Compile Data Set for Download or QSAR
Found 52 with Last Name = 'nomoto' and Initial = 'a'
TargetSolute carrier family 22 member 11(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50003019(8-(Hexahydro-2,5-methano-pentalen-3a-yl)-1,3-dipro...)copy SMILEScopy InChI
Affinity DataKi:  2.07E+4nMAssay Description:TP_TRANSPORTER: inhibition of E1S uptake in OAT4-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2V989BQPubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50420185(CHEMBL1233636)copy SMILEScopy InChI
Affinity DataKi:  2.27E+4nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake (PAH: 5 uM, indoxyl sulfate:500 uM) in S2 human-OAT1 expressing cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23R0V48PubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50420185(CHEMBL1233636)copy SMILEScopy InChI
Affinity DataKi:  2.30E+4nMAssay Description:TP_TRANSPORTER: uptake&inhibition of PAH in OAT1-S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23R0V48PubMed
TargetSolute carrier family 22 member 16(Homo sapiens (Human))
Kyorin University

Curated by ChEMBL
LigandPNGBDBM50037268((-)-Carnitine | (-)-L-Carnitine | (3R)-3-hydroxy-4...)copy SMILEScopy InChI
Affinity DataKi:  3.00E+4nMAssay Description:TP_TRANSPORTER: inhibition of carnitine in Xenopus laevis oocytesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20003CSPubMedDrugBank
TargetSolute carrier family 22 member 11(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataKi:  4.44E+4nMAssay Description:TP_TRANSPORTER: inhibition of Ochratoxin A uptake in OAT4-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DZ09JWPubMedDrugBank
TargetSolute carrier family 22 member 11(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataKi:  5.49E+4nMAssay Description:TP_TRANSPORTER: inhibition of E1S uptake in OAT4-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2V989BQPubMedDrugBank
TargetSolute carrier family 22 member 11(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM85245(CAS_36322-90-4 | NSC_4856 | Piroxicam)copy SMILEScopy InChI
Affinity DataKi:  1.08E+5nMAssay Description:TP_TRANSPORTER: inhibition of Ochratoxin A uptake in OAT4-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DZ09JWPubMedDrugBank
TargetSolute carrier family 22 member 8(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50420185(CHEMBL1233636)copy SMILEScopy InChI
Affinity DataKi:  1.69E+5nMAssay Description:TP_TRANSPORTER: inhibition of E1S uptake (E1S: 5 uM, indoxyl sulfate:500 uM) in S2 cells expressing human-OAT3More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23R0V48PubMed
TargetSolute carrier family 22 member 8(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50420185(CHEMBL1233636)copy SMILEScopy InChI
Affinity DataKi:  1.69E+5nMAssay Description:TP_TRANSPORTER: uptake&inhibition of estrone sulfate in OAT3-S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23R0V48PubMed
TargetSolute carrier family 22 member 11(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50420185(CHEMBL1233636)copy SMILEScopy InChI
Affinity DataKi:  1.81E+5nMAssay Description:TP_TRANSPORTER: uptake&inhibition of estrone sulfate in OAT4-S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23R0V48PubMed
TargetSolute carrier family 22 member 11(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50420185(CHEMBL1233636)copy SMILEScopy InChI
Affinity DataKi:  1.81E+5nMAssay Description:TP_TRANSPORTER: inhibition of E1S uptake (E1S: 5 uM, indoxyl sulfate:500 uM) in S2 cells expressing human-OAT4More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23R0V48PubMed
TargetSolute carrier family 22 member 11(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM23432(octanoate | octanoate, 1 | octanoic acid | octanoi...)copy SMILEScopy InChI
Affinity DataKi:  2.36E+5nMAssay Description:TP_TRANSPORTER: inhibition of Ochratoxin A uptake in OAT4-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DZ09JWPubMed
TargetSolute carrier family 22 member 11(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50344961(CHEMBL510139 | citrinin)copy SMILEScopy InChI
Affinity DataKi:  3.66E+5nMAssay Description:TP_TRANSPORTER: inhibition of Ochratoxin A uptake in OAT4-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DZ09JWPubMed
TargetSolute carrier family 22 member 11(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50344964(Betamipron | CHEMBL1231530 | N-(phenylcarbonyl)-be...)copy SMILEScopy InChI
Affinity DataKi:  5.02E+5nMAssay Description:TP_TRANSPORTER: inhibition of E1S uptake in OAT4-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2V989BQPubMed
TargetSolute carrier family 22 member 7(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataKi:  7.66E+5nMAssay Description:TP_TRANSPORTER: inhibition of PGF2alpha uptake in OAT2-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2V989BQPubMedDrugBank
TargetSolute carrier family 22 member 8(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataIC50: 4.93E+3nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in hOAT3-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMedDrugBank
TargetSolute carrier family 22 member 8(Rattus norvegicus)
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataIC50: 6.03E+3nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in rOAT3-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetCellular tumor antigen p53(Homo sapiens (Human))
Institute of Microbial Chemistry (BIKAKEN)

Curated by ChEMBL
LigandPNGBDBM50080451(CHEMBL3422267)copy SMILEScopy InChI
Affinity DataIC50: 6.20E+3nMAssay Description:Induction of p53-dependent growth suppression of human LNZTA3 cells after 72 hrs by MTT assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B046ZPubMed
TargetCellular tumor antigen p53(Homo sapiens (Human))
Institute of Microbial Chemistry (BIKAKEN)

Curated by ChEMBL
LigandPNGBDBM50080457(CHEMBL3422268)copy SMILEScopy InChI
Affinity DataIC50: 6.20E+3nMAssay Description:Induction of p53-dependent growth suppression of human LNZTA3 cells after 72 hrs by MTT assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B046ZPubMed
TargetSolute carrier family 22 member 8(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50344964(Betamipron | CHEMBL1231530 | N-(phenylcarbonyl)-be...)copy SMILEScopy InChI
Affinity DataIC50: 9.92E+3nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in hOAT3-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataIC50: 1.23E+4nMAssay Description:TP_TRANSPORTER: inhibition of PHA uptake (PHA: 5uM) in hOAT1-expressing S2 cellsMore data for this Ligand-Target Pair
TargetSolute carrier family 22 member 8(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM20688((3R,5R)-7-[(1S,2S,6S,8S,8aR)-6-hydroxy-2-methyl-8-...)copy SMILEScopy InChI
Affinity DataIC50: 1.37E+4nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in hOAT3-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMedDrugBank
TargetSolute carrier family 22 member 8(Rattus norvegicus)
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM20688((3R,5R)-7-[(1S,2S,6S,8S,8aR)-6-hydroxy-2-methyl-8-...)copy SMILEScopy InChI
Affinity DataIC50: 1.56E+4nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in rOAT3-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 11(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataIC50: 2.54E+4nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in hOAT4-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMedDrugBank
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50344964(Betamipron | CHEMBL1231530 | N-(phenylcarbonyl)-be...)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+4nMAssay Description:TP_TRANSPORTER: inhibition of PHA uptake (PHA: 5uM) in hOAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 8(Rattus norvegicus)
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50344964(Betamipron | CHEMBL1231530 | N-(phenylcarbonyl)-be...)copy SMILEScopy InChI
Affinity DataIC50: 4.75E+4nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in rOAT3-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 8(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22889((Cimetidine) N-Methyl-N''''-[2-(5-methyl-1H-imidaz...)copy SMILEScopy InChI
Affinity DataIC50: 9.24E+4nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in hOAT3-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 8(Rattus norvegicus)
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22889((Cimetidine) N-Methyl-N''''-[2-(5-methyl-1H-imidaz...)copy SMILEScopy InChI
Affinity DataIC50: 1.66E+5nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in rOAT3-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 8(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50367502(CILASTATIN)copy SMILEScopy InChI
Affinity DataIC50: 2.49E+5nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in hOAT3-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMedDrugBank
TargetSolute carrier family 22 member 7(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM20688((3R,5R)-7-[(1S,2S,6S,8S,8aR)-6-hydroxy-2-methyl-8-...)copy SMILEScopy InChI
Affinity DataIC50: 3.52E+5nMAssay Description:TP_TRANSPORTER: inhibition of PGF2alpha uptake (PGF2: 50nM) in hOAT2-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMedDrugBank
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM20688((3R,5R)-7-[(1S,2S,6S,8S,8aR)-6-hydroxy-2-methyl-8-...)copy SMILEScopy InChI
Affinity DataIC50: 4.08E+5nMAssay Description:TP_TRANSPORTER: inhibition of PHA uptake (PHA: 5uM) in hOAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMedDrugBank
TargetSolute carrier family 22 member 7(Rattus norvegicus)
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM20688((3R,5R)-7-[(1S,2S,6S,8S,8aR)-6-hydroxy-2-methyl-8-...)copy SMILEScopy InChI
Affinity DataIC50: 4.49E+5nMAssay Description:TP_TRANSPORTER: inhibition of PGF2alpha uptake (PGF2: 50nM) in rOAT2-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 11(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50344964(Betamipron | CHEMBL1231530 | N-(phenylcarbonyl)-be...)copy SMILEScopy InChI
Affinity DataIC50: 4.83E+5nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in hOAT4-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22889((Cimetidine) N-Methyl-N''''-[2-(5-methyl-1H-imidaz...)copy SMILEScopy InChI
Affinity DataIC50: 4.92E+5nMAssay Description:TP_TRANSPORTER: inhibition of PHA uptake (PHA: 5uM) in hOAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 11(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM20688((3R,5R)-7-[(1S,2S,6S,8S,8aR)-6-hydroxy-2-methyl-8-...)copy SMILEScopy InChI
Affinity DataIC50: 5.91E+5nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in hOAT4-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMedDrugBank
TargetSolute carrier family 22 member 7(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataIC50: 6.68E+5nMAssay Description:TP_TRANSPORTER: inhibition of PGF2alpha uptake (PGF2: 50nM) in hOAT2-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMedDrugBank
TargetSolute carrier family 22 member 8(Rattus norvegicus)
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50367502(CILASTATIN)copy SMILEScopy InChI
Affinity DataIC50: 7.42E+5nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in rOAT3-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 7(Rattus norvegicus)
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataIC50: 9.77E+5nMAssay Description:TP_TRANSPORTER: inhibition of PGF2alpha uptake (PGF2: 50nM) in rOAT2-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 7(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50390999(CEFOPERAZONE)copy SMILEScopy InChI
Affinity DataIC50: 1.33E+6nMAssay Description:TP_TRANSPORTER: inhibition of PGF2alpha in OAT2-S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CC11SXPubMed
TargetSolute carrier family 22 member 7(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM82898((6R,7R)-3-(acetoxymethyl)-8-keto-7-[[2-(2-thienyl)...)copy SMILEScopy InChI
Affinity DataIC50: 1.41E+6nMAssay Description:TP_TRANSPORTER: inhibition of PGF2alpha in OAT2-S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CC11SXPubMedDrugBank
TargetSolute carrier family 22 member 7(Rattus norvegicus)
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM82898((6R,7R)-3-(acetoxymethyl)-8-keto-7-[[2-(2-thienyl)...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+6nMAssay Description:TP_TRANSPORTER: inhibition of PGF2alpha in OAT2-S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CC11SXPubMed
TargetSolute carrier family 22 member 7(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50350468(CEFAMANDOLE)copy SMILEScopy InChI
Affinity DataIC50: 1.57E+6nMAssay Description:TP_TRANSPORTER: inhibition of PGF2alpha in OAT2-S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CC11SXPubMedDrugBank
TargetSolute carrier family 22 member 7(Rattus norvegicus)
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50390999(CEFOPERAZONE)copy SMILEScopy InChI
Affinity DataIC50: 1.62E+6nMAssay Description:TP_TRANSPORTER: inhibition of PGF2alpha in OAT2-S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CC11SXPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22889((Cimetidine) N-Methyl-N''''-[2-(5-methyl-1H-imidaz...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:TP_TRANSPORTER: inhibition of PHA uptake (PHA: 5uM) in rOAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 11(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM22889((Cimetidine) N-Methyl-N''''-[2-(5-methyl-1H-imidaz...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:TP_TRANSPORTER: inhibition of ES uptake (ES: 50nM) in hOAT4-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50367502(CILASTATIN)copy SMILEScopy InChI
Affinity DataIC50: 2.39E+6nMAssay Description:TP_TRANSPORTER: inhibition of PHA uptake (PHA: 5uM) in rOAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50367502(CILASTATIN)copy SMILEScopy InChI
Affinity DataIC50: 2.55E+6nMAssay Description:TP_TRANSPORTER: inhibition of PHA uptake (PHA: 5uM) in hOAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q27M0915PubMedDrugBank
TargetSolute carrier family 22 member 7(Rattus norvegicus)
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50350468(CEFAMANDOLE)copy SMILEScopy InChI
Affinity DataIC50: 3.18E+6nMAssay Description:TP_TRANSPORTER: inhibition of PGF2alpha in OAT2-S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CC11SXPubMed
TargetSolute carrier family 22 member 7(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50350473(Aliporina | CEFALORIDINE)copy SMILEScopy InChI
Affinity DataIC50: 4.48E+6nMAssay Description:TP_TRANSPORTER: inhibition of PGF2alpha in OAT2-S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CC11SXPubMed
TargetSolute carrier family 22 member 7(Homo sapiens (Human))
Nagoya University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50335523((6R,7R)-3-(acetoxymethyl)-7-(2-(2-aminothiazol-4-y...)copy SMILEScopy InChI
Affinity DataIC50: 4.68E+6nMAssay Description:TP_TRANSPORTER: inhibition of PGF2alpha in OAT2-S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CC11SXPubMed
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