BDBM50249689 2,10-Dihydroxy-6-({[6-(hydroxymethyl)pyridin-2-yl]methyl}amino)-13-(beta-D-glucopyranosyl)-12,13-dihydro-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione::CHEMBL474561

SMILES OC[C@H]1O[C@@H](On2c3cc(O)ccc3c3c4C(=O)N(NCc5cccc(CO)n5)C(=O)c4c4c5ccc(O)cc5[nH]c4c23)[C@H](O)[C@@H](O)[C@@H]1O

InChI Key InChIKey=RTWGXFRLCDXCRX-UHFFFAOYSA-N

Data  1 IC50  2 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50249689   

TargetEpidermal growth factor receptor(Human)
Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50249689(2,10-Dihydroxy-6-({[6-(hydroxymethyl)pyridin-2-yl]...)
Affinity DataIC50: 2.00E+5nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetDNA topoisomerase 1(Mouse)
Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50249689(2,10-Dihydroxy-6-({[6-(hydroxymethyl)pyridin-2-yl]...)
Affinity DataEC50:  73nMAssay Description:Inhibition of DNA topoisomerase 1 in mouse P388/S cells assessed as formation of topoisomerase 1-DNA complex by proteinase K/SDS methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetDNA topoisomerase 1(Human)
Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM50249689(2,10-Dihydroxy-6-({[6-(hydroxymethyl)pyridin-2-yl]...)
Affinity DataEC50:  3.30nMAssay Description:Inhibition of human DNA topoisomerase 1-mediated DNA cleavage assessed as relaxation of supercoiled pBR322 plasmid DNA after 15 mins by densitometerMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed