Cyclodiol | |
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Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C20H26O2[1] |
Molecular mass | 298.4 g/mol[1] |
Predicted LogP | 4.1[1] |
Chirality | absolute[2] |
Identifiers [] | |
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IUPAC name | (2R,11S,14S)-14-methylpentacyclo[13.2.2.01,14.02,11.05,10]nonadeca-5(10),6,8-triene-7,15-diol[1] |
SMILES | C[C@]12CC[C@H]3[C@H](C14CCC2(CC4)O)CCC5=C3C=CC(=C5)O[1] |
InChI | InChI=1S/C20H26O2/c1-18-7-6-16-15-4-3-14(21)12-13(15)2-5-17(16)19(18)8-10-20(18,22)11-9-19/h3-4,12,16-17,21-22H,2,5-11H2,1H3/t16-,17-,18+,19?,20?/m1/s1[1] |
InChIKey | YGXXZMDWSWSCSI-UYUJGIFYSA-N[1] |
Dosing | |
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Elimination half-life | 28.7 hours |
Cyclodiol
Cyclodiol (also known as ZK-115194, 14,21-Cyclo-19-norpregna-1,3,5(10)-triene-3,17-diol, CCRIS 9190, Zk 115194, 14,21-Cyclo-19-norpregn-1,3,5(10)-triene-3,11-diol, 14,17α-Ethano-1,3,5(10)-estratriene-3,17β-diol or 14,17-Ethano-14H-cyclopenta(a)phenanthrene, 14,21-cyclo-19-norpregna-1,3,5(10)-triene-3,17-diol deriv.) is a substance of the steroid class.
Chemistry
Stereochemistry
Cyclodiol is a absolute mixture