| Compound Information | SONAR Target prediction | | Name: | beta-AMYRIN | | Unique Identifier: | SPE00100360 | | MolClass: | Checkout models in ver1.5 and ver1.0 | | Molecular Formula: | | | Molecular Weight: | 376.32 g/mol | | X log p: | 2.864 (online calculus) | | Lipinksi Failures | 0 | | TPSA | 0 | | Hydrogen Bond Donor Count: | 0 | | Hydrogen Bond Acceptors Count: | 1 | | Rotatable Bond Count: | 0 | | Canonical Smiles: | CC1(C)CCC2(C)CCC3(C)C(=CCC4C5(C)CCC(O)C(C)(C)C5CCC43C)C2C1 | | Class: | triterpene | | Source: | widespread in plants | | Reference: | Phytochemistry 9: 1669 (1970) | | Generic_name: | 16,17-ANDROSTENE-3-OL | | Chemical_iupac_name: | 16,17-ANDROSTENE-3-OL | | Drug_type: | Experimental | | Drugbank_id: | EXPT00580 | | Logp: | 4.38 | | Drug_category: | Constitutive Androstane Receptor inhibitor | | Organisms_affected: | -1 |
| Species: |
4932 |
| Condition: |
TFP1 |
| Replicates: |
2 |
| Raw OD Value: r im |
0.7090±0.010253 |
| Normalized OD Score: sc h |
0.9541±0.019331 |
| Z-Score: |
-1.9138±0.781409 |
| p-Value: |
0.0935444 |
| Z-Factor: |
-10.3464 |
| Fitness Defect: |
2.3693 |
| Bioactivity Statement: |
Nonactive |
| Experimental Conditions | | | Library: | Spectrum | | Plate Number and Position: | 1|H10 | | Drug Concentration: | 50.00 nM | | OD Absorbance: | 600 nm | | Robot Temperature: | 24.30 Celcius | | Date: | 2007-08-31 YYYY-MM-DD | | Plate CH Control (+): | 0.041725±0.00094 | | Plate DMSO Control (-): | 0.707525±0.08144 | | Plate Z-Factor: | 0.5901 |
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ps
pdf |
| 634717 |
17-(5-ethyl-6-methyl-heptan-2-yl)-4,10,13-trimethyl-2,3,4,5,6,7,9,11,12,15,16,17-dodecahydro-1H-cyclopen
ta[a]phenanthren-3-ol |
| 635979 |
n/a |
| 1712010 |
(Z)-tetradec-11-en-1-ol |
| 1712011 |
(E)-tetradec-11-en-1-ol |
| 1747970 |
(2R)-2-methyl-4-[(1R)-2,2,3-trimethyl-1-cyclopent-3-enyl]butan-1-ol |
| 1747971 |
(2R)-2-methyl-4-[(1S)-2,2,3-trimethyl-1-cyclopent-3-enyl]butan-1-ol |
| internal high similarity DBLink | Rows returned: 8 | 1 2 Next >> |
| active | Cluster 1623 | Additional Members: 8 | Rows returned: 5 | |
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