Compile Data Set for Download or QSAR

Found 20 hits with Last Name = 'dyason' and Initial = 'jc'   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Sialidase-2 (Homo sapiens (Human))	BDBM50330326 ((4S,5R,6R)-5-Acetylamino-4-guanidino-6-((1R,3R)-1,...) Show SMILES [#6]-[#6](=O)-[#7]-[#6@@H]-1-[#6@H](-[#6]=[#6](-[#8]-[#6@H]-1-[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8])-[#6](-[#8])=O)\[#7]=[#6](\[#7])-[#7] |r,c:6| Show InChI InChI=1S/C12H20N4O7/c1-4(18)15-8-5(16-12(13)14)2-7(11(21)22)23-10(8)9(20)6(19)3-17/h2,5-6,8-10,17,19-20H,3H2,1H3,(H,15,18)(H,21,22)(H4,13,14,16)/t5-,6+,8+,9+,10+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank PDB Article PubMed	1.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
PF-IMSS-KEK-SBRC, Ibaraki 305-0801, Japan. Curated by ChEMBL					Assay Description Inhibition of human neuraminidase 2				J Med Chem 53: 2998-3002 (2010) Article DOI: 10.1021/jm100078r BindingDB Entry DOI: 10.7270/Q2N58NBM
					More data for this Ligand-Target Pair				3D Structure (crystal)
Sialidase-2 (Homo sapiens (Human))	BDBM4706 ((2R,3R,4S)-3-acetamido-4-hydroxy-2-[(1R,2R)-1,2,3-...) Show SMILES CC(=O)N[C@@H]1[C@@H](O)C=C(O[C@H]1[C@H](O)[C@H](O)CO)C(O)=O |r,c:7| Show InChI InChI=1S/C11H17NO8/c1-4(14)12-8-5(15)2-7(11(18)19)20-10(8)9(17)6(16)3-13/h2,5-6,8-10,13,15-17H,3H2,1H3,(H,12,14)(H,18,19)/t5-,6+,8+,9+,10+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Similars	PDB Article PubMed	1.40E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
PF-IMSS-KEK-SBRC, Ibaraki 305-0801, Japan. Curated by ChEMBL					Assay Description Inhibition of human neuraminidase 2				J Med Chem 53: 2998-3002 (2010) Article DOI: 10.1021/jm100078r BindingDB Entry DOI: 10.7270/Q2N58NBM
					More data for this Ligand-Target Pair				3D Structure (crystal)
Sialidase-2 (Homo sapiens (Human))	BDBM5024 ((-)-(1S,2S,3R,4R)-3-[(1S)-1-(Acetylamino)-2-ethylb...) Show SMILES [H][C@](NC(C)=O)(C(CC)CC)[C@@H]1[C@H](O)[C@H](C[C@H]1N=C(N)N)C(O)=O |r| Show InChI InChI=1S/C15H28N4O4/c1-4-8(5-2)12(18-7(3)20)11-10(19-15(16)17)6-9(13(11)21)14(22)23/h8-13,21H,4-6H2,1-3H3,(H,18,20)(H,22,23)(H4,16,17,19)/t9-,10+,11+,12-,13+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	3.30E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
PF-IMSS-KEK-SBRC, Ibaraki 305-0801, Japan. Curated by ChEMBL					Assay Description Inhibition of human neuraminidase 2				J Med Chem 53: 2998-3002 (2010) Article DOI: 10.1021/jm100078r BindingDB Entry DOI: 10.7270/Q2N58NBM
					More data for this Ligand-Target Pair				3D Structure (crystal)
Sialidase-2 (Homo sapiens (Human))	BDBM50314987 ((2S,3R,4R)-3-acetamido-4-hydroxy-2-(3-hydroxypropo...) Show SMILES CC(=O)N[C@@H]1[C@H](O)C=C(O[C@@H]1OCCCO)C(O)=O |r,c:7| Show InChI InChI=1S/C11H17NO7/c1-6(14)12-9-7(15)5-8(10(16)17)19-11(9)18-4-2-3-13/h5,7,9,11,13,15H,2-4H2,1H3,(H,12,14)(H,16,17)/t7-,9-,11+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.40E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
PF-IMSS-KEK-SBRC, Ibaraki 305-0801, Japan. Curated by ChEMBL					Assay Description Inhibition of human neuraminidase 2				J Med Chem 53: 2998-3002 (2010) Article DOI: 10.1021/jm100078r BindingDB Entry DOI: 10.7270/Q2N58NBM
					More data for this Ligand-Target Pair
Sialidase-2 (Homo sapiens (Human))	BDBM50314988 ((2S,3R,4R)-3-acetamido-4-hydroxy-2-isobutoxy-3,4-d...) Show SMILES CC(C)CO[C@H]1OC(=C[C@@H](O)[C@H]1NC(C)=O)C(O)=O |r,c:7| Show InChI InChI=1S/C12H19NO6/c1-6(2)5-18-12-10(13-7(3)14)8(15)4-9(19-12)11(16)17/h4,6,8,10,12,15H,5H2,1-3H3,(H,13,14)(H,16,17)/t8-,10-,12+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.80E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
