Compile Data Set for Download or QSAR
Report error Found 127 Enz. Inhib. hit(s) with all data for entry = 6468
LigandChemical structure of BindingDB Monomer ID 633373BDBM633373(4-(4-aminomethyl)phenyl)-2-methylphthalazin-1(2H)-...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633432BDBM633432(N-(4-(7-methoxy-4-oxo-3,4-dihydrophthalazin-1-yl)b...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633433BDBM633433(N-(4-(6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1-...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633379BDBM633379(4-(4-(aminomethyl)phenyl)-6-methoxyphthalazin-1(2H...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633374BDBM633374(4-(4-(aminomethyl)phenyl)-2-ethylphthalazin-1(2H)-...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633440BDBM633440(N-(4-(6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1-...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633418BDBM633418(N-(3-(3-methyl-4-oxo-3,4-dihydrophthalazin-1-yl)ph...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633482BDBM633482(N-(2-(trifluorobenzyl methyl)-4-((4-oxo-3,4-dihydr...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633419BDBM633419(N-(3-(3-benzyl-4-oxo-3,4-dihydrophthalazin-1-yl)ph...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633421BDBM633421(N-(4-(3-methyl-4-oxo-3,4-dihydrophthalazin-1-yl)ph...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633478BDBM633478(5-((6,7-dimethoxy-3-methyl-4-oxo-3,4-dihydrophthal...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633479BDBM633479(N-(3-fluoro-4-((4-oxo-3,4-dihydrophthalazin-1-yl)m...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633480BDBM633480(N-(2-fluoro-4-((4-oxo-3,4-dihydrophthalazin-1-yl)m...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633417BDBM633417(N-(3-(4-oxo-3,4-dihydrophthalazin-1-yl)phenyl)sulf...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633481BDBM633481(N-(3-(trifluorobenzyl methyl)-4-((4-oxo-3,4-dihydr...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633426BDBM633426(N-(4-(4-oxo-3,4-dihydrophthalazin-1-yl)benzyl) sul...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633427BDBM633427(N-(4-(3-methyl-4-oxo-3,4-dihydrophthalazin-1-yl)be...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633429BDBM633429(N-(4-(4-oxo-3-phenyl-3,4-dihydrophthalazin-1-yl)be...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633423BDBM633423(N-(3-(3-oxo-3,4-dihydrophthalazin-1-yl)benzyl)sulf...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633425BDBM633425(N-(3-(3-methyl-4-oxo-3,4-dihydrophthalazin-1-yl)be...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633462BDBM633462(N-((1-(6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633475BDBM633475(N-(4-((6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633476BDBM633476(N-(4-((6,7-dimethoxy-3-methyl-4-oxo-3,4-dihydropht...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633477BDBM633477(5-((6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1-yl...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633470BDBM633470(N-(4-((4-oxo-3,4-dihydrophthalazin-1-yl)methyl)phe...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633471BDBM633471(N-(4-((3-methyl-4-oxo-3,4-dihydrophthalazin-1-yl)m...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633472BDBM633472(N-(4-((6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633473BDBM633473(N-(4-((6,7-dimethoxy-3-methyl-4-oxo-3,4-dihydropht...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633450BDBM633450(7-(4-oxo-3,4-dihydrophthalazin-1-yl)-3,4-dihydrois...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633451BDBM633451(7-(6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1-yl)...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633387BDBM633387(4-(4-(aminomethyl)-3-(trifluoromethyl)phenyl) phth...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633452BDBM633452(N-(1-(4-(4-oxo-3,4-dihydrophthalazin-1-yl)phenyl)e...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633388BDBM633388(4-(1,2,3,4-tetrahydroisoquinolin-6-yl)phthalazin-1...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633453BDBM633453((R)-N-(1-(4-(4-oxo-3,4-dihydrophthalazin-1-yl)phen...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633382BDBM633382(4-(4-(aminomethyl)-phenyl)-7-methoxyphthalazin-1(2...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633383BDBM633383(4-(4-(aminomethyphenyl)-6,7-dimethoxyphthalazin-1(...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633384BDBM633384(4-(4-(aminomethyl)phenyl)-6,7-dimethoxy-2-methylph...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633385BDBM633385((R)-4-(4-(1-aminoethyl)phenyl)phthalazin-1(2H)-one...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633461BDBM633461(N-((1-(4-oxo-3,4-dihydrophthalazin-1-yl)piperidin-...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633455BDBM633455(N-(4-(4-oxo-3,4-dihydrophthalazin-1-yl)-2-(trifluo...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633456BDBM633456(N-methyl-N-(4-(4-oxo-3,4-dihydrophthalazin-1-yl)be...)
Affinity DataIC50: 1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633434BDBM633434(N-(4-(7-methoxy-3-methyl-4-oxo-3,4-dihydrophthalaz...)
Affinity DataIC50: 5.50E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633435BDBM633435(N-(4-(6-methoxy-4-oxo-3,4-dihydrophthalazin-1-yl)b...)
Affinity DataIC50: 5.50E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633437BDBM633437(N-(4-(6,7-dimethoxy-3-methyl-4-oxo-3,4-dihydrophth...)
Affinity DataIC50: 5.50E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633430BDBM633430(N-(4-(3-benzyl-4-oxo-3,4-dihydrophthalazin-1-yl)be...)
Affinity DataIC50: 5.50E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633431BDBM633431(N-(4-(3-(4-fluorobenzyl)-4-oxo-3,4-dihydrophthalaz...)
Affinity DataIC50: 5.50E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633442BDBM633442(N-(4-(6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1-...)
Affinity DataIC50: 5.50E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633378BDBM633378(4-(4-(aminomethyl)phenyl)-2-(4-fluorobenzyl) phtha...)
Affinity DataIC50: 5.50E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633443BDBM633443(N-(4-(6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1-...)
Affinity DataIC50: 5.50E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

LigandChemical structure of BindingDB Monomer ID 633444BDBM633444(N-(4-(6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1-...)
Affinity DataIC50: 5.50E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/25/2023
Entry Details
US Patent

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