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Substrate Report for: 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 ; 3,4-Dihydroxyquinoline ; 3-Hydroxy-1H-quinolin-4-one ; 3-hydroxyquinolin-4(1H)-one
________________________________________________________________________________________________
MW|161.16
Formula|C9H7NO2
CAS_number|90348-01-9
PubChem|440981
UniChem|BHTNYVRPYQQOMJ-UHFFFAOYSA-N
IUPHAR|
Wikipedia|

Target
Families | Quinoline-3,4-diol ligand of proteins in family: HOD-cofactorfree-dioxygenase
Protein | rhoer-aqdC1

References:
Search PubMed for references concerning: Quinoline-3,4-diol

4 more
    Title: Enzyme-Mediated Quenching of the Pseudomonas Quinolone Signal (PQS): A Comparison between Naturally Occurring and Engineered PQS-Cleaving Dioxygenases
    Arranz San Martin A, Vogel J, Wullich SC, Quax WJ, Fetzner S
    Ref: Biomolecules, 12:170, 2021 : PubMed

            

    Title: Quorum quenching revisited--from signal decays to signalling confusion
    Hong KW, Koh CL, Sam CK, Yin WF, Chan KG
    Ref: Sensors (Basel), 12:4661, 2012 : PubMed

            

    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 JS, Matuz A, Barath G, Kripli B, Giorgi M, Speier G, Kaizer J
    Ref: J Inorg Biochem, 108:15, 2012 : PubMed