Novobiocin calcium

A cell-permeable, potent, and selective blocker of necroptosis (EC 50 = 494 nM in FADD-deficient Jurkat cells treated with TNF-&#945), a nonapoptotic necrotic cell death pathway mediated by death-domain receptors (DRs) that offers neuroprotection

A DNA gyrase inhibitor that can be used for the production of positively supercoiled plasma DNA. Targets the nucleotide-binding site of gyrase B.

A cell-permeable isoxazolylpiperazine compound that is shown to inhibit influenza A H1N1 (A/WSN/33 strain), H3N2 (clinical isolate), and H5N1 (A/Vietnam/1194/04) replication in MDCK cells in vitro (EC 50 = 69, 160, and 330 nM, respectively) and

An ionophore-like polyether derivative of a C 38 fatty acid compound isolated from the dinoflagellates that have fed on the marine sponge Halinchrondria okadai . It is a potent non-comepetitive, reversible inhibitor of serine/threonine-specific

An ionophore-like polyether derivative of a C 38 fatty acid compound isolated from the dinoflagellates that have fed on the marine sponge Halinchrondria okadai . It is a potent non-comepetitive, reversible inhibitor of serine/threonine-specific

An ionophore-like polyether derivative of a C 38 fatty acid compound isolated from the dinoflagellates that have fed on the marine sponge Halinchrondria okadai . It is a potent non-comepetitive, reversible inhibitor of serine/threonine-specific

Casamino acids are all of the naturally occurring amino acids and particularly rich in essential amino acids. Casamino acids have undergone a nearly complete acid hydrolysis of the casein proteins until all of the nitrogen is converted to free

An orally bioavailable benzofuranylallylamine compound that acts as a potent, active site targeting, competitive and reversible inhibitor of 2,3-oxidosqualene:lanosterol cyclase activity (OSC IC 50 ~ 6.5 nM against mammalian) and reduces

Chromogenic substrate for &#946-glucosidase. Warning Toxicity: Standard Handling (A) Other Notes Lin, J.

A semi-synthetic form of Paclitaxel (Cat. No.

Developed for use in immunoassay applications. Dissolving one tablet in 1 liter of deionized H 2 O yields 140 mM NaCl, 2.

A cell-permeable inhibtor of protein kinase C (IC 50 = 20-50 &#181M). Activates Ca 2+ -activated K + channels in amphibian myelinated nerve fibers at micromolar concentrations.