null

SMILES OC[C@@H]1C[C@@H](NC(=O)c2ccc(Cl)s2)[C@H](C1)NC(=O)c1ccc(cc1)-n1ccccc1=O

InChI Key InChIKey=LWARIAPUYJUPKK-JCGIZDLHSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 7 hits for monomerid = 50218290   

TargetCoagulation factor X(Homo sapiens (Human))
Bristol-Myers Squibb Company

Curated by ChEMBL
LigandPNGBDBM50218290(5-chloro-N-((1R,2S,4S)-4-(hydroxymethyl)-2-(4-(2-o...)copy SMILEScopy InChI
Affinity DataKi:  0.560nMAssay Description:Inhibition of human factor 10aMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3CPQPubMed
TargetPlasma kallikrein(Homo sapiens (Human))
Bristol-Myers Squibb Company

Curated by ChEMBL
LigandPNGBDBM50218290(5-chloro-N-((1R,2S,4S)-4-(hydroxymethyl)-2-(4-(2-o...)copy SMILEScopy InChI
Affinity DataKi: >1.08E+4nMAssay Description:Inhibition of human plasma kallikreinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3CPQPubMed
TargetCoagulation factor VII(Homo sapiens (Human))
Bristol-Myers Squibb Company

Curated by ChEMBL
LigandPNGBDBM50218290(5-chloro-N-((1R,2S,4S)-4-(hydroxymethyl)-2-(4-(2-o...)copy SMILEScopy InChI
Affinity DataKi: >1.10E+4nMAssay Description:Inhibition of human factor 7aMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3CPQPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Bristol-Myers Squibb Company

Curated by ChEMBL
LigandPNGBDBM50218290(5-chloro-N-((1R,2S,4S)-4-(hydroxymethyl)-2-(4-(2-o...)copy SMILEScopy InChI
Affinity DataKi: >1.40E+4nMAssay Description:Inhibition of human urokinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3CPQPubMed
TargetVitamin K-dependent protein C(Homo sapiens (Human))
Bristol-Myers Squibb Company

Curated by ChEMBL
LigandPNGBDBM50218290(5-chloro-N-((1R,2S,4S)-4-(hydroxymethyl)-2-(4-(2-o...)copy SMILEScopy InChI
Affinity DataKi: >2.10E+4nMAssay Description:Inhibition of human activated protein CMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3CPQPubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Bristol-Myers Squibb Company

Curated by ChEMBL
LigandPNGBDBM50218290(5-chloro-N-((1R,2S,4S)-4-(hydroxymethyl)-2-(4-(2-o...)copy SMILEScopy InChI
Affinity DataKi: >2.10E+4nMAssay Description:Inhibition of human tissue plasminogen activatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3CPQPubMed
TargetPlasminogen(Homo sapiens (Human))
Bristol-Myers Squibb Company

Curated by ChEMBL
LigandPNGBDBM50218290(5-chloro-N-((1R,2S,4S)-4-(hydroxymethyl)-2-(4-(2-o...)copy SMILEScopy InChI
Affinity DataKi: >2.20E+4nMAssay Description:Inhibition of human PlasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3CPQPubMed