| 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: |
CLN2 |
| Replicates: |
2 |
| Raw OD Value: r im |
0.7250±0.00820244 |
| Normalized OD Score: sc h |
0.9942±0.00852077 |
| Z-Score: |
-0.7348±0.344241 |
| p-Value: |
0.475572 |
| Z-Factor: |
-4.89668 |
| Fitness Defect: |
0.7432 |
| Bioactivity Statement: |
Nonactive |
| Experimental Conditions | | | Library: | Spectrum_ED | | Plate Number and Position: | 1|G6 | | Drug Concentration: | 50.00 nM | | OD Absorbance: | 595 nm | | Robot Temperature: | 30.00 Celcius | | Date: | 2010-08-10 YYYY-MM-DD | | Plate CH Control (+): | 0.09625±0.00648 | | Plate DMSO Control (-): | 0.91±0.03692 | | Plate Z-Factor: | 0.7824 |
|  png
ps
pdf |
| 7054196 |
1-[(1S,2R,5S)-2-methyl-5-propan-2-yl-cyclopentyl]ethanone |
| 7054197 |
1-[(1S,2S,5S)-2-methyl-5-propan-2-yl-cyclopentyl]ethanone |
| 7054426 |
(1R,5R)-1,8,8-trimethylbicyclo[3.2.1]octan-2-one |
| 7054427 |
(1S,5S)-1,8,8-trimethylbicyclo[3.2.1]octan-2-one |
| 7054461 |
1-[(1R,2R,4R)-4,7,7-trimethylnorbornan-2-yl]propan-1-one |
| 7054462 |
1-[(1R,2S,4R)-4,7,7-trimethylnorbornan-2-yl]propan-1-one |
| internal high similarity DBLink | Rows returned: 17 | 1 2 3 Next >> |
| active | Cluster 10613 | Additional Members: 2 | Rows returned: 0 | |
|
