Aminoestradiol | |
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Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C18H25NO[1] |
Molecular mass | 271.4 g/mol[1] |
Predicted LogP | 3.8[1] |
Chirality | absolute[2] |
Identifiers [] | |
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IUPAC name | (8R,9S,13S,14S,17S)-17-amino-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-ol[1] |
SMILES | C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2N)CCC4=C3C=CC(=C4)O[1] |
InChI | InChI=1S/C18H25NO/c1-18-9-8-14-13-5-3-12(20)10-11(13)2-4-15(14)16(18)6-7-17(18)19/h3,5,10,14-17,20H,2,4,6-9,19H2,1H3/t14-,15-,16+,17+,18+/m1/s1[1] |
InChIKey | VPONVJPFULJPAN-ZBRFXRBCSA-N[1] |
Dosing |
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Aminoestradiol
Aminoestradiol (also known as 17βAE2, 17β-Aminoestradiol, (17β)-17-Aminoestra-1,3,5(10)-trien-3-ol, 17β-Aminoestra-1,3,5(10)-trien-3-ol, Estra-1,3,5(10)-trien-3-ol, 17β-amino-, (+)-17β-Aminoestra-1,3,5(10)-trien-3-ol, Estra-1,3,5(10)-trien-3-ol, 17-amino-, (17β)-, 17-Aminoestra-1,3,5(10)-trien-3-ol # or 3-Hydroxy-17-.β.-aminoestra-1,3,5(10)-triene) is a substance of the steroid class.
Chemistry
Stereochemistry
Aminoestradiol is a absolute mixture