60584 Results for: "Trisphenyl(3,3,3-trifluoroprop-1-yl)phosphonium+iodide&pageNo=8"
XBridge BEH C8 Column, 130Å, 2.5 µm, 3 mm X 30 mm 1 * 3 items
Supplier: WATERS
XBridge BEH C8 Column, 130Å, 2.5 µm, 3 mm X 30 mm 1 * 3 items
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CORTECS C8 Column, 90Å, 1.6 µm, 3 mm X 30 mm 1 * 3 items
Supplier: WATERS
CORTECS C8 Column, 90Å, 1.6 µm, 3 mm X 30 mm 1 * 3 items
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XTerra MS C8 Column, 125Å, 3.5 µm, 3.9 mm X 100 mm 1 * 1 items
Supplier: WATERS
XTerra MS C8 Column, 125Å, 3.5 µm, 3.9 mm X 100 mm 1 * 1 items
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Shodex KD-807 Column, 18 µm, 8 mm x 300 mm 1 * 1 items
Supplier: WATERS
Shodex KD-807 Column, 18 µm, 8 mm x 300 mm 1 * 1 items
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XBridge BEH C8 OBD Prep Column, 130Å, 10 µm, 50 mm X 250 mm 1 * 1 items
Supplier: WATERS
XBridge BEH C8 OBD Prep Column, 130Å, 10 µm, 50 mm X 250 mm 1 * 1 items
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XBridge Protein BEH SEC Column, 450Å, 3.5 µm, 7.8 mm X 150 mm 1 * 1 KIT
Supplier: WATERS
XBridge Protein BEH SEC Column, 450Å, 3.5 µm, 7.8 mm X 150 mm 1 * 1 KIT
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CORTECS C8 Method Validation Kit, 90Å, 2.7 µm, 4.6 mm X 30 mm 1 * 3 items
Supplier: WATERS
CORTECS C8 Method Validation Kit, 90Å, 2.7 µm, 4.6 mm X 30 mm 1 * 3 items
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SunFire Silica C8 Method Validation Kit, 100Å, 3.5 µm, 4.6 mm X 150 mm 1 * 3 items
Supplier: WATERS
SunFire Silica C8 Method Validation Kit, 100Å, 3.5 µm, 4.6 mm X 150 mm 1 * 3 items
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XSelect HSS C18 Method Transfer Kit, 100Å, 1.8 - 5 µm 1 * 2 items
Supplier: WATERS
XSelect HSS C18 Method Transfer Kit, 100Å, 1.8 - 5 µm 1 * 2 items
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8,8-Dimethyl-7-oxo-2-azaspiro[3.5]non-5-ene-6-carbonitrile hydrochloride 100mg pack 1 * 100 mg
Supplier: Apollo Scientific
8,8-Dimethyl-7-oxo-2-azaspiro[3.5]non-5-ene-6-carbonitrile hydrochloride 100mg pack 1 * 100 mg
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6,8-Difluoro-3,4-dihydronaphthalen-2(1H)-one 25g pack 1 * 25 g
Supplier: Apollo Scientific
6,8-Difluoro-3,4-dihydronaphthalen-2(1H)-one 25g pack 1 * 25 g
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Sphingomyelin ≥98% (by TLC)
Supplier: ENZO LIFE SCIENCES
Purified from bovine brain. Contains primarily stearic and nervoic acids. Precursor to ceramide second messengers via the action of sphingomyelinase.
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L-161-982 ≥98% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Prostanoid receptor ligand.
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SB-366791 ≥98% (by TLC)
Supplier: ENZO LIFE SCIENCES
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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Phosphatidylethanol ≥98% (by TLC)
Supplier: ENZO LIFE SCIENCES
Phosphatidylethanol ≥98% (by TLC)
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Phosphatidylbutanol ≥98% (by TLC)
Supplier: ENZO LIFE SCIENCES
Phosphatidylbutanol is a useful chromatographic standard for PLD assay.
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Haloenol lactone suicide substrate ≥98% (by TLC)
Supplier: ENZO LIFE SCIENCES
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)
Supplier: ENZO LIFE SCIENCES
Induces release of Ca²⁺ from intracellular stores
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Sphingosine-1-phosphate ≥98% (by TLC)
Supplier: ENZO LIFE SCIENCES
Endogenous signaling molecule.
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Luffariellolide (from Luffariella sp.) ≥98% (by TLC)
Supplier: ENZO LIFE SCIENCES
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.
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Corticosterone ≥98% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Corticosterone ≥98% (by HPLC)
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Puromycin dihydrochloride ≥98% (by HPLC)
Supplier: ENZO LIFE SCIENCES
Inhibits protein synthesis and induces apoptosis.
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Cyclopamine ≥98% (by TLC)
Supplier: ENZO LIFE SCIENCES
Blocks Hedgehog signaling
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2-Chloro-5-nitro-N-(4-pyridyl)benzamide ≥98% (by TLC)
Supplier: ENZO LIFE SCIENCES
Potent and selective PPARγ antagonist. T0070907 blocks PPARγ function in both cell-based reporter gene and adipocyte differentiation assays. It inhibits growth and survival of hepatocellular carcinoma cells and squamous cell carcinoma cell lines by interfering with cell adhesion "anoikis".
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: GRANT INSTRUMENTS
: BOCHEM
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: DWK Life Sciences
: Thermo Fisher Scientific
: VWR Collection
: Oxford Nanopore Technologies
: Industrial Physics
: AAT BIOQUEST
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: Palbam
: VWR Collection
: Integra
: VWR Collection
: FACELLITATE
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