null

SMILES COc1ccc2nc(sc2n1)N1[C@H]2CCN([C@@H]2[C@H](C)C1=O)C(=O)[C@@H]1CCCN1C(=O)Nc1ccc(cc1)C(C)C

InChI Key InChIKey=CHMFMINHSDVAEL-WLZNGNGHSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50133965   

TargetGenome polyprotein(Human rhinovirus B)
GlaxoSmithKline Research and Development

Curated by ChEMBL
LigandPNGBDBM50133965((S)-2-[(3aS,6S,6aR)-4-(5-Methoxy-thiazolo[5,4-b]py...)copy SMILEScopy InChI
Affinity DataKi:  117nMAssay Description:Potency against human cytomegalovirus protease in HCMV pNA assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2PD8PubMed
TargetCapsid scaffolding protein(Human cytomegalovirus (strain AD169) (HHV-5) (Huma...)
GlaxoSmithKline Research and Development

Curated by ChEMBL
LigandPNGBDBM50133965((S)-2-[(3aS,6S,6aR)-4-(5-Methoxy-thiazolo[5,4-b]py...)copy SMILEScopy InChI
Affinity DataIC50: 870nMAssay Description:Inhibition of human cytomegalovirus protease in HCMV pNA assay.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2PD8PubMed