Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H10O2 |
| Molecular Weight | 222.2387 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1OC2=C(C=CC=C2)C=C1C3=CC=CC=C3
InChI
InChIKey=HWDSXZLYIKESML-UHFFFAOYSA-N
InChI=1S/C15H10O2/c16-15-13(11-6-2-1-3-7-11)10-12-8-4-5-9-14(12)17-15/h1-10H
| Molecular Formula | C15H10O2 |
| Molecular Weight | 222.2387 |
| 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 |
|---|---|---|
| Effect of Erythrina variegata seed extract on hyperlipidemia elicited by high-fat diet in wistar rats. | 2010-10 |
|
| Structural characterization and comparison of switchgrass ball-milled lignin before and after dilute acid pretreatment. | 2010-09 |
|
| Inhibitory effect of flavonoids on mutant H-Rasp protein. | 2010-06-15 |
|
| Structure-based design of DevR inhibitor active against nonreplicating Mycobacterium tuberculosis. | 2009-10-22 |
|
| Inhibition of immune complex-mediated neutrophil oxidative metabolism: a pharmacophore model for 3-phenylcoumarin derivatives using GRIND-based 3D-QSAR and 2D-QSAR procedures. | 2008-05 |
|
| Inhibition of horseradish peroxidase catalytic activity by new 3-phenylcoumarin derivatives: synthesis and structure-activity relationships. | 2007-02-01 |
|
| Mammeigin. | 2006-06 |
|
| Solid phase synthesis of 3-(4-hydroxyphenyl)coumarin: preliminary experiments for combinatorial synthesis of substituted 3-phenylcoumarin derivatives. | 2004-08 |
|
| Prenylated isoflavonoids from Millettia pervilleana. | 2003-06 |
|
| Transcriptional suppression of the HIV promoter by natural compounds. | 2003-03 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:15:32 GMT 2025
by
admin
on
Mon Mar 31 22:15:32 GMT 2025
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| Record UNII |
WV24YNY4AU
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| Record Status |
Validated (UNII)
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