FH535 50 mg | 98.98%
TargetMol
FH535, a Wnt/β-catenin signaling and PPAR inhibitor, exhibits anti-tumor activities.
More Information Supplier PageFH535, a Wnt/β-catenin signaling and PPAR inhibitor, exhibits anti-tumor activities.
More Information Supplier PageFH535, a Wnt/β-catenin signaling and PPAR inhibitor, exhibits anti-tumor activities.
More Information Supplier PageTopiroxostat is a selective xanthine oxidase inhibitor developed for treatment and management of hyperuricemia and gout.
More Information Supplier PageTopiroxostat is a selective xanthine oxidase inhibitor developed for treatment and management of hyperuricemia and gout.
More Information Supplier PageTopiroxostat is a selective xanthine oxidase inhibitor developed for treatment and management of hyperuricemia and gout.
More Information Supplier Page6-Mercaptopurine anhydrous is a Nucleoside Metabolic Inhibitor. It interferes with nucleic acid synthesis by inhibiting purine metabolism and is used, usually in combination with other drugs, in the treatment of or in remission maintenance programs for leukemia.
More Information Supplier PageKenPaullone (9-Bromopaullone), a potent CDK1, CDK2 and CDK5 inhibitor, as new enhancer for iTreg cell differentiation. Kenpaullone promotes iTreg cell differentiation through increased and prolonged transcription of foxp3 gene by enhancing TGFβ-Smad3 signaling pathway.
More Information Supplier PageKenPaullone (9-Bromopaullone), a potent CDK1, CDK2 and CDK5 inhibitor, as new enhancer for iTreg cell differentiation. Kenpaullone promotes iTreg cell differentiation through increased and prolonged transcription of foxp3 gene by enhancing TGFβ-Smad3 signaling pathway.
More Information Supplier PageKenPaullone (9-Bromopaullone), a potent CDK1, CDK2 and CDK5 inhibitor, as new enhancer for iTreg cell differentiation. Kenpaullone promotes iTreg cell differentiation through increased and prolonged transcription of foxp3 gene by enhancing TGFβ-Smad3 signaling pathway.
More Information Supplier PagePX-12 (1-methylpropyl 2-imidazolyl disulfide) is a small-molecule inhibitor of Trx-1 (thioredoxin-1), stimulates apoptosis, down-regulates HIF-1α and vascular endothelial growth factor (VEGF) and inhibits tumor growth in animal models. Since high levels of Trx-1 have been associated with colorectal, gastric and lung cancers, PX-12 is indicated as a potential cancer treatment in combination with chemotherapy for […]
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