n
(pharmacology) A beta-adrenergic agonist.
n
A 5-HT_(1D) receptor agonist with migraine-preventative effects.
n
Aluminium acetylsalicylate, a drug used to treat pain and inflammation associated with muscular skeletal and joint disorders.
n
A compound that binds to the 5-HT_(2A) receptor in the brain, used as a radioligand when labelled with fluorine-18.
n
A particular epoxide compound and immunosuppressant.
n
(pharmacology) An antidepressant drug, never marketed.
n
A first-generation antihistamine drug used to relieve nasal congestion and in eye drops, usually in combination with naphazoline, to relieve the symptoms of allergic conjunctivitis.
n
(pharmacology) An antimuscarinic drug.
n
(pharmacology) An antiemetic drug C₂₃H₂₁F₇N₄O₃ taken orally to prevent nausea and vomiting occurring as a consequence of cancer chemotherapy or surgery. It acts as an antagonist of receptors for substance P. It is often taken in combination with other antiemetic drugs and is marketed under the trademark Emend.
n
A particular motilin receptor agonist.
n
(pharmacology) An antiemetic drug.
n
A xanthine drug that acts as a selective adenosine A₁ receptor antagonist.
n
A peripherally-acting aromatic ʟ-amino acid decarboxylase (AAAD) or DOPA decarboxylase inhibitor, used in the management of Parkinson's disease.
n
(pharmacology) Alternative form of benzatropine. [(pharmacology) An anticholinergic drug administered in the form of its mesylate C₂₁H₂₅NO·CH₄O₃S especially to treat the symptoms of Parkinson's disease (as tremors, spasms, or muscle weakness) or similar symptoms caused as side effects of other drugs (as phenothiazine derivatives).]
n
A nootropic drug developed for the treatment of Alzheimer's disease, acting as a blocker of voltage-sensitive sodium channels.
n
A serotonin-norepinephrine-dopamine reuptake inhibitor developed as an analgesic.
n
Alternative form of bromocriptine [(pharmacology) A drug used in the treatment of parkinsonism, galactorrhea, and other conditions. It is a synthetic analog of the ergot alkaloids and stimulates the dopaminergic receptors of the brain, inhibiting the release of prolactin.]
n
(pharmacology) An adrenergic antagonist.
n
A particular drug for the treatment of respiratory disorders.
n
(pharmacology) A parasympathomimetic gastrokinetic drug.
n
Alternative form of clonidine [(pharmacology) A drug that acts as an α₂-adrenoreceptor agonist, used in the treatment of hypertension, opiate withdrawal, and a variety of other conditions.]
n
(pharmacology) A drug that acts as an α₂-adrenoreceptor agonist, used in the treatment of hypertension, opiate withdrawal, and a variety of other conditions.
n
(medicine) A mixture of diphenoxylate and atropine used in the treatment of diarrhoea
n
A mixture of hypotensive alkaloids extracted from Veratrum album, used in the treatment of hypertension.
n
(pharmacology) An SSRI marketed for the treatment of premature ejaculation in men.
n
(pharmacology) An antispasmodic drug.
n
An alpha-adrenergic agonist.
n
An experimental drug being investigated for the treatment of amyotrophic lateral sclerosis.
n
(pharmacology) The laxative drug oxyphenisatine.
n
A histamine 1 receptor antagonist.
n
A phenothiazine used for the treatment of migraine.
n
A pharmaceutical drug used as an analgesic and antipyretic.
n
Alternative form of doxazosin [(pharmacology) A drug taken orally in the form of its mesylate C₂₃H₂₅N₅O₅·CH₄O₃S to relieve urethral obstruction in benign prostatic hyperplasia and to treat hypertension. It is a derivative of quinazoline that acts to relax smooth muscle by combining with and blocking the activity of an alpha-receptor.]
n
Alternative form of drotaverine [(pharmacology) An antispasmodic drug, structurally related to papaverine.]
n
(pharmacology) An antispasmodic drug, structurally related to papaverine.
n
An antiulcer and protease inhibitor.
n
(pharmacology) A particular dihydrofolate reductase inhibitor.
n
A triptan drug used to treat migraine.
n
A xanthine derivative used in the treatment of asthma as a bronchodilator.
n
An antidepressant drug resembling moclobemide.
n
(pharmacology) A particular drug derived from papaverine.
n
Alternative form of fencamfamine [A stimulant developed in the 1960s as an appetite suppressant, later withdrawn due to problems with dependence and abuse.]
n
Alternative form of fenethylline [A synthetic prodrug used as a stimulant.]
n
(pharmacology) A synthetic benzazepine drug used as an antihypertensive.
n
A piperazine drug with potential applications as an antidepressant and anxiolytic.
n
(medicine) A drug that may be used to treat decreased libido in women
n
A spasmolytic or antispasmodic drug.
n
A centrally-acting stimulant drug.
n
An alpha-adrenergic agonist.
n
Alternative form of indometacin. [(pharmacology) A compound with anti-inflammatory, antipyretic, and analgesic properties, used chiefly to treat rheumatoid arthritis and gout.]
n
(pharmacology) A prokinetic benzamide derivative used to treat gastrointestinal conditions.
n
(pharmacology) A dopamine agonist.
adj
That shows a response to levodopa
n
A cough-suppressing drug.
n
The levorotatory form of oxaprotiline.
n
(pharmacology) An aminotetralin drug.
n
(pharmacology) An antihistamine drug used to treat allergies.
n
A drug that inhibits the synthesis of prostaglandins, used to treat joint and muscle pain.
n
A drug used in urology as an antispasmodic.
n
Alternative form of metamizole [(organic chemistry) A non-steroidal anti-inflammatory drug used as a painkiller and fever reducer.]
n
An antihypertensive drug related to reserpine.
n
A drug that acts as a non-selective muscarinic acetylcholine receptor partial agonist.
n
(pharmacology) A particular antipsychotic drug.
n
A triptan drug, N-methyl-3-(1-methyl-4-piperidinyl)-1H-indole-5-ethanesulfonamide.
n
(pharmacology) An antispasmodic and anticholinergic drug C₂₂H₃₁NO₃ administered transdermally as a skin patch or orally in the form of its hydrochloride C₂₂H₃₁NO₃·HCl to relax the smooth muscles of the bladder in the treatment of urge incontinence, frequent urination, and urinary urgency.
n
Alternative form of papaverine [(organic chemistry, pharmacology) A nonaddictive derivative of opium used in medicine to relieve muscle spasms, as a vasodilator and in some forms of erectile dysfunction.]
n
(pharmacology) An adrenergic drug used to relieve allergic reactions, to treat respiratory infections and to suppress the appetite.
n
(pharmacology) An antispasmodic drug.
n
(pharmacology) An alpha-blocker used chiefly as a smooth muscle relaxant, especially in the treatment of hypertension and benign prostatic hyperplasia.
n
(pharmacology) An antispasmodic drug.
n
(pharmacology) A base of an amide related to procaine (trademark Pronestyl) that is used in the form of its hydrochloride C₁₃H₂₁N₃O·HCl as a cardiac depressant especially in the treatment of ventricular and atrial arrhythmias.
n
A particular tricyclic antidepressant, also used to treat ADHD.
n
(pharmacology) A particular H₂ receptor antagonist.
n
A drug under investigation for the treatment of Parkinson's disease.
n
(pharmacology) A particular serotonin receptor antagonist.
n
(pharmacology) An NK₁ receptor antagonist.
n
involuntary, repetitive movements as a side effect of dopamine antagonists.
n
An antihypertensive drug.
n
(pharmacology) An imidazopyridine derivative that is a proton pump inhibitor, used in Japan to treat gastroesophageal reflux and peptic ulcer.
n
Alternative form of terfenadine [An antihistamine drug formerly used to treat allergic conditions, superseded by fexofenadine in the 1990s due to the risk of cardiac arrhythmia.]
n
A mast cell stabilizer drug.
n
A particular antihistamine used as an antipruritic.
n
An experimental drug for the treatment of Huntington's disease
n
Initialism of Triple Reuptake Inhibitor.
n
(pharmacology) A ganglionic blocking agent used as a salt C₃₂H₄₀N₂O₅S₂ to lower blood pressure especially in hypertensive emergencies.
n
(pharmacology) A serotonin 5-HT₃ receptor antagonist used mainly as an antiemetic to treat nausea and vomiting following chemotherapy.
n
(pharmacology) A particular cardiac stimulant drug.
n
A muscarinic acetylcholine receptor agonist with reasonable selectivity for the M1 and M4 subtypes, possibly useful in treating Alzheimer's disease and schizophrenia.
n
(pharmacology) An anxiolytic drug that acts as an antagonist at the 5-HT₃ receptor.
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