphere, and inhibits the AKT/mTOR pathway.Formula:C19H16F3N3OPurity:99.72%Color and Shape:SoildMolecular weight:359.35Ref: TM-T60055
5mg50.00€10mg74.00€25mg140.00€50mg197.00€100mg306.00€200mg442.00€1mL*10mM (DMSO)51.00€PU-H71
CAS:PU-H71 is an effective selective HSP90 inhibitor with an IC50 of 51 nM.Formula:C18H21IN6O2SPurity:98.31%Color and Shape:SolidMolecular weight:512.37Delcasertib
CAS:Delcasertib (KAI-9803) is a potent and selective inhibitor of δ-protein kinase C (δPKC).Formula:C120H199N45O34S2Purity:99.96%Color and Shape:SolidMolecular weight:2880.28Ref: TM-T11740
1mg202.00€5mg512.00€10mg740.00€25mg1,121.00€50mg1,539.00€100mg2,072.00€1mL*10mM (DMSO)1,691.00€1-Oleoyl-2-acetyl-sn-glycerol
CAS:1-Oleoyl-2-acetyl-sn-glycerol (1-oleoyl-2-acetyl-glycerol) is a PKC activator that induces superoxide production.Formula:C23H42O5Color and Shape:SolidMolecular weight:398.58Nilotinib hydrochloride
CAS:Nilotinib HCl (AMN-107 HCl), an oral Bcr-Abl inhibitor, targets neuroinflammation, cognitive issues, and chronic myelogenous leukemia.Formula:C28H23ClF3N7OPurity:100%Color and Shape:SolidMolecular weight:565.98Hispidin
CAS:Hispidin is a polyphenol originally, including antioxidant, anti-inflammatory, and cytoprotective propertiesFormula:C13H10O5Purity:98.27%Color and Shape:White Crystalline PowderMolecular weight:246.22Ref: TM-T7792
1mg88.00€5mg187.00€10mg298.00€25mg533.00€50mg747.00€100mg1,017.00€1mL*10mM (DMSO)207.00€SB-743921 hydrochloride
CAS:SB-743921 hydrochloride (SB743921 HCl) is an effective inhibitor of kinesin spindle protein, KSP, (Ki =0.1 nM).Formula:C31H34Cl2N2O3Purity:95.58% - 99.70%Color and Shape:SolidMolecular weight:553.52Ref: TM-T2255
1mg42.00€5mg106.00€10mg163.00€25mg278.00€50mg429.00€100mg657.00€500mg1,501.00€1mL*10mM (DMSO)130.00€PPY A
CAS: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 cellsFormula:C22H20N4O2Purity:98.77%Color and Shape:SolidMolecular weight:372.42ILK-IN-2
CAS:ILK-IN-2 (OSU-T315) is a novel potent, orally active ILK (integrin-linked kinase) inhibitor with IC50 of 0.6 μM.Formula:C30H30F3N5OPurity:99.30%Color and Shape:SolidMolecular weight:533.59Ref: TM-T5488
1mg48.00€5mg97.00€10mg128.00€25mg162.00€50mg192.00€100mg281.00€200mg408.00€1mL*10mM (DMSO)137.00€Rosabulin
CAS:v Rosabulin (STA 5312) is an orally active microtubule inhibitor with potency.Formula:C22H16N4O2SPurity:98.06%Color and Shape:SolidMolecular weight:400.45Ref: TM-T16788
1mg97.00€5mg243.00€10mg364.00€25mg658.00€50mg938.00€100mg1,415.00€1mL*10mM (DMSO)265.00€Arg-Gly-Asp-Ser acetate
Arg-Gly-Asp-Ser acetate targets integrin, binding pro-caspase-8, -9, -3, but not -1; inhibits receptor function.Formula:C17H31N7O10Purity:98.14%Color and Shape:SolidMolecular weight:493.47Hsp90-IN-34
CAS:Hsp90-IN-34 (compound HAM-1) is a chemical inhibitor that targets the Aha1-Hsp90 chaperone complex with high affinity (KDapp=23.5 µM). It modulates the ATPase activity of Hsp90 by affecting the interaction between Hsp90 and Aha1.Formula:C22H14F2N6OColor and Shape:SolidMolecular weight:416.38Mivobulin
CAS:Mivobulin is an inhibitor of tubulin .Formula:C17H19N5O2Purity:98%Color and Shape:SolidMolecular weight:325.37FPA-124
CAS:FPA-124 is a cell-permeable copper complex that acts as a selective Akt (protein kinase B) inhibitor to induce apoptosis in a variety of cancer cell lines.Formula:C11H9Cl2CuN3O2SPurity:95.04%Color and Shape:SolidMolecular weight:381.73ZLY06
CAS:ZLY06 is a dual agonist of peroxisome proliferator-activated receptors (PPAR) δ and γ with oral activity (PPAR δ: EC50=341 nM; PPARγ: EC50=237 nM). It mediates the upregulation of CD36 and induces hepatic lipid accumulation by inhibiting the phosphorylation of AKT1. Moreover, ZLY06 significantly improves glucose and lipid metabolism without increasing body weight, primarily by enhancing the β-oxidation of fatty acids and reducing hepatic lipid synthesis, thereby alleviating fatty liver disease.Formula:C25H26O6Color and Shape:SolidMolecular weight:422.47ATN-161 trifluoroacetate salt
CAS:ATN-161 TFA salt, a new integrin α5β1 inhibitor, curbs angiogenesis, liver metastases growth, enhances survival in mice.Formula:C25H36F3N9O10SPurity:98% - 99.98%Color and Shape:SolidMolecular weight:711.67PND-1186
CAS:PND-1186 (VS-4718) is a reversible and specific FAK inhibitor (IC50: 1.5 nM).Formula:C25H26F3N5O3Purity:99.14% - 99.75%Color and Shape:SolidMolecular weight:501.5Catumaxomab
CAS:Catumaxomab is a rat-mouse hybrid lgG2 monoclonal and bispecific antibody that binds to the antigens CD3 and EpCAM for malignant ascites in cancer patients.Purity:95%Color and Shape:LiquidCK-869
CAS:CK-869 is an Actin-Related Protein 2/3 (ARP2/3) complex inhibitor(IC50 of 7 μM),and is useful tools for the investigation of the Arp2/3 complex.Formula:C17H16BrNO3SPurity:99.85%Color and Shape:SolidMolecular weight:394.28Zelavespib hydrochloride
Zelavespib (PU-H71) hydrochloride is a potent inhibitor of Hsp90, exhibiting an IC50 value of 51 nM in MDA-MB-468 cells.Purity:98%Color and Shape:Odour SolidSC79
CAS:SC79 is an AKT agonist with specificity and blood-brain barrier permeability.Formula:C17H17ClN2O5Purity:98% - 99.93%Color and Shape:SolidMolecular weight:364.78β-glycosidase-IN-1
CAS:β-glycosidase-IN-1 is a piperidine derivative, and is an inhibitor of β-glycosidase. It has hypoglycemic activity.Formula:C13H23NO5Purity:98%Color and Shape:SolidMolecular weight:273.33A-3 hydrochloride
CAS:A-3 hydrochloride: potent, reversible kinase antagonist; permeable; inhibits PKC, CKI, PKA, CKII, MLCK; Ki: 4.3-80 μM.Formula:C12H14Cl2N2O2SPurity:99.32%Color and Shape:SolidMolecular weight:321.22Ref: TM-T14069
1mg35.00€5mg66.00€10mg96.00€25mg170.00€50mg274.00€100mg439.00€500mg938.00€1mL*10mM (DMSO)90.00€(8R)-8-Hydroxyepoxyboetirane A
(8R)-8-Hydroxyepoxyboetirane A is a neuroactivating compound that interacts with PKCδ-C1B. This compound binds into the PKC enzyme pocket through hydrogen bonds with glycine-253, leucine-251, and threonine-242. It induces the release of NRG1 and promotes the differentiation of neural stem cells into neurons. (8R)-8-Hydroxyepoxyboetirane A holds potential for research into nervous system disorders.Color and Shape:Odour SolidTASP0415914
CAS:TASP0415914 is an orally potent inhibitor of phosphoinositide 3-kinase γ (PI3Kγ). TFormula:C13H17N5O3SPurity:98.14%Color and Shape:SolidMolecular weight:323.37Ref: TM-T7879
1mg55.00€5mg117.00€10mg187.00€25mg315.00€50mg449.00€100mg620.00€200mg835.00€1mL*10mM (DMSO)134.00€Orbofiban TFA
CAS:Orbofiban TFA is an orally active GPIIb/IIIa platelet receptor antagonist with inhibitory effects on platelet aggregation for the study of unstable coronaryFormula:C19H24F3N5O6Purity:97.45% - 98.43%Color and Shape:SolidMolecular weight:475.42HSP27 inhibitor J2
CAS:HSP27 inhibitor J2 (J2) (J2) is a HSP27 inhibitor, inhibits a production of HSP27 giant polymers, thereby having an effect of inhibiting a chaperone function ofFormula:C13H12O4SPurity:99.51%Color and Shape:SolidMolecular weight:264.3Ref: TM-T7265
1mg130.00€2mg185.00€5mg311.00€10mg472.00€25mg753.00€50mg1,064.00€100mg1,415.00€1mL*10mM (DMSO)455.00€Firategrast
CAS:Firategrast (SB 683699) is an orally active and specific α4β1/α4β7 integrin antagonist.Firategrast reduces the transport of lymphocytes into the central nervousFormula:C27H27F2NO6Purity:99.16%Color and Shape:SolidMolecular weight:499.5Ref: TM-TQ0291
1mg47.00€5mg87.00€10mg140.00€25mg283.00€50mg464.00€100mg747.00€200mg1,017.00€1mL*10mM (DMSO)97.00€Vevorisertib trihydrochloride
CAS:Vevorisertib trihydrochloride (ARQ 751 trihydrochloride) is ainhibitor of pan-AKT and AKT1-E17K mutations, inhibiting AKT1, AKT2 and AKT3.Formula:C35H41Cl3N8OPurity:98.28%Color and Shape:SolidMolecular weight:696.12Ref: TM-T38846
1mg70.00€5mg149.00€10mg230.00€25mg393.00€50mg552.00€100mg740.00€200mg1,130.00€1mL*10mM (DMSO)212.00€Teprenone
CAS:Teprenone (Geranylgeranylacetone) is a anti-ulcer drug, and works as an inducer of heat shock proteins (HSPs).Formula:C23H38OPurity:99.76% - 99.96%Color and Shape:SolidMolecular weight:330.55FAK-IN-14
CAS:FAK-IN-14 is a FAK inhibitor that induces apoptosis and cell cycle arrest. FAK-IN-14 has a more significant inhibitory effect on FAK, FGFR1 and Pyk2.Formula:C21H24BrN7OSPurity:99.7%Color and Shape:SoildMolecular weight:502.43BNC105
CAS:BNC105 is a tubulin polymerization inhibitor. It has potent antiproliferative and tumor vascular disrupting properties.Formula:C20H20O7Purity:96.57%Color and Shape:SolidMolecular weight:372.37Ref: TM-T14694
1mg84.00€5mg160.00€10mg226.00€25mg371.00€50mg520.00€100mg702.00€200mg944.00€1mL*10mM (DMSO)170.00€Teclistamab
CAS:Teclistamab(JNJ-64007957) is a human bispecific monoclonal antibody targeting the CD3 receptor on t-cells and the BCMA for relapsed and refractory multiple myeloma.Purity:95%Color and Shape:LiquidPentachloropseudilin
CAS:Pentachloropseudilin inhibits Myosin-1 and speeds up TGF-β receptor turnover, suppressing TGF-β activity.Formula:C10H4Cl5NOPurity:98.14%Color and Shape:SolidMolecular weight:331.41PF-562271
CAS:PF-562271 is an effective ATP-competitive, reversible inhibitor of FAK(IC50=1.5 nM) and Pyk2 kinase(IC50=13 nM).Formula:C21H20F3N7O3SPurity:100% - 97.65%Color and Shape:SolidMolecular weight:507.49Ref: TM-T2465
1mg59.00€5mg127.00€10mg159.00€25mg240.00€50mg378.00€100mg567.00€200mg793.00€1mL*10mM (DMSO)140.00€Akt1 and Akt2-IN-1
CAS:Akt1 and Akt2-IN-1 is an allosteric inhibitor of Akt1 (IC50=3.5 nM) and Akt2 (IC50=42 nM). It has potent and balanced activity.Formula:C33H29N7OColor and Shape:SolidMolecular weight:539.63cSRC/BCR-ABL-IN-1
cSRC/BCR-ABL-IN-1 (compound 21b) is a potent inhibitor of Bcr-Abl and C-Src, with IC50 values of 56.2 nM and 101 nM, respectively. It exhibits cytotoxicity.Formula:C29H31Cl2N5O4Molecular weight:584.494ε-V1-2, Cys-conjugated
Epsilon-V1-2, a Cys-conjugated, is a biologically active peptide known as the εPKC-specific inhibitor.Formula:C40H70N10O14SPurity:98%Color and Shape:SolidMolecular weight:947.11Miltefosine
CAS:Miltefosine (HePC), effective oral drug for both visceral and cutaneous leishmaniasis, in clinical trials worldwide.Formula:C21H46NO4PPurity:98% - 99.87%Color and Shape:White To Off-White PowderMolecular weight:407.57SMTIN-T140
CAS:SMTIN-T140: strong TRAP1 inhibitor, IC50=1.646μM, anticancer; disrupts mitochondria, boosts ROS, activates AMPK, shrinks PC3 tumors, no in vivo toxicity.Formula:C36H34BrClFN5OPPurity:98%Color and Shape:SolidMolecular weight:718.02HA-100
CAS:HA-100 is an inhibitor of protein kinaseFormula:C13H15N3O2SPurity:99.44%Color and Shape:Pale Yellow Crystalline SolidMolecular weight:277.3420-HETE
CAS:20-HETE is a CYP450 product, vasoconstrictor, modulates K+ channels, affects NADPH, ROS, NF-κB, NO synthase, and cell apoptosis/proliferation.Formula:C20H32O3Purity:99.79%Color and Shape:SolidMolecular weight:320.47Ref: TM-T14021
1mg (312.04μM*10mL in Ethanol)1,139.00€5mg (312.04μM*50mL in Ethanol)2,327.00€100μg (312.04μM*1mL in Ethanol)474.00€PKCiota-IN-2
CAS:PKCiota-IN-2 selectively inhibits PKC-ι (IC50=2.8nM) and also blocks PKC-α, ε (IC50s=71nM, 350nM).Formula:C24H21N5OPurity:99.74%Color and Shape:SolidMolecular weight:395.46Ref: TM-T9863
1mg115.00€2mg172.00€5mg255.00€10mg375.00€25mg562.00€50mg792.00€100mg1,064.00€1mL*10mM (DMSO)279.00€(E)-Akt inhibitor-IV
CAS:(E)-Akt inhibitor-IV ((E)-AKTIV) ((E)-AKTIV) is an inhibitor of PI3K-Akt.Formula:C31H29IN4SPurity:99.01% - 99.74%Color and Shape:SolidMolecular weight:616.56Ref: TM-T9393
1mg55.00€5mg116.00€10mg180.00€25mg338.00€50mg469.00€100mg655.00€200mg924.00€1mL*10mM (DMSO)157.00€Eupalinolide A
CAS:Eupalinolide B is a natural product ,and demonstrates potent cytotoxicity against A-549, BGC-823, SMMC-7721, and HL-60 tumour cell lines.Formula:C24H30O9Purity:98.18% - 99.22%Color and Shape:SolidMolecular weight:462.49Taurochenodeoxycholic acid sodium
CAS:Sodium taurochenodeoxycholate: induces apoptosis, anti-inflammatory, boosts insulin, stimulates α2-cells, increases [Ca(2+)](c).Formula:C26H44NNaO6SPurity:98.23% - 99.45%Color and Shape:White To Off-White PowderMolecular weight:521.68Arimoclomol maleate
CAS:Arimoclomol maleate (BRX-220) (BRX-220) is a heat shock protein (HSP) co-inducer.Formula:C18H24ClN3O7Purity:99.9% - 99.98%Color and Shape:SolidMolecular weight:429.85Ombrabulin hydrochloride
CAS:Ombrabulin hydrochloride is a synthetic, selective CA-4 phosphate ester or derivative of Ombrabulin to disrupt the tubulin cytoskeleton of endothelial cells andFormula:C21H27ClN2O6Purity:98%Color and Shape:SolidMolecular weight:438.9Roslin 2 bromide
CAS:Roslin 2 bromide (Benzylhexamethylenetetramine bromide) is a p53 reactivator that disrupts the binding of FAK and p5.Formula:C13H19BrN4Purity:97.07%Color and Shape:SolidMolecular weight:311.22FRAX486
CAS:FRAX486 is a potent p21-activated kinase (PAK) inhibitor with IC50 values of 14, 33, 39 and 575 nM for PAK1, PAK2, PAK3 and PAK4 respectively.Formula:C25H23Cl2FN6OPurity:98.81%Color and Shape:SolidMolecular weight:513.39AKT-IN-26
CAS:AKT-IN-26 (Compound 453) is an AKT inhibitor that binds to the Pleckstrin Homology (PH) domain of AKT. It is useful for research related to cell proliferation and cancer involving the AKT pathway.Formula:C21H17N5O4SColor and Shape:SolidMolecular weight:435.456JG-231
CAS:JG-231, a JG-98 analog, shows anticancer properties by blocking Hsp70-BAG3 interaction and hindering TNBC in MDA-MB-231 models.Formula:C22H18BrCl2N3OS4Purity:99.21%Color and Shape:SolidMolecular weight:619.47TN-16
CAS:TN-16 is a microtubule polymerization inhibitor (IC50 :0.4-1.7 μM)Formula:C19H18N2O2Purity:99.54%Color and Shape:SolidMolecular weight:306.36LXW7
CAS:LXW7 is an octamer disulfide cyclic peptide and αvβ3 integrin ligand, acts as a potent and specific endothelial progenitor cells (EPCs) and endothelial cells (Formula:C29H48N12O12S2Purity:100%Color and Shape:SolidMolecular weight:820.89Batatasin III
CAS:Batatasin III inhibits cancer migration and invasion by suppressing epithelial to mesenchymal transition and FAK-AKT signals and possesses anti-cancerFormula:C15H16O3Purity:99.16%Color and Shape:SolidMolecular weight:244.29HM03
CAS:HM03 is a potent and selective inhibitor of HSPA5, and has anticancer activity.Formula:C26H27ClN4O2Purity:97.15%Color and Shape:SolidMolecular weight:462.97AT7867
CAS:AT7867 inhibits Akt1/2/3 & p70S6K/PKA (IC50: 32/17/47 nM & 85/20 nM), minimal effect beyond AGC kinases.Formula:C20H20ClN3Purity:99.63%Color and Shape:SolidMolecular weight:337.85Ref: TM-T6304
2mg44.00€5mg65.00€10mg86.00€25mg135.00€50mg210.00€100mg313.00€200mg452.00€1mL*10mM (DMSO)65.00€2-Methylbutyrylcarnitine chloride
2-Methylbutyrylcarnitine (chloride) acts as a gut microbial metabolite that targets integrin α2β1 on platelets, facilitating the activation of cytosolic phospholipase A2 (cPLA2) and enhancing platelet hyperresponsiveness. This compound further augments platelet hyperreactivity and promotes thrombus formation in mice. It is also characterized as a branched-chain acylcarnitine.Formula:C12H24ClNO4Color and Shape:SolidMolecular weight:281.78Arginine-glycine-aspartic acid
CAS:RGD (RGD (Arg-Gly-Asp) Peptides) (Arg-Gly-Asp) Peptides is a cell adhesion motif which can mimic cell adhesion proteins and bind to integrins.Formula:C12H22N6O6Purity:99.11%Color and Shape:SolidMolecular weight:346.34Valategrast hydrochloride
CAS:Valategrast hydrochloride (R411), a dual antagonist of integrin α4β1 (VLA-4), is used for the potential treatment of asthma.Formula:C30H33Cl4N3O4Purity:98%Color and Shape:SolidMolecular weight:641.41Irigenin
CAS:Irigenin mediates its antimetastatic effect by specifically and selectively blocking the α9β1 and α4β1 integrin binding sites on the C-C loop of the ExtraFormula:C18H16O8Purity:99.50% - 99.85%Color and Shape:SolidMolecular weight:360.31Afuresertib hydrochloride
CAS:Afuresertib hydrochloride is an inhibitor of Akt kinase (Kis of 0.08/2/2.6 nM for Akt1/Akt2/Akt3 respectively)Formula:C18H18Cl3FN4OSPurity:99.96%Color and Shape:SolidMolecular weight:463.8Ref: TM-T7885
2mg52.00€5mg74.00€10mg95.00€25mg163.00€50mg253.00€100mg437.00€200mg568.00€1mL*10mM (DMSO)86.00€Bersanlimab
CAS:Bersanlimab (BI-505) is a fully human monoclonal antibody targeting Intercellular Adhesion Molecule-1 (ICAM-1).Bersanlimab has anticancer properties.Purity:> 95% - > 95%Color and Shape:LiquidMolecular weight:144.22 kDaDolastatin 10
CAS:Dolastatin 10 (DLS 10) is a powerful peptide with antimitotic properties, effectively inhibiting tubulin polymerization.Formula:C42H68N6O6SPurity:99.55%Color and Shape:SolidMolecular weight:785.09Shepherdin 79-87 acetate
Shepherdin 79-87 acetate is a peptidomimetic antagonist of the complex between Hsp90 and survivin, another key regulator of tumor cell viability.Formula:C43H68N12O14SPurity:98.08%Color and Shape:SolidMolecular weight:1009.14G-5555
CAS:G-5555 is a potent inhibitor of p21-activated kinase 1 (PAK1) (Kis: 3.7 nM and 11 nM for PAK1 and PAK2, respectively).Formula:C25H25ClN6O3Purity:99.76% - 99.87%Color and Shape:SolidMolecular weight:492.96Flumatinib
CAS:Flumatinib (HHGV678) is an orally bioavailable tyrosine kinase inhibitor flumatinib, with potential antineoplastic activity.Formula:C29H29F3N8OPurity:99.52% - 99.95%Color and Shape:SolidMolecular weight:562.59Ref: TM-T4320
1mg35.00€5mg66.00€10mg87.00€25mg127.00€50mg163.00€100mg273.00€200mg409.00€500mg677.00€1mL*10mM (DMSO)87.00€Betamethasone 17-benzoate
CAS:Betamethasone 17-benzoate is a representative steroid. It also can be used in the treatment of recurrent aphothous ulcers (RAU).Formula:C29H33FO6Purity:98%Color and Shape:SolidMolecular weight:496.57EC 144
CAS:EC 144, a second-generation selective inhibitor of Hsp90 , inhibits tumor growth for Hsp90α and degradation of Her-2 in MCF-7 cells.Formula:C21H24ClN5O2Color and Shape:SolidMolecular weight:413.9BRD9876
CAS:BRD9876 is a selective inhibitor of MM1S growth.Formula:C16H14N2Purity:97.81%Color and Shape:SolidMolecular weight:234.3FAK-IN-15
FAK-IN-15 is a highly potent focal adhesion kinase (FAK) inhibitor with antitumor activity.Formula:C21H24ClN7OSPurity:99.08%Color and Shape:SolidMolecular weight:457.98Palmitic acid
CAS:Palmitic acid (Cetylic acid) is a natural product, a common saturated fatty acid found in animals, plants and microorganisms.Formula:C16H32O2Purity:99.17% - 99.67%Color and Shape:White Crystalline Scales SolidMolecular weight:256.42Cyclo(RADfK)
CAS:Cyclo(RADfK) is a selective α(v)β(3) integrin ligand used in neoangiogenesis research, therapy, and diagnostics; it's a control for RGD peptides.Formula:C28H43N9O7Purity:100%Color and Shape:SolidMolecular weight:617.7Auristatin F
CAS:Auristatin F is an effective inhibitor of microtubule and vascular damaging agent. Auristatin F can be used in antibody-drug conjugates.Formula:C40H67N5O8Purity:98.41% - 99.25%Color and Shape:SolidMolecular weight:745.99AM-5308
CAS:AM-5308 is a kinesin KIF18A inhibitor that can be used to study cancer.Formula:C26H35N5O5SPurity:98.06% - 99.58%Color and Shape:SolidMolecular weight:529.65MMAF
CAS:MMAF (MonoMethyl auristatin F), an antimitotic agent, inhibits cell division by blocking the polymerization of tubulin.Formula:C39H65N5O8Purity:97.00%Color and Shape:SolidMolecular weight:731.96GRGDSPK
