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Sex hormones, Three-membered rings

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Antiandrogens (7)
Cyclic compounds (7)
Drugs acting on the genito-urinary system (7)
Hormonal agents (7)
Systemic hormonal preparations (7)
Epoxides (4)
Alkenes (3)
Antihypertensive agents (3)
Antimineralocorticoids (3)
Cycloalkanes (3)
Cycloalkenes (3)
Cyclopropanes (3)
Diuretics (3)
Drugs acting on the cardiovascular system (3)
Estrogens (3)
Neurotoxins (3)
Potassium-sparing diuretics (3)
Spiro compounds (3)
Xenoestrogens (3)
Cardiovascular system drug (1)
Drugs acting on the gastrointestinal system and metabolism (1)
PPAR agonists (1)
Pharmaceuticals (1)
Progestogens (1)

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dieldrin (128-10-9, 60-57-1, 72-20-8)  
Endrin is an organochloride with the chemical formula C12H8Cl6O that was first produced in 1950 by Shell and Velsicol Chemical Corporation. It was primarily used as an insecticide, as well as a rodenticide and piscicide. It is a colourless, odorless solid, although commercial samples are often off-white.
Endricol (72-20-8)  
Endrin  ·  Hexadrin
ENDRIN (72-20-8)  
Hexadrin
BISPHENOL A DIGLYCIDYL ETHER (1675-54-3, 500008-19-5)  
DGEBA  ·  DGEBPA  ·  2,2-bis(p-glycidyloxyphenyl)propane
Bisphenol A diglycidyl ether (commonly abbreviated BADGE or DGEBA) is an organic compound used as constituent of epoxy resins. The compound is a colorless solid (commercial samples can appear yellow) that melts slightly above room temperature.
Spirorenone (74220-07-8)  
6 beta, 7 beta, 15 beta, 16 beta-dimethylene-1,4-androstadiene-(17(beta-1')-spiro-5')-perhydrofuran-2',3-dione
Spirorenone (INN) (developmental code name ZK-35973) is a steroidal antimineralocorticoid of the spirolactone group that was never marketed. Spirorenone possesses 5–8 times the antimineralocorticoid activity of spironolactone in animal studies. The initial discovery of spirorenone was deemed a great success, as no compound with greater antimineralocorticoid activity had been developed since spironolactone in 1957.
Prorenone (49848-04-6)  
Prorenone (developmental code name SC-23133) is a steroidal antimineralocorticoid of the spirolactone group related to spironolactone that was never marketed. It is the lactonic form of prorenoic acid (prorenoate), and prorenoate potassium (SC-23992), the potassium salt of prorenoic acid, also exists. Prorenoate potassium is about 8 times more potent than spironolactone as an antimineralocorticoid in animals, and it may act as a prodrug to prorenone.
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Sex hormones
Three-membered rings