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TargetKynurenine 3-monooxygenase
LigandBDBM50061914
Substrate/Competitorn/a
Meas. Tech.ChEMBL_91740 (CHEMBL702202)
IC50 240±n/a nM
Citation Röver, SCesura, AMHuguenin, PKettler, RSzente, A Synthesis and biochemical evaluation of N-(4-phenylthiazol-2-yl)benzenesulfonamides as high-affinity inhibitors of kynurenine 3-hydroxylase. J Med Chem40:4378-85 (1998) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Kynurenine 3-monooxygenase
Name:Kynurenine 3-monooxygenase
Synonyms:KMO_RAT | Kmo
Type:PROTEIN
Mol. Mass.:54371.88
Organism:Rattus norvegicus
Description:ChEMBL_1487468
Residue:478
Sequence:
MASSDTEGKRVVVIGGGLVGALNACFLAKRNFQVDVYEAREDIRVANFMRGRSINLALSY
RGRQALKAVGLEDQIVSKGVPMKARMIHSLSGKKSAIPYGNKSQYILSISREKLNKDLLT
AVESYPNAKVHFGHKLSKCCPEEGILTMLGPNKVPRDITCDLIVGCDGAYSTVRAHLMKK
PRFDYSQQYIPHGYMELTIPPKNGEYAMEPNCLHIWPRNAFMMIALPNMDKSFTCTLFMS
FEEFEKLPTHSDVLDFFQKNFPDAIPLMGEQALMRDFFLLPAQPMISVKCSPFHLKSRCV
LMGDAAHAIVPFFGQGMNAGFEDCLVFDELMDKFNNDLSVCLPEFSRFRIPDDHAISDLS
MYNYIEMRAHVNSRWFLFQRLLDKFLHALMPSTFIPLYTMVAFTRIRYHEAVLRWHWQKK
VINRGLFVLGSLVAIGSAYILVHHLSPRPLELLRSAWTGTSGHWNRSADISPRVPWSH
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  Blast E-value cutoff:
BDBM50061914
n/a
NameBDBM50061914
Synonyms:CHEMBL342434 | N-[4-(4-Methoxy-phenyl)-thiazol-2-yl]-4-methyl-benzenesulfonamide
TypeSmall organic molecule
Emp. Form.C17H16N2O3S2
Mol. Mass.360.451
SMILESCOc1ccc(cc1)-c1csc(NS(=O)(=O)c2ccc(C)cc2)n1
Structure
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