CAS:GRGDSPK (EMD 56574) is an inhibitory peptide for RGD-mediated adhesion between integrin and extracellular matrix molecules.Formula:C28H49N11O11Purity:98%Color and Shape:SolidMolecular weight:715.76Amiprofos methyl
CAS:Amiprofos methyl (BAY-NTN 6867) is an organophosphorus herbicide that specifically and competitively inhibits microtubule polymerization in plant cells.Formula:C11H17N2O4PSPurity:99.66%Color and Shape:SolidMolecular weight:304.3Elarofiban
CAS:Elarofiban(RWJ-53308) is a novel and orally active GPIIb/IIIa antagonist.Formula:C22H32N4O4Purity:99.94%Color and Shape:SolidMolecular weight:416.51cemadotin free base
CAS:Cemadotin free base(LU103793 free base) is a novel anti-limiting peptide , an analog of Dolastatin 15, a naturally occurring cytotoxic peptide that blocksFormula:C35H56N6O5Purity:99% - 99.69%Color and Shape:SolidMolecular weight:640.86JH-VIII-157-02
CAS:JH-VIII-157-02 inhibits ALK, specifically EML4-ALK variants, with IC50s of 2 nM.Formula:C28H27N5O2Purity:98.02%Color and Shape:SolidMolecular weight:465.55Ref: TM-T15612
1mg116.00€5mg240.00€10mg358.00€25mg558.00€50mg753.00€100mg1,035.00€1mL*10mM (DMSO)246.00€N-Desmethyltamoxifen hydrochloride
CAS:N-Desmethyltamoxifen hydrochloride is the major tamoxifen metabolite in humans.Formula:C25H28ClNOPurity:99.15%Color and Shape:SolidMolecular weight:393.95Ref: TM-T12148
2mg35.00€5mg52.00€10mg78.00€25mg139.00€50mg202.00€100mg305.00€200mg426.00€1mL*10mM (DMSO)52.00€Dasatinib monohydrate
CAS:Dasatinib monohydrate, an oral SRC-kinase inhibitor, counters imatinib-resistant chronic myeloid leukemia.Formula:C22H28ClN7O3SPurity:100% - 99.68%Color and Shape:SolidMolecular weight:506.03Bisindolylmaleimide I
CAS:Bisindolylmaleimide I (GF109203X) is a potent and highly selective protein kinase C (PKC) inhibitor with a Ki of 14 nM.Formula:C25H24N4O2Purity:98.19% - 99.08%Color and Shape:Orange SolidMolecular weight:412.48C086
CAS:C086 is a novel and potent Hsp90 inhibitor that suppresses cell cycle progression, induces apoptosis, and exhibits anti-metastatic properties by modulating various mechanisms in different cell types.Formula:C29H28O8Color and Shape:SolidMolecular weight:504.53Mertansine
CAS:Mertansine is a tubulin inhibitor and an antibody-conjugable maytansinoid alkaloid. The IC50 of Mertansine against HCT-15 and A431 cells is 0.750 and 0.04nM.Cost-effective and quality-assured.Formula:C35H48ClN3O10SPurity:100% - 99.76%Color and Shape:SolidMolecular weight:738.29SB273005
CAS:SB273005 is a potent integrin inhibitor with Ki of 1.2 nM and 0.3 nM for αvβ3 receptor and αvβ5 receptor, respectively.Formula:C22H24F3N3O4Purity:99.58%Color and Shape:SolidMolecular weight:451.44Dynasore
CAS:Dynasore, a cell-permeable dynamin inhibitor, blocks GTPase of dynamin 1/2 and Drp1 (IC50: 15 μM) without affecting other small GTPases.Formula:C18H14N2O4Purity:95.85% - 99.22%Color and Shape:SolidMolecular weight:322.31Ref: TM-T1848
5mg49.00€10mg79.00€25mg140.00€50mg259.00€100mg374.00€200mg560.00€500mg883.00€1mL*10mM (DMSO)87.00€c-ABL-IN-5
C-ABL-IN-5, a selective c-Abl inhibitor, exhibits neuroprotective properties and has favorable characteristics including blood-brain barrier permeability,Formula:C19H17F2N3OPurity:98%Color and Shape:SolidMolecular weight:341.35KIF18A-IN-14
CAS:KIF18A-IN-14 (Compound Example 81) is an inhibitor of KIF18A that exists in two forms, EX81-A and its enantiomer EX81-B. EX81-A and EX81-B inhibit the viability of OVCAR-3 cells with IC50 values of 0-0.01 μM and 0.01-0.1 μM, respectively. KIF18A-IN-14 can be utilized in tumor research, including studies on colon cancer, breast cancer, and lung cancer.Formula:C26H32F3N5O6SColor and Shape:SolidMolecular weight:599.62REDV TFA
REDV TFA, the minimal active sequence of the CS5 site in the alternatively spliced type III connecting segment (IIICS) of fibronectin, mediates adhesion to theFormula:C20H35N7O9·xC2HF3O2Purity:98%Color and Shape:SolidMolecular weight:517.53 (free acid)Lyn-IN-1
CAS:Lyn-IN-1 (Bafetinib analog) is a selective and potent dual inhibitor of Bcr-Abl and LynFormula:C30H31F3N8OPurity:97% - 99.33%Color and Shape:SolidMolecular weight:576.62Ref: TM-T11916
1mg47.00€2mg56.00€5mg84.00€10mg124.00€25mg250.00€50mg393.00€100mg560.00€200mg815.00€1mL*10mM (DMSO)97.00€PVZB1194
CAS:PVZB1194, a biphenyl-type inhibitor of Kinesin spindle protein Eg5 (KIF11), exhibits anticancer potential by inducing cell cycle arrest and apoptosis throughFormula:C13H9F4NO2SPurity:98%Color and Shape:SolidMolecular weight:319.28Defactinib analogue-1
CAS:Defactinib analogue-1 (Compound 7) serves as a ligand for the target protein FAK, and is utilized in the synthesis of PROTAC FAK degrader 1.Formula:C20H20F3N5O3SColor and Shape:SolidMolecular weight:467.47Tubulysin D
