94231 Results for: "Benzyltributylammonium+bromide&pageNo=9"

A potent, irreversible inhibitor of various plant β-glucosidases and mammalian glucocerebrosidase. Has been employed in in vitro and animal models for Gaucher’s disease. It raises intracellular levels of glucosylceramide by inhibiting glucosylceramidase.

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L-161-982 ≥98% (by HPLC)

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Prostanoid receptor ligand.

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SB-366791 ≥98% (by TLC)

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A potent and selective vanilloid receptor (TRPV1) antagonist. An effective antagonist of hTRPV1 when stimulated by capsaicin, acid, or noxious heat.

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Gallocyanine ≥98% (by TLC)

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DKK1 inhibitor

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IQ-1 ≥98% (by TLC)

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Disrupts Wnt signaling

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GLUCAGON MONOCLONAL ANTIBODY (09) 1 * 1 mg

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GLUCAGON MONOCLONAL ANTIBODY (09) 1 * 1 mg

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NGAL (rat) ELISA kit

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For the quantitative determination of NGAL in rat urine, plasma, serum, tissue extracts, or culture supernatants.

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NGAL (pig) ELISA kit

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For the quantitative determination of NGAL in pig urine, plasma, serum, tissue extracts, or culture supernatants.

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Phosphatidylethanol ≥98% (by TLC)

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Phosphatidylethanol ≥98% (by TLC)

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Phosphatidylbutanol ≥98% (by TLC)

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Phosphatidylbutanol is a useful chromatographic standard for PLD assay.

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VU0155069 ≥98% (by TLC)

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PLD inhibitor

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U-73122 ≥99% (by TLC)

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Inhibitor of PLC activation

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Haloenol lactone suicide substrate ≥98% (by TLC)

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HELSS is a potent, irreversible, mechanism-based inhibitor of Ca2+-independent PLA2 (70% inhibition at 100 nM). It possesses a 1000-fold selectivity for Ca2+-independent PLA2 vs. Ca2+-dependent PLA2 . It has been used to identify the PLA2 involved in the release of arachidonate induced by vasopressin stimulation of A-10 smooth muscle cells (IC50=1 µM). It has also been shown to inhibit the Mg2+-dependent phophatidate phosphohydrolase from P388D1 macrophages (IC50~8 µM).

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Sphingosylphosphorylcholine ≥98% (by HPLC)

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Induces release of Ca²⁺ from intracellular stores

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Phytosphingosine ≥98%

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Ultra-pure

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Sphingosine-1-phosphate ≥98% (by TLC)

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Endogenous signaling molecule.

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Anisomycin ≥97% (by TLC)

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Activator of MAPK, Jnk and p38

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Luffariellolide (from Luffariella sp.) ≥98% (by TLC)

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Marine sesterterpenoid. Structurally related to manoalide. Anti-inflammatory phospholipase A2 (PLA2) inhibitor (IC50=0.23µM). Less potent than manoalide, but partially reversible (IC50=0.23µM, bee venom PLA2). Inhibits human recombinant sPLA2 (IC50=9.3µM) selectively over cPLA2.