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
Molecular Formula | C17H14O4 |
Molecular Weight | 282.2907 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
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 |
---|---|---|
5,7-Dimethoxyflavone and multiple flavonoids in combination alter the ABCG2-mediated tissue distribution of mitoxantrone in mice. | 2011 May |
|
5,7-Dimethoxyflavone, an activator of PPARα/γ, inhibits UVB-induced MMP expression in human skin fibroblast cells. | 2012 Mar |
|
Effect of the active ingredient of Kaempferia parviflora, 5,7-dimethoxyflavone, on the pharmacokinetics of midazolam. | 2018 Jun |
|
Effect of 5,7-dimethoxyflavone on Bcrp1-mediated transport of sorafenib in vitro and in vivo in mice. | 2018 May 30 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:13:40 GMT 2023
by
admin
on
Fri Dec 15 19:13:40 GMT 2023
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Record UNII |
J8HQQ4R4F2
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Record Status |
Validated (UNII)
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Record Version |
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