Compile Data Set for Download or QSAR
Report error Found 22 Enz. Inhib. hit(s) with all data for entry = 50036212
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046938BDBM50046938(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi:  4nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046922BDBM50046922(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi:  5nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046932BDBM50046932(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi:  5nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046940BDBM50046940(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi:  8nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046941BDBM50046941(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi:  10nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046920BDBM50046920(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi:  16nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50368830BDBM50368830(CHEMBL1790518)
Affinity DataKi:  22nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50368829BDBM50368829(CHEMBL1790517)
Affinity DataKi:  36nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046929BDBM50046929(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi:  48nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046921BDBM50046921(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi:  100nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046934BDBM50046934(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi:  100nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046935BDBM50046935(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi:  140nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046927BDBM50046927(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi:  200nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046925BDBM50046925(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi: >200nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046923BDBM50046923(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi: >200nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046924BDBM50046924(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi:  200nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046939BDBM50046939(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi: >200nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046936BDBM50046936(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi: >200nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046931BDBM50046931(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi: >200nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046933BDBM50046933(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi: >200nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046928BDBM50046928(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi: >200nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50046926BDBM50046926(N-(4-{1-[(1H-Benzoimidazol-2-ylmethyl)-carbamoyl]-...)
Affinity DataKi:  600nMAssay Description:Inhibition of HIV-1 protease in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed