Compile Data Set for Download or QSAR
Report error Found 33 Enz. Inhib. hit(s) with all data for entry = 50007237
LigandChemical structure of BindingDB Monomer ID 50060140BDBM50060140([(S)-1-{(4-Benzyloxy-benzyl)-[(2-cyano-2-phenyl-et...)
Affinity DataIC50: 2nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060144BDBM50060144([(S)-1-{(4-Benzyloxy-benzyl)-[((R)-1-methyl-2-phen...)
Affinity DataIC50: 3nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060141BDBM50060141([(S)-1-{(4-Benzyloxy-benzyl)-[(2-methyl-2-phenyl-p...)
Affinity DataIC50: 4nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060149BDBM50060149([(S)-1-{(4-Benzyloxy-benzyl)-[(2-phenyl-butylcarba...)
Affinity DataIC50: 5nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060145BDBM50060145([(S)-1-{(4-Benzyloxy-benzyl)-[((S)-2-phenyl-propyl...)
Affinity DataIC50: 5nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060139BDBM50060139([(S)-1-((4-Benzyloxy-benzyl)-{[(1-phenyl-cyclobuty...)
Affinity DataIC50: 6nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060146BDBM50060146([(S)-1-((4-Benzyloxy-benzyl)-{[(1-phenyl-cycloprop...)
Affinity DataIC50: 7nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060138BDBM50060138([(S)-1-{(4-Benzyloxy-benzyl)-[(2-phenyl-propylcarb...)
Affinity DataIC50: 8nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060150BDBM50060150([(S)-1-{(4-Benzyloxy-benzyl)-[((R)-2-phenyl-propyl...)
Affinity DataIC50: 16nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060142BDBM50060142([(S)-1-((4-Benzyloxy-benzyl)-{[(1-phenyl-cyclopent...)
Affinity DataIC50: 17nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060148BDBM50060148([(S)-1-{(4-Benzyloxy-benzyl)-[(2-phenyl-pentylcarb...)
Affinity DataIC50: 25nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060152BDBM50060152([(S)-1-{(4-Benzyloxy-benzyl)-[(2-ethyl-2-phenyl-bu...)
Affinity DataIC50: 32nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060143BDBM50060143([(S)-1-{(4-Benzyloxy-benzyl)-[((S)-1-methyl-2-phen...)
Affinity DataIC50: 41nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50059857BDBM50059857([(S)-1-[(4-Benzyloxy-benzyl)-(phenethylcarbamoyl-m...)
Affinity DataIC50: 62nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50059876BDBM50059876([(S)-1-[(S)-1-{(S)-2-Benzyloxy-1-[(S)-1-((R)-1-car...)
Affinity DataIC50: 76nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50060139BDBM50060139([(S)-1-((4-Benzyloxy-benzyl)-{[(1-phenyl-cyclobuty...)
Affinity DataIC50: 88nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50060141BDBM50060141([(S)-1-{(4-Benzyloxy-benzyl)-[(2-methyl-2-phenyl-p...)
Affinity DataIC50: 180nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50060146BDBM50060146([(S)-1-((4-Benzyloxy-benzyl)-{[(1-phenyl-cycloprop...)
Affinity DataIC50: 180nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50060140BDBM50060140([(S)-1-{(4-Benzyloxy-benzyl)-[(2-cyano-2-phenyl-et...)
Affinity DataIC50: 190nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060151BDBM50060151([(S)-1-{(4-Benzyloxy-benzyl)-[(1,1-dimethyl-2-phen...)
Affinity DataIC50: 270nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50060145BDBM50060145([(S)-1-{(4-Benzyloxy-benzyl)-[((S)-2-phenyl-propyl...)
Affinity DataIC50: 300nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50060138BDBM50060138([(S)-1-{(4-Benzyloxy-benzyl)-[(2-phenyl-propylcarb...)
Affinity DataIC50: 310nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50059879BDBM50059879([(S)-1-{(4-Benzyloxy-benzyl)-[(2-benzyloxy-ethylca...)
Affinity DataIC50: 320nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50060142BDBM50060142([(S)-1-((4-Benzyloxy-benzyl)-{[(1-phenyl-cyclopent...)
Affinity DataIC50: 330nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50060149BDBM50060149([(S)-1-{(4-Benzyloxy-benzyl)-[(2-phenyl-butylcarba...)
Affinity DataIC50: 400nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50060150BDBM50060150([(S)-1-{(4-Benzyloxy-benzyl)-[((R)-2-phenyl-propyl...)
Affinity DataIC50: 570nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50060144BDBM50060144([(S)-1-{(4-Benzyloxy-benzyl)-[((R)-1-methyl-2-phen...)
Affinity DataIC50: 710nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50060152BDBM50060152([(S)-1-{(4-Benzyloxy-benzyl)-[(2-ethyl-2-phenyl-bu...)
Affinity DataIC50: 1.00E+3nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50060148BDBM50060148([(S)-1-{(4-Benzyloxy-benzyl)-[(2-phenyl-pentylcarb...)
Affinity DataIC50: 1.00E+3nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50060147BDBM50060147([(S)-1-{(4-Benzyloxy-benzyl)-[(methyl-phenethyl-ca...)
Affinity DataIC50: 4.00E+3nMAssay Description:In vitro inhibition of rat farnesyltransferase.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50059857BDBM50059857([(S)-1-[(4-Benzyloxy-benzyl)-(phenethylcarbamoyl-m...)
Affinity DataIC50: 4.30E+3nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50060143BDBM50060143([(S)-1-{(4-Benzyloxy-benzyl)-[((S)-1-methyl-2-phen...)
Affinity DataIC50: 6.30E+3nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGTPase HRas(Human)
Warner-Lambert

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50059879BDBM50059879([(S)-1-{(4-Benzyloxy-benzyl)-[(2-benzyloxy-ethylca...)
Affinity DataIC50: 1.43E+4nMAssay Description:Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells. More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed