Compound Information | SONAR Target prediction | Name: | PERSEITOL | Unique Identifier: | SPE00202130 | MolClass: | Checkout models in ver1.5 and ver1.0 | Molecular Formula: | | Molecular Weight: | 196.071 g/mol | X log p: | -3.419 (online calculus) | Lipinksi Failures | 0 | TPSA | 0 | Hydrogen Bond Donor Count: | 0 | Hydrogen Bond Acceptors Count: | 7 | Rotatable Bond Count: | 6 | Canonical Smiles: | OCC(O)C(O)C(O)C(O)C(O)CO | Class: | carbohydrate | Source: | Persia spp. | Reference: | J Am Chem Soc 61: 339 (1939); Carbohydr Res 150: 35 (1986) |
Species: |
4932 |
Condition: |
TRK1 |
Replicates: |
2 |
Raw OD Value: r im |
0.5057±0.0133643 |
Normalized OD Score: sc h |
1.0002±0.0195016 |
Z-Score: |
-0.0017±0.598101 |
p-Value: |
0.672352 |
Z-Factor: |
-92.0931 |
Fitness Defect: |
0.397 |
Bioactivity Statement: |
Nonactive |
Experimental Conditions | | Library: | SPECMTS3 | Plate Number and Position: | 25|G10 | Drug Concentration: | 50.00 nM | OD Absorbance: | 600 nm | Robot Temperature: | 25.80 Celcius | Date: | 2008-03-14 YYYY-MM-DD | Plate CH Control (+): | 0.0405±0.00112 | Plate DMSO Control (-): | 0.48229999999999995±0.02093 | Plate Z-Factor: | 0.8643 |
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12001896 |
(3S,5S,6S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,3,4,6,7,8,9,11,12,14,15,1 6,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol |
14778391 |
(3S,5S,6R,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methyl-heptan-2-yl]-10,13-dimethyl-1,2,3,4,6,7,8, 9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol |
15942686 |
(1R,2S,4S,5R)-6-(hydroxymethyl)cyclohexane-1,2,3,4,5-pentol |
15946992 |
(1R,2S,3R,4R)-4-[(1R)-1,2-dihydroxyethyl]cyclopentane-1,2,3-triol |
15953493 |
(1S,2R,3S,4R,5S)-5-(hydroxymethyl)cyclohexane-1,2,3,4-tetrol |
16043508 |
(3S,5R,6R,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,3,4,6,7,8,9,11,12,14,1 5,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol |
internal high similarity DBLink | Rows returned: 2 | |
active | Cluster 2846 | Additional Members: 7 | Rows returned: 0 | |
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