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An organochlorine insecticide; active against a variety of insects including bollworms and tobacco budworms (LD50s = 4.14 and 4.95 mg/g, respectively); binds to GABA receptors (IC50 = 60 nM in rat brain membranes); toxic to rats (LD50 = 240 mg/kg)
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A potent anti-mitotic drug that is 100-fold more active than resveratrol at inhibiting the growth of human colon cancer Caco-2 cells; inhibits tubulin polymerization in a dose-dependent manner (IC50 = 4 μM) and enzymes involved in the synthesis of the polyamines, putrescine, and spermidine
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A substituted cathinone that is an analog to ethcathinone, differing by having propyl rather than methyl at the α position; intended for forensic and research purposes.
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A sterol glycoside with diverse biological activities; active against E. coli and S. aureus; inhibits α-amylase and α-glucosidase and scavenges DPPH radicals (IC50s = 46.4, 17, and 155 µM, respectively); inhibits the proliferation of HepG2 and SMMC-7721 hepatocellular carcinoma cells (IC50s = 143.4 and 138.73 UG/ml, respectively) and migration and invasion in the same cells at 50 or 100 UG/ml; increases survival and decreases the number of kidney CFUs in a mouse model of candidiasis induced by C. albicans
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An oxidative metabolite of cholesterol; formed via radical and non-radical oxidation of cholesterol at the 5,6-double bond; induces release of LDH and apoptosis in macrophage-differentiated U937 cells; has been found in human fatty streaks and advanced atherosclerotic lesions
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A prodrug form of methylprednisolone; nanoliposomes containing 6α-methylprednisolone 21-hemisuccinate decrease disease severity in a rat model of adjuvant-induced arthritis
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A nonapeptide hormone primarily synthesized in the hypothalamus with roles in uterine contraction and lactation, social memory and attachment, sexual and maternal behavior, aggression, learning, anxiety, feeding, and pain perception
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A 4-demethoxy analog of daunorubicin which intercalates in DNA and inhibits topoisomerase II, resulting in cancer cell cytotoxicity at low concentrations (IC50 = 20-120 nM); effective in combination therapy for the treatment of different types of leukemia
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A peptide agonist of the guanylate cyclase C receptor (Ki = 16.4 nM in a radioligand binding assay using mouse intestinal mucosa); stimulates fluid secretion and cGMP concentration in jejunal loops isolated from wild-type mice but not guanylate cyclase C receptor-null mice; increases intestinal transit rate in wild-type mice when administered at a dose of 100 μg/kg; reduces the number of phosphorylated ERK-positive dorsal horn neurons in the thoracolumbar spinal cord, a marker of nociceptive signaling, following noxious colorectal distension and mechanical hypersensitivity in a mouse model of TNBS-induced colitis
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