n
(pharmacology) A parathyroid hormone-related protein (PTHrP) analogue drug used to treat osteoporosis.
n
(organic chemistry) A derivative of inositol triphosphate that is a receptor agonist
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(pharmacology) A bisphosphonate C₄H₁₃NO₇P₂ used to inhibit bone resorption especially in the treatment of osteoporosis in postmenopausal women and Paget's disease of bone. Trade names include Fosamax and possibly others.
n
Alternative form of antipyrine [(pharmacology) The drug phenazone.]
n
(organic chemistry, medicine) A synthetic analogue of cytidine used in the treatment of myelodysplastic syndrome
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(medicine) Any of several pharmaceuticals having this structure; they are inhibitors of bone resorption, used to treat several diseases including Paget's disease and osteoporosis.
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(pharmacology) A synthetic derivative of calcitriol that is used to treat psoriasis.
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(pharmacology) A synthetic or recombinant form of calcitonin used to treat Paget disease of bone and postmenopausal osteoporosis.
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(medicine) The sodium salt of this compound used to prevent bone resorption
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Alternative form of chloraminophene [(medicine) A chemotherapy medication, 4-[4-[bis(2-chloroethyl)amino]phenyl]butanoic acid, used in treating chronic lymphocytic leukemia]
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A statin present in red yeast rice
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(medicine) The sodium salt of clodronic acid, used as a bone resorption inhibitor and antihypercalcemic agent.
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(pharmacology) The international nonproprietary name of cholecalciferol when used as a drug.
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(medicine) magnesium stearate when used in medicinal preparations
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(pharmacology) A synthetic analogue of ergocalciferol, used as a drug to treat secondary hyperparathyroidism and metabolic bone disease.
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(organic chemistry, biochemistry) Any of a group of hormones responsible for moulting in insects and other functions in other invertebrates and plants.
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A calcitonin derivative used as an antiparathyroid agent.
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(pharmacology) An analog of vitamin D, used to treat osteoporosis.
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(pharmacology) An analogue of calcitriol.
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(medicine) Abbreviation of fluid extract.
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An opioid peptide formed during the digestion of gliadin.
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Either of two eicosanoid hormones involved in inflammation, derived from arachidonic acid via oxidation by the enzyme 12-lipoxygenase.
n
(organic chemistry) A hydroxy derivative of testosterone; especially the anabolic steroid 4-hydroxytestosterone
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(chemistry) The conjugate base, or any salt or ester, of ibandronic acid. Used as a medication to inhibit bone loss in disorders of bone metabolism.
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(pharmacology) A bisphosphonate drug used in the prevention and treatment of osteoporosis.
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A particular intercalating compound.
n
(biochemistry) Any of several physiologically active lipids, related to the prostaglandins, that participate in allergic responses.
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Alternative form of levamisole [(organic chemistry) A synthetic imidazothiazole derivative whose hydrochloride is used as an antibiotic.]
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(pharmacology) A vitamin D analogue.
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(pharmacology) A synthetic mixture of levothyroxine and liothyronine, used to replenish thyroid hormones.
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(medicine) Synonym of flutamide
n
The conjugate base, or any salt or ester, of medronic acid, as (usually, especially) the technetium salt used as an radiotracer in medical imaging.
n
(organic chemistry) A triterpenoid derivative that inhibits glucosidase and amylase activity and is used in the treatment of diabetes mellitus.
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(pharmacology) A thioamide, closely related to propylthiouracil, used as an antithyroid preparation.
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(pharmacology) A bisphosphonate.
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(biochemistry) An estrogen produced by fungi.
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(biochemistry) A newly-discovered form of the peptide casomorphin
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(pharmacology) The conjugate base, or any salt or ester, of neridronic acid. Used as a medication to inhibit bone loss in disorders of bone metabolism.
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(pharmacology) A bisphosphonate drug to inhibit bone loss.
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(biochemistry, neuroscience) A neuroactive sterol
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(pharmacology) The conjugate base, or any salt or ester, of olpadronic acid. Used as a medication to inhibit bone loss in disorders of bone metabolism.
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(pharmacology) A bisphosphonate drug to inhibit bone loss.
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(biochemistry) An antitumor ribonuclease proposed for use in chemotherapy
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(pharmacology) The conjugate base, or any salt or ester, of pamidronic acid. Used as a medication to inhibit bone loss in disorders of bone metabolism.
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(pharmacology) (3-amino-1-hydroxy-1-phosphono-)phosphonic acid—a bisphosphonate drug to inhibit bone loss.
n
Alternative form of paricalcitol [(pharmacology) An analog of calcitriol (the active form of vitamin D) that is used for the prevention and treatment of secondary hyperparathyroidism.]
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(pharmacology) An analog of calcitriol (the active form of vitamin D) that is used for the prevention and treatment of secondary hyperparathyroidism.
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(biochemistry) Any ecdysteroid found in plants.
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A behenate polymer whose sucrose ester is used to measure intestinal fat
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A drug used as a stool stabilizer; a synthetic polymer of polyacrylic acid cross-linked with divinyl glycol, with calcium as a counterion.
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Abbreviation of progesterone. [(biochemistry, steroids, uncountable) A steroid hormone, secreted by the ovaries, whose function is to prepare the uterus for the implantation of a fertilized ovum and to maintain pregnancy.]
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(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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(organic chemistry) A phorbol that acts as an activator for a protein kinase.
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(biochemistry) Any of a class of compounds whose structure or effects on the body resemble retinol (vitamin A).
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A type of retinoid receptor
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(pharmacology) The conjugate base, or any salt or ester, of risedronic acid. Used as a medication to inhibit bone loss in disorders of bone metabolism.
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(pharmacology) A bisphosphonate C₇H₁₁NO₇P₂ taken orally to inhibit bone resorption especially in the prevention or treatment of osteoporosis in postmenopausal women. Trade names include Actonel, Atelvia, and possibly others.
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(pharmacology) Any of a class of drugs (chiefly lactones or pyrroles) that lower the amount of cholesterol in the blood by inhibiting an enzyme involved in its biosynthesis.
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(biochemistry, organic chemistry) A class of organic compounds having a structure of 17 carbon atoms arranged in four rings; they are lipids, and occur naturally as sterols, bile acids, adrenal and sex hormones, and some vitamins; many drugs are synthetic steroids.
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(pharmacology) A synthetic vitamin D₃ analogue.
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(pharmacology) A nonapeptide ACE inhibitor isolated from a snake of species Bothrops jararaca.
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A synthetic analogue of adrenocorticotropic hormone.
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(pharmacology) The conjugate base, or any salt or ester, of tiludronic acid. Used as a medication to inhibit bone loss in disorders of bone metabolism.
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(pharmacology) A bisphosphonate drug used for treatment of Paget's disease of bone.
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A particular kind of thyroid hormone analogue.
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(pharmacology) Initialism of tyrosine kinase inhibitor.
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A chemical compound, C₁₈H₂₃N.
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(medicine) Any of a class of tyrosine phosphorylation inhibitors.
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(biochemistry) A xenohormone that imitates androgen.
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(pharmacology) The conjugate base, or any salt or ester, of zoledronic acid. Used as a medication to inhibit bone loss in disorders of bone metabolism.
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