CAS:Tubulysin D is a tetrapeptide isolated from the myxobacterial species Archangium geophyra and Angiococcus disciformis, and displays potent antitumor activity.Formula:C43H65N5O9SPurity:98%Color and Shape:SolidMolecular weight:828.07Triciribine
CAS:Triciribine (NSC-154020) is a DNA synthesis inhibitor, and it also inhibits Akt and HIV-1/2.Formula:C13H16N6O4Purity:99.01% - 99.87%Color and Shape:SolidMolecular weight:320.3Ref: TM-T6065
1mg43.00€2mg57.00€5mg93.00€10mg135.00€25mg236.00€50mg394.00€100mg588.00€1mL*10mM (DMSO)93.00€S516
CAS:S516 is an active CKD-516 metabolite and is a potent inhibitor of tubulin polymerization(IC50 of 4.29 μM), has marked antitumor activity.Formula:C21H19N5O4SPurity:98%Color and Shape:SolidMolecular weight:437.47Nic-15
CAS:Nic-15 (compound 4n) serves as an anti-constrictive agent targeting the low vascular characteristics of pancreatic tumors. These characteristics enable cancer cells to adapt to the nutrient-deficient tumor microenvironment and develop resistance to treatment. Nic-15 modulates the PI3K/Akt/mTOR pathway and alleviates ER stress induced by Gemcitabine. It significantly inhibits migration and colony formation in MIA PaCa-2 and PANC-1 pancreatic cancer cells. When used in combination with Gemcitabine, Nic-15 effectively addresses resistance issues in pancreatic tumors. In xenograft models in vivo, Nic-15 notably enhances the efficacy of Gemcitabine.Formula:C25H26F2O3Color and Shape:SolidMolecular weight:412.47Dasatinib N-oxide
CAS:Dasatinib N-oxide is a key metabolite and potential impurity of the kinase inhibitor dasatinib.Formula:C22H26ClN7O3SPurity:98.54% - 99.85%Color and Shape:SolidMolecular weight:504Tubulin inhibitor 6
CAS:Tubulin inhibitor 6 (iHAP1) is an inhibitor of tubulin and a potent inhibitor of multiple cancer cell lines.Formula:C20H14ClNO2SPurity:99.05%Color and Shape:SolidMolecular weight:367.85Ref: TM-T13224
5mg50.00€10mg80.00€25mg117.00€50mg170.00€100mg259.00€200mg369.00€1mL*10mM (DMSO)51.00€PKC-θ inhibitor 1
CAS:PKC-theta inhibitor 1 is an inhibitor of PKCθ (Ki of 6 nM)Formula:C17H15F3N4OPurity:98%Color and Shape:SolidMolecular weight:348.32FGFRs-IN-1
FGFRs-IN-1 (Compound A16) is an orally active inhibitor targeting FGFR1/2/3/4, with IC50 values of 2.3, 7, 11, and 163 nM respectively. It also inhibits VEGFR1/2/3, Abl, and Flt3, with IC50 values of 61, 176, 112, 26, and 353 nM. The compound shows weak inhibition of CYP enzymes. FGFRs-IN-1 reduces the expression of α-SMA and collagen I, and it inhibits epithelial-mesenchymal transition (EMT) in A549 cells stimulated by TGF-β1. Additionally, FGFRs-IN-1 demonstrates anti-inflammatory activity in mouse models of lung fibrosis induced by Bleomycin and liver fibrosis induced by CCl4.Formula:C28H26Cl2N4O3Color and Shape:SolidMolecular weight:537.44HSP90-IN-27
CAS:HSP90-IN-27, also known as compound 19, is an inhibitor of HSP90 [1].Formula:C18H21N3O2SPurity:98%Color and Shape:SolidMolecular weight:343.44PF-431396
CAS:PF-431396 is a dual PYK2/FAK inhibitor (IC50: 11/2 nM).Formula:C22H21F3N6O3SPurity:98.83% - 99.82%Color and Shape:SolidMolecular weight:506.5Dynole 34-2
CAS:Dynole 34-2 is a non-competitive inhibitor of dynamin1 and dynamin2 GTPases that inhibits receptor-mediated endocytosis and synaptic vesicle endocytosis.Formula:C25H36N4OPurity:99.61%Color and Shape:SolidMolecular weight:408.58Tonabersat
CAS:Tonabersat (SB-220453) is a novel and orally available gap-junction modulator and CSD (Cortical spreading depression) inhibitor that,migraine and epilepsy.Formula:C20H19ClFNO4Purity:99.49%Color and Shape:SolidMolecular weight:391.82Uprosertib
CAS:Uprosertib (GSK2141795) is a potent, selective Akt broad-spectrum inhibitor for Akt1/Akt2/Akt3.Cost-effective and quality-assured.Formula:C18H16Cl2F2N4O2Purity:95.62% - 99.54%Color and Shape:SolidMolecular weight:429.25Ref: TM-T6849
1mg47.00€2mg59.00€5mg85.00€10mg124.00€25mg202.00€50mg324.00€100mg535.00€200mg752.00€1mL*10mM (DMSO)108.00€Xentuzumab
CAS:Xentuzumab (BI836845) is a recombinant monoclonal antibody to humanised IGF ligand that inhibits AKT activation and can be used to study solid tumours.Purity:95% - > 95%Color and Shape:LiquidMolecular weight:143.7 kDaEV206
CAS:EV206 is an effective inhibitor of Hsp70, exhibiting antiproliferative properties. This compound induces cell apoptosis (apoptosis) and enhances the protein expression of cleaved PARP and caspase-3. Additionally, EV206 demonstrates antitumor activity.Formula:C21H19N3OColor and Shape:SolidMolecular weight:329.40ILK-IN-3
CAS:ILK-IN-3 is an inhibitor of integrin linked kinase, and with antitumor activity.Formula:C10H12N6OPurity:99.69%Color and Shape:SolidMolecular weight:232.24(±)-1,2-Diolein
