| Compound Information | SONAR Target prediction | | Name: | 2-,2--BISEPIGALLOCATECHIN DIGALLATE | | Unique Identifier: | SPE00201507 | | MolClass: | Checkout models in ver1.5 and ver1.0 | | Molecular Formula: | | | Molecular Weight: | 880.458 g/mol | | X log p: | 26.014 (online calculus) | | Lipinksi Failures | 2 | | TPSA | 71.06 | | Hydrogen Bond Donor Count: | 0 | | Hydrogen Bond Acceptors Count: | 22 | | Rotatable Bond Count: | 9 | | Canonical Smiles: | Oc1cc(O)c2CC(OC(=O)c3cc(O)c(O)c(O)c3)C(Oc2c1)c1cc(O)c(O)c(O)c1c1c(O)c(
O)c(O)cc1C1Oc2cc(O)cc(O)c2CC1OC(=O)c1cc(O)c(O)c(O)c1 | | Source: | tea pigment |
| Species: |
4932 |
| Condition: |
VAM3 |
| Replicates: |
2 |
| Raw OD Value: r im |
0.4498±0.0440528 |
| Normalized OD Score: sc h |
0.6483±0.0437216 |
| Z-Score: |
-10.6646±0.834856 |
| p-Value: |
3.58822e-24 |
| Z-Factor: |
0.121642 |
| Fitness Defect: |
53.9844 |
| Bioactivity Statement: |
Active |
| Experimental Conditions | | | Library: | SPECMTS3 | | Plate Number and Position: | 25|C2 | | Drug Concentration: | 50.00 nM | | OD Absorbance: | 600 nm | | Robot Temperature: | 25.20 Celcius | | Date: | 2008-04-09 YYYY-MM-DD | | Plate CH Control (+): | 0.04035±0.00126 | | Plate DMSO Control (-): | 0.6912±0.03723 | | Plate Z-Factor: | 0.8555 |
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| DBLink | Rows returned: 4 | |
| 442543 |
[(2R,3R)-2-[2-[6-[(2R,3R)-5,7-dihydroxy-3-(3,4,5-trihydroxybenzoyl)oxy-chroman-2-yl]-2,3,4-trihydroxy-ph
enyl]-3,4,5-trihydroxy-phenyl]-5,7-dihydroxy-chroman-3-yl] 3,4,5-trihydroxybenzoate |
| 467315 |
[(2R,3R)-5,7-dihydroxy-2-[3,4,5-trihydroxy-2-[2,3,4-trihydroxy-6-[(2R,3R)-3,5,7-trihydroxychroman-2-yl]p
henyl]phenyl]chroman-3-yl] 3,4,5-trihydroxybenzoate |
| 5152597 |
[2-[2-[6-[5,7-dihydroxy-3-(3,4,5-trihydroxybenzoyl)oxy-chroman-2-yl]-2,3,4-trihydroxy-phenyl]-3,4,5-trih
ydroxy-phenyl]-5,7-dihydroxy-chroman-3-yl] 3,4,5-trihydroxybenzoate |
| 5152866 |
[5,7-dihydroxy-2-[3,4,5-trihydroxy-2-[2,3,4-trihydroxy-6-(3,5,7-trihydroxychroman-2-yl)phenyl]phenyl]chr
oman-3-yl] 3,4,5-trihydroxybenzoate |
| internal high similarity DBLink | Rows returned: 1 | |
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