Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C16H12O6 |
| Molecular Weight | 300.2629 |
| 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(O)=C3
InChI
InChIKey=RRRSSAVLTCVNIQ-UHFFFAOYSA-N
InChI=1S/C16H12O6/c1-21-9-5-12(19)16-13(20)7-14(22-15(16)6-9)8-2-3-10(17)11(18)4-8/h2-7,17-19H,1H3
| Molecular Formula | C16H12O6 |
| Molecular Weight | 300.2629 |
| 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 |
|---|---|---|
| Synergistic anti-glioma effect of Hydroxygenkwanin and Apigenin in vitro. | 2013-11-25 |
|
| [Studies on the chemical constituents from Lobelia chinensis]. | 2010-11 |
|
| [Studies on chemical constituents of Daphne genkwa]. | 2009-04 |
|
| Acasiane A and B and farnesirane A and B, diterpene derivatives from the roots of Acacia farnesiana. | 2009-02 |
|
| Iridoid glucosides and flavones from the aerial parts of Avicennia marina. | 2006-07 |
|
| HIV-1 integrase inhibitory substances from Coleus parvifolius. | 2003-03 |
|
| Antioxidant activity of chemical components from sage (Salvia officinalis L.) and thyme (Thymus vulgaris L.) measured by the oil stability index method. | 2002-03-27 |
|
| A weakly antimalarial biflavanone from Rhus retinorrhoea. | 2001-10 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:15:36 GMT 2025
by
admin
on
Mon Mar 31 19:15:36 GMT 2025
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| Record UNII |
732GA1Z079
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID50942365
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5318214
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admin on Mon Mar 31 19:15:36 GMT 2025 , Edited by admin on Mon Mar 31 19:15:36 GMT 2025
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732GA1Z079
Created by
admin on Mon Mar 31 19:15:36 GMT 2025 , Edited by admin on Mon Mar 31 19:15:36 GMT 2025
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PRIMARY |