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TargetIntestinal-type alkaline phosphatase 1
LigandBDBM53907
Substrate/Competitorn/a
Meas. Tech.Dose Response confirmation of uHTS hits from a small molecule inhibitors of mouse intestinal alkaline phosphatase via a luminescent assay
IC50 2790±n/a nM
Citation PubChem, PC Dose Response confirmation of uHTS hits from a small molecule inhibitors of mouse intestinal alkaline phosphatase via a luminescent assay PubChem Bioassay(2010)[AID]
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Intestinal-type alkaline phosphatase 1
Name:Intestinal-type alkaline phosphatase 1
Synonyms:Alpi | PPBI1_RAT
Type:Enzyme Catalytic Domain
Mol. Mass.:58396.39
Organism:Rattus norvegicus (Rat)
Description:P15693
Residue:540
Sequence:
MQGDWVLLLLLGLRIHLSFGVIPVEEENPVFWNQKAKEALDVAKKLQPIQTSAKNLILFL
GDGMGVPTVTATRILKGQLGGHLGPETPLAMDHFPFTALSKTYNVDRQVPDSAGTATAYL
CGVKANYKTIGVSAAARFNQCNSTFGNEVFSVMHRAKKAGKSVGVVTTTRVQHASPAGTY
AHTVNRDWYSDADMPSSALQEGCKDIATQLISNMDIDVILGGGRKFMFPKGTPDPEYPGD
SDQSGVRLDSRNLVEEWLAKYQGTRYVWNREQLMQASQDPAVTRLMGLFEPTEMKYDVNR
NASADPSLAEMTEVAVRLLSRNPQGFYLFVEGGRIDQGHHAGTAYLALTEAVMFDSAIEK
ASQLTNEKDTLTLITADHSHVFAFGGYTLRGTSIFGLAPLNAQDGKSYTSILYGNGPGYV
LNSGNRPNVTDAESGDVNYKQQAAVPLSSETHGGEDVAIFARGPQAHLVHGVQEQNYIAH
VMAFAGCLEPYTDCGLAPPADENRPTTPVQNSAITMNNVLLSLQLLVSMLLLVGTALVVS
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  Blast E-value cutoff:
BDBM53907
n/a
NameBDBM53907
Synonyms:2-(5-amino-1,3,4-thiadiazol-2-yl)-N'-{3-bromo-2-hydroxy-5-nitrobenzylidene}acetohydrazide | 2-(5-amino-1,3,4-thiadiazol-2-yl)-N'-[(E)-(5-bromo-3-nitro-6-oxo-1-cyclohexa-2,4-dienylidene)methyl]acetohydrazide | 2-(5-amino-1,3,4-thiadiazol-2-yl)-N'-[(E)-(5-bromo-3-nitro-6-oxocyclohexa-2,4-dien-1-ylidene)methyl]acetohydrazide | 2-(5-amino-1,3,4-thiadiazol-2-yl)-N'-[(E)-(5-bromo-6-keto-3-nitro-cyclohexa-2,4-dien-1-ylidene)methyl]acetohydrazide | 2-(5-azanyl-1,3,4-thiadiazol-2-yl)-N'-[(E)-(5-bromanyl-3-nitro-6-oxidanylidene-cyclohexa-2,4-dien-1-ylidene)methyl]ethanehydrazide | MLS000705091 | SMR000230750 | cid_16189248
TypeSmall organic molecule
Emp. Form.C11H9BrN6O4S
Mol. Mass.401.196
SMILESNc1nnc(CC(=O)N\[NH+]=C\[c-]2cc(cc(Br)c2=O)[N+]([O-])=O)s1
Structure
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