Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H14O4 |
| Molecular Weight | 282.2907 |
| 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=CC=C3)C(OC)=C1
InChI
InChIKey=JRFZSUMZAUHNSL-UHFFFAOYSA-N
InChI=1S/C17H14O4/c1-19-12-8-15(20-2)17-13(18)10-14(21-16(17)9-12)11-6-4-3-5-7-11/h3-10H,1-2H3
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL5393 Sources: https://www.ncbi.nlm.nih.gov/pubmed/21354800 |
9.2 µM [IC50] | ||
Target ID: CHEMBL2231 Sources: https://www.ncbi.nlm.nih.gov/pubmed/15661813 |
0.8 µM [IC50] | ||
Target ID: CHEMBL243 Sources: https://www.ncbi.nlm.nih.gov/pubmed/16964717 |
19.0 µM [IC50] | ||
Target ID: Q8CG03 Gene ID: 242202.0 Gene Symbol: Pde5a Target Organism: Mus musculus (Mouse) Sources: https://www.ncbi.nlm.nih.gov/pubmed/21884777 |
10.64 µM [IC50] |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Effect of the active ingredient of Kaempferia parviflora, 5,7-dimethoxyflavone, on the pharmacokinetics of midazolam. | 2018-06 |
|
| Effect of 5,7-dimethoxyflavone on Bcrp1-mediated transport of sorafenib in vitro and in vivo in mice. | 2018-05-30 |
|
| 5,7-Dimethoxyflavone, an activator of PPARα/γ, inhibits UVB-induced MMP expression in human skin fibroblast cells. | 2012-03 |
|
| 5,7-Dimethoxyflavone and multiple flavonoids in combination alter the ABCG2-mediated tissue distribution of mitoxantrone in mice. | 2011-05 |
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21392-57-4
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88881
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SUBSTANCE RECORD