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Human sera and related serum-derived preparations are used in cell culture, immunoassays, and other laboratory research. Depending on the preparation, they may supplement culture media or serve as blocking reagents and assay controls.
A histamine H1 receptor antagonist (Ki = 1.3 nM) and mast cell stabilizer; selective for H1 receptors over H2 and H3 receptors (Kis = 987 and 2,500 nM, respectively); inhibits compound 48/80-induced degranulation of rat peritoneal mast cells at 50 and 100 μM; inhibits the PCA reaction in rats by 54.6% at 20 mg/kg; inhibits the quick phase airway response in a rat ovalbumin-induced immediate airway response model at 30 mg/kg
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A dopamine D2 receptor antagonist (Ki = 0.3 nM in CHO cells expressing the rat receptor); selective for dopamine D2 over D3 receptors (Ki = 9.5 nM); inhibits dipropyl dopamine-induced femoral vasodilation in dogs at 0.5-5 μg/kg; prevents dopamine-induced decreases in pentagastrin-induced gastric antral motility in dogs at 0.5 mg/kg; inhibits apomorphine-induced emesis in dogs (ED50 = 0.031 mg/kg, p.o.); increases serum levels of prolactin in male rats
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A natural monocyclic sesquiterpene that potently inhibits the activation of Epstein-Barr virus by phorbol esters (IC50 = 140 nM); inhibits SHH signaling and induces apoptosis in cancer cell lines
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A mixture of closely related metabolites produced by A. teichomyceticus that are effective against Gram-positive bacteria; prevents bacterial cell-wall synthesis by binding and sequestering a cell-wall precursor with a D-alanine-containing peptide
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An agonist of dopamine D1A (D1R) and D1B (D5R) receptors (Kds = 17 and 11 nM, respectively); alters hemodynamic properties, including hypertension, in animals.
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A quinolone antibiotic that inhibits HIV-1 integrase (IC50 = 7.2 nM); has antiviral activity against laboratory strains and clinical isolates of HIV-1 in MAGI cells (EC50s = 0.1-1.26 nM) and HIV-2 in PBMCs (EC50s = 0.3-0.9)
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A prodrug form of temocaprilat; prevents impairment of acetylcholine-induced relaxation in aortic rings isolated from diabetic rats in a model of streptozotocin-induced diabetes; inhibits the angiotensin I-induced pressor response in normotensive rats at 0.1, 0.3, and 1 mg/kg; prevents coronary vascular remodeling induced by L-NAME in rats at 0.1 mg/ml in the drinking water; reduces plasma glucose levels in a KKAy mouse model of type 2 diabetes at 1 mg/kg
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A thiol-reactive fluorogenic probe; used to evaluate or quantify a variety of compounds containing reactive sulfur or thiol groups, including H2S, glutathione, proteins, and nucleotides
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A broad-spectrum herbicide; an irreversible inhibitor of GS1 and GS2 (Kis = 1.1. and 4.8 µM, respectively); reduces dry biomass of the weeds E. canadensis and L. rigidum (ED50s = 26 and 763 g/hectare, respectively); has no observed adverse effects in rats and mice at 4.1 and 17 mg/kg per day for three months
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A natural intermediate in the pteridine pathway that can be produced naturally from 7-oxobiopterin or in vitro by the oxidation of pterin by xanthine oxidase
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A cephalosporin antibiotic that is effective against E. coli (MIC values range from 0.25-2 mg/L depending on strain) as well as H. influenza and S. aureus
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A prodrug form of terbutaline; an inhibitor of BChE (IC50 = 3.9 nM for the human enzyme); increases the latency to histamine-induced collapse in guinea pigs at 1 and 2 mg/kg; completely inhibits ovalbumin-induced decreases in dynamic compliance and increases in pulmonary resistance in ovalbumin-sensitized guinea pigs at 10 mg/kg
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The main saponin constituent of C. asiatica that has been shown to improve wound healing including increasing collagen synthesis and elevating antioxidant levels in various normal and diabetic wound models
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