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=C2C(=O)C3=C(C=CC=C3)C(=O)C2=C(O)C=C1
InChI
InChIKey=GUEIZVNYDFNHJU-UHFFFAOYSA-N
InChI=1S/C14H8O4/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-6,15-16H
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Evaluation of the antiviral activity of anthraquinones, anthrones and anthraquinone derivatives against human cytomegalovirus. | 1992 Jan |
|
| Structure of a terbium(III)-quinizarine complex: the first crystallographic model for metalloanthracyclines. | 2003 May 19 |
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| Differential and special properties of the major human UGT1-encoded gastrointestinal UDP-glucuronosyltransferases enhance potential to control chemical uptake. | 2004 Jan 9 |
|
| Growth responses of Cassia obtusifolia toward human intestinal bacteria. | 2004 Jul |
|
| Ionic liquid-promoted ring-closure reactions between 1,4-dihydroxyanthraquinone and diamines. | 2006 Jun 21 |
|
| Kinetics of the substitution of dehydroacetic acid in tris (dehydroacetato) Fe(III) complex by 8-hydroxyquinoline, di- and tetra-hydroxyquinone. | 2007 Jun |
|
| Micellar electrokinetic chromatography method for the determination of several natural red dyestuff and lake pigments used in art work. | 2007 Jun 22 |
|
| Determination of lithium in pharmaceutical formulations used in the treatment of bipolar disorder by flow injection analysis with spectrophotometric detection. | 2007 Oct 15 |
|
| Involvement of Tetrahymena pyriformis and selected fungi in the elimination of anthracene, and toxicity assessment of the biotransformation products. | 2008 Feb |
|
| Estrogenic activity of anthraquinone derivatives: in vitro and in silico studies. | 2010 Aug 16 |
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8S496ZV3CS
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m9450
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201-368-7
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646569
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DTXSID8044464
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15367
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81-64-1
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37487
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5242
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6688
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1,4-DIHYDROXYANTHRAQUINONE
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C034890
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SUBSTANCE RECORD
