null

SMILES: CC(C)[C@H](N)C(=O)N(C)[C@H]1CN[C@@](CCCCB(O)O)(C1)C(O)=O

InChI Key:

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 568480   

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
Arginase-2, mitochondrial (Homo sapiens (Human))	BDBM568480 (US11420984, Example 30) Show SMILES CC(C)[C@H](N)C(=O)N(C)[C@H]1CN[C@@](CCCCB(O)O)(C1)C(O)=O |r,$;;;;;;;;;;;N;;;;;;;;;;;;$| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	2.42E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory effects of Examples 1 to 30 on the activity of Human Arginase 1 and Arginase 2 activity were quantified by measuring the formation of ...				Citation and Details BindingDB Entry DOI: 10.7270/Q2Q243GV
					More data for this Ligand-Target Pair
Arginase-1 (Homo sapiens (Human))	BDBM568480 (US11420984, Example 30) Show SMILES CC(C)[C@H](N)C(=O)N(C)[C@H]1CN[C@@](CCCCB(O)O)(C1)C(O)=O |r,$;;;;;;;;;;;N;;;;;;;;;;;;$| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.35E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The inhibitory effects of Examples 1 to 30 on the activity of Human Arginase 1 and Arginase 2 activity were quantified by measuring the formation of ...				Citation and Details BindingDB Entry DOI: 10.7270/Q2Q243GV
					More data for this Ligand-Target Pair