ethinylestradiol

Details

Instance of

type of chemical entity

Subclass of

steroid

Part of

response to 17alpha-ethynylestradiol, cellular response to 17alpha-ethynylestradiol

canonical SMILES

CC12CCC3C(C1CCC2(C#C)O)CCC4=C3C=CC(=C4)O

chemical formula

C₂₀H₂₄O₂

defined daily dose

1.5, 25

found in taxon

Tanacetum parthenium, Porophyllum ruderale, Tagetes lucida, Artemisia salsoloides, Elsholtzia ciliata, Elsholtzia fruticosa, Eucalyptus angulosa, Eucalyptus behriana, Eucalyptus brassiana, Eucalyptus bridgesiana, Eucalyptus camaldulensis, Eucalyptus ceratocorys

has use

medication

isomeric SMILES

C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@]2(C#C)O)CCC4=C3C=CC(=C4)O

mass

296.178

medical condition treated

prostate cancer, premature ovarian failure, breast cancer, ovarian disease, hypogonadism, premature menopause

physically interacts with

estrogen receptor 1, estrogen receptor 2

route of administration

oral administration, intravaginal administration, transdermal administration

stereoisomer of

17β-ethinylestradiol, (8R,9S,13S,14R,17R)-17-ethynyl-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthrene-3,17-diol

subject has role

estrogen, carcinogen