Compound Information | SONAR Target prediction | Name: | EPIANDROSTERONE | Unique Identifier: | SPE00310009 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | | Molecular Weight: | 261.21 g/mol | X log p: | -0.512 (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 | Class: | sterol | Source: | in normal human urine | Reference: | J Am Chem Soc 75: 2275 (9153) | Generic_name: | AETIOCHOLANOLONE | Chemical_iupac_name: | AETIOCHOLANOLONE | Drug_type: | Experimental | Drugbank_id: | EXPT00443 | Drug_category: | Alcohol Sulfotransferase inhibitor | Organisms_affected: | -1 |
Species: |
4932 |
Condition: |
BY4741-2nd |
Replicates: |
2 |
Raw OD Value: r im |
0.6675±0.0220617 |
Normalized OD Score: sc h |
0.8369±0.0166719 |
Z-Score: |
-6.4466±0.430768 |
p-Value: |
0.000000000414814 |
Z-Factor: |
0.315157 |
Fitness Defect: |
21.6032 |
Bioactivity Statement: |
Active |
Experimental Conditions | | Library: | Spectrum | Plate Number and Position: | 7|B7 | Drug Concentration: | 50.00 nM | OD Absorbance: | 600 nm | Robot Temperature: | 26.90 Celcius | Date: | 2006-04-05 YYYY-MM-DD | Plate CH Control (+): | 0.03875±0.00116 | Plate DMSO Control (-): | 0.769525±0.01649 | Plate Z-Factor: | 0.9201 |
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352070 |
17-hydroxy-1,5,13-trimethyl-1,2,4,6,7,8,9,10,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3- one |
354003 |
(4aS,6aR,6aR,8aR,9R,14bR)-14a-(hydroxymethyl)-2,2,4a,6a,6a,8a,9-heptamethyl-1,4,5,6,6b,7,8,9,11,12,12a,1 3,14,14b-tetradecahydropicene-3,10-dione |
354617 |
n/a |
385902 |
2-(12-hydroxydodecyl)-2,12,12-trimethyl-cyclododecan-1-one |
385904 |
2-(11-hydroxyundecyl)-2,8,8-trimethyl-cyclooctan-1-one |
439617 |
3-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one |
internal high similarity DBLink | Rows returned: 5 | |
active | Cluster 11774 | Additional Members: 14 | Rows returned: 5 | |
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