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Vagifem
PubChem Notes:
Estradiol Generally refers to 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. In humans, it is produced primarily by the cyclic ovaries and the PLACENTA. It is also produced by the adipose tissue of men and postmenopausal women. The 17-alpha-isomer of estradiol binds weakly to estrogen receptors (RECEPTORS, ESTROGEN) and exhibits little estrogenic activity in estrogen-responsive tissues. Various isomers can be synthesized.
Estradiol - definition from Biology-Online.org
[oestradiol a hormone (272 D) synthesised mainly in the ovary, but also in the placenta, testis and possibly adrenal cortex. a potent oestrogen.
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Molecular Formula:
C18H24O2
InChI: InChI=1/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3/t14-,15-,16+,17+,18+/m1/s1
InChIKey: InChIKey=VOXZDWNPVJITMN-ZBRFXRBCBJ
SMILES: [H][C@]12CC[C@]3(C)[C@@H](O)CC[C@@]3([H])[C@]1([H])CCc4cc(O)ccc24
CAS number 50-28-2
Names:
Aerodiol
Aquadiol
beta-Estradiol
cis-estradiol
Diogyn
Diogynets
Estrace
estradiol
Estradiol-17beta
Estradiol
Estradiol-17beta
estradiol-17β
Evorel
progynon
Vagifem
(17β)-estra-1,3,5(10)-triene-3,17-diol
(8S,9S,13S,14S,17S)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol
17beta-Estradiol
17beta-estradiol
17β-estradiol
17β-estra-1,3,5(10)-triene-3,17-diol
17β-oestradiol
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Registries:
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PubChem CID 5757
Beilstein =1914275
CAS 50-28-2 (from NIST)
ChEBI 16469
chemPDB EST
Gmelin 290805
Kegg C00951
PubChem ID 12012600
PubChem ID 4202
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