Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H8O4 |
| Molecular Weight | 240.2109 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC=CC2=C1C(=O)C3=CC=CC(O)=C3C2=O
InChI
InChIKey=JPICKYUTICNNNJ-UHFFFAOYSA-N
InChI=1S/C14H8O4/c15-9-5-1-3-7-11(9)14(18)8-4-2-6-10(16)12(8)13(7)17/h1-6,15-16H
| Molecular Formula | C14H8O4 |
| Molecular Weight | 240.2109 |
| 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 |
|---|---|---|
| Synchrotron radiation linear dichroism (SRLD) investigation of the electronic transitions of quinizarin, chrysazin, and anthrarufin. | 2010-09-15 |
|
| Structure-activity relationships of anthraquinones on the suppression of DNA-binding activity of the aryl hydrocarbon receptor induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin. | 2009-03 |
|
| Valence-state analysis through spectroelectrochemistry in a series of quinonoid-bridged diruthenium complexes [(acac)(2)Ru(mu-L)Ru(acac)(2)](n) (n=+2, +1, 0, -1, -2). | 2008 |
|
| C-Aryl glycosides via tandem intramolecular benzyne-furan cycloadditions. Total synthesis of vineomycinone B2 methyl ester. | 2006-10-25 |
|
| Electrocoagulation of quinone pigments. | 2006-07-14 |
|
| Interaction of anthracene and its oxidative derivatives with human serum albumin. | 2006 |
|
| Six-coordinate titanium complexes of a tripodal aminetris(phenoxide) ligand: synthesis, structure, and dynamics. | 2005-04-18 |
|
| The specificity of cross-reactivity: promiscuous antibody binding involves specific hydrogen bonds rather than nonspecific hydrophobic stickiness. | 2003-10 |
|
| Synthesis of symmetrical 1,5-bisacyloxyanthraquinone derivatives and their dual activity of cytotoxicity and lipid peroxidation. | 2002-12 |
|
| Hydroxyquinones are competitive non-peptide inhibitors of HIV-1 proteinase. | 1995-11-15 |
|
| Evaluation of the antiviral activity of anthraquinones, anthrones and anthraquinone derivatives against human cytomegalovirus. | 1992-01 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:39:03 GMT 2025
by
admin
on
Mon Mar 31 19:39:03 GMT 2025
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| Record UNII |
KPB60W5S3M
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| Record Status |
Validated (UNII)
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| Record Version |
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