Compound Information | SONAR Target prediction | Name: | Epiandrosterone | Unique Identifier: | Prest699 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | C19H30O2 | Molecular Weight: | 264.234 g/mol | X log p: | -0.281 (online calculus) | Lipinksi Failures | 0 | TPSA | 17.07 | Hydrogen Bond Donor Count: | 0 | Hydrogen Bond Acceptors Count: | 2 | Rotatable Bond Count: | 0 | Canonical Smiles: | CC12CCC(O)CC1CCC1C2CCC2(C)C1CCC2=O | Generic_name: | AETIOCHOLANOLONE | Chemical_iupac_name: | AETIOCHOLANOLONE | Drug_type: | Experimental | Drugbank_id: | EXPT00443 | Drug_category: | Alcohol Sulfotransferase inhibitor | Organisms_affected: | -1 |
Species: |
9606 |
Condition: |
TMPPre001 |
Replicates: |
2 |
Raw OD Value: r im |
2005.0000±0 |
Normalized OD Score: sc h |
0.9596±0 |
Z-Score: |
-0.9116±0 |
p-Value: |
0.361978 |
Z-Factor: |
-17.6957 |
Fitness Defect: |
1.0162 |
Bioactivity Statement: |
Nonactive |
Experimental Conditions | | Library: | Prestwick | Plate Number and Position: | 6|D11 | Drug Concentration: | 50.00 nM | OD Absorbance: | 0 nm | Robot Temperature: | 24.00 Celcius | Date: | 2006-10-10 YYYY-MM-DD | Plate CH Control (+): | 1009.5±953.84240 | Plate DMSO Control (-): | 2021±558.06298 | Plate Z-Factor: | -4.4864 |
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247863 |
(2R,3S,5S,8S,9S,10S,13S,14S)-3-hydroxy-2,10,13-trimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydro cyclopenta[a]phenanthren-17-one |
250212 |
17-hydroxy-4,4,10,13,14-pentamethyl-1,2,5,6,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-o ne |
250214 |
1-[(3S,5S,8R,9S,10S,13R,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,9,11,12,15,16,17-dodecah ydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone |
252049 |
n/a |
255701 |
(4S,5S,8R,9S,10S,13S,14S,17S)-17-hydroxy-4,13-dimethyl-2,4,5,6,7,8,9,10,11,12,14,15,16,17-tetradecahydro -1H-cyclopenta[a]phenanthren-3-one |
257410 |
n/a |
internal high similarity DBLink | Rows returned: 0 | |
active | Cluster 11774 | Additional Members: 14 | Rows returned: 6 | |
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