BDBM50451175 CHEMBL3138187
SMILES [H][C@@]12[#6]-[#6]-[#6@H](-[#6](-[#6])-[#6]-[#6]-[#6]-[#6](-[#6])-[#6])[C@@]1([#6])[#6]-[#6][C@@]1([H])[C@@]2([H])[#6]-[#6]-[#6]2-[#6]-[#6@@H](-[#6]-[#6]\[#6]=[#6](\c3cc(Cl)c(-[#8])c(c3)-[#6](-[#8])=O)-c3cc(Cl)c(-[#8])c(c3)-[#6](-[#8])=O)-[#6]-[#6][C@]12[#6]
InChI Key InChIKey=PCTSCNIWMNPBCS-UHFFFAOYSA-N
Data 3 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50451175
TargetC-C chemokine receptor type 1(Human)
National Cancer Istitute-Frederick Cancer Research and Development Center
Curated by ChEMBL
National Cancer Istitute-Frederick Cancer Research and Development Center
Curated by ChEMBL
Affinity DataIC50: 260nMAssay Description:Inhibition of RANTES-induced migration of human embryonic kidney (CCR1/HEK) cell transfectantsMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of HIV -1 proteaseMore data for this Ligand-Target Pair
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibition of HIV -1 IntegraseMore data for this Ligand-Target Pair