Luteinizing Hormone Releasing Hormone, salmon Luteinizing hormone-releasing hormone (LHRH or Gonadotropin-releasing hormone ) is an endogenous peptide hormone that binds the GnRH receptor, stimulating secretion of reproductive hormones (such as…
Luteinizing Hormone Releasing Hormone III, lamprey Luteinizing hormone-releasing hormone III (LHRH III) is a peptide hormone originally found in lamprey eels. LHRH III induces release of follicle-stimulating hormone (FSH), but…
Luteinizing Hormone Releasing Hormone Luteinizing hormone-releasing hormone (LHRH or Gonadotropin-releasing hormone ) is an endogenous peptide hormone that binds the GnRH receptor, stimulating secretion of reproductive hormones (such as luteinizing…
Lupinine Lupinine is a plant alkaloid found in species of Loranthus, Calia, and Lupinus. Lupinine exhibits immunostimulatory activity, potentially through the activation of CD69. Lupinine inhibits cholinesterases and may also…
Lumiracoxib Lumiracoxib is a non-steroidal anti-inflammatory drug (NSAID) that acts as an inhibitor of COX enzymes with specificity for COX-2. Like other NSAIDs, lumiracoxib exhibits anti-inflammatory, analgesic, antipyretic, and antinociceptive…
Loxoprofen Sodium Dihydrate Loxoprofen is a nonselective inhibitor of COX-1 and COX-2 that exhibits properties typical of most non-steroidal anti-inflammatory drugs (NSAIDs), including anti-inflammatory, analgesic, and antinociceptive activities. In vivo,…
Losartan Potassium Losartan is an inhibitor of the angiotensin II type 1 (AT1) receptor that exhibits antihypertensive, anti-fibrotic, and nephroprotective activities. In animal models of obstructive nephropathy, losartan decreases levels…
Lornoxicam Lornoxicam is a non-steroidal anti-inflammatory drug (NSAID) that inhibits COX-1 and COX-2. Lornoxicam exhibits both anti-inflammatory and analgesic activities. In vivo, lornoxicam decreases herpetic stromal keratitis induced by herpes…
Lopinavir Lopinavir is an HIV protease inhibitor that displays antiviral and anticancer activities. In vitro, lopinavir inhibits sarco/endoplasmic reticulum Ca2+-ATPase (SERCA), decreasing intracellular Ca2+ levels. In vivo, lopinavir’s inhibition of…
Loperamide Hydrochloride Loperamide is a μ-opioid receptor (μOR) agonist that exhibits gastrointestinal motility modulating, anorexigenic, analgesic, and antinociceptive activities; it also potentially inhibits HCN channels. Loperamide is clinically used as…