BDBM50086561 CHEMBL134536::NB-506 Analogue
SMILES C[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)n1c2cc(O)ccc2c2c3C(=O)N(NC(CO)CO)C(=O)c3c3c4ccc(O)cc4[nH]c3c12
InChI Key InChIKey=SVGBJMZKARIVJG-GBHIQSMOSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50086561
Affinity DataEC50: 140nMAssay Description:Inhibitory effect on topoisomerase-I mediated DNA cleavage using supercoiled pBR322 plasmid DNAMore data for this Ligand-Target Pair
TargetO94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139(Homo sapiens (Human))
Banyu Tsukuba Research Institute
Curated by ChEMBL
Banyu Tsukuba Research Institute
Curated by ChEMBL
Affinity DataIC50: 6.00E+4nMAssay Description:Inhibitory effect on protein kinase C using histone II-As as substrateMore data for this Ligand-Target Pair
TargetDNA topoisomerase 2-alpha/2-beta(Homo sapiens (Human))
Banyu Tsukuba Research Institute
Curated by ChEMBL
Banyu Tsukuba Research Institute
Curated by ChEMBL
Affinity DataEC50: >5.00E+4nMAssay Description:Tested for inhibitory effect on topoisomerase-2 mediated DNA cleavage using super coiled pBR322 plasmid DNAMore data for this Ligand-Target Pair