CAS:(±)-1,2-Diolein (1,2-Dioleoyl-rac-glycerol) (1,2-Dioleoyl-rac-glycerol) is a PKC activator. (±)-1,2-Diolein could increases myotubes Ca 2+ influx.Formula:C39H72O5Color and Shape:SolidMolecular weight:620.99Alvespimycin
CAS:Alvespimycin (17-DMAG) is a potent Hsp90 inhibitor with potential anticancer activity, which acts by binding to Hsp90.Formula:C32H48N4O8Purity:100%Color and Shape:SolidMolecular weight:616.75IIQLPEIVVV TFA
IIQLPEIVVV TFA serves as a specific inhibitor targeting the Drp1-Mff interaction. This compound discriminates between physiological and pathological fission, hindering physiological fission which leads to mitochondrial dysfunction. IIQLPEIVVV TFA is also utilized in research related to Huntington's disease.Formula:C54H95N11O14·xC2HF3O2Color and Shape:SolidMolecular weight:1122.40 (free base)Tyrosine kinase-IN-9
CAS:Tyrosine kinase-IN-9 (Compound B) is an inhibitor of c-Abl. It is useful for studying neurodegenerative diseases, such as Alzheimer's disease and Parkinson's disease.Formula:C20H14ClN3O3Color and Shape:SolidMolecular weight:379.796PF-03814735
CAS:PF-03814735 is a novel, potent and reversible inhibitor of Aurora A/B with IC50of 0.8 nM/5 nM, is less potent to Flt3, FAK, TrkA, and minimally active to Met and FGFR1. Phase 1.Formula:C23H25F3N6O2Purity:98%Color and Shape:SolidMolecular weight:474.48Tirofiban
CAS:Tirofiban (L700462) (MK-383) is a selective palate GPIIb/IIIa antagonist which inhibits platelet aggregation with IC50 of 9 nM.Formula:C22H36N2O5SPurity:99.87%Color and Shape:SolidMolecular weight:440.63-Hydroxyxanthone
CAS:3-Hydroxyxanthone (3-Hydroxy-xanthen-9-one), a xanthone derivative, exhibits inhibitory effects on NADPH-catalyzed lipid peroxidation in human umbilical veinFormula:C13H8O3Purity:98%Color and Shape:SolidMolecular weight:212.2NPX800
CAS:NPX800 is an inhibitor of heat shock factor 1 (HSF1) and can be used in studies about the treatment of cancer.Formula:C32H32FN5O4Purity:99.26%Color and Shape:SolidMolecular weight:569.63Ref: TM-T9804
1mg96.00€5mg240.00€10mg375.00€25mg627.00€50mg893.00€100mg1,216.00€1mL*10mM (DMSO)300.00€AKT-IN-6
CAS:AKT-IN-6 (INCB-047775) inhibits Akt, a key signaling protein linked to type 2 diabetes and cancer.Formula:C22H20FN5OPurity:98.83%Color and Shape:SolidMolecular weight:389.43Ref: TM-T36310
1mg35.00€5mg74.00€10mg111.00€25mg216.00€50mg354.00€100mg567.00€200mg805.00€1mL*10mM (DMSO)84.00€Radicicol
CAS:Radicicol is an antifungal antibiotic, a inhibitor of Hsp90 & FTO, Anti-malarial , inhibits iNOS gene expression by blocking the p38 kinase and NF-κB/Rel.Formula:C18H17ClO6Purity:98%Color and Shape:White/Yellow PowderMolecular weight:364.78Phorbol 12-myristate 13-acetate
CAS:Phorbol 12-myristate 13-acetate (PMA) belongs to the phorbol ester group of natural products and is an activator of PKC, SphK, and NF-κB.Formula:C36H56O8Purity:100% - 99.5%Color and Shape:White To Off-White SolidMolecular weight:616.83Eg5 Inhibitor V, trans-24
CAS:Eg5 Inhibitor V, trans-24 is a specific and potent Eg5 inhibitor that can be used in cancer research with an IC50 value of 0.65 uM.Formula:C26H21N3O3Purity:97.45%Color and Shape:SolidMolecular weight:423.46Ref: TM-T11155
1mg92.00€5mg205.00€10mg305.00€25mg495.00€50mg677.00€100mg905.00€200mg1,216.00€1mL*10mM (DMSO)227.00€A-286982
CAS:A 286982 blocks the LFA-1 and ICAM-1 integrin-ligand interaction.Formula:C24H27N3O4SPurity:97.81%Color and Shape:SolidMolecular weight:453.55Ref: TM-T21781
1mg35.00€2mg50.00€5mg74.00€10mg107.00€25mg210.00€50mg350.00€100mg522.00€1mL*10mM (DMSO)81.00€BX517
CAS:BX517 (PDK1 inhibitor 2) is a potent and selective inhibitor of PDK1.Formula:C15H14N4O2Purity:99.07%Color and Shape:SolidMolecular weight:282.3DTHIB
CAS:DTHIB robustly inhibits the HSF1 cancer gene signature and prostate cancer cell proliferation.Formula:C13H9ClFN3O3Purity:98.86% - 99.29%Color and Shape:SolidMolecular weight:309.68Ref: TM-T8858
1mg35.00€5mg70.00€10mg104.00€25mg210.00€50mg338.00€100mg540.00€500mg1,130.00€1mL*10mM (DMSO)78.00€AN-019
CAS:AN-019 (NRC-019) is a Bcr-Abl kinase inhibitor with antitumor activity for the study of chronic myelogenous leukemia (CML) and breast cancer.Formula:C25H17F6N5OPurity:98.01%Color and Shape:SolidMolecular weight:517.43ZIP acetate(863987-12-6 free base)
ZIP acetate inhibits PKMζ (protein kinase Mζ), affecting LTP maintenance and spatial memory, with an IC50 of 1-2.5 μM.Formula:C92H158N30O19Purity:94.68%Color and Shape:SolidMolecular weight:1988.43Tilavonemab
CAS:Tilavonemab (ABBV-8E12), a humanized anti-tau antibody, halts tau uptake in neurons and may help with Alzheimer's research.Purity:95% - 95%Color and Shape:LiquidSuprafenacine
CAS:Suprafenacine (N'-[(E)-(4-methylphenyl)methylidene]-4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide) is a cell-permeable microtubule destabilizer that inducesFormula:C16H18N4OPurity:99.72%Color and Shape:SolidMolecular weight:282.34GRGDSP acetate(91037-75-1 free base)
GRGDSP acetate(91037-75-1 free base) is a synthetic linear RGD peptide and is an integrin inhibitor.Formula:C24H41N9O12Purity:99.77%Color and Shape:SolidMolecular weight:647.64Auristatin E
CAS:Auristatin E, MMAE analog, blocks tubulin polymerisation, has cytotoxic and potent antitumor effects, used in ADCs.Formula:C40H69N5O7Purity:98.81%Color and Shape:SolidMolecular weight:732.01SB-216
CAS:SB-216, a potent anti-cancer compound, inhibits tubulin polymerization and curbs growth in various cancer cells.Formula:C17H18N4O2Purity:100%Color and Shape:SolidMolecular weight:310.35Ref: TM-T60757
1mg54.00€5mg116.00€10mg188.00€25mg331.00€50mg475.00€100mg655.00€1mL*10mM (DMSO)133.00€Dynamin inhibitory peptide, myristoylated acetate
Myristoylated acetate peptide inhibits DynaMin, blocking amphiphysin binding; myristoylated TFA variant hinders endocytosis.Formula:C63H111N19O16Purity:99.42%Color and Shape:SolidMolecular weight:1390.67SC-10
CAS:SC-10 is a direct activator of PKC with potential antiproliferative activity, useful in leukemia research.Formula:C17H22ClNO2SPurity:99.24% - 99.58%Color and Shape:SolidMolecular weight:339.88GRP78-IN-3
CAS:GRP78-IN-3: Potent Hsp70 blocker, selective Grp78 (HSPA5) inhib., IC50 0.59 μM, 7x more vs HspA9, 20x vs HspA2.Formula:C17H18N4O2SPurity:99.11%Color and Shape:SoildMolecular weight:342.42ALK inhibitor 1
CAS:ALK inhibitor 1 is a selective ALK kinase inhibitor.Formula:C23H28BrN7O3SPurity:98.27%Color and Shape:SolidMolecular weight:562.48Ref: TM-T10285
1mg52.00€5mg116.00€10mg170.00€25mg340.00€50mg472.00€100mg645.00€1mL*10mM (DMSO)143.00€KIF18A-IN-3
CAS: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.Formula:C28H38N4O5S2Purity:98.45%Color and Shape:SolidMolecular weight:574.76Combretastatin A-1
CAS:Combretastatin A-1 is a microtubule inhibitor with anti-tumour and can be used to study liver cancer.Formula:C18H20O6Purity:97.49% - 97.49%Color and Shape:SolidMolecular weight:332.35Lifitegrast
CAS:Lifitegrast (SAR 1118) is a lymphocyte, function-associated antigen-1 antagonist.Formula:C29H24Cl2N2O7SPurity:99.39% - 99.66%Color and Shape:SolidMolecular weight:615.48CGP 53353
CAS:CGP 53353 (DAPH-7) is a PKC inhibitor with inhibitory effects on PKCβII and PKCβI and can be used to study atherosclerosis.Formula:C20H13F2N3O2Purity:98.11%Color and Shape:SolidMolecular weight:365.33PKC-θ inhibitor
CAS:PKC-theta inhibitor is PKC-θinhibitor, with an IC50 of 12 nM.Formula:C20H25F3N6O3Purity:98%Color and Shape:SolidMolecular weight:454.45Ref: TM-T5423
1mg106.00€5mg250.00€10mg329.00€25mg467.00€50mg612.00€100mg944.00€200mg1,264.00€1mL*10mM (DMSO)274.00€Borussertib
CAS:Borussertib is a covalent-allosteric and first-in-class inhibitor of protein kinase Akt(IC50 of 0.8 nM and a Ki of 2.2 nM for Aktwt)Formula:C36H32N6O3Purity:99.00%Color and Shape:SolidMolecular weight:596.68Ref: TM-T8427
1mg133.00€5mg274.00€10mg432.00€25mg715.00€50mg1,008.00€100mg1,359.00€1mL*10mM (DMSO)360.00€FAK-IN-11
FAK-IN-11 (Compound 4l), a FAK inhibitor, specifically targets the ATP binding pocket of FAK to prevent its phosphorylation.Formula:C25H41NO3Purity:98%Color and Shape:SolidMolecular weight:403.6Tirbanibulin Mesylate
CAS:Tirbanibulin Mesylate (KX01 Mesylate) is an inhibitor of Src that targets the peptide substrate site of Src (GI50: 9-60 nM in cancer cell lines).Formula:C27H33N3O6SPurity:99.42%Color and Shape:SolidMolecular weight:527.63Ref: TM-T15675
2mg38.00€5mg56.00€10mg70.00€25mg126.00€50mg243.00€100mg416.00€200mg562.00€1mL*10mM (DMSO)65.00€IPI-493
CAS:IPI-493 is a bioactive chemical.Formula:C28H39N3O8Purity:100%Color and Shape:SolidMolecular weight:545.62WAY-118959-A
CAS:WAY-118959-A is a potential microtubule acetylation inhibitor.Formula:C16H14N4OS2Purity:99.86%Color and Shape:SolidMolecular weight:342.44Ref: TM-T60065
1mg115.00€5mg255.00€10mg375.00€25mg562.00€50mg787.00€100mg1,074.00€200mg1,454.00€1mL*10mM (DMSO)261.00€Sangivamycin
CAS:Sangivamycin (NSC-65346) inhibits PKC (Ki=10μM) and hinders growth in various human cancers.Formula:C12H15N5O5Purity:98.11%Color and Shape:SolidMolecular weight:309.28Ref: TM-T9605
1mg126.00€5mg274.00€10mg416.00€25mg677.00€50mg944.00€100mg1,264.00€1mL*10mM (DMSO)360.00€AKT-IN-2
CAS:AKT-IN-2 is a selective, and orally bioavailable AKT inhibitor (IC50: 5 nM for AKT1).Formula:C25H34F3N7OPurity:98%Color and Shape:SolidMolecular weight:505.583CAI
CAS:3CAI inhibits AKT1/2, reduces mTOR/GSK3β, and triggers apoptosis in colon cancer cells.Formula:C10H8ClNOPurity:98.13%Color and Shape:SolidMolecular weight:193.63Ref: TM-T14034
5mg55.00€10mg77.00€25mg125.00€50mg220.00€100mg330.00€200mg485.00€500mg787.00€1mL*10mM (DMSO)64.00€
