BDBM50509085 TAUROACIDIN A

SMILES OC(CNC(=O)c1cc(Br)c(Br)[nH]1)\C=C1/NC(=N)N=C1NCCS(O)(=O)=O

InChI Key InChIKey=HXXOFJVFKMAZGM-UHFFFAOYSA-N

Data  3 IC50

  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 = 50509085   

TargetEpidermal growth factor receptor(Human)
Southwest Jiaotong University

Curated by ChEMBL
LigandPNGBDBM50509085(TAUROACIDIN A)
Affinity DataIC50: 3.78E+4nMAssay Description:Inhibition of EGFR (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/19/2021
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Southwest Jiaotong University

Curated by ChEMBL
LigandPNGBDBM50509085(TAUROACIDIN A)
Affinity DataIC50: 4.46E+4nMAssay Description:Inhibition of EGFR (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/21/2024
Entry Details
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
University of Kwazulu-Natal (Westville)

Curated by ChEMBL
LigandPNGBDBM50509085(TAUROACIDIN A)
Affinity DataIC50: 3.79E+4nMAssay Description:Inhibition of c-ErbB-2 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/21/2024
Entry Details
PubMed