Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H14O5 |
| Molecular Weight | 298.2901 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C=C1)C2=COC3=C(C2=O)C(O)=CC(OC)=C3
InChI
InChIKey=DQNLRFRBAWCJHQ-UHFFFAOYSA-N
InChI=1S/C17H14O5/c1-20-11-5-3-10(4-6-11)13-9-22-15-8-12(21-2)7-14(18)16(15)17(13)19/h3-9,18H,1-2H3
| Molecular Formula | C17H14O5 |
| Molecular Weight | 298.2901 |
| 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/20460823 |
5.7 null [pIC50] |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Free Radical-Scavenging Capacities, Phenolics and Capsaicinoids in Wild Piquin Chili (Capsicum annuum var. Glabriusculum). | 2018-10-16 |
|
| Inhibitory effects of herbal extracts on breast cancer resistance protein (BCRP) and structure-inhibitory potency relationship of isoflavonoids. | 2010 |
|
| Quinone reductase 2 substrate specificity and inhibition pharmacology. | 2005-02-10 |
|
| An isoflavone from Myristica malabarica. | 2000-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:23:34 GMT 2025
by
admin
on
Mon Mar 31 19:23:34 GMT 2025
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| Record UNII |
O617EDC7HT
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| Record Status |
Validated (UNII)
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| Record Version |
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