BDBM50053620 1-phenylguanidine::1N-amino(immino)methylaniline::CHEMBL14047::N-Phenyl-guanidine::N-phenylguanidine

SMILES [#7]\[#6](-[#7])=[#7]\c1ccccc1

InChI Key InChIKey=ZOAGAHYTQDWGPT-UHFFFAOYSA-N

Data  7 KI  6 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 13 hits for monomerid = 50053620   

TargetUrokinase-type plasminogen activator(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50053620(1N-amino(immino)methylaniline | 1-phenylguanidine ...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against Urokinase-type plasminogen activatorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAmine oxidase [copper-containing] 3(Human)
Astellas Pharma

Curated by ChEMBL
LigandPNGBDBM50053620(1N-amino(immino)methylaniline | 1-phenylguanidine ...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human VAP-1 expressed in CHO cells using [14C]-benzylamine as substrate preincubated for 30 mins prior to substrate addition measured a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetMembrane primary amine oxidase(Rat)
Astellas Pharma

Curated by ChEMBL
LigandPNGBDBM50053620(1N-amino(immino)methylaniline | 1-phenylguanidine ...)
Affinity DataIC50: 7.80E+4nMAssay Description:Inhibition of rat VAP-1 expressed in CHO cells using [14C]-benzylamine as substrate preincubated for 30 mins prior to substrate addition measured aft...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetSolute carrier family 22 member 1(Human)
Virginia Commonwealth University

Curated by ChEMBL
LigandPNGBDBM50053620(1N-amino(immino)methylaniline | 1-phenylguanidine ...)
Affinity DataIC50: 4.11E+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 Depth
Date in BDB:
1/17/2020
Entry Details Article
PubMed
TargetSolute carrier family 22 member 3(Human)
Virginia Commonwealth University

Curated by ChEMBL
LigandPNGBDBM50053620(1N-amino(immino)methylaniline | 1-phenylguanidine ...)
Affinity DataIC50: 9.98E+4nMAssay Description:Inhibition of OCT3 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/17/2020
Entry Details Article
PubMed
TargetSolute carrier family 22 member 2(Human)
Virginia Commonwealth University

Curated by ChEMBL
LigandPNGBDBM50053620(1N-amino(immino)methylaniline | 1-phenylguanidine ...)
Affinity DataIC50: 8.90E+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 Depth
Date in BDB:
1/17/2020
Entry Details Article
PubMed
Target5-hydroxytryptamine receptor 3A/3B/3C/3D/3E(Human)
Virginia Commonwealth University

Curated by ChEMBL
LigandPNGBDBM50053620(1N-amino(immino)methylaniline | 1-phenylguanidine ...)
Affinity DataKi:  2.34E+3nMAssay Description:Compound was tested for the inhibition of [3H]GR-65630 binding to 5-hydroxytryptamine 3 receptor expressed in NG 108-15 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50053620(1N-amino(immino)methylaniline | 1-phenylguanidine ...)
Affinity DataKi:  2.06E+4nMAssay Description:Inhibition against Urokinase-type plasminogen activatorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/19/2012
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50053620(1N-amino(immino)methylaniline | 1-phenylguanidine ...)
Affinity DataKi:  2.06E+4nMAssay Description:Inhibition against Urokinase-type plasminogen activatorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/19/2012
Entry Details Article
PubMed
TargetSerine protease 1(Bovine)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50053620(1N-amino(immino)methylaniline | 1-phenylguanidine ...)
Affinity DataKi:  1.63E+5nMAssay Description:Inhibition against TrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/19/2012
Entry Details Article
PubMed
TargetTissue-type plasminogen activator(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50053620(1N-amino(immino)methylaniline | 1-phenylguanidine ...)
Affinity DataKi:  7.33E+5nMAssay Description:The compound was tested for its inhibition against Tissue plasminogen activator at 1 mM when assayed against 0.3 mM S-2288 (Km = 0.673 mM)More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/19/2012
Entry Details Article
PubMed
TargetPlasminogen(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50053620(1N-amino(immino)methylaniline | 1-phenylguanidine ...)
Affinity DataKi:  2.61E+6nMAssay Description:Inhibition against human plasmin was determined at 0.5 mMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/19/2012
Entry Details Article
PubMed
TargetSerine protease 1(Bovine)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50053620(1N-amino(immino)methylaniline | 1-phenylguanidine ...)
Affinity DataKi:  1.63E+5nMAssay Description:log1/Ki value was calculated against TrypsinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/19/2012
Entry Details Article
PubMed