Oja, M.; Sild, S.; Piir, G.; Maran, U. Intrinsic aqueous solubility: mechanistically transparent data-driven modeling of drug substances. Pharmaceutics 2022, 14, 2248.
Compound
| ID: | t89 | |
|---|---|---|
| Name: | estradiol | |
| Description: | ||
| Labels: | ||
| CAS: | 50-28-2 | |
| InChi Code: | InChI=1S/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 |
Properties
logS0a: Intrinsic aqueous solubility from multiple sources [log(mol/L)]
| Value | Source or prediction |
|---|---|
| -4.85 |
Bergström, C. A. S.; Wassvik, C. M.; Norinder, U.; Luthman, K.; Artursson, P. Global and local computational models for aqueous solubility prediction of drug-like molecules. J. Chem. Inf. Comput. Sci. 2004, 44, 1477–1488. http://dx.doi.org/https://doi.org/10.1021/ci049909h |
| -4.096 |
M2: Model with RDKit descriptors from training set 2 (Training set) |
| -4.244 |
M3: Model with PaDEL and XLOGS descriptors from training set 2 (Training set) |
| -4.087 |
M_cons: Consensus model (average of predictions from M1, M2 and M3) (Training set) |