null

SMILES CC(C)[C@@H](NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](Cc1ccc(O)cc1)NC(=O)[C@@H](N)CC(O)=O)C(=O)NCC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](CCCNC(N)=N)C(O)=O

InChI Key InChIKey=FKGMYQLIIAUAEG-WAYDFHHGSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50407450   

Target7-dehydrocholesterol reductase(Homo sapiens (Human))TBA
LigandPNGBDBM50407450(CHEMBL4544901)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Histamine-induced inhibition of forskolin- stimulated cAMP accumulation in SK-N-MC cells overexpressing the human Histamine H3 receptorMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50407450(CHEMBL4544901)copy SMILEScopy InChI
Affinity DataIC50: 97nMAssay Description:Antagonistic affinity tested against isolated Rat Thoracic Aorta Alpha-1D adrenergic receptorMore data for this Ligand-Target Pair
In DepthDetails