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An inhibitor of glucosylceramide synthase; inhibits glucosylceramide synthase by 70, 41, and 62% in MDCK cell homogenates, mouse liver microsomes, and mouse brain homogenates, respectively, at 20 µM; inhibits sphingomyelin synthase activity in P. falciparum-infected erythrocytes and inhibits growth of P. falciparum (IC50 = 0.85 µM)
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Human Vimentin Profiling ELISA Kit is a Quantitative ELISA kit for the measurement of Human Vimentin Profiling in Human in Tissue Lysate, Suspension cells, Tissue Homogenate, Adherent cells samples.
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An antimalarial agent; active against six P. falciparum drug-sensitive or -resistant strains (IC50s = 1.53-3.94 nM); reduces parasitemia in P. chabaudi-infected mice at 3, 6, and 8 mg/kg in combination with artesunate; inhibits SARS-CoV-2 replication in infected A459-ACE2 cells (IC50 = 198 nM); cytotoxic against a panel of human cancer cells lines (CC50s = 1.6-4.9 µM)
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A dihydrofolate reductase inhibitor that prevents the production of tetrahydrofolic acid in P. falciparum and other protozoa; displays a prophylactic effect (ED50 = 0.5 mg/kg) in in vivo antimalarial mouse models
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A reversible inhibitor of both Aurora A and B kinases (IC50s = 0.8 and 5 nM, respectively); also inhibits FLT1, FAK, TrkA, Met, and FGFR1 (IC50s = 10, 22, 30, 100, and 100 nM, respectively)
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An antagonist of VEGFR1, VEGFR2, and VEGFR3 with IC50 values of 77, 37, and 190 nM, respectively; less potently inhibits PDGF and c-Kit (IC50 = 600 and 700 nM) and has no effect on additional kinases; completely blocks retinal neovascularization in oxygen-induced ischemic retinopathy in mice
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A noncompetitive nicotinic acetylcholine receptor antagonist with preferential activity at the α3β4 subtype (IC50 = 90-640 nM) compared to α4β2, α3β2, and α7 subtypes (IC50s range from 1-7 μM)
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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 broad-spectrum antibiotic that inhibits protein synthesis by inducing miscoding; commonly used as a dominant selection antibiotic for genetically modified bacteria, yeasts, fungi, protozoa, plants, and mammalian cells
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An ω-7 fatty acid; dietary administration reduces total body fat, mesenteric fat, and adipocyte size, increases inguinal fat mass, and decreases intestinal and hepatic triglyceride secretion in a rat model of obesity with features of metabolic syndrome at 1% w/w; decreases hepatocellular ballooning and steatosis in the same model; dietary administration of a butter enriched with trans-vaccenic acid decreases serum cholesterol levels and the formation of aortic atherosclerotic lesions in Ldlr-/- mice
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A chalcone and flavonoid with diverse biological activities; active against C. albicans and C. neoformans (IC50s = 3 and 7 UG/ml, respectively), as well as T. rubrum and M. audouinii (MIC = 1.2 UG/ml for both); active against various bacteria (MICs = 4.9-39.1 UG/ml); induces mitochondrial-mediated apoptosis in IMR-32 and NB-39 human neuroblastoma cells; inhibits the proliferation of OVCAR-8 ovarian, PC3 prostate, MCF-7 breast, and A549 lung cancer cell lines; reduces dopaminergic neuronal cell death and increases the stay time in the rotarod test in a mouse model of MPTP-induced Parkinson’s disease at 50 mg/kg
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An asymmetric bis-pyridinium aldoxime that functions as an AChE reactivator through nucleophilic attack of oximate anions on organophosphate-AChE conjugates; demonstrates therapeutic activity in experimental models of organophosphate poisoning
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An asymmetric phospholipid that can interdigitate with equal length (symmetric) acyl chain phospholipids in bilayer membranes to potentially minimize the hydrophobic mismatch between acyl chains
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