Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H14O6 |
| Molecular Weight | 314.2895 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(O)=C2C(=O)C=C(OC2=C1)C3=CC=C(O)C(OC)=C3
InChI
InChIKey=ROCUOVBWAWAQFD-UHFFFAOYSA-N
InChI=1S/C17H14O6/c1-21-10-6-12(19)17-13(20)8-14(23-16(17)7-10)9-3-4-11(18)15(5-9)22-2/h3-8,18-19H,1-2H3
| Molecular Formula | C17H14O6 |
| Molecular Weight | 314.2895 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:59:02 UTC 2023
by
admin
on
Sat Dec 16 09:59:02 UTC 2023
|
| Record UNII |
CT1Q4E0I0W
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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Code | English | ||
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| Code System | Code | Type | Description | ||
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DTXSID90180421
Created by
admin on Sat Dec 16 09:59:02 UTC 2023 , Edited by admin on Sat Dec 16 09:59:02 UTC 2023
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CT1Q4E0I0W
Created by
admin on Sat Dec 16 09:59:02 UTC 2023 , Edited by admin on Sat Dec 16 09:59:02 UTC 2023
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25739-41-7
Created by
admin on Sat Dec 16 09:59:02 UTC 2023 , Edited by admin on Sat Dec 16 09:59:02 UTC 2023
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Velutin
Created by
admin on Sat Dec 16 09:59:02 UTC 2023 , Edited by admin on Sat Dec 16 09:59:02 UTC 2023
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5464381
Created by
admin on Sat Dec 16 09:59:02 UTC 2023 , Edited by admin on Sat Dec 16 09:59:02 UTC 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> CONSTITUENT ALWAYS PRESENT |
Velutin significantly
inhibited p38 and JNK phosphorylation at 5 and 10 uM.The SEAP reporter assay was conducted to evaluate the inhibitory
effects of velutin in inhibiting NF-.KAPPA.B activation in our
previous report. The IC50 values of this compound was
estimated at 2.0 uM for velutin.
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PARENT -> CONSTITUENT ALWAYS PRESENT |
ORAC value expressed as umol TE/g for this compound 13643.3 +/- 1119.5.
ORAC is a chemical antioxidant assay that is based on the inhibition of the peroxyl-radical induced oxidation initiated by thermal decomposition of AAPH.
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