Drug results: 100
| benzoyl peroxide | A peroxide derivative that has been used topically for BURNS and as a dermatologic agent in the treatment of ACNE and POISON IVY DERMATITIS. It is used also as a bleach in the food industry. |
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| clindamycin phosphate |
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| adapalene | A naphthalene derivative that has specificity for RETINOIC ACID RECEPTORS. It is used as a DERMATOLOGIC AGENT for the treatment of ACNE. |
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| nicotinamide | An important compound functioning as a component of the coenzyme NAD. Its primary significance is in the prevention and/or cure of blacktongue and PELLAGRA. Most animals cannot manufacture this compound in amounts sufficient to prevent nutritional deficiency and it therefore must be supplemented through dietary intake. |
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| tretinoin | An important regulator of GENE EXPRESSION during growth and development, and in NEOPLASMS. Tretinoin, also known as retinoic acid and derived from maternal VITAMIN A, is essential for normal GROWTH; and EMBRYONIC DEVELOPMENT. An excess of tretinoin can be teratogenic. It is used in the treatment of PSORIASIS; ACNE VULGARIS; and several other SKIN DISEASES. It has also been approved for use in promyelocytic leukemia (LEUKEMIA, PROMYELOCYTIC, ACUTE). |
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| spironolactone | A potassium sparing diuretic that acts by antagonism of aldosterone in the distal renal tubules. It is used mainly in the treatment of refractory edema in patients with congestive heart failure, nephrotic syndrome, or hepatic cirrhosis. Its effects on the endocrine system are utilized in the treatments of hirsutism and acne but they can lead to adverse effects. (From Martindale, The Extra Pharmacopoeia, 30th ed, p827) |
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| salicylic acid | A compound obtained from the bark of the white willow and wintergreen leaves. It has bacteriostatic, fungicidal, and keratolytic actions. |
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| erythromycin | A bacteriostatic antibiotic macrolide produced by Streptomyces erythreus. Erythromycin A is considered its major active component. In sensitive organisms, it inhibits protein synthesis by binding to 50S ribosomal subunits. This binding process inhibits peptidyl transferase activity and interferes with translocation of amino acids during translation and assembly of proteins. |
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| sulfur | An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine. |
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| hydrocortisone | The main glucocorticoid secreted by the ADRENAL CORTEX. Its synthetic counterpart is used, either as an injection or topically, in the treatment of inflammation, allergy, collagen diseases, asthma, adrenocortical deficiency, shock, and some neoplastic conditions. |
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| fludiazepam |
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| benperidol | A butyrophenone with general properties similar to those of HALOPERIDOL. It has been used in the treatment of aberrant sexual behavior. (From Martindale, The Extra Pharmacopoeia, 30th ed, p567) |
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| trifluperidol | A butyrophenone with general properties similar to those of HALOPERIDOL. It is used in the treatment of PSYCHOSES including MANIA and SCHIZOPHRENIA. (From Martindale, The Extra Pharmacopoeia, 30th ed, p621) |
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| clopamide | A sulfamoylbenzamide piperidine. It is considered a thiazide-like diuretic. |
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| loxiglumide | cholecystokinin receptor antagonist; RN refers to (+-)-isomer |
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| pinazepam |
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| doxefazepam |
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| tripamide |
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| bietaserpine | hypotensive agent; structure |
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| rosaprostol |
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| methoserpidine |
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| omapatrilat |
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| sulfachrysoidine |
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| rolitetracycline | A pyrrolidinylmethyl TETRACYCLINE. |
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| clomocycline |
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| meclocycline |
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| oxytetracycline | A TETRACYCLINE analog isolated from the actinomycete STREPTOMYCES RIMOSUS and used in a wide variety of clinical conditions. |
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| sancycline |
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| guamecycline |
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| sulfamazone |
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| diseptal B |
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| clobenzepam |
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| sitaxentan | endothelin A receptor antagonist |
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| succinylsulfathiazole | intestinal antimicrobial agent; structure |
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| eptazocine |
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| perflenapent | a phase shift contrast agent that uses dodecafluoropentane as the enhancing gas |
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| etallobarbital |
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| reposal |
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| buthalital |
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| tetrabarbital |
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| cyclopentobarbital |
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| hexobarbital | A barbiturate that is effective as a hypnotic and sedative. |
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| proxibarbal |
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| enallylpropymal |
