BDBM50589246 CHEMBL5184316

SMILES C[C@@H](O)[C@@H]1NC(=O)[C@@H]2CSSC[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](Cc3ccc(O)c(I)c3)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CSSC[C@H](NC(=O)CN)C(=O)N2)NC(=O)[C@H](CCCNC(N)=O)NC(=O)[C@@H]2CCCN2C(=O)[C@H](CC(O)=O)NC1=O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O

InChI Key InChIKey=VVORNPTYPFGYRF-QTICAQMXSA-N

Data  1 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 1 hit for monomerid = 50589246   

TargetNeuronal acetylcholine receptor; alpha9/alpha10(Homo sapiens (Human))
Wroclaw University Of Science And Technology

Curated by ChEMBL
LigandPNGBDBM50589246(CHEMBL5184316)
Affinity DataIC50:  1.5nMAssay Description:Inhibition of human nAChR alpha9alpha10 expressed in Xenopus laevis oocytes holding potential of -70 mV by voltage-clamp based electrophysiological m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed