Quinoline-3,4-diol

General

Type : Quinoline

Chemical_Nomenclature : 3-hydroxy-1H-quinolin-4-one

Canonical SMILES : C1=CC=C2C(=C1)C(=O)C(=CN2)O

InChI : InChI=1S\/C9H7NO2\/c11-8-5-10-7-4-2-1-3-6(7)9(8)12\/h1-5,11H,(H,10,12)

InChIKey : BHTNYVRPYQQOMJ-UHFFFAOYSA-N

Other name(s) : HQ,     3-hydroxy-4(1H)-quinolone,     1-H-3-hydroxy-4-oxoquinoline,     3,4-Dihydroxyquinoline,     3-Hydroxy-1H-quinolin-4-one,     QNL,     3-hydroxyquinolin-4(1H)-one


MW : 161.16

Formula : C9H7NO2

CAS_number : 90348-01-9

PubChem :

UniChem :

Iuphar :

Target

References (8)

Title : Enzyme-Mediated Quenching of the Pseudomonas Quinolone Signal (PQS): A Comparison between Naturally Occurring and Engineered PQS-Cleaving Dioxygenases - Arranz San Martin_2022_Biomolecules_12_170
Author(s) : Arranz San Martin A , Vogel J , Wullich SC , Quax WJ , Fetzner S
Ref : Biomolecules , 12 :170 , 2021
Abstract : Arranz San Martin_2022_Biomolecules_12_170
ESTHER : Arranz San Martin_2022_Biomolecules_12_170
PubMedSearch : Arranz San Martin_2022_Biomolecules_12_170
PubMedID:
Gene_locus related to this paper: artsp-hod , strbb-d7bw96 , mycab-x8en65 , nocfa-q5yp20

Title : Bio-inspired flavonol and quinolone dioxygenation by a non-heme iron catalyst modeling the action of flavonol and 3-hydroxy-4(1H)-quinolone 2,4-dioxygenases - Pap_2012_J.Inorg.Biochem_108_15
Author(s) : Pap JS , Matuz A , Barath G , Kripli B , Giorgi M , Speier G , Kaizer J
Ref : J Inorg Biochem , 108 :15 , 2012
Abstract : Pap_2012_J.Inorg.Biochem_108_15
ESTHER : Pap_2012_J.Inorg.Biochem_108_15
PubMedSearch : Pap_2012_J.Inorg.Biochem_108_15
PubMedID: 22265834

Title : Quorum quenching revisited--from signal decays to signalling confusion - Hong_2012_Sensors.(Basel)_12_4661
Author(s) : Hong KW , Koh CL , Sam CK , Yin WF , Chan KG
Ref : Sensors (Basel) , 12 :4661 , 2012
Abstract : Hong_2012_Sensors.(Basel)_12_4661
ESTHER : Hong_2012_Sensors.(Basel)_12_4661
PubMedSearch : Hong_2012_Sensors.(Basel)_12_4661
PubMedID: 22666051

Title : Structural basis for cofactor-independent dioxygenation of N-heteroaromatic compounds at the alpha\/beta-hydrolase fold - Steiner_2010_Proc.Natl.Acad.Sci.U.S.A_107_657
Author(s) : Steiner RA , Janssen HJ , Roversi P , Oakley AJ , Fetzner S
Ref : Proc Natl Acad Sci U S A , 107 :657 , 2010
Abstract : Steiner_2010_Proc.Natl.Acad.Sci.U.S.A_107_657
ESTHER : Steiner_2010_Proc.Natl.Acad.Sci.U.S.A_107_657
PubMedSearch : Steiner_2010_Proc.Natl.Acad.Sci.U.S.A_107_657
PubMedID: 20080731
Gene_locus related to this paper: artsp-hod , psepu-QDO

Title : Cofactor-independent oxidases and oxygenases - Fetzner_2010_Appl.Microbiol.Biotechnol_86_791
Author(s) : Fetzner S , Steiner RA
Ref : Applied Microbiology & Biotechnology , 86 :791 , 2010
Abstract : Fetzner_2010_Appl.Microbiol.Biotechnol_86_791
ESTHER : Fetzner_2010_Appl.Microbiol.Biotechnol_86_791
PubMedSearch : Fetzner_2010_Appl.Microbiol.Biotechnol_86_791
PubMedID: 20157809

Title : Crystallization and diffraction data of 1H-3-hydroxy-4-oxoquinoline 2,4-dioxygenase: a cofactor-free oxygenase of the alpha\/beta-hydrolase family - Qi_2007_Acta.Crystallogr.Sect.F.Struct.Biol.Cryst.Commun_63_378
Author(s) : Qi R , Fetzner S , Oakley AJ
Ref : Acta Crystallographica Sect F Struct Biol Cryst Commun , 63 :378 , 2007
Abstract : Qi_2007_Acta.Crystallogr.Sect.F.Struct.Biol.Cryst.Commun_63_378
ESTHER : Qi_2007_Acta.Crystallogr.Sect.F.Struct.Biol.Cryst.Commun_63_378
PubMedSearch : Qi_2007_Acta.Crystallogr.Sect.F.Struct.Biol.Cryst.Commun_63_378
PubMedID: 17565175

Title : Dioxygenases without requirement for cofactors and their chemical model reaction: compulsory order ternary complex mechanism of 1H-3-hydroxy-4-oxoquinaldine 2,4-dioxygenase involving general base catalysis by histidine 251 and single-electron oxidation of the substrate dianion - Frerichs-Deeken_2004_Biochemistry_43_14485
Author(s) : Frerichs-Deeken U , Ranguelova K , Kappl R , Huttermann J , Fetzner S
Ref : Biochemistry , 43 :14485 , 2004
Abstract : Frerichs-Deeken_2004_Biochemistry_43_14485
ESTHER : Frerichs-Deeken_2004_Biochemistry_43_14485
PubMedSearch : Frerichs-Deeken_2004_Biochemistry_43_14485
PubMedID: 15533053
Gene_locus related to this paper: artsp-hod

Title : 2,4-dioxygenases catalyzing N-heterocyclic-ring cleavage and formation of carbon monoxide. Purification and some properties of 1H-3-hydroxy-4-oxoquinaldine 2,4-dioxygenase from Arthrobacter sp. Ru61a and comparison with 1H-3-hydroxy-4-oxoquinoline 2,4-dioxygenase from Pseudomonas putida 33\/1 - Bauer_1996_Eur.J.Biochem_240_576
Author(s) : Bauer I , Max N , Fetzner S , Lingens F
Ref : European Journal of Biochemistry , 240 :576 , 1996
Abstract : Bauer_1996_Eur.J.Biochem_240_576
ESTHER : Bauer_1996_Eur.J.Biochem_240_576
PubMedSearch : Bauer_1996_Eur.J.Biochem_240_576
PubMedID: 8856057
Gene_locus related to this paper: artsp-hod , psepu-QDO