Compound Information | SONAR Target prediction | Name: | Corticosterone | Unique Identifier: | LOPAC 00759 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | C21H30O4 | Molecular Weight: | 319.246 g/mol | X log p: | 0.527 (online calculus) | Lipinksi Failures | 0 | TPSA | 34.14 | Hydrogen Bond Donor Count: | 0 | Hydrogen Bond Acceptors Count: | 4 | Rotatable Bond Count: | 2 | Canonical Smiles: | CC12CC(O)C3C(CCC4=CC(=O)CCC34C)C1CCC2C(=O)CO | Class: | Hormone | Selectivity: | Glucocorticoid |
Species: |
4932 |
Condition: |
MRC1 |
Replicates: |
2 |
Raw OD Value: r im |
0.8249±0.0046669 |
Normalized OD Score: sc h |
1.0068±0.000683994 |
Z-Score: |
0.5008±0.0971659 |
p-Value: |
0.617342 |
Z-Factor: |
-4.75478 |
Fitness Defect: |
0.4823 |
Bioactivity Statement: |
Nonactive |
Experimental Conditions | | Library: | Lopac | Plate Number and Position: | 3|F11 | Drug Concentration: | 50.00 nM | OD Absorbance: | 600 nm | Robot Temperature: | 24.40 Celcius | Date: | 2005-12-06 YYYY-MM-DD | Plate CH Control (+): | 0.11487499999999999±0.15809 | Plate DMSO Control (-): | 0.798225±0.01215 | Plate Z-Factor: | 0.9437 |
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4122713 |
8-hydroxy-17-(2-hydroxyacetyl)-13-methyl-1,2,6,7,9,10,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanth ren-3-one |
5316088 |
(4aR,5S,6aR,7S)-5-hydroxy-7-(2-hydroxyacetyl)-4a,6a-dimethyl-4,4b,5,6,7,8,9,10,10a,10b,11,12-dodecahydro -3H-chrysen-2-one |
6540812 |
(8S,9R,10R,11S,13S,14S,17R)-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17 -dodecahydrocyclopenta[a]phenanthren-3-one |
6603769 |
(8S,9S,10S,11R,13S,14R,17R)-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17 -dodecahydrocyclopenta[a]phenanthren-3-one |
6918887 |
(8R,9S,10S,11R,13R,14R,17S)-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17 -dodecahydrocyclopenta[a]phenanthren-3-one |
internal high similarity DBLink | Rows returned: 6 | |
active | Cluster 10196 | Additional Members: 12 | Rows returned: 0 | |
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