PF-IMSS-KEK-SBRC, Ibaraki 305-0801, Japan. Curated by ChEMBL					Assay Description Inhibition of human neuraminidase 2				J Med Chem 53: 2998-3002 (2010) Article DOI: 10.1021/jm100078r BindingDB Entry DOI: 10.7270/Q2N58NBM
					More data for this Ligand-Target Pair
Sialidase-2 (Homo sapiens (Human))	BDBM50314986 ((2S,3R,4R)-3-acetamido-2-(2,3-dihydroxypropoxy)-4-...) Show SMILES CC(=O)N[C@@H]1[C@H](O)C=C(O[C@@H]1OCC(O)CO)C(O)=O |r,c:7| Show InChI InChI=1S/C11H17NO8/c1-5(14)12-9-7(16)2-8(10(17)18)20-11(9)19-4-6(15)3-13/h2,6-7,9,11,13,15-16H,3-4H2,1H3,(H,12,14)(H,17,18)/t6?,7-,9-,11+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.40E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
PF-IMSS-KEK-SBRC, Ibaraki 305-0801, Japan. Curated by ChEMBL					Assay Description Inhibition of human neuraminidase 2				J Med Chem 53: 2998-3002 (2010) Article DOI: 10.1021/jm100078r BindingDB Entry DOI: 10.7270/Q2N58NBM
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497276 (CHEMBL3330708) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#7]=[N+]=[#7-])-[#6@H]1-[#7]-[#6](=O)-[#6](-[#6])-[#6])-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C13H20N4O7.Na/c1-5(2)12(21)15-9-6(16-17-14)3-8(13(22)23)24-11(9)10(20)7(19)4-18;/h3,5-7,9-11,18-20H,4H2,1-2H3,(H,15,21)(H,22,23);/q;+1/p-1/t6-,7+,9+,10+,11+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497281 (CHEMBL3330844) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#7]=[N+]=[#7-])-[#6@H]1-[#7]-[#6](=O)-[#6]-1-[#6]-[#6]-1)-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C13H18N4O7.Na/c14-17-16-6-3-8(13(22)23)24-11(10(20)7(19)4-18)9(6)15-12(21)5-1-2-5;/h3,5-7,9-11,18-20H,1-2,4H2,(H,15,21)(H,22,23);/q;+1/p-1/t6-,7+,9+,10+,11+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	910	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497279 (CHEMBL3330846) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#7]=[N+]=[#7-])-[#6@H]1-[#7]-[#6](=O)-[#6](-[#6])-[#6]-[#6])-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C14H22N4O7.Na/c1-3-6(2)13(22)16-10-7(17-18-15)4-9(14(23)24)25-12(10)11(21)8(20)5-19;/h4,6-8,10-12,19-21H,3,5H2,1-2H3,(H,16,22)(H,23,24);/q;+1/p-1/t6?,7-,8+,10+,11+,12+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.58E+3	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497280 (CHEMBL3330845) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#7]=[N+]=[#7-])-[#6@H]1-[#7]-[#6](=O)-[#6]-1-[#6]-[#6]-[#6]-1)-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C14H20N4O7.Na/c15-18-17-7-4-9(14(23)24)25-12(11(21)8(20)5-19)10(7)16-13(22)6-2-1-3-6;/h4,6-8,10-12,19-21H,1-3,5H2,(H,16,22)(H,23,24);/q;+1/p-1/t7-,8+,10+,11+,12+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.92E+3	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497275 (CHEMBL3330709) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#8])-[#6@H]1-[#7]-[#6](=O)-[#6](-[#6])-[#6])-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C13H21NO8.Na/c1-5(2)12(19)14-9-6(16)3-8(13(20)21)22-11(9)10(18)7(17)4-15;/h3,5-7,9-11,15-18H,4H2,1-2H3,(H,14,19)(H,20,21);/q;+1/p-1/t6-,7+,9+,10+,11+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.82E+3	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497285 (CHEMBL3330704) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#7]=[N+]=[#7-])-[#6@H]1-[#7]-[#6](-[#6])=O)-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C11H16N4O7.Na/c1-4(17)13-8-5(14-15-12)2-7(11(20)21)22-10(8)9(19)6(18)3-16;/h2,5-6,8-10,16,18-19H,3H2,1H3,(H,13,17)(H,20,21);/q;+1/p-1/t5-,6+,8+,9+,10+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.92E+3	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497278 (CHEMBL3330847) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#7]=[N+]=[#7-])-[#6@H]1-[#7]-[#6](=O)-[#6](\[#6])=[#6]\[#6])-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C14H20N4O7.Na/c1-3-6(2)13(22)16-10-7(17-18-15)4-9(14(23)24)25-12(10)11(21)8(20)5-19;/h3-4,7-8,10-12,19-21H,5H2,1-2H3,(H,16,22)(H,23,24);/q;+1/p-1/b6-3+;/t7-,8+,10+,11+,12+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	7.76E+3	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497277 (CHEMBL3330849) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#7]=[N+]=[#7-])-[#6@H]1-[#7]-[#6](=O)-[#6](-[#6])-[#6]-[#8])-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C13H20N4O8.Na/c1-5(3-18)12(22)15-9-6(16-17-14)2-8(13(23)24)25-11(9)10(21)7(20)4-19;/h2,5-7,9-11,18-21H,3-4H2,1H3,(H,15,22)(H,23,24);/q;+1/p-1/t5?,6-,7+,9+,10+,11+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	9.49E+3	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497283 (CHEMBL3330705) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#8])-[#6@H]1-[#7]-[#6](-[#6])=O)-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C11H17NO8.Na/c1-4(14)12-8-5(15)2-7(11(18)19)20-10(8)9(17)6(16)3-13;/h2,5-6,8-10,13,15-17H,3H2,1H3,(H,12,14)(H,18,19);/q;+1/p-1/t5-,6+,8+,9+,10+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.38E+4	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497282 (CHEMBL3330848) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#7]=[N+]=[#7-])-[#6@H]1-[#7]-[#6](=O)-[#6](-[#6])-[#8])-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C12H18N4O8.Na/c1-4(18)11(21)14-8-5(15-16-13)2-7(12(22)23)24-10(8)9(20)6(19)3-17;/h2,4-6,8-10,17-20H,3H2,1H3,(H,14,21)(H,22,23);/q;+1/p-1/t4?,5-,6+,8+,9+,10+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.81E+4	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497286 (CHEMBL3330710) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#7])-[#6@H]1-[#7]-[#6](=O)-[#6](-[#6])-[#6])-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C13H22N2O7.Na/c1-5(2)12(19)15-9-6(14)3-8(13(20)21)22-11(9)10(18)7(17)4-16;/h3,5-7,9-11,16-18H,4,14H2,1-2H3,(H,15,19)(H,20,21);/q;+1/p-1/t6-,7+,9+,10+,11+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.61E+5	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497284 (CHEMBL3330843) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#7]-[#6](-[#7])=[#7])-[#6@H]1-[#7]-[#6](=O)-[#6](-[#6])-[#6])-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C14H24N4O7.Na/c1-5(2)12(22)18-9-6(17-14(15)16)3-8(13(23)24)25-11(9)10(21)7(20)4-19;/h3,5-7,9-11,19-21H,4H2,1-2H3,(H,18,22)(H,23,24)(H4,15,16,17);/q;+1/p-1/t6-,7+,9+,10+,11+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497274 (CHEMBL3330706) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#7])-[#6@H]1-[#7]-[#6](-[#6])=O)-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C11H18N2O7.Na/c1-4(15)13-8-5(12)2-7(11(18)19)20-10(8)9(17)6(16)3-14;/h2,5-6,8-10,14,16-17H,3,12H2,1H3,(H,13,15)(H,18,19);/q;+1/p-1/t5-,6+,8+,9+,10+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair
Neuraminidase (Influenza A virus)	BDBM50497287 (CHEMBL3330707) Show SMILES [Na;v0+].[H][C@]1([#8]-[#6](=[#6]-[#6@H](-[#7]-[#6](-[#7])=[#7])-[#6@H]1-[#7]-[#6](-[#6])=O)-[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:3| Show InChI InChI=1S/C12H20N4O7.Na/c1-4(18)15-8-5(16-12(13)14)2-7(11(21)22)23-10(8)9(20)6(19)3-17;/h2,5-6,8-10,17,19-20H,3H2,1H3,(H,15,18)(H,21,22)(H4,13,14,16);/q;+1/p-1/t5-,6+,8+,9+,10+;/m0./s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Griffith University Curated by ChEMBL					Assay Description Inhibition of neuraminidase activity of human parainfluenza virus 1 C35 hemagglutinin-neuraminidase pre-incubated for 20 mins before MUN substrate by...				J Med Chem 57: 7613-23 (2014) Article DOI: 10.1021/jm500759v BindingDB Entry DOI: 10.7270/Q2DB84VP
					More data for this Ligand-Target Pair