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LigandPNGBDBM50514847(CHEMBL4558745)
Affinity DataKd:  3.07E+3nMAssay Description:Binding affinity to AIMP2 D2X isoform (unknown origin) by fluorescence-based equilibrium binding assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2021
Entry Details Article
PubMed
LigandPNGBDBM50527599(CHEMBL4562996)
Affinity DataKd:  3.85E+3nMAssay Description:Binding affinity to AIMP2 DX2 isoform (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/25/2021
Entry Details Article
PubMed
LigandPNGBDBM50527600(CHEMBL4576024)
Affinity DataKd:  1.43E+4nMAssay Description:Binding affinity to AIMP2 DX2 isoform (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/25/2021
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50130539(2,2-Dimethyl-propionic acid 2-(3,4-dimethyl-benzyl...)
Affinity DataEC50:  790nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50130544(Benzoic acid 2-(4-tert-butyl-benzyl)-3-[3-(4-metha...)
Affinity DataEC50:  252nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50130545(Benzoic acid 2-(4-tert-butyl-benzyl)-3-[3-(4-metha...)
Affinity DataEC50:  2.79E+3nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50130548(2,2-Dimethyl-propionic acid 2-(3,4-dimethyl-benzyl...)
Affinity DataEC50:  22nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50130538(2,2-Dimethyl-propionic acid 3-[3-(4-acetylamino-be...)
Affinity DataEC50:  450nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50130546(2,2-Dimethyl-propionic acid 2-(4-tert-butyl-benzyl...)
Affinity DataEC50:  40nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50130552(Benzoic acid 2-(3,4-dimethyl-benzyl)-3-[3-(4-metha...)
Affinity DataEC50:  166nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50130551(2,2-Dimethyl-propionic acid 2-(3,4-dimethyl-benzyl...)
Affinity DataEC50:  1.70E+3nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50196337(2-((3-(4-hydroxy-3-methoxybenzyl)thioureido)methyl...)
Affinity DataEC50:  1.97nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50196343(2-((3-(4-hydroxy-3-methoxybenzyl)thioureido)methyl...)
Affinity DataEC50:  2.83nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM20461(Zostrix | (E)-N-[(4-hydroxy-3-methoxyphenyl)methyl...)
Affinity DataEC50:  44.8nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50130556(Benzoic acid 2-(3,4-dimethyl-benzyl)-3-[3-(4-metha...)
Affinity DataEC50:  1.73E+3nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50130554(2,2-Dimethyl-propionic acid 2-(3,4-dimethyl-benzyl...)
Affinity DataEC50:  1.14E+3nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rat)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50130555(2,2-Dimethyl-propionic acid 2-(3,4-dimethyl-benzyl...)
Affinity DataEC50:  990nMAssay Description:In vitro [Ca2+] influx relative to capsaicin by Rat Vanilloid receptor (VR1) expressing CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetLysine--tRNA ligase(Human)
Cha University

Curated by ChEMBL
LigandPNGBDBM50571529(CHEMBL4862068)
Affinity DataKd:  4.92E+4nMAssay Description:Binding affinity to human N-terminal His6-tagged 15N-labelled KRS (1 to 207 residues) expressed in Escherichia coli BL21(DE3) measured by flourescenc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2022
Entry Details Article
PubMed
TargetLysine--tRNA ligase(Human)
Cha University

Curated by ChEMBL
LigandPNGBDBM50571530(CHEMBL4852870)
Affinity DataKd:  5.75E+3nMAssay Description:Binding affinity to human N-terminal His6-tagged 15N-labelled KRS (1 to 207 residues) expressed in Escherichia coli BL21(DE3) measured by flourescenc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2022
Entry Details Article
PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM20321(JYL1421 | CHEMBL388824 | 3-[(4-tert-butylphenyl)me...)
Affinity DataEC50:  8nMAssay Description:Concentration required to antagonized capsaicin-induced calcium uptake at the transient receptor potential cation channel (subfamily V member 1) expr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213177((2S)-2-ethoxy-3-(4-(3-phenyl-3-(propylcarbamothioy...)
Affinity DataEC50:  3.94E+3nMAssay Description:Agonist activity at human PPARalpha in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213178((2S)-3-(4-(3-((cyclohexylmethyl)carbamothioyloxy)-...)
Affinity DataEC50:  1.07E+4nMAssay Description:Agonist activity at human PPARalpha in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213179((2R)-3-(4-(3-((4-tert-butylbenzyl)carbamothioyloxy...)
Affinity DataEC50:  380nMAssay Description:Agonist activity at human PPARalpha in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213180((2S)-2-ethoxy-3-(4-(3-(ethylcarbamothioyloxy)-3-ph...)
