n
(pharmacology) A pyridine-substituted sterol used as a drug against prostate cancer.
n
Alternative form of abiraterone [(pharmacology) A pyridine-substituted sterol used as a drug against prostate cancer.]
n
(pharmacology) A particular selective estrogen receptor modulator.
n
(pharmacology) A prostaglandin analogue.
n
A therapeutic progestin.
n
(pharmacology) A nonsteroidal aromatase inhibitor C₁₇H₁₉N₅ (trademark Arimidex) used to treat breast cancer after surgery and for metastases in postmenopausal women.
n
(biochemistry) A prostaglandin inhibitor.
n
(pharmacology) A nonsteroidal antiandrogen used to treat prostate cancer.
n
(pharmacology) A prostaglandin analogue.
n
(pharmacology) An investigational selective progesterone receptor modulator.
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(pharmacology) A prostaglandin analogue.
n
(pharmacology) A drug that is a thyrotropin-releasing hormone analogue.
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(pharmacology) A SERM medication used to treat bone problems.
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(pharmacology) A potent glucocorticoid steroid use to treat asthma.
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A derivative of thiamine (vitamin B1) used to treat sciatica and other painful nerve conditions.
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(pharmacology) A synthetic analogue of prostacyclin.
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(pharmacology) A prostaglandin analog C₂₅H₃₇NO₄ used topically to reduce elevated intraocular pressure (as in the treatment of open-angle glaucoma) and promote the growth of longer and thicker eyelashes. It is marketed under the trademarks Latisse and Lumigan.
n
(pharmacology) α-bromo-α,β-diphenyl-β-p-ethylphenylethylene, a synthetic, non-steroidal selective estrogen receptor modulator of the triphenylethylene group.
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(pharmacology) A prostaglandin analogue.
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(pharmacology) A synthetic prostaglandin analogue of PGF_(2α), with oxytocic properties.
n
(pharmacology) A prostaglandin analogue.
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(pharmacology) A prostaglandin analogue.
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(pharmacology) A synthetic glucocorticoid.
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(pharmacology) A particular prostaglandin analogue.
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A selective estrogen receptor modulator.
n
A nonsteroidal anti-inflammatory drug.
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(pharmacology) A particular antiandrogen.
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(pharmacology) A particular prostaglandin analogue.
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(pharmacology) A synthetic progestogen C₂₂H₃₀O used in birth control pills in combination with ethinylestradiol.
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A synthetic, non-steroidal, highly selective agonist of ERβ (estrogen receptor beta), used in scientific research.
n
(pharmacology) prostaglandin F2α, used in medicine to induce labour and as an abortifacient
n
(pharmacology) A synthetic drug C₂₇H₃₀F₆N₂O₂ that inhibits 5-alpha-reductase to convert testosterone into dihydrotestosterone and is used to treat benign prostatic hyperplasia.
n
(pharmacology) A synthetic prostaglandin designed to resemble dinoprostone.
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(pharmacology) A synthetic, non-steroidal pure antiandrogen developed for the treatment of metastatic castration-resistant prostate cancer.
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(pharmacology) A selective, transition-state, non-competitive inhibitor of the type II isoform of the enzyme 5α-reductase.
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A particular nonsteroidal antimineralocorticoid
n
Alternative form of etacrynic acid [(pharmacology) A powerful diuretic drug used in the treatment of fluid retention, especially that associated with heart, liver, and kidney disorders.]
n
A particular synthetic, non-steroidal antiestrogen.
n
(pharmacology) A prostaglandin analogue.
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(pharmacology) An aromatase inhibitor used in the treatment of breast cancer.
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A nonsteroidal anti-inflammatory drug.
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Alternative form of phenprocoumon [A long-acting oral anticoagulant drug, derived from coumarin, used for the prophylaxis and treatment of thromboembolic disorders.]
n
(pharmacology) A prostaglandin analogue.
n
(pharmacology) A drug which acts as aromatase inhibitor thus reducing estrogen production; used e.g. in treating breast cancer.
n
(pharmacology) An antiestrogen drug.
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A nonsteroidal anti-inflammatory drug.
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(pharmacology) A prostaglandin analogue.
n
(pharmacology) A prostaglandin analogue.
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(pharmacology) An analogue of prostaglandin E1, used as a treatment for obstetric bleeding.
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(medicine) A solution of prostaglandin used to control postpartum bleeding
n
(pharmacology) A drug used to treat pulmonary arterial hypertension, scleroderma, Raynaud phenomenon and ischemia.
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(pharmacology) A particular antiandrogen.
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(pharmacology) An experimental selective estrogen receptor modulator, the enantiomer of ormeloxifene.
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(pharmacology) A prostaglandin analogue.
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(pharmacology) A corticosteroid used in optometry and ophthalmology.
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(pharmacology) An H₂ receptor antagonist used as an antiulcer agent.
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(pharmacology) A prostaglandin analogue.
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(pharmacology) A synthetic analogue of ergonovine with oxytocic properties.
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(pharmacology) A prostaglandin analogue.
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(pharmacology) A steroidal aromatase inhibitor.
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(pharmacology) A selective estrogen receptor modulator.
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(pharmacology) A drug used for various purposes including the prevention of drug-induced gastric ulcers and the inducement of abortions, having the chemical formula C₂₂H₃₈O₅.
n
A nonsteroidal antiestrogenic drug that has been investigated to treat advanced breast cancer.
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A drug used for joint and muscular pain.
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(pharmacology) A prostaglandin analogue.
n
(pharmacology) An antiandrogen medication used in the treatment of advanced-stage prostate cancer.
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A particular antiandrogen.
n
A drug for the treatment of Cushing's disease.
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(pharmacology) An oral medication used to treat dyspareunia.
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(pharmacology) An anti-inflammatory and analgesic drug used to treat arthritis and gout.
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(pharmacology) A particular lipooxygenase inhibitor.
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A drug that acts as a highly selective agonist of the ERβ subtype of the estrogen receptor, used in scientific research.
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(pharmacology) A drug that is administered in an inactive form that is metabolised in the body into a biologically active compound
n
Alternative form of prostacyclin [(organic chemistry) A prostaglandin produced in the walls of blood vessels; it acts as a vasodilator and inhibits the aggregation of platelets]
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A prostaglandin analogue.
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A drug used in gynecology.
n
A nonsteroidal anti-inflammatory drug.
n
A therapeutic corticotropin drug.
n
(pharmacology) Initialism of selective estrogen receptor modulator.
n
(pharmacology) A prostaglandin analogue used topically (as eyedrops) to control the progression of glaucoma and in the management of ocular hypertension.
n
An experimental non-steroidal progestin.
n
A particular drug used in chemotherapy.
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(pharmacology) A prostaglandin analogue.
n
(pharmacology) An antiandrogen drug.
n
(pharmacology) An oral selective estrogen receptor modulator.
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(pharmacology) A drug used to treat Cushing's syndrome in dogs.
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(pharmacology) A selective inhibitor of the enzyme 5α-reductase.
n
(pharmacology) A prostaglandin analogue whose isopropyl ester is used to treat glaucoma and ocular hypertension.
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(pharmacology) A particular drug, a steroidal androgen receptor antagonist.
n
(pharmacology) The more active isomer of clomiphene, which binds to estrogen receptors and stays bound for long periods of time, preventing normal receptor recycling and causing an effective reduction in hypothalamic estrogen receptor number.
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