Calcium carbimide

A cell-permeable potent analog of Cyclopamine (Cat. No.

A cell-permeable potent analog of Cyclopamine (Cat. No.

A cell-permeable quinoline compound that selectively targets ArfGEF GBF1, but not BIG1/2, and attenuates GBF1-mediated cellular vesicle traffickings in a reversible manner. Phenotypic comparisons in Vero (African Green Monkey Kidney epithelial)

A cell-permeable amidino-guanidinium compound that acts as a potent, reversible and substrate competitive LSD1 selective inhibitor (IC 50 = 5.27 &#181M for hLSD1) and efficiently blocks LSD1-mediated demethylation of H3K4Me2 and H3K4Me (IC 50

Cell Line Origin Human brain astrocytoma Cell Line Description Established from an anaplastic astrocytoma of normal adult brain. Application Tumourigenicity studies DNA Profile STR-PCR Data: Amelogenin: X CSF1PO: 10 D13S317: 11 D16S539: 12,13

Precursor of the coenzymes NAD + and NADP + . Warning Toxicity: Irritant (B) Legal Information CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

A cell-permeable selective inhibitor of COX-2 in vitro . Inhibits sheep placental COX-2 (IC 50 = 3.

A cell-permeable chemically stable cytidine analog that displays antitumor properties. Acts as transition state analog inhibitor of cytidine deaminase by binding at the active site as covalent hydrates.

A cell-permeable chemically stable cytidine analog that displays antitumor properties. Acts as transition state analog inhibitor of cytidine deaminase by binding at the active site as covalent hydrates.