null

SMILES CC(C)SC[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C

InChI Key InChIKey=PMGSGSRYNICBHS-BFHWGTDASA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50022375   

TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50022375(BDBM50022873 | CHEMBL348469 | {1-[1-(1-Cyclohexylm...)copy SMILEScopy InChI
Affinity DataIC50: 9.90nMAssay Description:Evaluated in vitro for inhibitory potency against renin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2RJ4K2DPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50022375(BDBM50022873 | CHEMBL348469 | {1-[1-(1-Cyclohexylm...)copy SMILEScopy InChI
Affinity DataIC50: 9nMpH: 6.0Assay Description:Inhibition of human renal renin at pH 6More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D1XPubMed