BDBM3985 2,2 -Dithiobis(7-methyl-1H-indole-3-propanoic acid)::3-(2-{[3-(2-carboxyethyl)-7-methyl-1H-indol-2-yl]disulfanyl}-7-methyl-1H-indol-3-yl)propanoic acid::dithiobis(1H-indole-3-alkanoic acid) deriv. 33
SMILES: Cc1cccc2c(CCC(O)=O)c(SSc3[nH]c4c(C)cccc4c3CCC(O)=O)[nH]c12
InChI Key: InChIKey=VSGQCGRYAAEEEL-UHFFFAOYSA-N
Data: 1 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Epidermal growth factor receptor (Homo sapiens (Human)) | BDBM3985 (2,2 -Dithiobis(7-methyl-1H-indole-3-propanoic acid...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | KEGG PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Auckland | Assay Description IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe... | J Med Chem 36: 2459-69 (1993) Article DOI: 10.1021/jm00069a003 BindingDB Entry DOI: 10.7270/Q2RJ4GNS | |||||||||||
More data for this Ligand-Target Pair |