Affinity DataEC50:  5.39E+3nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213181((2S)-2-ethoxy-3-(4-(3-hydroxy-3-phenylpropyl)pheny...)
Affinity DataEC50:  300nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213180((2S)-2-ethoxy-3-(4-(3-(ethylcarbamothioyloxy)-3-ph...)
Affinity DataEC50:  2.04E+4nMAssay Description:Agonist activity at human PPARalpha in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213182((2S)-3-(4-(2-(benzylcarbamothioyloxy)-2-phenyletho...)
Affinity DataEC50:  6.21E+3nMAssay Description:Agonist activity at human PPARalpha in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM28681(cid_5281055 | [3H]rosiglitazone | CHEMBL121 | ROSI...)
Affinity DataEC50:  3.46E+3nMAssay Description:Agonist activity at human PPARalpha in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213177((2S)-2-ethoxy-3-(4-(3-phenyl-3-(propylcarbamothioy...)
Affinity DataEC50:  3.48E+3nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213183((2S)-3-(4-(3-(butylcarbamothioyloxy)-3-phenylpropy...)
Affinity DataEC50:  3.60E+3nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213184((2S)-3-(4-(3-(benzylcarbamoyloxy)-3-phenylpropyl)p...)
Affinity DataEC50:  1.42E+3nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213184((2S)-3-(4-(3-(benzylcarbamoyloxy)-3-phenylpropyl)p...)
Affinity DataEC50:  6.05E+3nMAssay Description:Agonist activity at human PPARalpha in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213185((2S)-3-(4-(3-(benzylcarbamothioyloxy)-3-phenylprop...)
Affinity DataEC50:  580nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213186((2R)-3-(4-(3-(benzylcarbamothioyloxy)-3-phenylprop...)
Affinity DataEC50:  350nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213187((2R)-2-ethoxy-3-(4-(3-(phenethylcarbamothioyloxy)-...)
Affinity DataEC50:  1.05E+3nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213189((2S)-2-ethoxy-3-(4-(3-(phenethylcarbamothioyloxy)-...)
Affinity DataEC50:  490nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50110590(5-(2,5-dimethylphenoxy)-2,2-dimethylpentanoic acid...)
Affinity DataEC50:  1.48E+5nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213188((2S)-3-(4-(3-((4-tert-butylbenzyl)carbamothioyloxy...)
Affinity DataEC50:  160nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213185((2S)-3-(4-(3-(benzylcarbamothioyloxy)-3-phenylprop...)
Affinity DataEC50:  70nMAssay Description:Agonist activity at human PPARalpha in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213190((2S)-2-ethoxy-3-(4-(3-phenyl-3-(phenylcarbamothioy...)
Affinity DataEC50:  5.25E+3nMAssay Description:Agonist activity at human PPARalpha in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213183((2S)-3-(4-(3-(butylcarbamothioyloxy)-3-phenylpropy...)
Affinity DataEC50:  7.26E+3nMAssay Description:Agonist activity at human PPARalpha in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213182((2S)-3-(4-(2-(benzylcarbamothioyloxy)-2-phenyletho...)
Affinity DataEC50:  7.17E+3nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213179((2R)-3-(4-(3-((4-tert-butylbenzyl)carbamothioyloxy...)
Affinity DataEC50:  140nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213191((S)-3-(4-(3-(benzylcarbamothioyloxy)propyl)phenyl)...)
Affinity DataEC50:  1.40E+3nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM28681(cid_5281055 | [3H]rosiglitazone | CHEMBL121 | ROSI...)
Affinity DataEC50:  30nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213188((2S)-3-(4-(3-((4-tert-butylbenzyl)carbamothioyloxy...)
Affinity DataEC50:  3.27E+3nMAssay Description:Agonist activity at human PPARalpha in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50110590(5-(2,5-dimethylphenoxy)-2,2-dimethylpentanoic acid...)
Affinity DataEC50:  1.93E+5nMAssay Description:Agonist activity at human PPARalpha in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213178((2S)-3-(4-(3-((cyclohexylmethyl)carbamothioyloxy)-...)
Affinity DataEC50:  1.06E+3nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor alpha(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213186((2R)-3-(4-(3-(benzylcarbamothioyloxy)-3-phenylprop...)
Affinity DataEC50:  260nMAssay Description:Agonist activity at human PPARalpha in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50213190((2S)-2-ethoxy-3-(4-(3-phenyl-3-(phenylcarbamothioy...)
Affinity DataEC50:  4.58E+3nMAssay Description:Agonist activity at human PPARgamma in CV1 cells by GAL4 transactivation assay after 24 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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