Compile Data Set for Download or QSAR
Report error Found 247 with Last Name = 'de martino' and Initial = 'g'
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Sapienza University of Rome

Curated by ChEMBL
LigandPNGBDBM50169065(2-Methyl-5-nitro-1-[2-(phenyl-thiophen-2-yl-methox...)
Affinity DataEC50:  30nMAssay Description:Concentration required to inhibit HIV-1 reverse transcriptase activity (wild-type) enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Sapienza University of Rome

Curated by ChEMBL
LigandPNGBDBM50169063(Benzhydryl-[2-(2-methyl-5-nitro-imidazol-1-yl)-eth...)
Affinity DataEC50:  8.00E+3nMAssay Description:Concentration required to inhibit HIV-1 reverse transcriptase activity (wild-type) by 50%More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Sapienza University of Rome

Curated by ChEMBL
LigandPNGBDBM2483(Sustiva | DMP-266 | (4S)-6-chloro-4-(2-cyclopropyl...)
Affinity DataEC50:  4nMAssay Description:Concentration required to inhibit HIV-1 reverse transcriptase activity (wild-type) by 50%More data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Sapienza University of Rome

Curated by ChEMBL
LigandPNGBDBM50169066(1-(2-Benzhydrylsulfanyl-ethyl)-2-methyl-5-nitro-1H...)
Affinity DataEC50:  2.30E+3nMAssay Description:Concentration required to inhibit HIV-1 reverse transcriptase activity of wild-type enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Sapienza University of Rome

Curated by ChEMBL
LigandPNGBDBM1434(BI-RG-587 | 2-cyclopropyl-7-methyl-2,4,9,15-tetraa...)
Affinity DataEC50:  250nMAssay Description:Concentration required to inhibit HIV-1 reverse transcriptase activity (wild-type) by 50%More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2278(5Cl3PhSO2-2IndolCONH2 | 3-(benzenesulfonyl)-5-chlo...)
Affinity DataIC50: 25nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2482(5-chloro-3-[(3,5-dimethylbenzene)sulfonyl]-1H-indo...)
Affinity DataIC50: 31nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2483(Sustiva | DMP-266 | (4S)-6-chloro-4-(2-cyclopropyl...)
Affinity DataIC50: 33nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2481(5-chloro-3-[(4-methylbenzene)sulfonyl]-1H-indole-2...)
Affinity DataIC50: 72nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1127,Y768C]/[588-1147,Y768C](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2483(Sustiva | DMP-266 | (4S)-6-chloro-4-(2-cyclopropyl...)
Affinity DataIC50: 85nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
TargetGag-Pol polyprotein [588-1127,Y768C]/[588-1147,Y768C](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2481(5-chloro-3-[(4-methylbenzene)sulfonyl]-1H-indole-2...)
Affinity DataIC50: 110nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1127,Y768C]/[588-1147,Y768C](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2482(5-chloro-3-[(3,5-dimethylbenzene)sulfonyl]-1H-indo...)
Affinity DataIC50: 130nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1127,Y768C]/[588-1147,Y768C](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2278(5Cl3PhSO2-2IndolCONH2 | 3-(benzenesulfonyl)-5-chlo...)
Affinity DataIC50: 160nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2409(2-methyl-1-{2-[(2-methylphenyl)(phenyl)methoxy]eth...)
Affinity DataIC50: 200nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2412(2-methyl-1-{2-[(3-methylphenyl)(phenyl)methoxy]eth...)
Affinity DataIC50: 300nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2415(1-{2-[alpha-(3-Nitrophenyl)phenylmethoxy]ethyl}-2-...)
Affinity DataIC50: 300nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2410(1-{2-[alpha-(2-Fluorophenyl)phenylmethoxy]ethyl}-2...)
Affinity DataIC50: 400nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2413(1-{2-[alpha-(3-Fluorophenyl)phenylmethoxy]ethyl}-2...)
Affinity DataIC50: 500nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2414(1-{2-[(3-chlorophenyl)(phenyl)methoxy]ethyl}-2-met...)
Affinity DataIC50: 500nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2411(1-{2-[(2-chlorophenyl)(phenyl)methoxy]ethyl}-2-met...)
Affinity DataIC50: 600nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM1434(BI-RG-587 | 2-cyclopropyl-7-methyl-2,4,9,15-tetraa...)
Affinity DataIC50: 2.80E+3nMpH: 7.9 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027,K690N]/[588-1147,K690N](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2483(Sustiva | DMP-266 | (4S)-6-chloro-4-(2-cyclopropyl...)
Affinity DataIC50: 3.40E+3nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
TargetN-acylethanolamine-hydrolyzing acid amidase(Human)
University of Salerno

Curated by ChEMBL
LigandPNGBDBM50171299(N-pentadecylcyclohexanecarboxamide | Cyclohexaneca...)
Affinity DataIC50: 4.50E+3nMAssay Description:Inhibition of NAAAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027,K690N]/[588-1147,K690N](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2481(5-chloro-3-[(4-methylbenzene)sulfonyl]-1H-indole-2...)
Affinity DataIC50: 5.00E+3nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027,K690N]/[588-1147,K690N](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2482(5-chloro-3-[(3,5-dimethylbenzene)sulfonyl]-1H-indo...)
Affinity DataIC50: 5.00E+3nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027,K690N]/[588-1147,K690N](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2278(5Cl3PhSO2-2IndolCONH2 | 3-(benzenesulfonyl)-5-chlo...)
Affinity DataIC50: 5.00E+3nMpH: 7.8 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetN-acylethanolamine-hydrolyzing acid amidase(Human)
University of Salerno

Curated by ChEMBL
LigandPNGBDBM50309176(N-Pentadecyl-benzamide | N-pentadecylbenzamide | C...)
Affinity DataIC50: 8.30E+3nMAssay Description:Inhibition of NAAAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetN-acylethanolamine-hydrolyzing acid amidase(Human)
University of Salerno

Curated by ChEMBL
LigandPNGBDBM50309177(cyclopentyl palmitate | CHEMBL590884)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant NAAA expressed in human HEK293 cells assessed as conversion of [1,2-14C]palmitoylethanolamine to [1,2-14C]ethanolamin...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetN-acylethanolamine-hydrolyzing acid amidase(Human)
University of Salerno

Curated by ChEMBL
LigandPNGBDBM50171299(N-pentadecylcyclohexanecarboxamide | Cyclohexaneca...)
Affinity DataIC50: 1.70E+4nMAssay Description:Inhibition of human recombinant NAAA expressed in human HEK293 cells assessed as conversion of [1,2-14C]palmitoylethanolamine to [1,2-14C]ethanolamin...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetN-acylethanolamine-hydrolyzing acid amidase(Human)
University of Salerno

Curated by ChEMBL
LigandPNGBDBM50171291(cyclohexyl palmitate | Hexadecanoic acid cyclohexy...)
Affinity DataIC50: 1.90E+4nMAssay Description:Inhibition of NAAAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rat)
Institute of Biomolecular Chemistry

Curated by ChEMBL
LigandPNGBDBM50175107((5Z,8Z,11Z,14Z)-N-(4-morpholinophenyl)icosa-5,8,11...)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory activity against rat brain FAAH by [14C]anandamide hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rat)
Institute of Biomolecular Chemistry

Curated by ChEMBL
LigandPNGBDBM50175120(N-(4-methoxyphenethyl)oleamide | CHEMBL199702)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory activity against rat brain FAAH by [14C]anandamide hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rat)
Institute of Biomolecular Chemistry

Curated by ChEMBL
LigandPNGBDBM50175119(N-(3,5-dimethoxyphenethyl)oleamide | CHEMBL199402)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory activity against rat brain FAAH by [14C]anandamide hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rat)
Institute of Biomolecular Chemistry

Curated by ChEMBL
LigandPNGBDBM50175108((5Z,8Z,11Z,14Z)-1-(4-(4-fluorophenyl)piperazin-1-y...)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory activity against rat brain FAAH by [14C]anandamide hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rat)
Institute of Biomolecular Chemistry

Curated by ChEMBL
LigandPNGBDBM50175117(N-(4-methoxybenzyl)oleamide | CHEMBL372530)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory activity against rat brain FAAH by [14C]anandamide hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rat)
Institute of Biomolecular Chemistry

Curated by ChEMBL
LigandPNGBDBM50175122(N-(4-methoxyphenyl)oleamide | CHEMBL199960)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory activity against rat brain FAAH by [14C]anandamide hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rat)
Institute of Biomolecular Chemistry

Curated by ChEMBL
LigandPNGBDBM50175126((5Z,8Z,11Z,14Z)-N-(2,4-dimethoxybenzyl)icosa-5,8,1...)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory activity against rat brain FAAH by [14C]anandamide hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rat)
Institute of Biomolecular Chemistry

