| Compound Information | SONAR Target prediction | | Name: | Oleic Acid | | Unique Identifier: | LOPAC 01105 | | MolClass: | Checkout models in ver1.5 and ver1.0 | | Molecular Formula: | C18H34O2 | | Molecular Weight: | 248.191 g/mol | | X log p: | 3.318 (online calculus) | | Lipinksi Failures | 1 | | TPSA | 17.07 | | Hydrogen Bond Donor Count: | 0 | | Hydrogen Bond Acceptors Count: | 2 | | Rotatable Bond Count: | 15 | | Canonical Smiles: | CCCCCCCC=CCCCCCCCCC(O)=O | | Class: | Phosphorylation | | Action: | Activator | | Selectivity: | PKC | | Generic_name: | OLEIC ACID | | Chemical_iupac_name: | OLEIC ACID | | Drug_type: | Experimental | | Kegg_compound_id: | C00712 | | Drugbank_id: | EXPT02430 | | Logp: | 6.036 | | Cas_registry_number: | 112-80-1 | | Drug_category: | Serum Albumin inhibitor | | Organisms_affected: | -1 |
| Species: |
4932 |
| Condition: |
WHI5 |
| Replicates: |
2 |
| Raw OD Value: r im |
0.6366±0.031537 |
| Normalized OD Score: sc h |
1.0140±0.0425344 |
| Z-Score: |
0.5002±1.33687 |
| p-Value: |
0.402284 |
| Z-Factor: |
-5.06018 |
| Fitness Defect: |
0.9106 |
| Bioactivity Statement: |
Nonactive |
| Experimental Conditions | | | Library: | Lopac | | Plate Number and Position: | 12|B4 | | Drug Concentration: | 50.00 nM | | OD Absorbance: | 600 nm | | Robot Temperature: | 0.00 Celcius | | Date: | 2005-04-20 YYYY-MM-DD | | Plate CH Control (+): | 0.045875±0.00087 | | Plate DMSO Control (-): | 0.6643749999999999±0.09786 | | Plate Z-Factor: | 0.7360 |
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| 160156 |
(4R)-4-[(5R,8S,9S,10R,13R,14S)-10,13-dimethyl-2,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]
phenanthren-17-yl]pentanoic acid |
| 164601 |
11-[(1R)-1-cyclopent-2-enyl]undecanoic acid |
| 177655 |
octadec-15-enoic acid |
| 195858 |
9-(6-propyl-1-cyclohex-3-enyl)nonanoic acid |
| 220039 |
6-(1-cyclohexenyl)hexanoic acid |
| 220339 |
7-ethyl-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid |
| internal high similarity DBLink | Rows returned: 5 | |
| active | Cluster 13466 | Additional Members: 2 | Rows returned: 0 | |
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