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=CC2=C(C(=O)C=C(O2)C3=CC(O)=C(O)C=C3)C(O)=C1
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
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| A weakly antimalarial biflavanone from Rhus retinorrhoea. | 2001 Oct |
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| Antioxidant activity of chemical components from sage (Salvia officinalis L.) and thyme (Thymus vulgaris L.) measured by the oil stability index method. | 2002 Mar 27 |
|
| HIV-1 integrase inhibitory substances from Coleus parvifolius. | 2003 Mar |
|
| Iridoid glucosides and flavones from the aerial parts of Avicennia marina. | 2006 Jul |
|
| [Studies on chemical constituents of Daphne genkwa]. | 2009 Apr |
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| Acasiane A and B and farnesirane A and B, diterpene derivatives from the roots of Acacia farnesiana. | 2009 Feb |
|
| [Studies on the chemical constituents from Lobelia chinensis]. | 2010 Nov |
|
| Synergistic anti-glioma effect of Hydroxygenkwanin and Apigenin in vitro. | 2013 Nov 25 |
Patents
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| Code System | Code | Type | Description | ||
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20243-59-8
Created by
admin on Fri Dec 15 18:34:34 GMT 2023 , Edited by admin on Fri Dec 15 18:34:34 GMT 2023
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DTXSID50942365
Created by
admin on Fri Dec 15 18:34:34 GMT 2023 , Edited by admin on Fri Dec 15 18:34:34 GMT 2023
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5318214
Created by
admin on Fri Dec 15 18:34:34 GMT 2023 , Edited by admin on Fri Dec 15 18:34:34 GMT 2023
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732GA1Z079
Created by
admin on Fri Dec 15 18:34:34 GMT 2023 , Edited by admin on Fri Dec 15 18:34:34 GMT 2023
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PRIMARY |
SUBSTANCE RECORD