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| heptobarbital |
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| bucolome |
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| metharbital |
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| caplacizumab | In patients with aTTP, levels of a substance called von Willebrand factor are increased. von Willebrand factor acts on platelets to cause them to stick together and form blood clots. Caplacizumab, the active substance in Cablivi, is a nanobody (a small antibody) which has been designed to attach to von Willebrand factor in a way that stops it acting on platelets. This reduces platelets sticking together and forming clots in blood vessels and, as a result, platelet levels in the blood rise because they are no longer taken up to form clots. | |
| protizinic acid |
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| femoxetine | serotonin uptake inhibitor; RN given refers to (3R-trans)-isomer |
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| ibuprofen guaiacol ester |
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| zorubicin |
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| dapoxetine | selective serotonin reuptake inhibitor (SSRI) that was designed specifically for premature ejaculation |
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| fenclofenac |
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| ornoprostil |
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| enprostil | A synthetic PGE2 analog that has an inhibitory effect on gastric acid secretion, a mucoprotective effect, and a postprandial lowering effect on gastrin. It has been shown to be efficient and safe in the treatment of gastroduodenal ulcers. |
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| thurfyl nicotinate |
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| hydroxymethylnicotinamide |
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| fentiazac |
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| zomepirac |
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| disofenin |
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| lidofenin |
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| medazepam | A benzodiazepine derivative used in the treatment of anxiety. It has sedative, muscle relaxant, and anticonvulsant properties. One of its metabolites is DIAZEPAM and one of its excretion products is OXAZEPAM. |
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| sulfathiourea |
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| piketoprofen |
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| nizofenone | Nizofenone is a neuroprotective drug which protects neurons from death following cerebral anoxia (interruption of oxygen supply to the brain). It might thus be useful in the treatment of acute neurological conditions such as stroke. |
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| sulfamethoxypyridazine | A sulfanilamide antibacterial agent. |
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| narcobarbital |
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| aminohydroxybutyric acid |
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| glucametacin | indomethacin analog; structure |
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| ibuprofen piconol | pyridyl ester of ibuprofen; structure given in first source; RN given refers to cpd without isomeric designation |
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| bermoprofen |
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| vedaprofen |
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| alminoprofen |
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| loxoprofen |
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| pheniodol sodium |
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| clevudine |
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| epervudine |
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| fenbutrazate |
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| isonixin |
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| bidisomide |
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| droxidopa | A synthetic precursor of norepinephrine that is used in the treatment of PARKINSONIAN DISORDERS and ORTHOSTATIC HYPOTENSION. |
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| picilorex |
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| fenproporex | an anorectic drug used in the treatment of obesity |
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| lobenzarit | prevents autoimmune kidney disease in hybrid mice; RN given refers to parent cpd |
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| etilamfetamine |
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| aminorex | An amphetamine-like anorectic agent. It may cause pulmonary hypertension. |
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| clorprenaline |
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| levisoprenaline |
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| eptotermin alfa | an osteoinductive initiates bone formation through the induction of cellular differentiation in mesenchymal cells, which are recruited to the implant site from bone marrow periosteum and muscle, used for treatment of non-union of bone fractures | |
| clobuzarit |
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| actarit |
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| heptabarb |
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| selamectin | A broad-spectrum endectocide; |
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| oxymesterone |
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| oxabolone |
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| tiomesterone |
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| prasterone acetate |
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| bromochlorosalicylanilide |
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| nikethamide | A central nervous system stimulant. It was formerly used in the treatment of barbiturate overdose but is now considered to be of no value for such purposes and may be dangerous. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1229) |
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