| Compound Information | SONAR Target prediction | | Name: | Genistein | | Unique Identifier: | LOPAC 00433 | | MolClass: | Checkout models in ver1.5 and ver1.0 | | Molecular Formula: | C15H10O5 | | Molecular Weight: | 260.158 g/mol | | X log p: | 14.737 (online calculus) | | Lipinksi Failures | 1 | | TPSA | 26.3 | | Hydrogen Bond Donor Count: | 0 | | Hydrogen Bond Acceptors Count: | 5 | | Rotatable Bond Count: | 1 | | Canonical Smiles: | Oc1ccc(cc1)C1=COc2cc(O)cc(O)c2C1=O | | Class: | Phosphorylation | | Action: | Inhibitor | | Selectivity: | Tyrosine kinase | | Generic_name: | 5,7-DIHYDROXY-3-(4-HYDROXYPHENYL)-4H-1-B | | Chemical_iupac_name: | GENISTEIN | | Drug_type: | Experimental | | Kegg_compound_id: | C06563 | | Drugbank_id: | EXPT01582 | | Logp: | 1.89 | | Cas_registry_number: | 446-72-0 | | Drug_category: | Estrogen Receptor Beta inhibitor | | Organisms_affected: | -1 |
| Species: |
4932 |
| Condition: |
KRE1 |
| Replicates: |
2 |
| Raw OD Value: r im |
0.6318±0.00176777 |
| Normalized OD Score: sc h |
0.9961±0.00493438 |
| Z-Score: |
-0.1621±0.204852 |
| p-Value: |
0.872542 |
| Z-Factor: |
-26.7101 |
| Fitness Defect: |
0.1363 |
| Bioactivity Statement: |
Nonactive |
| Experimental Conditions | | | Library: | Lopac | | Plate Number and Position: | 7|D11 | | Drug Concentration: | 50.00 nM | | OD Absorbance: | 600 nm | | Robot Temperature: | 27.90 Celcius | | Date: | 2005-11-22 YYYY-MM-DD | | Plate CH Control (+): | 0.038474999999999995±0.00138 | | Plate DMSO Control (-): | 0.6494500000000001±0.02124 | | Plate Z-Factor: | 0.8665 |
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| DBLink | Rows returned: 2 | |
| 5280961 |
5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one |
| 11000304 |
6,8-dideuterio-5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one |
| internal high similarity DBLink | Rows returned: 17 | 1 2 3 Next >> |
| active | Cluster 14679 | Additional Members: 9 | Rows returned: 5 | |
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