Sie suchten nach: Formamid

Artikel-Nr: (ENZOBMLHP0120050)

Lieferant: ENZO LIFE SCIENCES

Hersteller Artikel Nummer : BMLHP0120050

Beschreibung: Primary metabolite of arachidonic acid via the 12-lipoxygenase pathway. Inhibits thromboxane synthase. Inhibits platelet aggregation via activation of guanylate cyclase (100% at 5µM). Stimulates leukotriene biosynthesis. Potent and selective inhibitor of Ca2+-calmodulin-dependent protein kinase II (IC50=0.7µM). Endogenous TRPV1 agonist (Ki=0.35µM).

UOM: 1 * 50 µG

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Lieferant: ENZO LIFE SCIENCES

Beschreibung: Apoptosis inducer.

Lieferant: ENZO LIFE SCIENCES

Beschreibung: DMOG is a cell permeable prolyl-4-hydroxylase inhibitor which upregulates HIF activity. HIF activation stimulates angiogenesis in several different models. DMOG also inhibits FIH (Factor Inhibiting HIF), an asparaginyl hydroxylase, which enhances the HIF response. It is active in vivo and attenuates myocardial injury in a rabbit ischemia reperfusion model (20mg/kg). Is expected to act pro-angiogenic.

Artikel-Nr: (ENZOALX380235M002)

Lieferant: ENZO LIFE SCIENCES

Hersteller Artikel Nummer : ALX380235M002

Beschreibung: Antibiotic. Specific and potent inhibitor of NADH-ubiquinone oxidoreductase (complex I) that binds to ubiquinone binding site(s). Inhibits both mitochondrial and bacterial NADH ubiquinone oxidoreductase. Anticancer agent that prevents up-regulation of GRP78, and exhibits cytotoxic activity for etoposide resistant cancer cells under glucose-deprived conditions.

UOM: 1 * 2 mg

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Lieferant: ENZO LIFE SCIENCES

Beschreibung: Potent and selective protein kinase C inhibitor which has been used effectively in platelets, Swiss 3T3 fibroblasts and macrophages. Inhibitory profile: PKC, IC50=0.02µM (inhibits α, ßI, ßII and γ subtypes with similar potency); PKA, IC50=2.0µM; phosphorylase kinase, IC50=0.7µM; insulin, EGF and PDGF receptor tyrosine kinases are not inhibited at concentrations up to 50µM.

Lieferant: ENZO LIFE SCIENCES

Beschreibung: Water soluble and stable nitric oxide radical scavenger that shows in chemical and biological systems antagonistic action against the free nitric oxide radical (NO·). The inhibitory effects were almost 2-fold stronger than those of NMMA and NOARG. Reacts with nitric oxide in a stoichometric manner. Can be used for an improved detection of nitric oxide in activated macrophage cultures in combination with the Griess reagent. Protects against endotoxin shock.

Lieferant: G-Biosciences

Beschreibung: Diese vorgemischten, gebrauchsfertigen Gel-Ladepuffer wurden entwickelt, um den Gebrauch von Ethidiumbromid zu minimieren. Glow-Farbstoffe liefern intensive DNA/RNA-Banden mit geringem Hintergrund und minimaler Bandenverzerrung auf jeder Art von Agarose- oder Acrylamid-Gel.

Lieferant: Cayman Chemical

Beschreibung: Tenofovir disoproxil is a prodrug of the acyclic nucleoside phosphonate, tenofovir. Tenofovir is converted by cellular enzymes to tenofovir diphosphate, an obligate chain terminator that inhibits the activity of HIV reverse transcriptase and hepatitis B virus polymerase. Due to its rapid intracellular uptake, the anti-HIV activity of tenofovir disoproxil is reportedly >100-fold greater than that of the negatively charged tenofovir in a T cell line and primary blood lymphocytes.

Artikel-Nr: (PHBLPBTHL0293-1G)

Lieferant: Pharmablock (USA)

Hersteller Artikel Nummer : PBTHL0293-1G

Beschreibung: N-[(4-METHYLBENZENESULFONYL)METHYL]FORMA 1 * 1 g

UOM: 1 * 1 g

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Lieferant: MP Biomedicals

Beschreibung: 2-Hydroxypropyl-beta-cyclodextrin are non-toxic solubilisers. The solubility of drugs increases linearly with the concentration of 2-Hydroxypropyl-b-cyclodextrin in aqueous buffer. The formation of drug/cyclodextrin complexes is a rapidly reversible reaction and complexes exist both in solution and crystalline states.

Artikel-Nr: (AMBDA733528-100MG)

Lieferant: AMBEED

Hersteller Artikel Nummer : A733528-100MG

Beschreibung: N-(1-HYDROXY-2-METHYLPROPAN-2-YL)FORMAMI 1 * 0,1 g

UOM: 1 * 0,1 g

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Artikel-Nr: (PHBLPBLL1485-1G)

Lieferant: Pharmablock (USA)

Hersteller Artikel Nummer : PBLL1485-1G

Beschreibung: N-(3-HYDROXYAZETIDIN-1-YL)(TERT-BUTOXY)F 1 * 1 g

UOM: 1 * 1 g

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Artikel-Nr: (AMBDA237451-5G)

Lieferant: AMBEED

Hersteller Artikel Nummer : A237451-5G

Beschreibung: N-(2-AMINO-4,6-DICHLOROPYRIMIDINE-5-YL)F 1 * 5 g

UOM: 1 * 5 g

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Artikel-Nr: (AMBDA151702-250MG)

Lieferant: AMBEED

Hersteller Artikel Nummer : A151702-250MG

Beschreibung: N-(4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOR 1 * 0,25 g

UOM: 1 * 0,25 g

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Artikel-Nr: (ENZOBMLEI3270025)

Lieferant: ENZO LIFE SCIENCES

Hersteller Artikel Nummer : BMLEI3270025

Beschreibung: URB-597 is a potent and selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH), which is involved in the hydrolysis of endogenous cannabinoids such as anandamide. Inhibition of FAAH may serve to enhance the analgesic effects of endogenous cannabinoids. URB-597 has been shown to inhibit FAAH in rat cortical neuron membranes and in intact neurons with IC50 values of 4.6nM and 0.5nM, respectively. The compound has also been shown to have anxiolytic effects in rats (ID50=0.15mg/kg). Because URB-597 acts on FAAH and does not interfere with the binding of anandamide to the CB1 and CB2 receptors, it is a novel tool for drug development.

UOM: 1 * 25 mg

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Artikel-Nr: (PHBLPBN20122103-5G)

Lieferant: Pharmablock (USA)

Hersteller Artikel Nummer : PBN20122103-5G

Beschreibung: N-(2-CYANO-1H-PYRROL-1-YL)(TERT-BUTOXY)F 1 * 5 g

UOM: 1 * 5 g

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