Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C21H22O5 |
| Molecular Weight | 354.3964 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C2C=C(COC2=CC(O)=C1CC=C(C)C)C3=C(O)C=C(O)C=C3
InChI
InChIKey=UACNRZUVCUEUPY-UHFFFAOYSA-N
InChI=1S/C21H22O5/c1-12(2)4-6-16-19(24)10-20-17(21(16)25-3)8-13(11-26-20)15-7-5-14(22)9-18(15)23/h4-5,7-10,22-24H,6,11H2,1-3H3
| Molecular Formula | C21H22O5 |
| Molecular Weight | 354.3964 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Cytotoxic activity of low molecular weight polyphenols against human oral tumor cell lines. | 2000 Jul-Aug |
|
| A licorice ethanolic extract with peroxisome proliferator-activated receptor-gamma ligand-binding activity affects diabetes in KK-Ay mice, abdominal obesity in diet-induced obese C57BL mice and hypertension in spontaneously hypertensive rats. | 2003 Nov |
|
| Dehydroglyasperin C isolated from licorice caused Nrf2-mediated induction of detoxifying enzymes. | 2010 Feb 10 |
|
| Neuroprotective effects of dehydroglyasperin C through activation of heme oxygenase-1 in mouse hippocampal cells. | 2012 Jun 6 |
|
| Dehydroglyasperin C, a component of liquorice, attenuates proliferation and migration induced by platelet-derived growth factor in human arterial smooth muscle cells. | 2013 Aug 28 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:28:26 GMT 2023
by
admin
on
Sat Dec 16 08:28:26 GMT 2023
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| Record UNII |
80H8MSZ44I
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| Record Status |
Validated (UNII)
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| Record Version |
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480775
Created by
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80H8MSZ44I
Created by
admin on Sat Dec 16 08:28:26 GMT 2023 , Edited by admin on Sat Dec 16 08:28:26 GMT 2023
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199331-35-6
Created by
admin on Sat Dec 16 08:28:26 GMT 2023 , Edited by admin on Sat Dec 16 08:28:26 GMT 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> CONSTITUENT ALWAYS PRESENT |
The compound showed strong ferric reducing activities and effectively scavenged DPPH, ABTS+, and singlet oxygen radicals.
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