Compile Data Set for Download or QSAR
Found 139 of ki data for polymerid = 50004012,50004761,50004762
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50350468(CEFAMANDOLE)copy SMILEScopy InChI
Affinity DataKi:  30nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2N87C2CPubMedDrugBank
TargetSolute carrier family 22 member 6(Mus musculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50206441(2-(2,4,5,7-tetrabromo-3-hydroxy-6-oxo-6H-xanthen-9...)copy SMILEScopy InChI
Affinity DataKi:  89nMAssay Description:Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W95B35PubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50370587(CEFAZOLIN)copy SMILEScopy InChI
Affinity DataKi:  180nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2N87C2CPubMedDrugBank
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50390999(CEFOPERAZONE)copy SMILEScopy InChI
Affinity DataKi:  210nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2N87C2CPubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM82898((6R,7R)-3-(acetoxymethyl)-8-keto-7-[[2-(2-thienyl)...)copy SMILEScopy InChI
Affinity DataKi:  220nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2N87C2CPubMedDrugBank
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50049707((6R,7R)-7-{2-(2-Amino-thiazol-4-yl)-2-[(Z)-methoxy...)copy SMILEScopy InChI
Affinity DataKi:  230nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2N87C2CPubMedDrugBank
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM50485601(CHEMBL2075007)copy SMILEScopy InChI
Affinity DataKi:  400nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN76RKPubMed
TargetSolute carrier family 22 member 6(Mus musculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50270022(O2C(CH2)4CO2 dianion | adipate | adipate dianion |...)copy SMILEScopy InChI
Affinity DataKi:  410nMAssay Description:Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W95B35PubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50350473(Aliporina | CEFALORIDINE)copy SMILEScopy InChI
Affinity DataKi:  740nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2N87C2CPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM50485602(CHEMBL2075010)copy SMILEScopy InChI
Affinity DataKi:  1.10E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN76RKPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM50012957(1-((p-(2-(5-chloro-o-anisamido)ethyl)phenyl)sulfon...)copy SMILEScopy InChI
Affinity DataKi:  1.60E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7W83PubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM50485603(CHEBI:7426 | CHEMBL2074738)copy SMILEScopy InChI
Affinity DataKi:  1.90E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN76RKPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM50339185((2S)-2-(6-methoxynaphthalen-2-yl)propanoic acid | ...)copy SMILEScopy InChI
Affinity DataKi:  2.00E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q28053WWPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM50420231(CHEMBL2074600)copy SMILEScopy InChI
Affinity DataKi:  2.74E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Oat1-expressing LLC-PK1 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FQ9XW4PubMed
TargetSolute carrier family 22 member 6(Mus musculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50143424(2-(3-hydroxy-6-oxo-6H-xanthen-9-yl)benzoic acid | ...)copy SMILEScopy InChI
Affinity DataKi:  2.95E+3nMAssay Description:Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W95B35PubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50335523((6R,7R)-3-(acetoxymethyl)-7-(2-(2-aminothiazol-4-y...)copy SMILEScopy InChI
Affinity DataKi:  3.13E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2N87C2CPubMed
TargetSolute carrier family 22 member 6(Mus musculus)
University of California

Curated by ChEMBL
LigandPNGBDBM35847((15S)-prostaglandin E2 | (5Z,11alpha,13E,15S)-11,1...)copy SMILEScopy InChI
Affinity DataKi:  3.40E+3nMAssay Description:Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W95B35PubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM50009859((+-)-2-(p-isobutylphenyl)propionic acid | (+-)-alp...)copy SMILEScopy InChI
Affinity DataKi:  3.50E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q28053WWPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM17638(2-{1-[(4-chlorophenyl)carbonyl]-5-methoxy-2-methyl...)copy SMILEScopy InChI
Affinity DataKi:  4.20E+3nMAssay Description:TP_TRANSPORTER: inhibition of MTX uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20Z74JRPubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataKi:  4.30E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in OAT1-expressing CHO cellsMore data for this Ligand-Target Pair
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataKi:  4.41E+3nMAssay Description:TP_TRANSPORTER: inhibition of Ochratoxin A uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
TargetSolute carrier family 22 member 6(Mus musculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50009859((+-)-2-(p-isobutylphenyl)propionic acid | (+-)-alp...)copy SMILEScopy InChI
Affinity DataKi:  4.70E+3nMAssay Description:Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W95B35PubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50485608(CHEBI:28837 | Caprylic acid | EDENOR C 8-98-100 | ...)copy SMILEScopy InChI
Affinity DataKi:  5.41E+3nMAssay Description:TP_TRANSPORTER: inhibition of Ochratoxin A uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XD14JBPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM25903(3-(butylamino)-4-phenoxy-5-sulfamoylbenzoic acid |...)copy SMILEScopy InChI
Affinity DataKi:  5.50E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W66N2SPubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50270006(2-(4-aminobenzamido)acetate | AMINOHIPPURATE)copy SMILEScopy InChI
Affinity DataKi:  6.02E+3nMAssay Description:Inhibition of human Oat1 expressed in Drosophila S2 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TB17WFPubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50240008(Aminohippuric Acid | CHEBI:104011 | PAHA | Para-Am...)copy SMILEScopy InChI
Affinity DataKi:  6.02E+3nMAssay Description:TP_TRANSPORTER: inhibition of Ochratoxin A uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50350467(BL-S578 | CEFADROXIL | Cefadrops)copy SMILEScopy InChI
Affinity DataKi:  6.14E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2N87C2CPubMedDrugBank
TargetSolute carrier family 22 member 6(Mus musculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataKi:  6.31E+3nMAssay Description:Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hrMore data for this Ligand-Target Pair
TargetSolute carrier family 22 member 6(Mus musculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50269998((S)-2-((R)-5-chloro-8-hydroxy-3-methyl-1-oxoisochr...)copy SMILEScopy InChI
Affinity DataKi:  6.31E+3nMAssay Description:Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W95B35PubMed
TargetSolute carrier family 22 member 6(Mus musculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50270021(glutarate | glutarate(2-) | pentanedioate)copy SMILEScopy InChI
Affinity DataKi:  6.70E+3nMAssay Description:Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W95B35PubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50538736(CHEMBL4640580)copy SMILEScopy InChI
Affinity DataKi:  7.20E+3nMAssay Description:Inhibition of human OAT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20C50BSPubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50003019(8-(Hexahydro-2,5-methano-pentalen-3a-yl)-1,3-dipro...)copy SMILEScopy InChI
Affinity DataKi:  7.82E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2S183SPPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM50485600(CHEMBL2074714)copy SMILEScopy InChI
Affinity DataKi:  9.00E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN76RKPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM50344967(2-[(4-Isopropyl-cyclohexanecarbonyl)-amino]-3-phen...)copy SMILEScopy InChI
Affinity DataKi:  9.20E+3nMAssay Description:Inhibition of rat Oat1 expressed in Xenopus oocytesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TB17WFPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM50344967(2-[(4-Isopropyl-cyclohexanecarbonyl)-amino]-3-phen...)copy SMILEScopy InChI
Affinity DataKi:  9.20E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7W83PubMed
TargetSolute carrier family 22 member 6(Mus musculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50270006(2-(4-aminobenzamido)acetate | AMINOHIPPURATE)copy SMILEScopy InChI
Affinity DataKi:  9.40E+3nMAssay Description:Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W95B35PubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM25902(4-chloro-2-[(furan-2-ylmethyl)amino]-5-sulfamoylbe...)copy SMILEScopy InChI
Affinity DataKi:  9.50E+3nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W66N2SPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM17638(2-{1-[(4-chlorophenyl)carbonyl]-5-methoxy-2-methyl...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+4nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q28053WWPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM50328021((2-Hydroxy-benzoylamino)-acetic acid | 2-(2-hydrox...)copy SMILEScopy InChI
Affinity DataKi:  1.10E+4nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q28053WWPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM50328021((2-Hydroxy-benzoylamino)-acetic acid | 2-(2-hydrox...)copy SMILEScopy InChI
Affinity DataKi:  1.10E+4nMAssay Description:Inhibition of rat Oat1 expressed in Xenopus oocytesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TB17WFPubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataKi:  1.21E+4nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50344963(1-Methylpyrenyl mercapturic acid | CHEMBL1778337)copy SMILEScopy InChI
Affinity DataKi:  1.45E+4nMAssay Description:Inhibition of human Oat1 expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TB17WFPubMed
TargetSolute carrier family 22 member 6(Rattus norvegicus)
University of Rochester School of Medicine and Dentistry

Curated by ChEMBL
LigandPNGBDBM50206509(4-Dipropylsulfamoyl-benzoic acid | 4-Dipropylsulfa...)copy SMILEScopy InChI
Affinity DataKi:  1.58E+4nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
TargetSolute carrier family 22 member 6(Mus musculus)
University of California

Curated by ChEMBL
LigandPNGBDBM50240408(1-hexanecarboxylate | CH3-[CH2]5-COO(-) | enanthat...)copy SMILEScopy InChI
Affinity DataKi:  1.67E+4nMAssay Description:Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W95B35PubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM85245(CAS_36322-90-4 | NSC_4856 | Piroxicam)copy SMILEScopy InChI
Affinity DataKi:  1.98E+4nMAssay Description:TP_TRANSPORTER: inhibition of Ochratoxin A uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XD14JBPubMedDrugBank
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50420189(CHEMBL1624767)copy SMILEScopy InChI
Affinity DataKi:  2.24E+4nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R78GGZPubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin 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))
Kyorin 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 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50344964(Betamipron | CHEMBL1231530 | N-(phenylcarbonyl)-be...)copy SMILEScopy InChI
Affinity DataKi:  2.36E+4nMAssay Description:TP_TRANSPORTER: inhibition of PAH uptake in OAT1-expressing S2 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2S183SPPubMed
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
Kyorin University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50344964(Betamipron | CHEMBL1231530 | N-(phenylcarbonyl)-be...)copy SMILEScopy InChI
Affinity DataKi:  2.36E+4nMAssay Description:Inhibition of human Oat1 expressed in Drosophila S2 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TB17WFPubMed
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