BDBM50140085 CHEMBL266702::GCCSLPPCAANNPDYC*

SMILES CC(C)C[C@@H](NC(=O)[C@@H](CO)NC(=O)[C@@H](CS)NC(=O)[C@@H](CS)NC(=O)CN)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CS)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N1CCC[C@@H]1C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc1ccc(S)cc1)C(=O)N[C@@H](CS)C(N)=O

InChI Key InChIKey=VHZCCIRHQVLGCE-UHFFFAOYSA-N

Data  2 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 2 hits for monomerid = 50140085   

TargetNeuronal acetylcholine receptor subunit alpha-3/beta-2(Rat)
The University of Queensland

Curated by ChEMBL
LigandPNGBDBM50140085(GCCSLPPCAANNPDYC* | CHEMBL266702)
Affinity DataIC50: 9.60nMAssay Description:Inhibition of rat Nicotinic acetylcholine receptor alpha3-beta2 expressed in Xenopus OocytesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetG2/mitotic-specific cyclin-B1(Rat)
The University of Queensland

Curated by ChEMBL
LigandPNGBDBM50140085(GCCSLPPCAANNPDYC* | CHEMBL266702)
Affinity DataIC50: 252nMAssay Description:Compound was evaluated for inhibition of rat Nicotinic acetylcholine receptor alpha7 (nAChR) in Xenopus OocytesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed