Compound Information | SONAR Target prediction | Name: | Androsterone | Unique Identifier: | LOPAC 00697 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | C19H30O2 | Molecular Weight: | 263.226 g/mol | X log p: | -0.358 (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: | Hormone | Selectivity: | Androgen | Generic_name: | AETIOCHOLANOLONE | Chemical_iupac_name: | AETIOCHOLANOLONE | Drug_type: | Experimental | Drugbank_id: | EXPT00443 | Drug_category: | Alcohol Sulfotransferase inhibitor | Organisms_affected: | -1 |
Species: |
4932 |
Condition: |
DEP1 |
Replicates: |
2 |
Raw OD Value: r im |
0.5809±0.0166877 |
Normalized OD Score: sc h |
0.8948±0.0304884 |
Z-Score: |
-4.3491±1.44685 |
p-Value: |
0.000440462 |
Z-Factor: |
-0.870248 |
Fitness Defect: |
7.7277 |
Bioactivity Statement: |
Active |
Experimental Conditions | | Library: | Lopac | Plate Number and Position: | 2|G5 | Drug Concentration: | 50.00 nM | OD Absorbance: | 600 nm | Robot Temperature: | 26.90 Celcius | Date: | 2005-11-16 YYYY-MM-DD | Plate CH Control (+): | 0.03855±0.00129 | Plate DMSO Control (-): | 0.64055±0.02116 | Plate Z-Factor: | 0.8634 |
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5024895 |
14a-(hydroxymethyl)-2,2,4a,6a,6a,8a,9-heptamethyl-1,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydropic ene-3,10-dione |
5061847 |
17-hydroxy-10,13-dimethyl-1,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-2-one |
5123765 |
1-(17-hydroxy-5,10,13-trimethyl-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren -3-yl)ethanone |
5165408 |
17-hydroxy-6,10,13-trimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3- one |
5233916 |
1-(8-hydroxy-10a-methyl-2,3,4,4a,4b,5,6,6a,7,8,9,10,10b,11,12,12a-hexadecahydro-1H-chrysen-1-yl)ethanone |
5255015 |
n/a |
internal high similarity DBLink | Rows returned: 5 | |
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