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

InChI Key:

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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 568467   
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
Arginase-2, mitochondrial


(Homo sapiens (Human))
BDBM568467
PNG
(US11420984, Example 17)
Show SMILES N[C@@H](CO)C(=O)N[C@H]1CN[C@](CCCCB(O)O)(C1)C(O)=O |r,$;;;;;;;;;N;;;;;;;;;;;;$|
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 230n/an/an/an/an/an/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))
BDBM568467
PNG
(US11420984, Example 17)
Show SMILES N[C@@H](CO)C(=O)N[C@H]1CN[C@](CCCCB(O)O)(C1)C(O)=O |r,$;;;;;;;;;N;;;;;;;;;;;;$|
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 200n/an/an/an/an/an/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