null

SMILES: [H][C@]1(OC(=C[C@H](O)[C@H]1NC(C)=O)C(O)=O)[C@H](O)[C@H](O)Cn1cc(nn1)-c1ccc(NC(C)=O)cc1

InChI Key: InChIKey=VSZSVCUULZGSNI-APQLOABGSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50270455   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Sialidase-4 (Homo sapiens (Human))	BDBM50270455 (CHEMBL4076383) Show SMILES [H][C@]1(OC(=C[C@H](O)[C@H]1NC(C)=O)C(O)=O)[C@H](O)[C@H](O)Cn1cc(nn1)-c1ccc(NC(C)=O)cc1 |r,c:3| Show InChI InChI=1S/C21H25N5O8/c1-10(27)22-13-5-3-12(4-6-13)14-8-26(25-24-14)9-16(30)19(31)20-18(23-11(2)28)15(29)7-17(34-20)21(32)33/h3-8,15-16,18-20,29-31H,9H2,1-2H3,(H,22,27)(H,23,28)(H,32,33)/t15-,16+,18+,19+,20+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Alberta Curated by ChEMBL					Assay Description Inhibition of human N-terminal MBP-fused NEU4 expressed in Escherichia coli using 4MU-NANA as substrate preincubated for 15 mins followed by substrat...				J Med Chem 61: 1990-2008 (2018) Article DOI: 10.1021/acs.jmedchem.7b01574 BindingDB Entry DOI: 10.7270/Q2XS5XV6
					More data for this Ligand-Target Pair
Sialidase-1 (Homo sapiens (Human))	BDBM50270455 (CHEMBL4076383) Show SMILES [H][C@]1(OC(=C[C@H](O)[C@H]1NC(C)=O)C(O)=O)[C@H](O)[C@H](O)Cn1cc(nn1)-c1ccc(NC(C)=O)cc1 |r,c:3| Show InChI InChI=1S/C21H25N5O8/c1-10(27)22-13-5-3-12(4-6-13)14-8-26(25-24-14)9-16(30)19(31)20-18(23-11(2)28)15(29)7-17(34-20)21(32)33/h3-8,15-16,18-20,29-31H,9H2,1-2H3,(H,22,27)(H,23,28)(H,32,33)/t15-,16+,18+,19+,20+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Alberta Curated by ChEMBL					Assay Description Inhibition of human CathA-IRES-6His-tagged NEU1 expressed in HEK293T cells using 4MU-NANA as substrate preincubated for 15 mins followed by substrate...				J Med Chem 61: 1990-2008 (2018) Article DOI: 10.1021/acs.jmedchem.7b01574 BindingDB Entry DOI: 10.7270/Q2XS5XV6
					More data for this Ligand-Target Pair
Sialidase-2 (Homo sapiens (Human))	BDBM50270455 (CHEMBL4076383) Show SMILES [H][C@]1(OC(=C[C@H](O)[C@H]1NC(C)=O)C(O)=O)[C@H](O)[C@H](O)Cn1cc(nn1)-c1ccc(NC(C)=O)cc1 |r,c:3| Show InChI InChI=1S/C21H25N5O8/c1-10(27)22-13-5-3-12(4-6-13)14-8-26(25-24-14)9-16(30)19(31)20-18(23-11(2)28)15(29)7-17(34-20)21(32)33/h3-8,15-16,18-20,29-31H,9H2,1-2H3,(H,22,27)(H,23,28)(H,32,33)/t15-,16+,18+,19+,20+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Alberta Curated by ChEMBL					Assay Description Inhibition of human N-terminal MBP-fused NEU2 expressed in Escherichia coli using 4MU-NANA as substrate preincubated for 15 mins followed by substrat...				J Med Chem 61: 1990-2008 (2018) Article DOI: 10.1021/acs.jmedchem.7b01574 BindingDB Entry DOI: 10.7270/Q2XS5XV6
					More data for this Ligand-Target Pair
Sialidase-3 (Homo sapiens (Human))	BDBM50270455 (CHEMBL4076383) Show SMILES [H][C@]1(OC(=C[C@H](O)[C@H]1NC(C)=O)C(O)=O)[C@H](O)[C@H](O)Cn1cc(nn1)-c1ccc(NC(C)=O)cc1 |r,c:3| Show InChI InChI=1S/C21H25N5O8/c1-10(27)22-13-5-3-12(4-6-13)14-8-26(25-24-14)9-16(30)19(31)20-18(23-11(2)28)15(29)7-17(34-20)21(32)33/h3-8,15-16,18-20,29-31H,9H2,1-2H3,(H,22,27)(H,23,28)(H,32,33)/t15-,16+,18+,19+,20+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alberta Curated by ChEMBL					Assay Description Inhibition of human N-terminal MBP-fused NEU3 expressed in Escherichia coli using 4MU-NANA as substrate preincubated for 15 mins followed by substrat...				J Med Chem 61: 1990-2008 (2018) Article DOI: 10.1021/acs.jmedchem.7b01574 BindingDB Entry DOI: 10.7270/Q2XS5XV6
					More data for this Ligand-Target Pair