BDBM50036754 (1Z)-N'-(aminosulfonyl)-3-[({2-[(diaminomethylene)amino]-1,3-thiazol-4-yl}methyl)thio]propanimidamide::(1Z)-N'-(aminosulfonyl)-3-[({2-[(diaminomethylene)amino]-1,3-thiazol-4-yl}methyl)thio]propanimidamide (Famotidine)::3-(2-Guanidino-thiazol-4-ylmethylsulfanyl)-N-sulfonylamino-propionamidine::CHEMBL902::FAMOTIDINE::Fluxid::MK-208::N'-(aminosulfonyl)-3-(((2-((diaminomethylene)amino)-4-thiazolyl)methyl)thio)propanimidamide::N-sulfomoyl-3-(2-Guanidino-2H-1lambda*4*-thiazol-4-ylmethylsulfanyl)-propionamidine::Pepcid::Pepcid ac::Pepcid ac (geltab)::Pepcid rpd

SMILES [#7]\[#6](-[#7])=[#7]/c1nc(-[#6]-[#16]-[#6]-[#6]-[#6](=[#7])-[#7]S([#7])(=O)=O)cs1

InChI Key InChIKey=XUFQPHANEAPEMJ-UHFFFAOYSA-N

Data  2 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 8 hits for monomerid = 50036754   

TargetSolute carrier family 22 member 8(Homo sapiens (Human))
Kyoto University Hospital

Curated by ChEMBL
LigandPNGBDBM50036754((1Z)-N'-(aminosulfonyl)-3-[({2-[(diaminomethylene)...)
Affinity DataKi:  3.00E+5nMAssay Description:TP_TRANSPORTER: inhibition of E1S uptake in OAT3 expressing oocytesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSolute carrier family 22 member 2(Homo sapiens (Human))
Kyoto University Hospital

Curated by ChEMBL
LigandPNGBDBM50036754((1Z)-N'-(aminosulfonyl)-3-[({2-[(diaminomethylene)...)
Affinity DataKi:  1.80E+6nMAssay Description:TP_TRANSPORTER: inhibition of TEA uptake in OCT2 expressing oocytesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMultidrug and toxin extrusion protein 1(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50036754((1Z)-N'-(aminosulfonyl)-3-[({2-[(diaminomethylene)...)
Affinity DataIC50:  760nMAssay Description:Inhibition of human MATE1-mediated ASP+ uptake expressed in HEK293 cells after 1.5 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSolute carrier family 22 member 1(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50036754((1Z)-N'-(aminosulfonyl)-3-[({2-[(diaminomethylene)...)
Affinity DataIC50: >3.00E+5nMAssay Description:Inhibition of human OCT1-mediated ASP+ uptake expressed in HEK293 cells after 3 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSolute carrier family 22 member 2(Homo sapiens (Human))
Kyoto University Hospital

Curated by ChEMBL
LigandPNGBDBM50036754((1Z)-N'-(aminosulfonyl)-3-[({2-[(diaminomethylene)...)
Affinity DataIC50:  3.61E+4nMAssay Description:Inhibition of human OCT2-mediated ASP+ uptake expressed in HEK293 cells after 3 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMultidrug and toxin extrusion protein 2(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50036754((1Z)-N'-(aminosulfonyl)-3-[({2-[(diaminomethylene)...)
Affinity DataIC50:  3.62E+4nMAssay Description:Inhibition of human MATE2K-mediated ASP+ uptake expressed in HEK293 cells after 1.5 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H2 receptor(Cavia porcellus (domestic guinea pig))
Fujisawa Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50036754((1Z)-N'-(aminosulfonyl)-3-[({2-[(diaminomethylene)...)
Affinity DataIC50:  300nMAssay Description:Compound was tested for H2 receptor antagonistic activity against histamine stimulated chronotropic response in isolated guinea pig right atriumMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSolute carrier family 22 member 3(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50036754((1Z)-N'-(aminosulfonyl)-3-[({2-[(diaminomethylene)...)
Affinity DataIC50:  1.07E+4nMAssay Description:Inhibition of human OCT3-mediated ASP+ uptake expressed in HEK293 cells after 3 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed