545395-94-6 | AMG-9810 (Catalog# : 179117)AMG 9810 is a competitive antagonist of capsaicin activation of the vanilloid receptor 1 (TRPV1). Additionally, it has been shown to compete with other modes of TRPV1 activation.
52328-98-0 | ASC-J9 (Catalog# : 179816)<span style="color:#34495E;font-family:"font-size:14px;background-color:#FFFFFF;">ASC-J9, also known as GO-Y025 and Dimethylcurcumin, is an AR degradation en
5854-93-3 | Alanosine (Catalog# : 161227117)Alanosine, also known as L-alanosine, is an amino acid analogue and antibiotic derived from the bacterium Streptomyces alanosinicus with antimetabolite and potential antineoplast
537034-17-6 | BML-210 (Catalog# : 16122901)BML-210, also known as CAY10433, is HDAC inhibitor. BML-210 induces growth inhibition and apoptosis and regulates HDAC and DAPC complex expression levels in cervical cancer cells
501437-28-1 | BI-D1870 (Catalog# : 122914)BI-D1870 is an ATP-competitive inhibitor of S6 ribosome for RSK1/2/3/4 with IC50 of 31 nM/24 nM/18 nM/15 nM, respectively; 10- to 100-fold selectivity for RSK than MST2, GSK-3, M
52794-97-5 | Carubicin HCl (Catalog# : 17914)Carubicin HCl is an anthracycline antineoplastic antibiotic isolated from the bacterium Actinomadura carminata. Carubicin intercalates into DNA and interacts with topoisomerase II.
521937-07-5 | CID755673 (Catalog# : 73104)CID 755673 is a selective and potent protein kinase D1-D3, PKC, CAK, PLK1 and CAMKII inhibitor. CID 755673 has been reported to inhibit PKD-mediated protein transport and inhibit
591778-68-6 | CP-640186 (Catalog# : 52229)CP-640186 is an isozyme-nonselective acetyl-CoA carboxylase (ACCase) inhibitor with IC50s of 53 nM and 61 nM for rat liver ACC1 and rat skeletal muscle ACC2 respectively; with im
55224-05-0 | Davercin (Catalog# : 17030310)Davercin, also known as Erythromycin Cyclocarbonate, is a bacteriostatic antibiotic macrolide produced by Streptomyces erythreus. It inhibits protein synthesis by binding to 50S
522-17-8 | Deguelin (Catalog# : 16122701)Deguelin, a natural product isolated from plants in the Mundulea sericea family, is an PI3K/AKT Inhibitor.Deguelin increases sensitivity of human leukaemia cells to chemotherapeu