Compile Data Set for Download or QSAR
Report error Found 42 Enz. Inhib. hit(s) with all data for entry = 9166
TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446509BDBM446509(2-(9-nitro-5-oxopyrido[2′,3′:4,5]pyrim...)
Affinity DataIC50: 5.5nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446508BDBM446508(N,N-dimethyl-2-(9-nitro-5-oxopyrido[2′,3R...)
Affinity DataIC50: 5.5nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 50154611BDBM50154611(2-Nitro-4b,9,10-triaza-benzo[b]fluorene-5,11-dione...)
Affinity DataIC50: 5.5nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446492BDBM446492(9-(trifluoromethoxy)pyrido[2′,3′:4,5]p...)
Affinity DataIC50: 5.5nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446493BDBM446493(9-chloropyrido[2′,3′:4,5]pyrimido[1,2-...)
Affinity DataIC50: 5.5nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 50300305BDBM50300305(4-Amino-N-(3-chloro-4-fluorophenyl)-N'-hydroxy-1,2...)
Affinity DataIC50: 5.5nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446517BDBM446517(pyrido[2,3-D]pyrido[3 ‘,4’: 4,5]pyrrolo[...)
Affinity DataIC50: 5.5nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 50154611BDBM50154611(2-Nitro-4b,9,10-triaza-benzo[b]fluorene-5,11-dione...)
Affinity DataIC50: 5.5nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446503BDBM446503(11-((2-(dimethylamino)ethoxy)imino)-9-nitropyrido[...)
Affinity DataIC50: 5.5nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 50154616BDBM50154616(4-aza-8-fluorotryptanthrin | 2-Fluoro-4b,9,10-tria...)
Affinity DataIC50: 5.5nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446515BDBM446515(2-(9-nitro-5-oxopyrido[2′,3′:4,5]pyrim...)
Affinity DataIC50: 5.5nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 50154616BDBM50154616(4-aza-8-fluorotryptanthrin | 2-Fluoro-4b,9,10-tria...)
Affinity DataIC50: 5.5nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446483BDBM446483(pyrido[2′,3′:4,5]pyrimido[1,2-α]i...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446511BDBM446511(11-(methoxyimino)-9-nitropyrido[2′,3′:...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446510BDBM446510((((9-nitro-5-oxopyrido[2′,3′:4,5]pyrim...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446484BDBM446484(pyrido[3′,4′:4,5]pyrimido[1,2-c]indole...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446505BDBM446505(11-((2-(dimethylamino)ethoxy)imino)-9-fluoropyrido...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446504BDBM446504(9-chloro-11-((2-(dimethylamino)ethoxy)imino)pyrido...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446507BDBM446507(11-((2-hydroxyethoxy)imino)-9-nitropyrido[2′...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446502BDBM446502(11-((2-(dimethylamino)ethoxy)imino)pyrido[2′...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446489BDBM446489(9-fluoropyrido[3′,4′:4,5]pyrimido[1,2-...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446498BDBM446498(9-chloro-11-(hydroxyimino)pyrido[2′,3′...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446484BDBM446484(pyrido[3′,4′:4,5]pyrimido[1,2-c]indole...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446486BDBM446486(9-methylpyrido[2′,3′:4,5]pyrimido[1,2-...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446496BDBM446496(9-chloropyrido[3′,4′: 4,5]pyrimido[1,2...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446494BDBM446494(9-methoxypyrido[2′,3′:4,5]pyrimido[1,2...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 50442991BDBM50442991(GNF-Pf-3777 | CHEMBL432537 | US10669273, Compound ...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446483BDBM446483(pyrido[2′,3′:4,5]pyrimido[1,2-α]i...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 48009BDBM48009(SMR000544298 | 8-fluoranylindolo[2,1-b]quinazoline...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446486BDBM446486(9-methylpyrido[2′,3′:4,5]pyrimido[1,2-...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446489BDBM446489(9-fluoropyrido[3′,4′:4,5]pyrimido[1,2-...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446514BDBM446514(11-((carboxymethoxyimino)-9-nitropyridine[2′...)
Affinity DataIC50: 550nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 50240612BDBM50240612(CHEMBL306946 | Indolo[2,1-b]quinazoline-6,12-dione...)
Affinity DataIC50: 5.50E+3nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446495BDBM446495(9-methoxypyrido[3′,4′:4,5]pyrimido[1,2...)
Affinity DataIC50: 5.50E+3nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446506BDBM446506(9-chloro-11-((3-(dimethylamino)propoxy)imino)pyrid...)
Affinity DataIC50: 5.50E+3nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446500BDBM446500(11-(hydroxyimino)-9-methoxypyrido[2′,3′...)
Affinity DataIC50: 5.50E+3nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446516BDBM446516(2-(9-methoxy-5-oxopyrido[2′,3′:4,5]pyr...)
Affinity DataIC50: 5.50E+3nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446497BDBM446497(11-(hydroxyimino)pyrido[2′,3′:4,5]pyri...)
Affinity DataIC50: 5.50E+3nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446513BDBM446513(11-((allyloxy)imino)-9-nitropyrido[2′,3̸...)
Affinity DataIC50: 5.50E+3nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446512BDBM446512(11-(ethoxyimino)-9-nitropyrido[2′,3′:4...)
Affinity DataIC50: 5.50E+3nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 446499BDBM446499(11-(hydroxyimino)-9-methylpyrido[2′,3′...)
Affinity DataIC50: 5.50E+3nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
Peking University

US Patent
LigandChemical structure of BindingDB Monomer ID 50442994BDBM50442994(CHEMBL312537 | US10669273, Compound 5b)
Affinity DataIC50: 1.00E+4nMAssay Description:Experimental method: IDO-1 can oxidatively cleave the indole ring of tryptophan to form N-formylkynurenine. Referring to the method in the literature...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details
US Patent