AMG-208
AMG 208 is a highly selective c-Met inhibitor with IC50 of 9 nM. Phase 1.
Showing 5425–5440 of 5738 results
AMG 208 is a highly selective c-Met inhibitor with IC50 of 9 nM. Phase 1.
Ki16425 is a competitive, potent and reversible antagonist to LPA1, LPA2 and LPA3 with Ki of 0.34 μM, 6.5 μM and 0.93 μM in RH7777 cell lines, respectively, shows no activity at LPA4, LPA5, LPA6.
Zoledronic acid (ZA), a potent osteoclast inhibitor, induces apoptosis in osteoclasts by inhibiting enzymes of the mevalonate pathway and preventing the isoprenylation of small GTP-binding proteins such as Ras and Rho.
Streptozotocin is a glucosamine-nitrosourea derivative, which is a methylating, carcinogenic, antibiotic and diabetes inducing agent.
Pamidronate Disodium is a nitrogen containing bisphosphonate, used to prevent osteoporosis.
Mercaptopurine is a widely used antileukemic agent and immunosuppressive drug that inhibits de novo purine synthesis through incorporation of thiopurine methyltransferase metabolites into DNA and RNA.
Megestrol acetate is a synthetic progestogen, used to treat breast cancer and loss of appetite.
Ifosfamide is a nitrogen mustard alkylating agent used in the treatment of cancer.
Tegafur (FT-207, NSC 148958) is a substance being used in the treatment of some types of cancer.
Floxuridine is an antineoplastic antimetabolite, used in the treatment of colon carcinoma and colorectal cancer that has metastasized to the liver.
Epothilone A is a paclitaxel-like microtubule-stabilizing agent with EC0.01 of 2 μM.
Cilostazol is a potent cyclic nucleotide phosphodiesterase type 3 (PDE3) inhibitor with IC50 of 0.2 μM and inhibitor of adenosine uptake.
Cilnidipine is a unique L-type and N-type calcium channel blocker, used for high blood pressure treatment.
Chelerythrine is a potent, selective antagonist of PKC with IC50 of 0.66 mM.
Cetirizine DiHCl is an antihistamine.
Celastrol is a potent proteasome inhibitor for the chymotrypsin-like activity of a purified 20S proteasome with IC50 of 2.5 μM.