Compound Information | SONAR Target prediction | Name: | 5alpha-ANDROSTAN-3,17-DIONE | Unique Identifier: | SPE00107108 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | | Molecular Weight: | 261.21 g/mol | X log p: | -0.364 (online calculus) | Lipinksi Failures | 0 | TPSA | 34.14 | 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: | human urine & adrenal cortex | Therapeutics: | androgen | Generic_name: | 5ALPHA-ANDROSTAN-3,17-DIONE | Chemical_iupac_name: | 5ALPHA-ANDROSTAN-3,17-DIONE | Drug_type: | Experimental | Drugbank_id: | EXPT00262 | Drug_category: | Estradiol 17 Beta-Dehydrogenase 1 inhibitor | Organisms_affected: | -1 |
Species: |
4932 |
Condition: |
TRK1 |
Replicates: |
2 |
Raw OD Value: r im |
0.4289±0.00473762 |
Normalized OD Score: sc h |
0.8507±0.00367484 |
Z-Score: |
-4.6103±0.092849 |
p-Value: |
0.00000421522 |
Z-Factor: |
0.211107 |
Fitness Defect: |
12.3768 |
Bioactivity Statement: |
Active |
Experimental Conditions | | Library: | SPECMTS3 | Plate Number and Position: | 9|C8 | Drug Concentration: | 50.00 nM | OD Absorbance: | 600 nm | Robot Temperature: | 25.60 Celcius | Date: | 2008-03-14 YYYY-MM-DD | Plate CH Control (+): | 0.0403±0.00051 | Plate DMSO Control (-): | 0.477825±0.01695 | Plate Z-Factor: | 0.8747 |
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7056784 |
(5S,8R,9S,10S,13R,14R,17R)-10,13-dimethyl-17-[(2S)-6-methylheptan-2-yl]-1,2,4,5,6,7,8,9,11,12,14,15,16,1 7-tetradecahydrocyclopenta[a]phenanthren-3-one |
7057894 |
(5S,8S,9S,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,4,5,6,7,8,9,11,12,14,15,16,1 7-tetradecahydrocyclopenta[a]phenanthren-3-one |
7057963 |
(2S)-2-methylcyclohexan-1-one |
7057964 |
(3S)-3-methylcyclohexan-1-one |
7057991 |
(2S,6S)-2,6-dimethylcyclohexan-1-one |
7060916 |
(2R)-2-methylcyclododecan-1-one |
internal high similarity DBLink | Rows returned: 17 | 1 2 3 Next >> |
active | Cluster 11774 | Additional Members: 14 | Rows returned: 5 | |
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