Curated by ChEMBL
LigandPNGBDBM50175109(N-(2,4-dimethoxyphenethyl)oleamide | CHEMBL199649)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory activity against rat brain FAAH by [14C]anandamide hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetN-acylethanolamine-hydrolyzing acid amidase(Human)
University of Salerno

Curated by ChEMBL
LigandPNGBDBM50171286(N-(3-hydroxy-propionyl)pentadecanamide | 3-Hydroxy...)
Affinity DataIC50: 3.20E+4nMAssay Description:Inhibition of NAAAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGag-Pol polyprotein [588-1027]/[588-1147](Human immunodeficiency virus type 1)
Sapienza University of Rome

LigandPNGBDBM2484(1-(benzenesulfonyl)-2-nitrobenzene | 2NO2Ph-SO2-Ph...)
Affinity DataIC50: 5.05E+4nMpH: 7.9 T: 2°CAssay Description:The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetN-acylethanolamine-hydrolyzing acid amidase(Human)
University of Salerno

Curated by ChEMBL
LigandPNGBDBM50171294(CHEMBL138543 | Propionic acid hexadecyl ester | HE...)
Affinity DataIC50: 5.40E+4nMAssay Description:Inhibition of NAAAMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSodium-dependent dopamine transporter(Human)
Niddk

Curated by ChEMBL
LigandPNGBDBM50183549((S)-(+)-4-[2-[bis-(4-fluorophenyl)methoxy]ethyl]-1...)
Affinity DataKi:  0.400nMAssay Description:Displacement of [125I]RTI-55 from DATMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSodium-dependent dopamine transporter(Human)
Niddk

Curated by ChEMBL
LigandPNGBDBM50183539(CHEMBL381256 | CHEMBL429492 | trans-(R,R)-4-[2-[bi...)
Affinity DataKi:  0.5nMAssay Description:Displacement of [125I]RTI-55 from DATMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCannabinoid receptor 2(Human)
Institute of Biomolecular Chemistry

Curated by ChEMBL
LigandPNGBDBM50072775(ChEMBL_75020 | 5-(1,1-Dimethyl-heptyl)-2-[(1R,2R,5...)
Affinity DataKi:  0.700nMAssay Description:Displacement of [3H]CP-55940 from human recombinant CB2 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
TargetSodium-dependent dopamine transporter(Human)
Niddk

Curated by ChEMBL
LigandPNGBDBM50183535((R)-(+)-4-[2-[bis-(4-fluorophenyl)methoxy]ethyl]-1...)
Affinity DataKi:  0.800nMAssay Description:Displacement of [125I]RTI-55 from DATMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSodium-dependent dopamine transporter(Human)
Niddk

Curated by ChEMBL
LigandPNGBDBM50183540((S)-(-)-4-[2-[bis-(4-fluorophenyl)methoxy]ethyl]-1...)
Affinity DataKi:  0.900nMAssay Description:Displacement of [125I]RTI-55 from DATMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSodium-dependent dopamine transporter(Human)
Niddk

Curated by ChEMBL
LigandPNGBDBM50183545(R-(-)-4-[2-[bis-(4-fluorophenyl)methoxy]ethyl]-1-(...)
Affinity DataKi:  0.900nMAssay Description:Displacement of [125I]RTI-55 from DATMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSodium-dependent dopamine transporter(Human)
Niddk

Curated by ChEMBL
LigandPNGBDBM50183532(4-[2-[bis-(4-fluorophenyl)methoxy]ethyl]-1-(3,4-di...)
Affinity DataKi:  1.10nMAssay Description:Displacement of [125I]RTI-55 from DATMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSodium-dependent dopamine transporter(Human)
Niddk

Curated by ChEMBL
LigandPNGBDBM50183546(S-(+)-4-[2-[bis-(4-fluorophenyl)methoxy]ethyl]-1-(...)
Affinity DataKi:  1.30nMAssay Description:Displacement of [125I]RTI-55 from DATMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSodium-dependent dopamine transporter(Human)
Niddk

Curated by ChEMBL
LigandPNGBDBM50183547(CHEMBL206128 | CHEMBL255065 | trans-(S,S)-4-[2-[bi...)
Affinity DataKi:  1.40nMAssay Description:Displacement of [125I]RTI-55 from DATMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Displayed 1 to 50 (of 247 total ) | Next | Last >>
Jump to: