Compound Information | SONAR Target prediction | Name: | Retinoic acid p-hydroxyanilide | Unique Identifier: | LOPAC 00957 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | C26H33NO2 | Molecular Weight: | 358.284 g/mol | X log p: | 20.884 (online calculus) | Lipinksi Failures | 1 | TPSA | 17.07 | Hydrogen Bond Donor Count: | 0 | Hydrogen Bond Acceptors Count: | 3 | Rotatable Bond Count: | 7 | Canonical Smiles: | CC1CCCC(C)(C)C=1C=CC(C)=CC=CC(C)=CC(=O)Nc1ccc(O)cc1 | Class: | Cell Cycle | Action: | Inhibitor | Generic_name: | N-(4-HYDROXYPHENYL)ALL-TRANS RETINAMIDE | Chemical_iupac_name: | N-(4-HYDROXYPHENYL)ALL-TRANS RETINAMIDE | Drug_type: | Experimental | Drugbank_id: | EXPT01420 | Logp: | 5.99 | Drug_category: | Retinol Binding Protein Complexed With Fenre inhibitor | Organisms_affected: | -1 |
Species: |
4932 |
Condition: |
NOP16 |
Replicates: |
2 |
Raw OD Value: r im |
0.7406±0.00799031 |
Normalized OD Score: sc h |
1.0205±0.00601029 |
Z-Score: |
0.9755±0.393605 |
p-Value: |
0.347788 |
Z-Factor: |
-3.4676 |
Fitness Defect: |
1.0562 |
Bioactivity Statement: |
Nonactive |
Experimental Conditions | | Library: | Lopac | Plate Number and Position: | 8|G6 | Drug Concentration: | 50.00 nM | OD Absorbance: | 600 nm | Robot Temperature: | 0.00 Celcius | Date: | 2005-04-22 YYYY-MM-DD | Plate CH Control (+): | 0.044925±0.00230 | Plate DMSO Control (-): | 0.706275±0.04392 | Plate Z-Factor: | 0.8266 |
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DBLink | Rows returned: 4 | |
1744 |
N-(4-hydroxyphenyl)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)nona-2,4,6,8-tetraenamide |
5288209 |
(2Z,4E,6Z,8E)-N-(4-hydroxyphenyl)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)nona-2,4,6,8-tetraenami de |
6440160 |
(2Z,4E,6Z,8E)-N-(4-hydroxyphenyl)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)nona-2,4,6,8-tetraenami de |
6603872 |
(2Z,4E,6Z,8E)-N-(4-hydroxyphenyl)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)nona-2,4,6,8-tetraenami de |
internal high similarity DBLink | Rows returned: 0 | |
active | Cluster 820 | Additional Members: 15 | Rows returned: 3 | |
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