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A β-AR antagonist (IC50s = 8.9 and 5.2 μM for β1- and β2-ARs, respectively) and a class III antiarrhythmic agent; decreases IK in guinea pig ventricular cells and prolongs action potential duration in electrically stimulated isolated guinea pig papillary muscles at 100 μM; decreases heart rate and increases blood pressure and the cardiac FRP in a canine model of PES-induced ventricular tachycardia
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A bioactive sphingolipid; inhibits IL-4 production by 16% in PMA-stimulated EL4 T cells at 10 μM; cytotoxic to SK-BR-3 and MCF-7/Adr breast cancer cells (IC50s = 15.9 and 19.9 μM, respectively); increases maturation and stability of F508del-CFTR proteins, enhances cAMP-activated chloride secretion, and suppresses secretion of IL-8 in primary epithelial cells isolated from patients with cystic fibrosis
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A fluorescent marker for autophagic vacuoles; autofluorescent substance incorporated into multilamellar bodies by both an ion trapping mechanism and interaction with membrane lipids; exhibits Stokes shift and increased relative fluorescence in hydrophobic environments; selectively accumulates in PaTu 8902 subcellular fractions containing the lysosomal enzymes acid phosphatase and cathepsin D, but not those containing the rough and smooth endoplasmic reticulum markers TRAM and cytochrome P450, respectively
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An acylated amino acid that is used as a urinary biomarker for several indications; increased urinary excretion is indicative of MCAD deficiency; can also be used as a biomarker for exposure to gamma radiation
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A tricyclic antidepressant that blocks norepinephrine and serotonin transporters (KDs = 4.4 and 18 nM, respectively) more potently than the dopamine transporter (KD = 1.1 µM)
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A peripherally acting, antihypertensive compound that competes with norepinephrine for transport into presynaptic terminals of adrenergic neurons by the norepinephrine transporter, reducing the release of norepinephrine in response to action potentials
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A broad-spectrum tetracycline antibiotic; active against E. faecium in vitro (MIC = 16 mg/L); reduces the number of bacteria in the lung in a mouse model of multi-drug resistant A. baumannii-induced pneumonia at 20 mg/kg every 12 hours; reduces spinal cord lesion size and improves hindlimb function post-injury in a mouse model of acute spinal cord injury at an initial dose of 50 mg/kg and subsequent doses of 25 mg/kg per day for 5 days
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A major urinary metabolite of the selective serotonin reuptake inhibitor paroxetine; may be used as a control in LC/MS or GC/MS paroxetine testing applications
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A redox-sensitive tetrazolium salt used primarily to detect metabolic activity in microorganisms; readily taken up by living cells and reduced by respiratory activity to produce a red fluorescent, water-insoluble formazan crystal (absorption maximum at 450 nm)
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A potassium channel opener, activating the ATP-modulated potassium channels of guinea pig bladder and heart with Ki values of 104 and 251 nM, respectively; completely relaxes coronary artery rings preconstricted with serotonin (IC50 = 1.26 µM)
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A potassium channel opener, activating the ATP-modulated potassium channels of guinea pig bladder and heart with Ki values of 104 and 251 nM, respectively; completely relaxes coronary artery rings preconstricted with serotonin (IC50 = 1.26 µM)
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More