Compound Information | SONAR Target prediction | Name: | Androsterone | Unique Identifier: | Prest689 | 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 |
1917.0000±0 |
Normalized OD Score: sc h |
0.9023±0 |
Z-Score: |
-2.2022±0 |
p-Value: |
0.0276484 |
Z-Factor: |
-62.9691 |
Fitness Defect: |
3.5882 |
Bioactivity Statement: |
Nonactive |
Experimental Conditions | | Library: | Prestwick | Plate Number and Position: | 6|B2 | 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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6427606 |
(6S)-6-hydroxydecalin-2-one |
6429569 |
(3R,5S)-3-hydroxy-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16-hexadecahydrocyclopenta[a]phenanthren-17-one |
6429570 |
(3R,5R)-3-hydroxy-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16-hexadecahydrocyclopenta[a]phenanthren-17-one |
6429828 |
(5R,17R)-17-hydroxy-10,13,17-trimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanth ren-3-one |
6429831 |
(5R,7R,17R)-17-hydroxy-7,10,13,17-tetramethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]p henanthren-3-one |
6429847 |
(5R,7R,17S)-17-hydroxy-7,10,13,17-tetramethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]p henanthren-3-one |
internal high similarity DBLink | Rows returned: 0 | |
active | Cluster 11774 | Additional Members: 14 | Rows returned: 6 | |
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