BDBM50045291 CHEMBL88340::i2-[2-(Morpholine-4-sulfonylamino)-3-phenyl-propionylamino]-pent-4-enoic acid [1-cyclohexylmethyl-3,3-difluoro-2-hydroxy-3-(2-morpholin-4-yl-ethylcarbamoyl)-propyl]-amide

SMILES O[C@H]([C@H](CC1CCCCC1)NC(=O)[C@H](CC=C)NC(=O)[C@H](Cc1ccccc1)NS(=O)(=O)N1CCOCC1)C(F)(F)C(=O)NCCN1CCOCC1

InChI Key InChIKey=PVHMTQKFPXCDJQ-XHPANXIASA-N

Data  4 KI  1 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50045291   

TargetCathepsin D(Human)
University of Florida

Curated by ChEMBL
LigandPNGBDBM50045291(CHEMBL88340 | i2-[2-(Morpholine-4-sulfonylamino)-3...)
Affinity DataKi:  0.800nMAssay Description:Binding affinity against human cathepsin DMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetCathepsin E(Human)
University of Florida

Curated by ChEMBL
LigandPNGBDBM50045291(CHEMBL88340 | i2-[2-(Morpholine-4-sulfonylamino)-3...)
Affinity DataKi:  21nMAssay Description:Binding affinity against human cathepsin EMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetPepsin A-5(Human)
University of Florida

Curated by ChEMBL
LigandPNGBDBM50045291(CHEMBL88340 | i2-[2-(Morpholine-4-sulfonylamino)-3...)
Affinity DataKi:  1.24E+3nMAssay Description:Binding affinity against human pepsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetGastricsin(Human)
University of Florida

Curated by ChEMBL
LigandPNGBDBM50045291(CHEMBL88340 | i2-[2-(Morpholine-4-sulfonylamino)-3...)
Affinity DataKi: >4.00E+3nMAssay Description:Binding affinity against human gastricsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetRenin(Human)
University of Florida

Curated by ChEMBL
LigandPNGBDBM50045291(CHEMBL88340 | i2-[2-(Morpholine-4-sulfonylamino)-3...)
Affinity DataIC50:  0.700nMAssay Description:Inhibitory activity against monkey reninMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed