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Target5'-nucleotidase
LigandBDBM222262
Substrate/Competitorn/a
Meas. Tech.Ecto-5'-Nucleotidase Inhibition Assay
pH7.4±n/a
Temperature310.15±n/a K
IC50 2.6e+2± 1e+1 nM
Commentsextracted
Citation Ejaz, SASaeed, ASiddique, MNNisa, ZUKhan, SLecka, JSévigny, JIqbal, J Synthesis, characterization and biological evaluation of novel chalcone sulfonamide hybrids as potent intestinal alkaline phosphatase inhibitors. Bioorg Chem70:229-236 (2017) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
5'-nucleotidase
Name:5'-nucleotidase
Synonyms:5'-NT | 5'-nucleotidase (CD73) | 5NTD_HUMAN | CD_antigen=CD73 | Ecto-5'-nucleotidase | Ecto-5-nucleotidase (e5'NT) | NT5 | NT5E | NTE
Type:Enzyme
Mol. Mass.:63371.54
Organism:Homo sapiens (Human)
Description:P21589
Residue:574
Sequence:
MCPRAARAPATLLLALGAVLWPAAGAWELTILHTNDVHSRLEQTSEDSSKCVNASRCMGG
VARLFTKVQQIRRAEPNVLLLDAGDQYQGTIWFTVYKGAEVAHFMNALRYDAMALGNHEF
DNGVEGLIEPLLKEAKFPILSANIKAKGPLASQISGLYLPYKVLPVGDEVVGIVGYTSKE
TPFLSNPGTNLVFEDEITALQPEVDKLKTLNVNKIIALGHSGFEMDKLIAQKVRGVDVVV
GGHSNTFLYTGNPPSKEVPAGKYPFIVTSDDGRKVPVVQAYAFGKYLGYLKIEFDERGNV
ISSHGNPILLNSSIPEDPSIKADINKWRIKLDNYSTQELGKTIVYLDGSSQSCRFRECNM
GNLICDAMINNNLRHTDEMFWNHVSMCILNGGGIRSPIDERNNGTITWENLAAVLPFGGT
FDLVQLKGSTLKKAFEHSVHRYGQSTGEFLQVGGIHVVYDLSRKPGDRVVKLDVLCTKCR
VPSYDPLKMDEVYKVILPNFLANGGDGFQMIKDELLRHDSGDQDINVVSTYISKMKVIYP
AVEGRIKFSTGSHCHGSFSLIFLSLWAVIFVLYQ
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM222262
n/a
NameBDBM222262
Synonyms:(Z)-4-(2-((E)-4-(3,4-dimethoxyphenyl)-1-morpholino-2-oxobut-3-enylidene) hydrazinyl) benzenesulfonamide (4e)
TypeSmall organic molecule
Emp. Form.C22H26N4O6S
Mol. Mass.474.53
SMILESCOc1ccc(\C=C\C(=O)C(=N\Nc2ccc(cc2)S(N)(=O)=O)\N2CCOCC2)cc1OC
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: