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=COC2=CC3=C1C=CC(=O)O3
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 |
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Suksdorfin: an anti-HIV principle from Lomatium suksdorfii, its structure-activity correlation with related coumarins, and synergistic effects with anti-AIDS nucleosides. | 1994 Oct |
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Coumarins are competitive inhibitors of cytochrome P450 1B1, with equal potency for allelic variants. | 2005 Mar |
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Potent protective effect of isoimperatorin against aflatoxin B1-inducible cytotoxicity in H4IIE cells: bifunctional effects on glutathione S-transferase and CYP1A. | 2006 Dec |
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The effects of isoimperatorin isolated from Angelicae dahuricae on cyclooxygenase-2 and 5-lipoxygenase in mouse bone marrow-derived mast cells. | 2008 Feb |
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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 Aug |
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Furocoumarins affect hepatic cytochrome P450 and renal organic ion transporters in mice. | 2012 Feb 25 |
|
Mechanism-based inactivation of cytochrome P450 2B6 by isoimperatorin. | 2015 Jan 25 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:49:49 GMT 2023
by
admin
on
Fri Dec 15 19:49:49 GMT 2023
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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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admin on Fri Dec 15 19:49:49 GMT 2023 , Edited by admin on Fri Dec 15 19:49:49 GMT 2023
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Related Record | Type | Details | ||
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