607-67-0 | 2-Methylquinolin-4-ol

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$19.00	$13.00
10g	95%	in stock	$33.00	$24.00
100g	95%	in stock	$281.00	$197.00

Description

• Catalog Number: AB67615
• Chemical Name: 2-Methylquinolin-4-ol
• CAS Number: 607-67-0
• Molecular Formula: C10H9NO
• Molecular Weight: 159.1846
• MDL Number: MFCD00006758
• SMILES: Cc1cc(O)c2c(n1)cccc2
• NSC Number: 21483

Computed Properties

• Complexity: 232
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• XLogP3: 1.9

Literature

• Cloning and heterologous expression of the aurachin RE biosynthesis gene cluster afford a new cytochrome P450 for quinoline N-hydroxylation.

  Chembiochem : a European journal of chemical biology 20130617

• Integrated organic-aqueous biocatalysis and product recovery for quinaldine hydroxylation catalyzed by living recombinant Pseudomonas putida.

  Journal of industrial microbiology & biotechnology 20120701

• Regioselective aromatic hydroxylation of quinaldine by water using quinaldine 4-oxidase in recombinant Pseudomonas putida.

  Journal of industrial microbiology & biotechnology 20110801

• AuaA, a membrane-bound farnesyltransferase from Stigmatella aurantiaca, catalyzes the prenylation of 2-methyl-4-hydroxyquinoline in the biosynthesis of aurachins.

  Chembiochem : a European journal of chemical biology 20110725

• Copy number determination, expression analysis of genes potentially involved in replication, and stability assays of pAL1--the linear megaplasmid of Arthrobacter nitroguajacolicus Rü61a.

  Microbiological research 20110120

• Evolutionary relationships of microbial aromatic prenyltransferases.

  PloS one 20110101

• Endochin optimization: structure-activity and structure-property relationship studies of 3-substituted 2-methyl-4(1H)-quinolones with antimalarial activity.

  Journal of medicinal chemistry 20101014

• Convenient and efficient microwave-assisted synthesis of a methyl derivative of the fused indoloquinoline alkaloid cryptosanguinolentine.

  Molecules (Basel, Switzerland) 20100429

• Iron- and 4-hydroxy-2-alkylquinoline-containing periplasmic inclusion bodies of Pseudomonas aeruginosa: a chemical analysis.

  Bioorganic chemistry 20070401

• Spectroscopic and biochemical studies on protein variants of quinaldine 4-oxidase: Role of E736 in catalysis and effects of serine ligands on the FeSI and FeSII clusters.

  Biochemistry 20061212

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

• Gene cluster of Arthrobacter ilicis Ru61a involved in the degradation of quinaldine to anthranilate: characterization and functional expression of the quinaldine 4-oxidase qoxLMS genes.

  The Journal of biological chemistry 20030725

• Microbial metabolism of quinoline and related compounds. XVI. Quinaldine oxidoreductase from Arthrobacter spec. Rü 61a: a molybdenum-containing enzyme catalysing the hydroxylation at C-4 of the heterocycle.

  Biological chemistry Hoppe-Seyler 19930201

• Microbial metabolism of quinoline and related compounds. VI. Degradation of quinaldine by Arthrobacter sp.

  Biological chemistry Hoppe-Seyler 19901001