Compile Data Set for Download or QSAR
Report error Found 24 Enz. Inhib. hit(s) with all data for entry = 50035474
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027132BDBM50027132(1-[5-Benzoylamino-6-(3,4-dimethoxy-phenyl)-4-oxo-h...)
Affinity DataIC50: 1.40nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027142BDBM50027142(1-{5-[(Furan-2-carbonyl)-amino]-4-oxo-6-phenyl-hex...)
Affinity DataIC50: 1.40nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027344BDBM50027344(1-(5-Benzoylamino-4-oxo-6-phenyl-hexanoyl)-pyrroli...)
Affinity DataIC50: 3.20nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027147BDBM50027147(1-[5-Benzoylamino-6-(4-hydroxy-phenyl)-4-oxo-hexan...)
Affinity DataIC50: 4.70nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027144BDBM50027144(1-(5-Benzoylamino-4-oxo-6-pyridin-3-yl-hexanoyl)-p...)
Affinity DataIC50: 5.70nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 21642BDBM21642((2S)-1-[(2S)-2-methyl-3-sulfanylpropanoyl]pyrrolid...)
Affinity DataIC50: 9nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027146BDBM50027146(1-[5-Benzoylamino-6-(4-benzyloxy-phenyl)-4-oxo-hex...)
Affinity DataIC50: 10nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027154BDBM50027154(1-(5-Benzoylamino-4-oxo-6-pyridin-3-yl-hexanoyl)-p...)
Affinity DataIC50: 15nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027133BDBM50027133(1-{4-Oxo-6-phenyl-5-[(tetrahydro-furan-2-carbonyl)...)
Affinity DataIC50: 20nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027152BDBM50027152(2-(5-Benzoylamino-4-oxo-6-phenyl-hexanoylamino)-3-...)
Affinity DataIC50: 28nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027153BDBM50027153(1-(6-Benzoylamino-5-oxo-7-phenyl-heptanoyl)-pyrrol...)
Affinity DataIC50: 42nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027150BDBM50027150(1-[5-(2-Methyl-benzoylamino)-4-oxo-6-phenyl-hexano...)
Affinity DataIC50: 46nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027148BDBM50027148(1-(5-Benzoylamino-4-oxo-6-phenyl-hexanoyl)-pyrroli...)
Affinity DataIC50: 82nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027140BDBM50027140(1-[5-Benzoylamino-6-(4-benzyloxy-phenyl)-4-oxo-hex...)
Affinity DataIC50: 86nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027134BDBM50027134(1-(5-Benzoylamino-4-oxo-6-phenyl-hexanoyl)-pyrroli...)
Affinity DataIC50: 150nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027149BDBM50027149(2-(5-Benzoylamino-4-oxo-6-phenyl-hexanoylamino)-3-...)
Affinity DataIC50: 180nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027145BDBM50027145(1-(5-Benzyloxycarbonylamino-4-oxo-6-phenyl-hexanoy...)
Affinity DataIC50: 240nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027151BDBM50027151(1-(5-Benzoylamino-4-oxo-hexanoyl)-pyrrolidine-2-ca...)
Affinity DataIC50: 300nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027143BDBM50027143(1-(5-Acetylamino-4-oxo-6-phenyl-hexanoyl)-pyrrolid...)
Affinity DataIC50: 330nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027138BDBM50027138(1-(5-Benzoylamino-4-oxo-6-phenyl-hexanoyl)-4-hydro...)
Affinity DataIC50: 540nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027137BDBM50027137(1-(5-Benzoylamino-4-hydroxyimino-6-phenyl-hexanoyl...)
Affinity DataIC50: 1.20E+3nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027139BDBM50027139(1-[5-(2-Methyl-benzoylamino)-4-oxo-6-phenyl-hexano...)
Affinity DataIC50: 1.60E+3nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027135BDBM50027135(1-[5-Benzoylamino-6-(4-benzyloxy-phenyl)-4-oxo-hex...)
Affinity DataIC50: 8.60E+3nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme 2(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027136BDBM50027136(1-(5-Amino-4-oxo-6-phenyl-hexanoyl)-pyrrolidine-2-...)
Affinity DataIC50: 2.50E+4nMAssay Description:Concentration required to inhibit the activity of Angiotensin I converting enzyme by 50%More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed