BDBM50053608 1N-amino(immino)methyl-3-chloroaniline::CHEMBL13823::N-(3-Chloro-phenyl)-guanidine::N-(3-chlorophenyl)guanidine

SMILES [#7]\[#6](-[#7])=[#7]\c1cccc(Cl)c1

InChI Key InChIKey=DWLMIHRZURMFAQ-UHFFFAOYSA-N

Data  7 KI  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 50053608   

Target5-hydroxytryptamine receptor 3A(Homo sapiens (Human))
Virginia Commonwealth University

Curated by ChEMBL
LigandPNGBDBM50053608(1N-amino(immino)methyl-3-chloroaniline | CHEMBL138...)
Affinity DataKi:  32nMAssay Description:Displacement of [3H]GR65630 from 5-HT3 receptor (unknown origin) expressed in mouse/rat NG108-15 cells after 30 mins by by liquid scintillation count...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 3A/3B/3C/3D/3E(Homo sapiens (Human))
Virginia Commonwealth University

Curated by ChEMBL
LigandPNGBDBM50053608(1N-amino(immino)methyl-3-chloroaniline | CHEMBL138...)
Affinity DataKi:  35nMAssay Description:Compound was tested for the inhibition of [3H]-GR-65,630 binding to 5-hydroxytryptamine 3 receptor expressed in NG 108-15 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50053608(1N-amino(immino)methyl-3-chloroaniline | CHEMBL138...)
Affinity DataKi:  6.17E+4nMAssay Description:log1/Ki value was calculated against Urokinase-type plasminogen activatorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50053608(1N-amino(immino)methyl-3-chloroaniline | CHEMBL138...)
Affinity DataKi:  6.18E+4nMAssay Description:Inhibition against Urokinase-type plasminogen activatorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50053608(1N-amino(immino)methyl-3-chloroaniline | CHEMBL138...)
Affinity DataKi:  1.10E+6nMAssay Description:Inhibition against TrypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50053608(1N-amino(immino)methyl-3-chloroaniline | CHEMBL138...)
Affinity DataKi:  1.10E+6nMAssay Description:Inhibition against TrypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50053608(1N-amino(immino)methyl-3-chloroaniline | CHEMBL138...)
Affinity DataKi: <1.00E+7nMAssay Description:Inhibition against human plasmin was determined at 0.5 mMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSolute carrier family 22 member 1(Homo sapiens (Human))
Virginia Commonwealth University

Curated by ChEMBL
LigandPNGBDBM50053608(1N-amino(immino)methyl-3-chloroaniline | CHEMBL138...)
Affinity DataIC50:  1.37E+4nMAssay Description:Inhibition of human OCT1 expressed in HEK293 cells assessed as decrease in uptake of substrate [3H]MPP+ after 1 min by liquid scintillation counting ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSolute carrier family 22 member 3(Homo sapiens (Human))
Virginia Commonwealth University

Curated by ChEMBL
LigandPNGBDBM50053608(1N-amino(immino)methyl-3-chloroaniline | CHEMBL138...)
Affinity DataIC50:  7.60E+3nMAssay Description:Inhibition of human OCT3 expressed in HEK293 cells assessed as decrease in uptake of substrate [3H]MPP+ after 1 min by liquid scintillation counting ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSolute carrier family 22 member 2(Homo sapiens (Human))
Virginia Commonwealth University

Curated by ChEMBL
LigandPNGBDBM50053608(1N-amino(immino)methyl-3-chloroaniline | CHEMBL138...)
Affinity DataIC50:  6.05E+4nMAssay Description:Inhibition of human OCT2 expressed in HEK293 cells assessed as decrease in uptake of substrate [3H]MPP+ after 1 min by liquid scintillation counting ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed