n
(pharmacology) An antiinfective drug.
n
(pharmacology) A COX-2 inhibitor with possible anticancer properties.
n
A particular antihistamine drug used to treat hay fever and allergic conjunctivitis.
n
(pharmacology) An anti-inflammatory drug used in the treatment of bowel disease.
n
An oral medication for the treatment of Von Hippel-Lindau disease-associated renal cell carcinoma.
n
A peptide used as a screening test for exocrine pancreatic insufficiency and to monitor the adequacy of supplemental pancreatic therapy.
n
(pharmacology) A particular cough suppressant.
n
(medicine) A drug, (3Z)-N-(2-hydroxy-3-piperidin-1-ylpropoxy)pyridine-3-carboximidoyl chloride that induces heat shock proteins
n
A phosphodiesterase inhibitor.
n
A medication used to stop bleeding in patients with a rare clotting disorder, congenital factor XIII A-subunit deficiency.
n
(pharmacology) A low-molecular-weight heparin, used to prevent deep vein thrombosis.
n
A parasympathomimetic and muscarinic agonist used to treat dry mouth.
n
(pharmacology) An antiulcer drug.
n
(medicine) A mixture of amiloride and frusemide used to treat fluid retention
n
(pharmacology) A chemical substance, acting as a mast cell stabilizer.
n
Abbreviation of cortivazol. [(pharmacology) A high-affinity agonist ligand for the glucocorticoid receptor.]
n
(medicine) A sulfonamide drug that is a carbonic anhydrase inhibitor used to treat glaucoma
n
A neuroprotective agent used to aid neurological recovery following acute brain ischemia and subsequent cerebral infarction.
n
An allosteric effector of haemoglobin that increases its oxygen-carrying capacity and can be used to increase the efficacy of certain chemotherapy drugs.
n
A naturally-occurring selective proteasome inhibitor with anti-inflammatory activity.
n
(pharmacology) A retinoid drug C₂₃H₃₀O₃ used especially to treat severe psoriasis that has been withdrawn from use in the U.S. for its tendency to cause birth defects and is typically replaced in treatment by acitretin.
n
A lipooxygenase inhibitor.
n
A topical antiinfective drug.
n
An aldose reductase inhibitor.
n
A nonsteroidal anti-inflammatory drug, analgesic, and antipyretic used in horses.
n
(pharmacology) A serine protease inhibitor ethyl 4-[6-(diaminomethylideneamino-)hexanoyloxy]benzoate that is used in the treatment of pancreatitis.
n
(pharmacology) A psychoactive drug derived from tenocyclidine.
n
(pharmacology) A diuretic drug.
n
An antihypertensive agent.
n
Abbreviation of isobutylmethylxanthine. [(chemistry) A certain non-specific inhibitor of phosphodiesterases, which also possesses adenosine antagonist activity.]
n
A particular inhibitor of P-glycoprotein.
n
Alternative form of lansoprazole [(pharmacology) A particular proton pump inhibitor C₁₆H₁₄F₃N₃O₂S (trademark Prevacid) similar to omeprazole that prevents the stomach from producing acid.]
n
(pharmacology) An inhibitor of pyrimidine synthesis, used to treat some forms of arthritis.
n
(pharmacology) The benzimidazole drug 2-(1H-benzimidazol-2-ylsulfinylmethyl)-N-methyl-N-(2-methylpropyl)aniline.
n
An inhibitor of certain receptor tyrosine kinases, vascular endothelial growth factor, and platelet-derived growth factor.
n
A failed experimental drug for the treatment of HIV.
n
An experimental drug for the treatment of cystic fibrosis.
n
(pharmacology) An antidiarrheal drug.
n
An aldose reductase inhibitor.
n
A veterinary drug for the treatment of obese dogs.
n
(pharmacology) Contraction of morpholinoethyl.
n
A drug originally developed as a herbicide but now used to treat hereditary tyrosinemia type 1.
n
A thymidylate synthase inhibitor.
n
(pharmacology) Initialism of nucleoside reverse transcriptase inhibitor; as opposed to NtRTIs.
n
A medication for the treatment of polyneuropathy in people with hereditary transthyretin-mediated amyloidosis.
n
(pharmacology) A long-acting ACE inhibitor.
n
A proton pump inhibitor.
n
(medicine, uncountable) A drug cocktail used to treat gastroesophageal reflux.
n
A medication used in the possible treatment and prevention of cataracts.
n
(pharmacology) An anticancer drug.
n
(pharmacology) A synthetic sulfur-containing compound which promotes increased excretion of uric acid and is used to treat gout.
n
A lipooxygenase inhibitor.
n
(pharmacology) A proton pump inhibitor (trademark AcipHex) that inhibits gastric acid secretion and is taken orally in the form of its sodium salt C₁₈H₂₀NaN₃O₃S especially to treat gastroesophageal reflux disease, duodenal ulcers, and disorders (such as Zollinger–Ellison syndrome) involving gastric acid hypersecretion.
n
(pharmacology) A steroid drug which acts as an antimineralocorticoid (for which purpose it is used in the treatment of certain types of edema and hypertension) and an antiandrogen (for which purpose it is used as part of some types of hormone therapy, especially for transgender women).
n
(pharmacology) A histamine 2 receptor antagonist.
n
A chemical compound derived from Streptomyces bacteria, closely related to phosphoramidon.
n
A particular inhibitor of P-glycoprotein.
n
(pharmacology) A topical retinoid used to treat psoriasis, acne, and photodamage.
n
An immunosuppressant drug.
n
(pharmacology) An ACE inhibitor.
n
An inhibitor of IMP dehydrogenase under investigation for use in the treatment of cancer.
n
(pharmacology) A COX-2 inhibitor, an effective chemopreventive agent against rat experimental liver fibrosis.
n
A phosphodiesterase inhibitor.
n
A particular phosphodiesterase inhibitor.
n
(pharmacology) A drug that is a potent leukotriene D4 antagonist.
n
An aldose reductase inhibitor.
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