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( )-Perillaldehyde has an antidepressant effect by modulating the olfactory nervous system in a mouse model of stress-induced depression ( )-Perillaldehyde also has anti-inflammatory activity inducing JNK activation in RAW264 7 cells and inhibiting the expression of TNF- with an IC50 of 171 7 M[1][2]
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Hydrocortisone Acetate (Cortisol 21-acetate) is the synthetic acetate salt form of hydrocortisone a corticosteroid with anti-inflammatory and immunosuppressive properties
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MW 430.7 Da, Purity >98%. Fat-soluble antioxidant. Peroxyl radical scavenger that protects polyunsaturated fatty acids in membranes and lipoproteins. Anticarcinogen.
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A long-chain ω-3 fatty acid ethyl ester; dietary administration increases the ex vivo activity of hepatic β-oxidation enzymes at 41.4 g/100 g of total dietary fatty acids; reduces total hepatic triglyceride levels and increases the ω-3 fatty acid content of hepatic triglycerides and phospholipids, as well as increases the total levels of ω-3 fatty acids in rats; reverses increases in plasma cholesterol levels and reduces circulating triglyceride levels in rats fed a high-fat diet at 1 g/kg
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Luteinizing hormone releasing hormone human acetate salt (LHRH) is a neuropeptide hormone targeting anterior pituitary signaling pathways It is designed to stimulate the anterior pituitary gland thereby promoting secretion of follicle-stimulating hormone (FSH) and luteinizing hormone (LH) LHRH exerts its biological activity primarily by selectively activating matrix metalloproteinase-2 (MMP-2) and matrix metalloproteinase-9 (MMP-9) key enzymes involved in extracellular matrix remodeling In studies with human endometrial cancer cell lines and decidual stromal cells LHRH mediates induction of MMP-9 expression and activation Based on these pharmacological properties LHRH holds research potential in reproductive biology embryo implantation tumor cell invasiveness and metastasis studies
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L-796778 acetate is a selective agonist of the sst3 receptor In CHO-K1 cells expressing the hsst3 receptor L-796778 acetate is a partial agonist that inhibits Forskolin (HY-15371)-stimulated cAMP production with an IC50 value of 18 nM L-796778 acetate has anticonvulsant effect[1]
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