48170 Results for: "Sodium+alginate&pageNo=8"

Binds to calmodulin, inhibiting Ca²⁺-calmodulin-regulated enzyme activity. It inhibits the Ca²⁺/calmodulin-induced activation of myosin light chain kinase in a concentration dependent manner (IC50=25 µM). Cell permeable.

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8,8-Dimethyl-7-oxo-2-azaspiro[3.5]non-5-ene-6-carbonitrile hydrochloride 250mg pack 1 * 250 mg

Supplier: Apollo Scientific

8,8-Dimethyl-7-oxo-2-azaspiro[3.5]non-5-ene-6-carbonitrile hydrochloride 250mg pack 1 * 250 mg

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(R)-(-)-a-Methoxy-a-trifluoromethylphenylacetyl chloride, ca. 18% solution in Dichloromethane (ca. 1 100mg pack 1 * 100 mg

Supplier: Apollo Scientific

(R)-(-)-a-Methoxy-a-trifluoromethylphenylacetyl chloride, ca. 18% solution in Dichloromethane (ca. 1 100mg pack 1 * 100 mg

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2,8-Diiododibenzo[B,D]Furan 1g pack 1 * 1 g

Supplier: Apollo Scientific

2,8-Diiododibenzo[B,D]Furan 1g pack 1 * 1 g

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2,8-Dichloro-Quinoline-3-Carbaldehyde 1g pack 1 * 1 g

Supplier: Apollo Scientific

2,8-Dichloro-Quinoline-3-Carbaldehyde 1g pack 1 * 1 g

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2,8-Diiododibenzo[B,D]Furan 5g pack 1 * 5 g

Supplier: Apollo Scientific

2,8-Diiododibenzo[B,D]Furan 5g pack 1 * 5 g

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2-Amino-9-((2R,4S,5R)-4-Hydroxy-5-(Hydroxymethyl)Tetrahydrofuran-2-Yl)-3H-Purine-6,8(7H,9H)-Dione 1g pack 1 * 1 g

Supplier: Apollo Scientific

2-Amino-9-((2R,4S,5R)-4-Hydroxy-5-(Hydroxymethyl)Tetrahydrofuran-2-Yl)-3H-Purine-6,8(7H,9H)-Dione 1g pack 1 * 1 g

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SC-51089 ≥98%

Supplier: Enzo Life Sciences

Prostanoid receptor inhibitor

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NGAL (PIG) MONOCLONAL ANTIBODY (28) (BIOTIN CONJUGATE) 1 * 150 µG

Supplier: Enzo Life Sciences

NGAL (PIG) MONOCLONAL ANTIBODY (28) (BIOTIN CONJUGATE) 1 * 150 µG

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Mycalolide B ≥98%

Supplier: Enzo Life Sciences

Depolymerizes actin

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N,N-Dimethylsphingosine, D-erythro ≥98% (by TLC)

Supplier: Enzo Life Sciences

Sphingosine kinase inhibitor

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N-Hexanoyl-D-erythro-sphingosine ≥98% (by TLC)

Supplier: Enzo Life Sciences

A biologically active, cell-permeable, but nonphysiologic ceramide analog. It activates protein phosphatase 2A and MAP kinase (MAPK/ERK), suppresses insulin-induced tyrosine phosphorylation and inhibits glycoprotein traffic by the secretory pathway. It inhibits diacylglycerol accumulation and phospholipase D activation in fibroblasts. It induces an arrest at the G0/G1 transition of the cell cycle (10μM) and causes apoptosis (15μM or greater) in Molt-4 leukemia cells.

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Phytoceramide C2 ≥98% (by TLC)

Supplier: Enzo Life Sciences

Inhibits yeast growth and activates ceramide-activated protein phosphatase (CAPP).

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Adenosine-5'-O-(3-thiotriphosphate) tetralithium salt ≥85% (by HPLC) ATP analog

Supplier: Enzo Life Sciences

An ATP analog that can substitute for ATP in various kinase reactions. The resulting thiophosphorylated proteins are resistant to dephosphorylation by protein phosphatases.

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N-(2-Hydroxyethyl)oleamide ≥98% (by TLC)

Supplier: Enzo Life Sciences

Activates TRPV1. Endogenous anandamide-like lipid which regulates appetite but does not bind to cannabinoid receptors. In rats, food intake is inhibited by oral oleylethanolamide. Induces satiety by activation of PPARα. Inhibits ceramidase.

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Ono-RS-082 ≥98% (by TLC)

Supplier: Enzo Life Sciences

Phospholipase A2 inhibitor (IC50=7 µM for purified guinea pig lung PLA2). Inhibits epinephrine-stimulated thromboxane production in human platelets (86% at 3.5µM). Also blocks insulin secretion in pancreatic islets in response to glucose. Disrupts membrane tubule-mediated reassembly and maintenance of the Golgi complex.