117-12-4 | 1,5-Dihydroxyanthraquinone

Packsize	Purity	Availability	Price	Discounted Price
5g	85%	in stock	$14.00	$10.00
10g	85%	in stock	$17.00	$12.00
25g	85%	in stock	$29.00	$21.00
100g	85%	in stock	$97.00	$68.00

Description

• Catalog Number: AA17290
• Chemical Name: 1,5-Dihydroxyanthraquinone
• CAS Number: 117-12-4
• Molecular Formula: C14H8O4
• Molecular Weight: 240.21092
• MDL Number: MFCD00001210
• SMILES: Oc1cccc2c1C(=O)c1cccc(c1C2=O)O

Computed Properties

• Complexity: 342
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• XLogP3: 3.7

Literature

• Synchrotron radiation linear dichroism (SRLD) investigation of the electronic transitions of quinizarin, chrysazin, and anthrarufin.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20100915

• 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.

  Journal of bioscience and bioengineering 20090301

• 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).

  Chemistry (Weinheim an der Bergstrasse, Germany) 20080101

• C-Aryl glycosides via tandem intramolecular benzyne-furan cycloadditions. Total synthesis of vineomycinone B2 methyl ester.

  Journal of the American Chemical Society 20061025

• Electrocoagulation of quinone pigments.

  Molecules (Basel, Switzerland) 20060714

• Interaction of anthracene and its oxidative derivatives with human serum albumin.

  Acta biochimica Polonica 20060101

• Six-coordinate titanium complexes of a tripodal aminetris(phenoxide) ligand: synthesis, structure, and dynamics.

  Inorganic chemistry 20050418

• The specificity of cross-reactivity: promiscuous antibody binding involves specific hydrogen bonds rather than nonspecific hydrophobic stickiness.

  Protein science : a publication of the Protein Society 20031001

• Synthesis of symmetrical 1,5-bisacyloxyanthraquinone derivatives and their dual activity of cytotoxicity and lipid peroxidation.

  Archiv der Pharmazie 20021201

• Phytoestrogens from the roots of Polygonum cuspidatum (Polygonaceae): structure-requirement of hydroxyanthraquinones for estrogenic activity.

  Bioorganic & medicinal chemistry letters 20010723

• Hydroxyquinones are competitive non-peptide inhibitors of HIV-1 proteinase.

  Biochimica et biophysica acta 19951115

• Evaluation of the antiviral activity of anthraquinones, anthrones and anthraquinone derivatives against human cytomegalovirus.

  Antiviral research 19920101