Compound Information | SONAR Target prediction | Name: | 3-alpha,21-Dihydroxy-5-alpha-pregnan-20-one | Unique Identifier: | LOPAC 01126 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | C21H34O3 | Molecular Weight: | 301.231 g/mol | X log p: | -0.154 (online calculus) | Lipinksi Failures | 0 | TPSA | 17.07 | Hydrogen Bond Donor Count: | 0 | Hydrogen Bond Acceptors Count: | 3 | Rotatable Bond Count: | 2 | Canonical Smiles: | CC12CCC(O)CC1CCC1C3CCC(C(=O)CO)C3(C)CCC12 | Class: | GABA | Action: | Modulator | Selectivity: | GABA-A |
Species: |
4932 |
Condition: |
MT2481-pdr1pdr3 |
Replicates: |
2 |
Raw OD Value: r im |
0.7044±0.00106066 |
Normalized OD Score: sc h |
1.0334±0.0051143 |
Z-Score: |
1.8714±0.160992 |
p-Value: |
0.0629674 |
Z-Factor: |
-1.66832 |
Fitness Defect: |
2.7651 |
Bioactivity Statement: |
Nonactive |
Experimental Conditions | | Library: | Lopac | Plate Number and Position: | 12|B8 | Drug Concentration: | 50.00 nM | OD Absorbance: | 600 nm | Robot Temperature: | 27.80 Celcius | Date: | 2005-04-08 YYYY-MM-DD | Plate CH Control (+): | 0.046825000000000006±0.00100 | Plate DMSO Control (-): | 0.6559250000000001±0.01369 | Plate Z-Factor: | 0.9297 |
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7056541 |
(3R,5S,8R,9R,10S,13S,14S)-3-acetyl-3-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H- cyclopenta[a]phenanthren-17-one |
7056542 |
(3S,5S,8S,9R,10S,13S,14S)-3-acetyl-3-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H- cyclopenta[a]phenanthren-17-one |
7056543 |
(3R,5S,8S,9R,10S,13S,14S)-3-acetyl-3-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H- cyclopenta[a]phenanthren-17-one |
7064610 |
(2S)-1-(1-adamantyl)-2-hydroxy-propan-1-one |
7064611 |
(2R)-1-(1-adamantyl)-2-hydroxy-propan-1-one |
7092964 |
(2R,4aR,6aR,6aS,6bS,8aS,12aS,14aS,14bS)-2-hydroxy-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4a,5,6,6b,7,8,9,10 ,12,12a,13,14,14a-tetradecahydro-1H-picen-3-one |
internal high similarity DBLink | Rows returned: 1 | |
active | Cluster 17389 | Additional Members: 4 | Rows returned: 2 | |
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