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SMILES: Fc1ccc(cc1)C(=O)CC(=O)C(=O)NC1CCC(CC1)NC(=O)C(=O)CC(=O)c1ccc(F)cc1

InChI Key: InChIKey=WHNLRJKWXWOXFO-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 = 50479060   
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)
BDBM50479060
PNG
(CHEMBL469070)
Show SMILES Fc1ccc(cc1)C(=O)CC(=O)C(=O)NC1CCC(CC1)NC(=O)C(=O)CC(=O)c1ccc(F)cc1 |(8.82,-41.88,;10.15,-42.65,;11.48,-41.88,;12.81,-42.65,;12.81,-44.19,;11.49,-44.96,;10.16,-44.2,;14.14,-44.96,;14.14,-46.5,;15.47,-44.19,;16.81,-44.96,;16.82,-46.51,;18.15,-44.19,;18.15,-42.65,;19.48,-44.96,;20.8,-44.15,;22.14,-44.88,;23.46,-44.08,;23.42,-42.55,;22.07,-41.81,;20.74,-42.61,;24.73,-41.75,;24.69,-40.21,;23.34,-39.46,;26.01,-39.4,;27.36,-40.13,;25.96,-37.86,;27.28,-37.05,;28.63,-37.79,;27.24,-35.51,;28.55,-34.72,;28.52,-33.19,;27.16,-32.46,;27.13,-30.92,;25.85,-33.26,;25.89,-34.8,)|
Show InChI InChI=1S/C26H24F2N2O6/c27-17-5-1-15(2-6-17)21(31)13-23(33)25(35)29-19-9-11-20(12-10-19)30-26(36)24(34)14-22(32)16-3-7-18(28)8-4-16/h1-8,19-20H,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 3.55E+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
Integrase


(Human immunodeficiency virus 1)
BDBM50479060
PNG
(CHEMBL469070)
Show SMILES Fc1ccc(cc1)C(=O)CC(=O)C(=O)NC1CCC(CC1)NC(=O)C(=O)CC(=O)c1ccc(F)cc1 |(8.82,-41.88,;10.15,-42.65,;11.48,-41.88,;12.81,-42.65,;12.81,-44.19,;11.49,-44.96,;10.16,-44.2,;14.14,-44.96,;14.14,-46.5,;15.47,-44.19,;16.81,-44.96,;16.82,-46.51,;18.15,-44.19,;18.15,-42.65,;19.48,-44.96,;20.8,-44.15,;22.14,-44.88,;23.46,-44.08,;23.42,-42.55,;22.07,-41.81,;20.74,-42.61,;24.73,-41.75,;24.69,-40.21,;23.34,-39.46,;26.01,-39.4,;27.36,-40.13,;25.96,-37.86,;27.28,-37.05,;28.63,-37.79,;27.24,-35.51,;28.55,-34.72,;28.52,-33.19,;27.16,-32.46,;27.13,-30.92,;25.85,-33.26,;25.89,-34.8,)|
Show InChI InChI=1S/C26H24F2N2O6/c27-17-5-1-15(2-6-17)21(31)13-23(33)25(35)29-19-9-11-20(12-10-19)30-26(36)24(34)14-22(32)16-3-7-18(28)8-4-16/h1-8,19-20H,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