| 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: |
APC9 |
| Replicates: |
2 |
| Raw OD Value: r im |
0.7045±0.0013435 |
| Normalized OD Score: sc h |
0.9922±0.00456371 |
| Z-Score: |
-0.4244±0.24153 |
| p-Value: |
0.675772 |
| Z-Factor: |
-8.62218 |
| Fitness Defect: |
0.3919 |
| Bioactivity Statement: |
Nonactive |
| Experimental Conditions | | | Library: | Spectrum | | Plate Number and Position: | 9|E9 | | Drug Concentration: | 50.00 nM | | OD Absorbance: | 600 nm | | Robot Temperature: | 23.00 Celcius | | Date: | 2007-11-22 YYYY-MM-DD | | Plate CH Control (+): | 0.041624999999999995±0.00032 | | Plate DMSO Control (-): | 0.684675±0.01815 | | Plate Z-Factor: | 0.9186 |
|  png
ps
pdf |
| 7053598 |
(1R,3R,4R)-1,7,7-trimethyl-3-propyl-norbornan-2-one |
| 7053599 |
(1R,3S,4R)-1,7,7-trimethyl-3-propyl-norbornan-2-one |
| 7053604 |
(1R,3R,4R)-1,3,7,7-tetramethylnorbornan-2-one |
| 7053605 |
(1R,3S,4R)-1,3,7,7-tetramethylnorbornan-2-one |
| 7054194 |
1-[(1S,2R,5R)-2-methyl-5-propan-2-yl-cyclopentyl]ethanone |
| 7054195 |
1-[(1S,2S,5R)-2-methyl-5-propan-2-yl-cyclopentyl]ethanone |
| internal high similarity DBLink | Rows returned: 17 | 1 2 3 Next >> |
| active | Cluster 10613 | Additional Members: 2 | Rows returned: 0 | |
|
