null

SMILES CCc1cn([C@@H]2O[C@H](CNC(=O)[C@H](C)Oc3cc(OC)c(Cl)cc3Cl)[C@@H](O)[C@@H]2F)c(=O)[nH]c1=O

InChI Key InChIKey=NQXYZAIBCVSURW-KZEOBUNESA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50101067   

TargetThymidine kinase(Human herpesvirus 1 (strain SC16) (HHV-1) (Human h...)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101067((S)-2-(2,4-Dichloro-5-methoxy-phenoxy)-N-[(2R,3R,4...)copy SMILEScopy InChI
Affinity DataIC50: 1.80nMAssay Description:Inhibitory activity against HSV-1 Thymidine Kinase (HSV-1 TK)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BZ65B6PubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101067((S)-2-(2,4-Dichloro-5-methoxy-phenoxy)-N-[(2R,3R,4...)copy SMILEScopy InChI
Affinity DataIC50: 0.190nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BZ65B6PubMed