Compound Information | SONAR Target prediction | Name: | CAMPHOR (1R) | Unique Identifier: | SPE01500156 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | | Molecular Weight: | 136.106 g/mol | X log p: | -0.875 (online calculus) | Lipinksi Failures | 0 | TPSA | 17.07 | Hydrogen Bond Donor Count: | 0 | Hydrogen Bond Acceptors Count: | 1 | Rotatable Bond Count: | 0 | Canonical Smiles: | CC1(C)C2CCC1(C)C(=O)C2 | Class: | terpene | Source: | Cinnamomum camphora | Therapeutics: | analgesic, antiinfective, antipruritic | 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: |
BCK2 |
Replicates: |
2 |
Raw OD Value: r im |
0.7410±0.0495682 |
Normalized OD Score: sc h |
0.9916±0.0230999 |
Z-Score: |
-0.2956±0.935819 |
p-Value: |
0.526338 |
Z-Factor: |
-12.1884 |
Fitness Defect: |
0.6418 |
Bioactivity Statement: |
Nonactive |
Experimental Conditions | | Library: | Spectrum | Plate Number and Position: | 9|E9 | Drug Concentration: | 50.00 nM | OD Absorbance: | 600 nm | Robot Temperature: | 25.80 Celcius | Date: | 2006-03-29 YYYY-MM-DD | Plate CH Control (+): | 0.037875±0.00166 | Plate DMSO Control (-): | 0.730375±0.01398 | Plate Z-Factor: | 0.9595 |
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7140382 |
(5R,8S,9R,10R,13R,14S)-10,13-dimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthr ene-3,17-dione |
7140383 |
(5R,8S,9R,10S,13R,14S)-10,13-dimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthr ene-3,17-dione |
7160826 |
(3R)-3-methylcyclopentadecan-1-one |
7160827 |
(3S)-3-methylcyclopentadecan-1-one |
7163286 |
n/a |
7164431 |
(1R,4R,6R)-5,5,6-trimethylnorbornan-2-one |
internal high similarity DBLink | Rows returned: 17 | 1 2 3 Next >> |
active | Cluster 10613 | Additional Members: 2 | Rows returned: 0 | |
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