Sie suchten nach: Formamid

Artikel-Nr: (HONCR1478-10MG)

Lieferant: Honeywell Chemicals

Hersteller Artikel Nummer : R1478-10MG

Beschreibung: High quality inorganic and organic reference materials produced according to ISO 9001.

UOM: 1 * 10 mg

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Lieferant: ENZO LIFE SCIENCES

Beschreibung: Irreversible, cell permeable broad-spectrum caspase inhibitor.

Lieferant: ENZO LIFE SCIENCES

Beschreibung: A cell-permeable cGMP analog which is more resistant to phosphodiesterases than cGMP and which preferentially activates cGMP-dependent protein kinase. It inhibits thrombin stimulated arachidonic acid release in human platelets.

Artikel-Nr: (ENZOALX270429M005)

Lieferant: ENZO LIFE SCIENCES

Hersteller Artikel Nummer : ALX270429M005

Beschreibung: A cell permeable, selective, and ATP-competitive inhibitor of Rho kinase (ROCK) activity (IC50=25µM). Does not inhibit the activation of Rho nor does it affect the in vitro activities of MLCK, PKCα, and SAPK2a/p38α. Shown to be less potent than Y-27632.

UOM: 1 * 5 mg

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Lieferant: ENZO LIFE SCIENCES

Beschreibung: Bcl-2 ligand

Artikel-Nr: (ENZOBMLCN1200001)

Lieferant: ENZO LIFE SCIENCES

Hersteller Artikel Nummer : BMLCN1200001

Beschreibung: PKA activator.

UOM: 1 * 1 mg

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Lieferant: ENZO LIFE SCIENCES

Beschreibung: Novel immune modulator that alters migration and homing of lymphocytes. Acts as a potent agonist of sphingosine 1-phosphate receptors (S1P) after phosphorylation by sphingosine kinase. Also inhibits cytosolic phospholipase A2 independently of sphingosine 1-phosphate receptors.

Artikel-Nr: (ENZOALX450011M100)

Lieferant: ENZO LIFE SCIENCES

Hersteller Artikel Nummer : ALX450011M100

Beschreibung: Heavy metal chelator.

UOM: 1 * 100 mg

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Artikel-Nr: (ENZOALX270427M005)

Lieferant: ENZO LIFE SCIENCES

Hersteller Artikel Nummer : ALX270427M005

Beschreibung: Selective COX-1 inhibitor (IC50=9nM). Shows 700-fold more selectivity over COX-2 (IC50=6.3µM). Inhibits COX-1-derived platelet thromboxane B2, gastric PGE2, and dermal PGE2 production. Orally active in rat.

UOM: 1 * 5 mg

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Artikel-Nr: (HONCR1468-10MG)

Lieferant: Honeywell Chemicals

Hersteller Artikel Nummer : R1468-10MG

Beschreibung: High quality inorganic and organic reference materials produced according to ISO 9001.

UOM: 1 * 10 mg

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Lieferant: ENZO LIFE SCIENCES

Beschreibung: Endogenous [1] ligand for the CB1 receptor (CB1: Ki=52nm; CB2: Ki=1930nm [2]) and TRPV1 (Ki=5.78µM [3,4]). Inhibits NF-κB activation through direct binding to IKKβ [5] and induces apoptosis independently of cannabinoid or vanilloid receptors [6]. Activates the MAP kinase (MAPK/ERK) signalling pathway [7].

Artikel-Nr: (ENZOALX380222MC25)

Lieferant: ENZO LIFE SCIENCES

Hersteller Artikel Nummer : ALX380222MC25

Beschreibung: Inhibitor of protein kinase C (PKC) and cyclin-dependent kinases (CDKs) resulting in accumulation of cells in the G1 phase and induction of apoptosis. Enhances the cytotoxicity of other anticancer drugs, such as DNA-damaging agents and anti-metabolite drugs, through putative abrogation of G2 and/or S phase accumulation induced by these agents.

UOM: 1 * 0,25 mg

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Artikel-Nr: (ENZOALX270396M005)

Lieferant: ENZO LIFE SCIENCES

Hersteller Artikel Nummer : ALX270396M005

Beschreibung: Selective inhibitor of CDK1/cyclin B (IC50=20nM). Potent cytotoxin in tumor cells: IC50=5.3µM against MCF7 cells, IC50=11.1µM against K562 cells, IC50=3.0µM against CEM cells, IC50=6.3µM against HOS cells, and IC50=6.3µM against G361 cells.

UOM: 1 * 5 mg

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Lieferant: ENZO LIFE SCIENCES

Beschreibung: Precursor to a large family of eicosanoids. Acts as a second messenger independent of metabolism. Retrograde messenger in long-term potentiation in the nervous system. Inhibits ras-GAP. Activator for several protein kinase C (PKC) isotypes.

Lieferant: ENZO LIFE SCIENCES

Beschreibung: Cyclooxygenase inhibitor. Selectively inhibits PGH synthase-2 (IC50=1 µM) with no inhibition of PGH synthase-1 at concentrations up to 100 µM. Protects neuronal cultures from LPS-induced neurotoxicity.

Lieferant: ENZO LIFE SCIENCES

Beschreibung: Antibiotic. Dominant analog of the reveromycin complex. Inhibitor of the mitogenic activity of epidermal growth factor (EGF). G1 phase cell cycle inhibitor, selectively inhibiting isoleucyl-tRNA synthetase. Displays antiproliferative as well as potent antifungal activity. Induces apoptosis in osteoclasts thus inhibiting bone resorption.