Compound Information | SONAR Target prediction | Name: | AMBRETTOLIDE | Unique Identifier: | SPE00310003 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | C16H28O2 | Molecular Weight: | 224.17 g/mol | X log p: | 4.152 (online calculus) | Lipinksi Failures | 0 | TPSA | 26.3 | Hydrogen Bond Donor Count: | 0 | Hydrogen Bond Acceptors Count: | 2 | Rotatable Bond Count: | 0 | Canonical Smiles: | O=C1CCCCCC=CCCCCCCCCO1 | Source: | ex Abelmoschus moschatus and bees | Reference: | Food Cosmet Toxicol 13: 707 (1975) |
Species: |
4932 |
Condition: |
KAR3 |
Replicates: |
2 |
Raw OD Value: r im |
0.6353±0.00494975 |
Normalized OD Score: sc h |
0.9909±0.00290654 |
Z-Score: |
-0.4212±0.124068 |
p-Value: |
0.674784 |
Z-Factor: |
-17.0341 |
Fitness Defect: |
0.3934 |
Bioactivity Statement: |
Nonactive |
Experimental Conditions | | Library: | Spectrum | Plate Number and Position: | 23|E11 | Drug Concentration: | 50.00 nM | OD Absorbance: | 600 nm | Robot Temperature: | 27.50 Celcius | Date: | 2007-09-06 YYYY-MM-DD | Plate CH Control (+): | 0.04205±0.00117 | Plate DMSO Control (-): | 0.6291±0.01824 | Plate Z-Factor: | 0.9008 |
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5317881 |
(8E)-1-oxacycloheptadec-8-en-2-one |
5318312 |
[(3S,6aR,8aR,12S,14bR)-4,4,4a,6a,6b,8a,11,12,14b-nonamethyl-1,2,3,5,6,7,8,9,10,11,12,12a,14,14a-tetradec ahydropicen-3-yl] dodecanoate |
5318316 |
[(3S,6aR,8aR,14bR)-4,4,4a,6a,6b,8a,11,11,14b-nonamethyl-2,3,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-pi cen-3-yl] dodecanoate |
5318340 |
[(3S,6aR,8aR,12S,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecah ydro-1H-picen-3-yl] tetradecanoate |
5318351 |
[(3S,6aR,8aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydrop icen-3-yl] tetradecanoate |
5318360 |
[(3S,6aR,8aR,12S,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecah ydro-1H-picen-3-yl] hexadecanoate |
internal high similarity DBLink | Rows returned: 5 | |
active | Cluster 983 | Additional Members: 1 | Rows returned: 0 | |
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