Compound Information | SONAR Target prediction | Name: | DIHYDROJASMONIC ACID | Unique Identifier: | SPE01504104 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | | Molecular Weight: | 192.127 g/mol | X log p: | -1.077 (online calculus) | Lipinksi Failures | 0 | TPSA | 34.14 | Hydrogen Bond Donor Count: | 0 | Hydrogen Bond Acceptors Count: | 3 | Rotatable Bond Count: | 6 | Canonical Smiles: | CCCCCC1C(CCC1=O)CC(O)=O | Class: | alkane | Source: | Jasminium spp and Vicia faba | Reference: | Helv Chim Acta 57: 1301 (1974); Tet Lett 3413 (1974); JACS 97: 6144 (1975); PNAS 98: 4788 (2001) | Therapeutics: | plant growth regulator |
Species: |
4932 |
Condition: |
TOR1 |
Replicates: |
2 |
Raw OD Value: r im |
0.9552±0.0122329 |
Normalized OD Score: sc h |
0.9667±0.00148916 |
Z-Score: |
0.3078±0.0855591 |
p-Value: |
0.758698 |
Z-Factor: |
-1.02769 |
Fitness Defect: |
0.2762 |
Bioactivity Statement: |
Nonactive |
Experimental Conditions | | Library: | Spectrum_ED | Plate Number and Position: | 22|B2 | Drug Concentration: | 50.00 nM | OD Absorbance: | 595 nm | Robot Temperature: | 30.00 Celcius | Date: | 2012-09-18 YYYY-MM-DD | Plate CH Control (+): | -0.00012500000000000006±0.00279 | Plate DMSO Control (-): | 0.997225±0.02285 | Plate Z-Factor: | 0.9176 |
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5282979 |
5-oxoheptanoic acid |
5282980 |
5-oxononanoic acid |
5282999 |
5-oxohexadecanoic acid |
5283958 |
(4R)-4-[(3S,5S,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-7,12-dioxo-2,3,4,5,6,8,9,11,14,15,16,17-d odecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid |
5283961 |
(4R)-4-[(5S,8R,9S,10R,12S,13R,14S,17R)-12-hydroxy-10,13-dimethyl-3,7-dioxo-2,4,5,6,8,9,11,12,14,15,16,17 -dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid |
5283962 |
(4R)-4-[(5R,8R,9S,10R,12S,13R,14S,17R)-12-hydroxy-10,13-dimethyl-3,7-dioxo-2,4,5,6,8,9,11,12,14,15,16,17 -dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid |
internal high similarity DBLink | Rows returned: 13 | 1 2 3 Next >> |
active | Cluster 11884 | Additional Members: 2 | Rows returned: 1 | |
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