Compound Information | SONAR Target prediction | Name: | Cortexolone | Unique Identifier: | LOPAC 01179 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | C21H30O4 | Molecular Weight: | 319.246 g/mol | X log p: | 0.635 (online calculus) | Lipinksi Failures | 0 | TPSA | 34.14 | Hydrogen Bond Donor Count: | 0 | Hydrogen Bond Acceptors Count: | 4 | Rotatable Bond Count: | 2 | Canonical Smiles: | CC12CCC(=O)C=C1CCC1C2CCC2(C)C1CCC2(O)C(=O)CO | Class: | Hormone | Action: | Precursor | Selectivity: | Cortisol |
Species: |
4932 |
Condition: |
CIN2 |
Replicates: |
2 |
Raw OD Value: r im |
0.8253±0.00933381 |
Normalized OD Score: sc h |
1.0022±0.000948071 |
Z-Score: |
0.1728±0.0888775 |
p-Value: |
0.863098 |
Z-Factor: |
-48.1525 |
Fitness Defect: |
0.1472 |
Bioactivity Statement: |
Nonactive |
Experimental Conditions | | Library: | Lopac | Plate Number and Position: | 13|H11 | Drug Concentration: | 50.00 nM | OD Absorbance: | 600 nm | Robot Temperature: | 27.00 Celcius | Date: | 2005-12-07 YYYY-MM-DD | Plate CH Control (+): | 0.171075±0.19517 | Plate DMSO Control (-): | 0.8003±0.01034 | Plate Z-Factor: | 0.9382 |
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9050 |
(17R)-17-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a] phenanthren-3-one |
227112 |
17-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenan thren-3-one |
252011 |
17-hydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]ph enanthren-3-one |
440707 |
(8R,9S,10R,13S,14S,17R)-17-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydr o-1H-cyclopenta[a]phenanthren-3-one |
657187 |
(8R,9S,10S,13S,14S,17S)-17-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydr o-1H-cyclopenta[a]phenanthren-3-one |
5318189 |
(10R,13S,17S)-17-hydroxy-17-(2-hydroxyacetyl)-10,13,14-trimethyl-1,2,6,7,8,9,11,12,15,16-decahydrocyclop enta[a]phenanthren-3-one |
internal high similarity DBLink | Rows returned: 15 | 1 2 3 Next >> |
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