Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C16H14O4 |
| Molecular Weight | 270.28 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3
InChI
InChIKey=IGWDEVSBEKYORK-UHFFFAOYSA-N
InChI=1S/C16H14O4/c1-10(2)5-7-19-16-11-3-4-15(17)20-14(11)9-13-12(16)6-8-18-13/h3-6,8-9H,7H2,1-2H3
| Molecular Formula | C16H14O4 |
| Molecular Weight | 270.28 |
| 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 |
|---|---|---|
| Mechanism-based inactivation of cytochrome P450 2B6 by isoimperatorin. | 2015-01-25 |
|
| Furocoumarins affect hepatic cytochrome P450 and renal organic ion transporters in mice. | 2012-02-25 |
|
| Notopterygium forbesii Boiss extract and its active constituent phenethyl ferulate attenuate pro-inflammatory responses to lipopolysaccharide in RAW 264.7 macrophages. A "protective" role for oxidative stress? | 2009-08 |
|
| The effects of isoimperatorin isolated from Angelicae dahuricae on cyclooxygenase-2 and 5-lipoxygenase in mouse bone marrow-derived mast cells. | 2008-02 |
|
| Potent protective effect of isoimperatorin against aflatoxin B1-inducible cytotoxicity in H4IIE cells: bifunctional effects on glutathione S-transferase and CYP1A. | 2006-12 |
|
| Coumarins are competitive inhibitors of cytochrome P450 1B1, with equal potency for allelic variants. | 2005-03 |
|
| Suksdorfin: an anti-HIV principle from Lomatium suksdorfii, its structure-activity correlation with related coumarins, and synergistic effects with anti-AIDS nucleosides. | 1994-10 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:58:05 GMT 2025
by
admin
on
Mon Mar 31 19:58:05 GMT 2025
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| Record UNII |
0ZMV066080
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| Record Status |
Validated (UNII)
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| Record Version |
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0ZMV066080
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DTXSID60197460
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482-45-1
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