13207-66-4 | 5-Aminoquinolin-8-ol

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$20.00	$14.00
250mg	95%	in stock	$39.00	$27.00
1g	95%	in stock	$102.00	$71.00
5g	95%	in stock	$386.00	$270.00

Description

• Catalog Number: AA46658
• Chemical Name: 5-Aminoquinolin-8-ol
• CAS Number: 13207-66-4
• Molecular Formula: C9H8N2O
• Molecular Weight: 160.1726
• MDL Number: MFCD00185837
• SMILES: Nc1ccc(c2c1cccn2)O

Computed Properties

• Complexity: 163
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• XLogP3: 1.6

Literature

• Substituted oxines inhibit endothelial cell proliferation and angiogenesis.

  Organic & biomolecular chemistry 20120421

• Novel proteasome inhibitors to overcome bortezomib resistance.

  Journal of the National Cancer Institute 20110706

• Synthesis and antifungal activity of furo[2,3-f]quinolin-5-ols.

  Bioorganic & medicinal chemistry letters 20110201

• Redox-based inactivation of cysteine cathepsins by compounds containing the 4-aminophenol moiety.

  PloS one 20110101

• Electrospun mats from styrene/maleic anhydride copolymers: modification with amines and assessment of antimicrobial activity.

  Macromolecular bioscience 20100811

• Effect of noncompetitive proteasome inhibition on bortezomib resistance.

  Journal of the National Cancer Institute 20100721

• Rational design of indoleamine 2,3-dioxygenase inhibitors.

  Journal of medicinal chemistry 20100211

• Synthesis and antifungal activity of 1H-pyrrolo[3,2-g]quinoline-4,9-diones and 4,9-dioxo-4,9-dihydro-1H-benzo[f]indoles.

  Bioorganic & medicinal chemistry letters 20090101

• Progress in developing polymerized crystalline colloidal array sensors for point-of-care detection of myocardial ischemia.

  The Analyst 20080301

• Preparation of open tubular solid-phase extraction column with 5-amino-8-hydroxyquinoline-modified gold nanoparticle phase for the enrichment of heavy metal ions.

  Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20080201

• (E)-5-(2-Thienylmethyl-eneamino)quinolin-8-ol.

  Acta crystallographica. Section E, Structure reports online 20080101

• Quinoline-8-ol-immobilized Amberlite XAD-4: synthesis, characterization, and uranyl ion uptake properties suitable for analytical applications.

  Analytical and bioanalytical chemistry 20020401