Compound Information | SONAR Target prediction | Name: | MENTHONE | Unique Identifier: | SPE00300564 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | | Molecular Weight: | 136.106 g/mol | X log p: | -0.199 (online calculus) | Lipinksi Failures | 0 | TPSA | 17.07 | Hydrogen Bond Donor Count: | 0 | Hydrogen Bond Acceptors Count: | 1 | Rotatable Bond Count: | 1 | Canonical Smiles: | CC(C)C1CCC(C)CC1=O | Class: | terpene | Source: | pennyroyal and peppermint oils | Reference: | J Org Chem 25: 1434 (1960) | 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: |
APC9 |
Replicates: |
2 |
Raw OD Value: r im |
0.7002±0.00961665 |
Normalized OD Score: sc h |
0.9972±0.0100966 |
Z-Score: |
-0.1488±0.546267 |
p-Value: |
0.702448 |
Z-Factor: |
-5425.06 |
Fitness Defect: |
0.3532 |
Bioactivity Statement: |
Nonactive |
Experimental Conditions | | Library: | Spectrum | Plate Number and Position: | 5|E9 | Drug Concentration: | 50.00 nM | OD Absorbance: | 600 nm | Robot Temperature: | 21.70 Celcius | Date: | 2007-11-22 YYYY-MM-DD | Plate CH Control (+): | 0.041374999999999995±0.00052 | Plate DMSO Control (-): | 0.687425±0.02326 | Plate Z-Factor: | 0.8902 |
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7061774 |
n/a |
7061775 |
n/a |
7061776 |
n/a |
7067821 |
(4R,4aR,6aS,6aS,6bR,8aR,12aR,14aR,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13 ,14,14b-tetradecahydro-1H-picen-3-one |
7067822 |
(4R,4aR,6aS,6aS,6bR,8aR,12aR,14aR,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13 ,14,14b-tetradecahydro-1H-picen-3-one |
7067823 |
(4R,4aR,6aS,6aR,6bR,8aR,12aR,14aR,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13 ,14,14b-tetradecahydro-1H-picen-3-one |
internal high similarity DBLink | Rows returned: 17 | 1 2 3 Next >> |
active | Cluster 10481 | Additional Members: 1 | Rows returned: 0 | |
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