Procurou por: N-(1,1,3,3-Tetramethylbutyl)formamide

Código de Artigo: (ENZOALX270481G005)

Fornecedor: ENZO LIFE SCIENCES

Descrição: PPARα activator.

UOM: 1 * 5 g

Promoção

Fornecedor: ENZO LIFE SCIENCES

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

Código de Artigo: (ENZOBMLCR1080010)

Fornecedor: ENZO LIFE SCIENCES

Descrição: Cannabinoid receptor ligand.

UOM: 1 * 10 mg

Promoção

Fornecedor: ENZO LIFE SCIENCES

Descrição: 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.

Código de Artigo: (ENZOALX270429M005)

Fornecedor: ENZO LIFE SCIENCES

Descrição: 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

Promoção

Código de Artigo: (ENZOALX450011M100)

Fornecedor: ENZO LIFE SCIENCES

Descrição: Heavy metal chelator.

UOM: 1 * 100 mg

Promoção

Fornecedor: ENZO LIFE SCIENCES

Descrição: 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.

Código de Artigo: (HONCR1478-10MG)

Fornecedor: Honeywell Chemicals

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

UOM: 1 * 10 mg

Promoção

Código de Artigo: (ENZOBMLCN1200001)

Fornecedor: ENZO LIFE SCIENCES

Descrição: PKA activator.

UOM: 1 * 1 mg

Promoção

Fornecedor: ENZO LIFE SCIENCES

Descrição: Bcl-2 ligand

Fornecedor: ENZO LIFE SCIENCES

Descrição: 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].

Código de Artigo: (ENZOALX270427M005)

Fornecedor: ENZO LIFE SCIENCES

Descrição: 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

Promoção

Código de Artigo: (ENZOALX380222MC25)

Fornecedor: ENZO LIFE SCIENCES

Descrição: 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

Promoção

Código de Artigo: (ENZOALX270396M005)

Fornecedor: ENZO LIFE SCIENCES

Descrição: 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

Promoção

Código de Artigo: (PRSI58-652)

Fornecedor: ProSci Inc.

Descrição: For WB starting dilution is: 1:1000.

UOM: 1 * 400 µl

Novo produto Promoção

Fornecedor: ENZO LIFE SCIENCES

Descrição: 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.