Reaction Details | |||
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Target | Hexokinase HKDC1 [W721R] | ||
Ligand | BDBM76184 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Dose Response confirmation of inhibitors of hexokinase domain containing I (HKDC1) in the hexokinase 1 selectivity assay | ||
IC50 | 12400±n/a nM | ||
Citation | PubChem, PC Dose Response confirmation of inhibitors of hexokinase domain containing I (HKDC1) in the hexokinase 1 selectivity assay PubChem Bioassay(2011)[AID] | ||
More Info.: | Get all data from this article, Solution Info, Assay Method | ||
Hexokinase HKDC1 [W721R] | |||
Name: | Hexokinase HKDC1 [W721R] | ||
Synonyms: | HKDC1 | HKDC1_HUMAN | putative hexokinase HKDC1 | ||
Type: | Enzyme Catalytic Domain | ||
Mol. Mass.: | 102520.24 | ||
Organism: | Homo sapiens (Human) | ||
Description: | gi_156151420 | ||
Residue: | 917 | ||
Sequence: |
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BDBM76184 | |||
n/a | |||
Name | BDBM76184 | ||
Synonyms: | 4-[(2,9-dioxo-1,2,4,5,6,7,8,9-octahydropyrazolo[5,1-b]quinazolin-3-yl)diazenyl]benzenesulfonamide | 4-[2-(2,9-dioxo-5,6,7,8-tetrahydro-1H-pyrazolo[5,1-b]quinazolin-3-ylidene)hydrazinyl]benzenesulfonamide | 4-[2-[2,9-bis(oxidanylidene)-5,6,7,8-tetrahydro-1H-pyrazolo[5,1-b]quinazolin-3-ylidene]hydrazinyl]benzenesulfonamide | 4-[N'-(2,9-diketo-5,6,7,8-tetrahydro-1H-pyrazolo[5,1-b]quinazolin-3-ylidene)hydrazino]benzenesulfonamide | MLS000705743 | SMR000231775 | cid_16189729 | ||
Type | Small organic molecule | ||
Emp. Form. | C16H16N6O4S | ||
Mol. Mass. | 388.401 | ||
SMILES | NS(=O)(=O)c1ccc(cc1)N=Nc1c2[nH]c3CCCCc3c(=O)n2[nH]c1=O |w:11.12| | ||
Structure |