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SMILES: Fc1ccccc1C(=O)CC(=O)C(=O)NC1CCC(CC1)NC(=O)C(=O)CC(=O)c1ccccc1F

InChI Key: InChIKey=NVDZWFJOKRQWOY-UHFFFAOYSA-N

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50479074   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Integrase


(Human immunodeficiency virus 1)
BDBM50479074
PNG
(CHEMBL467169)
Show SMILES Fc1ccccc1C(=O)CC(=O)C(=O)NC1CCC(CC1)NC(=O)C(=O)CC(=O)c1ccccc1F |(4.24,-28.05,;5.54,-27.24,;5.5,-25.7,;6.82,-24.9,;8.17,-25.64,;8.21,-27.16,;6.89,-27.96,;6.93,-29.49,;8.28,-30.24,;5.61,-30.3,;5.66,-31.84,;7.01,-32.58,;4.34,-32.65,;2.99,-31.9,;4.39,-34.19,;3.07,-34.99,;3.11,-36.52,;1.8,-37.33,;.45,-36.6,;.4,-35.05,;1.72,-34.26,;-.86,-37.4,;-2.2,-36.63,;-2.2,-35.09,;-3.54,-37.4,;-3.53,-38.95,;-4.87,-36.63,;-6.2,-37.4,;-6.2,-38.95,;-7.54,-36.63,;-8.86,-37.41,;-10.19,-36.64,;-10.2,-35.09,;-8.86,-34.33,;-7.53,-35.09,;-6.2,-34.33,)|
Show InChI InChI=1S/C26H24F2N2O6/c27-19-7-3-1-5-17(19)21(31)13-23(33)25(35)29-15-9-11-16(12-10-15)30-26(36)24(34)14-22(32)18-6-2-4-8-20(18)28/h1-8,15-16H,9-14H2,(H,29,35)(H,30,36)
PDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of wild-type HIV1 integrase 3'-processing activity using [32P]-labeled linear oligonucleotide substrate by polyacrylamide gel electrophore...


Bioorg Med Chem 16: 7777-87 (2008)


Article DOI: 10.1016/j.bmc.2008.07.008
BindingDB Entry DOI: 10.7270/Q2M90CG4
More data for this
Ligand-Target Pair
Integrase


(Human immunodeficiency virus 1)
BDBM50479074
PNG
(CHEMBL467169)
Show SMILES Fc1ccccc1C(=O)CC(=O)C(=O)NC1CCC(CC1)NC(=O)C(=O)CC(=O)c1ccccc1F |(4.24,-28.05,;5.54,-27.24,;5.5,-25.7,;6.82,-24.9,;8.17,-25.64,;8.21,-27.16,;6.89,-27.96,;6.93,-29.49,;8.28,-30.24,;5.61,-30.3,;5.66,-31.84,;7.01,-32.58,;4.34,-32.65,;2.99,-31.9,;4.39,-34.19,;3.07,-34.99,;3.11,-36.52,;1.8,-37.33,;.45,-36.6,;.4,-35.05,;1.72,-34.26,;-.86,-37.4,;-2.2,-36.63,;-2.2,-35.09,;-3.54,-37.4,;-3.53,-38.95,;-4.87,-36.63,;-6.2,-37.4,;-6.2,-38.95,;-7.54,-36.63,;-8.86,-37.41,;-10.19,-36.64,;-10.2,-35.09,;-8.86,-34.33,;-7.53,-35.09,;-6.2,-34.33,)|
Show InChI InChI=1S/C26H24F2N2O6/c27-19-7-3-1-5-17(19)21(31)13-23(33)25(35)29-15-9-11-16(12-10-15)30-26(36)24(34)14-22(32)18-6-2-4-8-20(18)28/h1-8,15-16H,9-14H2,(H,29,35)(H,30,36)
PDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 5.50E+4n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of wild-type HIV1 integrase strand transfer activity using [32P]-labeled linear oligonucleotide substrate by polyacrylamide gel electropho...


Bioorg Med Chem 16: 7777-87 (2008)


Article DOI: 10.1016/j.bmc.2008.07.008
BindingDB Entry DOI: 10.7270/Q2M90CG4
More data for this
Ligand-Target Pair