Compound Information | SONAR Target prediction | Name: | 5alpha-Pregnan-3alpha-ol-20-one | Unique Identifier: | LOPAC 01166 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | C21H34O2 | Molecular Weight: | 285.231 g/mol | X log p: | 0.313 (online calculus) | Lipinksi Failures | 0 | TPSA | 17.07 | Hydrogen Bond Donor Count: | 0 | Hydrogen Bond Acceptors Count: | 2 | Rotatable Bond Count: | 1 | Canonical Smiles: | CC(=O)C1CCC2C3CCC4CC(O)CCC4(C)C3CCC21C | Class: | GABA | Action: | Modulator | Selectivity: | GABA-A | 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 |
Replicates: |
8 |
Raw OD Value: r im |
0.7604±0.0402769 |
Normalized OD Score: sc h |
1.0029±0.0245073 |
Z-Score: |
0.1491±0.785467 |
p-Value: |
0.49216 |
Z-Factor: |
-26.5975 |
Fitness Defect: |
0.709 |
Bioactivity Statement: |
Nonactive |
Experimental Conditions | | Library: | Lopac | Plate Number and Position: | 13|E5 | Drug Concentration: | 50.00 nM | OD Absorbance: | 600 nm | Robot Temperature: | 27.80 Celcius | Date: | 2005-04-07 YYYY-MM-DD | Plate CH Control (+): | 0.04800625000000002±0.00227 | Plate DMSO Control (-): | 0.7375000000000003±0.02694 | Plate Z-Factor: | 0.9214 |
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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 17389 | Additional Members: 4 | Rows returned: 2 | |
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