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: |
RNR3 |
Replicates: |
2 |
Raw OD Value: r im |
0.4899±0.0333047 |
Normalized OD Score: sc h |
0.6284±0.020365 |
Z-Score: |
-11.0768±0.437701 |
p-Value: |
2.45934e-27 |
Z-Factor: |
0.618541 |
Fitness Defect: |
61.2699 |
Bioactivity Statement: |
Active |
Experimental Conditions | | Library: | Spectrum | Plate Number and Position: | 7|B7 | Drug Concentration: | 50.00 nM | OD Absorbance: | 600 nm | Robot Temperature: | 23.90 Celcius | Date: | 2006-04-26 YYYY-MM-DD | Plate CH Control (+): | 0.03805±0.00106 | Plate DMSO Control (-): | 0.76675±0.01989 | Plate Z-Factor: | 0.9271 |
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7092505 |
1-[(3R,5S,8S,9R,10S,13R,14R,17S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahyd ro-1H-cyclopenta[a]phenanthren-17-yl]ethanone |
7092506 |
1-[(3R,5S,8S,9S,10S,13R,14S,17S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahyd ro-1H-cyclopenta[a]phenanthren-17-yl]ethanone |
7092507 |
1-[(3R,5S,8S,9S,10S,13R,14R,17S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahyd ro-1H-cyclopenta[a]phenanthren-17-yl]ethanone |
7166458 |
n/a |
7166459 |
n/a |
7166460 |
n/a |
internal high similarity DBLink | Rows returned: 5 | |
active | Cluster 11774 | Additional Members: 14 | Rows returned: 5 | |
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