Tegafur (FT-207) 10mg | Purity Not Available
Selleck Chemicals
Tegafur (NSC 148958,Fluorafur,FT-207) is a substance being used in the treatment of some types of cancer.
More Information Supplier PageTegafur (NSC 148958,Fluorafur,FT-207) is a substance being used in the treatment of some types of cancer.
More Information Supplier PageIfosfamide is a nitrogen mustard alkylating agent used in the treatment of cancer.
More Information Supplier PageMegestrol acetate (BDH1298, SC10363) is a synthetic progestogen, used to treat breast cancer and loss of appetite.
More Information Supplier PageMercaptopurine(6-MP) 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.
More Information Supplier PageMercaptopurine(6-MP) 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.
More Information Supplier PageZoledronic acid (Zoledronate), 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. Zoledronic acid (ZA) also induces autophagy.
More Information Supplier PageZoledronic acid (Zoledronate), 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. Zoledronic acid (ZA) also induces autophagy.
More Information Supplier PageKi16425 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.
More Information Supplier PageAMG 208 is a highly selective dual c-Met and RON inhibitor with IC50 of 9 nM for c-Met.
More Information Supplier PageCamptothecin (CPT) is a specific inhibitor of DNA topoisomerase I (Topo I) with IC50 of 0.68 μM in a cell-free assay. Camptothecin induces apoptosis in cancer cells via microRNA-125b-mediated mitochondrial pathways. Phase 2.
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