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=CC(OC)=CC(O)=C3C2=O
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 |
---|---|---|
An isoflavone from Myristica malabarica. | 2000 Jan |
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Quinone reductase 2 substrate specificity and inhibition pharmacology. | 2005 Feb 10 |
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Inhibitory effects of herbal extracts on breast cancer resistance protein (BCRP) and structure-inhibitory potency relationship of isoflavonoids. | 2010 |
|
Free Radical-Scavenging Capacities, Phenolics and Capsaicinoids in Wild Piquin Chili (Capsicum annuum var. Glabriusculum). | 2018 Oct 16 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:52:38 GMT 2023
by
admin
on
Fri Dec 15 18:52:38 GMT 2023
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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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