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=CC2=C(C(=O)C=C(O2)C3=CC(OC)=C(O)C=C3)C(O)=C1
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
PubMed
| Title | Date | PubMed |
|---|---|---|
| Differential abilities of the mushroom ribosome-inactivating proteins hypsin and velutin to perturb normal development of cultured mouse embryos. | 2010-06 |
|
| A phenethyl bromo ester from Citharexylum fruticosum. | 2010-03 |
|
| Chemical constituents from tiger's betel, Piper porphyrophyllum N.E.Br. (Fam. Piperaceae). | 2010-03 |
|
| Trypsin isoinhibitors with antiproliferative activity toward leukemia cells from Phaseolus vulgaris cv "White Cloud Bean". | 2010 |
|
| Binding modes of two novel non-nucleoside reverse transcriptase inhibitors, YM-215389 and YM-228855, to HIV type-1 reverse transcriptase. | 2008 |
|
| Flavonoids from Daphne giraldii Nitsche. | 2008 |
|
| Iridoid glucosides and flavones from the aerial parts of Avicennia marina. | 2006-07 |
|
| Isolation of flavonoids, a biscoumarin and an amide from the flower buds of Daphne genkwa and the evaluation of their anti-complement activity. | 2006-07 |
|
| The pharmacological potential of mushrooms. | 2005-09 |
|
| Cytotoxic triterpenoids from Acridocarpus vivy from the Madagascar rain forest. | 2004-06 |
|
| Ent-pimarane type diterpenes from Gnaphalium gaudichaudianum. | 2003-02 |
|
| Isolation of pleuturegin, a novel ribosome-inactivating protein from fresh sclerotia of the edible mushroom Pleurotus tuber-regium. | 2001-11-02 |
|
| Isolation and characterization of velutin, a novel low-molecular-weight ribosome-inactivating protein from winter mushroom (Flammulina velutipes) fruiting bodies. | 2001-03-23 |
|
| Evaluation of natural products as inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase. | 1991-01-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:56:45 GMT 2025
by
admin
on
Mon Mar 31 22:56:45 GMT 2025
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| Record UNII |
CT1Q4E0I0W
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| Record Status |
Validated (UNII)
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| Record Version |
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| Code System | Code | Type | Description | ||
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DTXSID90180421
Created by
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CT1Q4E0I0W
Created by
admin on Mon Mar 31 22:56:45 GMT 2025 , Edited by admin on Mon Mar 31 22:56:45 GMT 2025
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25739-41-7
Created by
admin on Mon Mar 31 22:56:45 GMT 2025 , Edited by admin on Mon Mar 31 22:56:45 GMT 2025
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Velutin
Created by
admin on Mon Mar 31 22:56:45 GMT 2025 , Edited by admin on Mon Mar 31 22:56:45 GMT 2025
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5464381
Created by
admin on Mon Mar 31 22:56:45 GMT 2025 , Edited by admin on Mon Mar 31 22:56:45 GMT 2025
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| 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.
|
