BDBM50253790 (2S,3R)-2-amino-N-(2-{[7-({2-[(2S,3R)-2-amino-3-hydroxybutanamido]ethyl}carbamoyl)-9,10-dioxo-9,10-dihydroanthracen-2-yl]formamido}ethyl)-3-hydroxybutanamide::CHEMBL454902

SMILES C[C@@H](O)[C@H](N)C(=O)NCCNC(=O)c1ccc2C(=O)c3ccc(cc3C(=O)c2c1)C(=O)NCCNC(=O)[C@@H](N)[C@@H](C)O

InChI Key InChIKey=FLFVCOYRMLTFJO-UHFFFAOYSA-N

Data  2 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50253790   

TargetDNA polymerase I, thermostable(Thermus aquaticus)
University of Padova

Curated by ChEMBL
LigandPNGBDBM50253790((2S,3R)-2-amino-N-(2-{[7-({2-[(2S,3R)-2-amino-3-hy...)
Affinity DataEC50: >4.00E+4nMAssay Description:Inhibition of Taq polymeraseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetTelomerase reverse transcriptase(Human)
University of Padova

Curated by ChEMBL
LigandPNGBDBM50253790((2S,3R)-2-amino-N-(2-{[7-({2-[(2S,3R)-2-amino-3-hy...)
Affinity DataEC50: >4.00E+4nMAssay Description:Inhibition of telomerase in human JR8 cells by TRAP assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed