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: |
TMPPre003 |
Replicates: |
2 |
Raw OD Value: r im |
17567.0000±0 |
Normalized OD Score: sc h |
0.9796±0 |
Z-Score: |
-0.5688±0 |
p-Value: |
0.569514 |
Z-Factor: |
-60.1552 |
Fitness Defect: |
0.563 |
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 (+): | 18603±2417.22394 | Plate DMSO Control (-): | 18347.5±2353.75180 | Plate Z-Factor: | -21.3877 |
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5320371 |
(4R,4aR,6bR,8S,8aS,12aR,14aS)-8-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13 ,14,14b-tetradecahydro-1H-picen-3-one |
5459009 |
(4aS,6aR,6aR,6bR,8aR,9R,12aR,14aR,14bR)-14a-(hydroxymethyl)-2,2,4a,6a,6a,8a,9-heptamethyl-1,4,5,6,6b,7,8 ,9,11,12,12a,13,14,14b-tetradecahydropicene-3,10-dione |
5459041 |
n/a |
5701989 |
(3R,5R,10S,13S)-3-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phe nanthren-17-one |
6420080 |
(3R,5R,8R,10S,13S,14S)-3-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopent a[a]phenanthren-17-one |
6427588 |
(6R)-6-hydroxydecalin-2-one |
internal high similarity DBLink | Rows returned: 0 | |
active | Cluster 11774 | Additional Members: 14 | Rows returned: 6 | |
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