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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Neuraminidase' and Ligand = 'BDBM50365365'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Neuraminidase


(Influenza A virus)
BDBM50365365
PNG
(CHEMBL4175711)
Show SMILES CCC(CC)O[C@@H]1C=C(C[C@H](NCCCNc2cccc(Cl)c2C)[C@H]1NC(C)=O)C(O)=O |r,c:7|
Show InChI InChI=1S/C24H36ClN3O4/c1-5-18(6-2)32-22-14-17(24(30)31)13-21(23(22)28-16(4)29)27-12-8-11-26-20-10-7-9-19(25)15(20)3/h7,9-10,14,18,21-23,26-27H,5-6,8,11-13H2,1-4H3,(H,28,29)(H,30,31)/t21-,22+,23+/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 0.590n/an/an/an/an/an/a



Shandong University

Curated by ChEMBL


Assay Description
Inhibition of Influenza A virus (H1N1) neuraminidase activity


J Med Chem 61: 6379-6397 (2018)


Article DOI: 10.1021/acs.jmedchem.8b00929
BindingDB Entry DOI: 10.7270/Q2H41V0C
More data for this
Ligand-Target Pair
Neuraminidase


(Influenza A virus (strain A/Memphis/1/1971 H3N2))
BDBM50365365
PNG
(CHEMBL4175711)
Show SMILES CCC(CC)O[C@@H]1C=C(C[C@H](NCCCNc2cccc(Cl)c2C)[C@H]1NC(C)=O)C(O)=O |r,c:7|
Show InChI InChI=1S/C24H36ClN3O4/c1-5-18(6-2)32-22-14-17(24(30)31)13-21(23(22)28-16(4)29)27-12-8-11-26-20-10-7-9-19(25)15(20)3/h7,9-10,14,18,21-23,26-27H,5-6,8,11-13H2,1-4H3,(H,28,29)(H,30,31)/t21-,22+,23+/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 31n/an/an/an/an/an/a



Shandong University

Curated by ChEMBL


Assay Description
Inhibition of Influenza A virus (H3N2) neuraminidase activity


J Med Chem 61: 6379-6397 (2018)


Article DOI: 10.1021/acs.jmedchem.8b00929
BindingDB Entry DOI: 10.7270/Q2H41V0C
More data for this
Ligand-Target Pair