BDBM50066350 3-Morpholin-4-yl-N-[4-(3-morpholin-4-yl-propionylamino)-9,10-dioxo-9,10-dihydro-anthracen-1-yl]-propionamide; hydrochloride::CHEMBL144827::CHEMBL544111
SMILES: O=C(CCN1CCOCC1)Nc1ccc(NC(=O)CCN2CCOCC2)c2C(=O)c3ccccc3C(=O)c12
InChI Key: InChIKey=FSMRMUDCRVGEFR-UHFFFAOYSA-N
Data: 2 IC50
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Telomerase reverse transcriptase (Homo sapiens (Human)) | BDBM50066350 (3-Morpholin-4-yl-N-[4-(3-morpholin-4-yl-propionyla...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 3.35E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Cancer Research Curated by ChEMBL | Assay Description Inhibition of telomerase activity | J Med Chem 41: 3253-60 (1998) Article DOI: 10.1021/jm9801105 BindingDB Entry DOI: 10.7270/Q2TX3G1R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Telomerase reverse transcriptase (Homo sapiens (Human)) | BDBM50066350 (3-Morpholin-4-yl-N-[4-(3-morpholin-4-yl-propionyla...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 3.35E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Cancer Research Curated by ChEMBL | Assay Description Inhibitory activity of telomerase was measured using the TRAP assay. | J Med Chem 41: 4873-84 (1998) Article DOI: 10.1021/jm981067o BindingDB Entry DOI: 10.7270/Q2WW7GSD | |||||||||||
More data for this Ligand-Target Pair |