Compile Data Set for Download or QSAR
Report error Found 75 Enz. Inhib. hit(s) with all data for entry = 50046200
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099406BDBM50099406(CHEMBL3344272)
Affinity DataIC50: 19nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(malaria parasite P. vivax)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099406BDBM50099406(CHEMBL3344272)
Affinity DataIC50: 24nMAssay Description:Inhibition of Plasmodium vivax plasmepsin V by fluorogenic PEXEL cleavage assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099378BDBM50099378(CHEMBL3344165)
Affinity DataIC50: 26nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099272BDBM50099272(CHEMBL3344164)
Affinity DataIC50: 29nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetCathepsin D(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099242BDBM50099242(CHEMBL3344159)
Affinity DataIC50: 43nMAssay Description:Inhibition of human cathepsin D assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099380BDBM50099380(CHEMBL3344166)
Affinity DataIC50: 77nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099381BDBM50099381(CHEMBL3344261)
Affinity DataIC50: 230nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099391BDBM50099391(CHEMBL3344266)
Affinity DataIC50: 348nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099395BDBM50099395(CHEMBL3344270)
Affinity DataIC50: 378nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetCathepsin D(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099378BDBM50099378(CHEMBL3344165)
Affinity DataIC50: 447nMAssay Description:Inhibition of human cathepsin D assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099387BDBM50099387(CHEMBL3344262)
Affinity DataIC50: 530nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099394BDBM50099394(CHEMBL3344269)
Affinity DataIC50: 550nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099148BDBM50099148(CHEMBL3344151)
Affinity DataIC50: 556nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099390BDBM50099390(CHEMBL3344265)
Affinity DataIC50: 569nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099171BDBM50099171(CHEMBL3344152)
Affinity DataIC50: 613nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099240BDBM50099240(CHEMBL3344157)
Affinity DataIC50: 614nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099388BDBM50099388(CHEMBL3344263)
Affinity DataIC50: 622nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099403BDBM50099403(CHEMBL3344271)
Affinity DataIC50: 625nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetCathepsin D(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099272BDBM50099272(CHEMBL3344164)
Affinity DataIC50: 713nMAssay Description:Inhibition of human cathepsin D assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099389BDBM50099389(CHEMBL3344264)
Affinity DataIC50: 772nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099393BDBM50099393(CHEMBL3344268)
Affinity DataIC50: 774nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099236BDBM50099236(CHEMBL3344153)
Affinity DataIC50: 865nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099237BDBM50099237(CHEMBL3344154)
Affinity DataIC50: 967nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099392BDBM50099392(CHEMBL3344267)
Affinity DataIC50: 2.01E+3nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetCathepsin D(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099381BDBM50099381(CHEMBL3344261)
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of human cathepsin D assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetCathepsin D(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099380BDBM50099380(CHEMBL3344166)
Affinity DataIC50: 5.10E+3nMAssay Description:Inhibition of human cathepsin D assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099241BDBM50099241(CHEMBL3344158)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099242BDBM50099242(CHEMBL3344159)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099243BDBM50099243(CHEMBL3344160)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099247BDBM50099247(CHEMBL3344161)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099249BDBM50099249(CHEMBL3344162)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099252BDBM50099252(CHEMBL3344163)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099238BDBM50099238(CHEMBL3344155)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetPlasmepsin V(Plasmodium falciparum (isolate 3D7))
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099239BDBM50099239(CHEMBL3344156)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Plasmodium falciparum plasmepsin V assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetCathepsin D(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099388BDBM50099388(CHEMBL3344263)
Affinity DataIC50: 2.90E+4nMAssay Description:Inhibition of human cathepsin D assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetCathepsin D(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099406BDBM50099406(CHEMBL3344272)
Affinity DataIC50: 3.20E+4nMAssay Description:Inhibition of human cathepsin D assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetBeta-secretase 1(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099389BDBM50099389(CHEMBL3344264)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human BACE1 assessed as cleavage of TRF substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetBeta-secretase 1(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099390BDBM50099390(CHEMBL3344265)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human BACE1 assessed as cleavage of TRF substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetBeta-secretase 1(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099171BDBM50099171(CHEMBL3344152)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human BACE1 assessed as cleavage of TRF substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetBeta-secretase 1(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099236BDBM50099236(CHEMBL3344153)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human BACE1 assessed as cleavage of TRF substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetCathepsin D(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099391BDBM50099391(CHEMBL3344266)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human cathepsin D assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetBeta-secretase 1(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099391BDBM50099391(CHEMBL3344266)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human BACE1 assessed as cleavage of TRF substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetCathepsin D(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099392BDBM50099392(CHEMBL3344267)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human cathepsin D assessed as cleavage of wtKAHRP fluorogenic substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetBeta-secretase 1(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099392BDBM50099392(CHEMBL3344267)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human BACE1 assessed as cleavage of TRF substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetBeta-secretase 1(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099237BDBM50099237(CHEMBL3344154)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human BACE1 assessed as cleavage of TRF substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetBeta-secretase 1(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099393BDBM50099393(CHEMBL3344268)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human BACE1 assessed as cleavage of TRF substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetBeta-secretase 1(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099238BDBM50099238(CHEMBL3344155)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human BACE1 assessed as cleavage of TRF substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetBeta-secretase 1(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099394BDBM50099394(CHEMBL3344269)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human BACE1 assessed as cleavage of TRF substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetBeta-secretase 1(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099395BDBM50099395(CHEMBL3344270)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human BACE1 assessed as cleavage of TRF substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
TargetBeta-secretase 1(Human)
The Walter and Eliza Hall Institute of Medical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50099403BDBM50099403(CHEMBL3344271)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human BACE1 assessed as cleavage of TRF substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/27/2016
Entry Details Article
PubMed
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