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Synthesis of C-homo-B-nor-estrone. 1974

H Ila, and V Dabral, and N Anand

UI MeSH Term Description Entries
D009654 Norsteroids Steroids which have undergone contraction in ring size or reduction in side chains.
D004958 Estradiol The 17-beta-isomer of estradiol, an aromatized C18 steroid with hydroxyl group at 3-beta- and 17-beta-position. Estradiol-17-beta is the most potent form of mammalian estrogenic steroids. 17 beta-Estradiol,Estradiol-17 beta,Oestradiol,17 beta-Oestradiol,Aerodiol,Delestrogen,Estrace,Estraderm TTS,Estradiol Anhydrous,Estradiol Hemihydrate,Estradiol Hemihydrate, (17 alpha)-Isomer,Estradiol Monohydrate,Estradiol Valerate,Estradiol Valeriante,Estradiol, (+-)-Isomer,Estradiol, (-)-Isomer,Estradiol, (16 alpha,17 alpha)-Isomer,Estradiol, (16 alpha,17 beta)-Isomer,Estradiol, (17-alpha)-Isomer,Estradiol, (8 alpha,17 beta)-(+-)-Isomer,Estradiol, (8 alpha,17 beta)-Isomer,Estradiol, (9 beta,17 alpha)-Isomer,Estradiol, (9 beta,17 beta)-Isomer,Estradiol, Monosodium Salt,Estradiol, Sodium Salt,Estradiol-17 alpha,Estradiol-17beta,Ovocyclin,Progynon-Depot,Progynova,Vivelle,17 beta Estradiol,17 beta Oestradiol,Estradiol 17 alpha,Estradiol 17 beta,Estradiol 17beta,Progynon Depot
D006718 Homosteroids Steroids whose structure has been expanded by the addition of one or more carbon atoms to the ring skeleton in any of the four rings.
D045166 Estradiol Congeners Steroidal compounds related to ESTRADIOL, the major mammalian female sex hormone. Estradiol congeners include important estradiol precursors in the biosynthetic pathways, metabolites, derivatives, and synthetic steroids with estrogenic activities. Estradiol Congener,Estrogen Analog,Estrogen Analogue,Synthetic Estrogen,Estrogen Analogs,Estrogen Analogues,Estrogens, Synthetic,Synthetic Estrogens,Analog, Estrogen,Analogs, Estrogen,Analogue, Estrogen,Analogues, Estrogen,Congener, Estradiol,Estrogen, Synthetic

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