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hydroxyprogesterone การใช้

ประโยคมือถือ
  • Progestins used for luteal support include dydrogesterone and 17?-hydroxyprogesterone caproate
  • It is the 3-cyclopentyl enol ether of 17?-hydroxyprogesterone acetate.
  • It can be synthesized from 17?-hydroxyprogesterone.
  • In animals, it is approximately 25 times more potent than progesterone or hydroxyprogesterone caproate.
  • Levels of 17?-hydroxyprogesterone, androstenedione, and cortisol may play a role in screening.
  • It is a 17?-hydroxyprogesterone derivative and a derivative of the less potent chlormadinone acetate.
  • One promising ester, [ 17?-hydroxyprogesterone acetate ], marketed as Prodox, was found.
  • During the period of administration, the testosterone concentrations decreased and the serum 17?-hydroxyprogesterone concentrations increased.
  • :progesterone + reduced ferredoxin + O 2 \ rightleftharpoons 15beta-hydroxyprogesterone + oxidized ferredoxin + H 2 O
  • Medroxyprogesterone acetate ( Provera ) entered clinical use and became widely marketed, largely superseding the 17?-hydroxyprogesterone esters.
  • In addition, whereas 9?-fluoro-11?-hydroxyprogesterone has pronounced mineralocorticoid effects, BKP lacks such effects.
  • 17?-OHP is also the parent compound of a class of progestins referred to as the 17?-hydroxyprogesterone derivatives.
  • "' Flumedroxone "'is a steroidal progestogen of the 17?-hydroxyprogesterone group that was never marketed.
  • The human enzyme efficiently acts on progesterone, 17?-hydroxyprogesterone, androstenedione, and testosterone to 5?-reduced metabolites.
  • Unlike many other 17?-hydroxyprogesterone derivatives but similarly to hydroxyprogesterone caproate, algestone acetophenide is reported to possess no glucocorticoid activity.
  • Unlike many other 17?-hydroxyprogesterone derivatives but similarly to hydroxyprogesterone caproate, algestone acetophenide is reported to possess no glucocorticoid activity.
  • Progesterone in turn is the precursor of the mineralocorticoid aldosterone, and after conversion to 17?-hydroxyprogesterone, of cortisol and androstenedione.
  • Among others, this class of drugs includes chlormadinone acetate, cyproterone acetate, hydroxyprogesterone caproate, medroxyprogesterone acetate, and megestrol acetate.
  • "' Gestonorone caproate "'( synthetic, steroidal progestin of the 19-norprogesterone and 17?-hydroxyprogesterone groups.
  • Clinical development of ethynerone was discontinued, and many of the 17?-hydroxyprogesterone derivatives were withdrawn for the indication of hormonal contraception.
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