Compile Data Set for Download or QSAR
Found 48 with Last Name = 'boechat' and Initial = 'n'
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50521944(CHEMBL4204512)copy SMILEScopy InChI
Affinity DataKi:  1.30E+3nMAssay Description:Competitive inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli assessed as reduction in urea production by measu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2ZJFPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50521942(CHEMBL4216180)copy SMILEScopy InChI
Affinity DataKi:  5.10E+3nMAssay Description:Competitive inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli assessed as reduction in urea production by measu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2ZJFPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50510706(CHEMBL4515068)copy SMILEScopy InChI
Affinity DataKi:  1.70E+4nMAssay Description:Non-competitive inhibition of Leishmania amazonensis arginase using L-arginine as substrate incubated for 15 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6HJQPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50521943(CHEMBL4574177)copy SMILEScopy InChI
Affinity DataKi:  2.60E+4nMAssay Description:Competitive inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli assessed as reduction in urea production by measu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2ZJFPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50521947(CHEMBL4530523)copy SMILEScopy InChI
Affinity DataKi:  3.20E+4nMAssay Description:Competitive inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli assessed as reduction in urea production by measu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2ZJFPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50137118(CHEMBL3753575)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50137117(CHEMBL3754535)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50137116(CHEMBL378856)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50137113(CHEMBL3753096)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50137112(CHEMBL309896)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM2899((4S)-6-chloro-4-[(E)-2-cyclopropylethenyl]-4-(trif...)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM27577(5-[(3-ethyl-5-fluoro-1H-indazol-4-yl)oxy]benzene-1...)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM2898((4S)-6-chloro-4-(2-cyclopropylethynyl)-4-(trifluor...)copy SMILEScopy InChI
Affinity DataIC50: 32nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM2483((4S)-6-chloro-4-(2-cyclopropylethynyl)-4-(trifluor...)copy SMILEScopy InChI
Affinity DataIC50: 38nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM2483((4S)-6-chloro-4-(2-cyclopropylethynyl)-4-(trifluor...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Biological assay using HIV-1 reverse transcriptase.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DZ06W4
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM2955(GW420867X | HBY1293 | propan-2-yl (2S)-2-ethyl-7-f...)copy SMILEScopy InChI
Affinity DataIC50: 45nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM2912((3S,5S)-7-chloro-5-[(E)-2-cyclopropylethenyl]-3-me...)copy SMILEScopy InChI
Affinity DataIC50: 46nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM27576(5-[(5-fluoro-3-methyl-1H-indazol-4-yl)oxy]benzene-...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50137114(CHEMBL3753238)copy SMILEScopy InChI
Affinity DataIC50: 56nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50137119(CHEMBL3753009)copy SMILEScopy InChI
Affinity DataIC50: 59nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM2906((3S,5S)-7-chloro-5-(2-cyclopropylethynyl)-3-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 82nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM1434(11-cyclopropyl-5,11-dihydro-4-methyl-6H-dipyrido[3...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Biological assay using HIV-1 reverse transcriptase.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DZ06W4
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50137120(CHEMBL3753006)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM50137115(CHEMBL3754170)copy SMILEScopy InChI
Affinity DataIC50: 950nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM93122(3-Hydroxy-2-oxo-3-trifluoromethylindole, 25)copy SMILEScopy InChI
Affinity DataIC50: 3.41E+3nMAssay Description:Biological assay using HIV-1 reverse transcriptase.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DZ06W4
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM93122(3-Hydroxy-2-oxo-3-trifluoromethylindole, 25)copy SMILEScopy InChI
Affinity DataIC50: 3.41E+3nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM93121(3-Hydroxy-2-oxo-3-trifluoromethylindole, 21)copy SMILEScopy InChI
Affinity DataIC50: 3.61E+3nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM93121(3-Hydroxy-2-oxo-3-trifluoromethylindole, 21)copy SMILEScopy InChI
Affinity DataIC50: 3.61E+3nMAssay Description:Biological assay using HIV-1 reverse transcriptase.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DZ06W4
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM93119(3-Hydroxy-2-oxo-3-trifluoromethylindole, 16)copy SMILEScopy InChI
Affinity DataIC50: 6.07E+3nMAssay Description:Biological assay using HIV-1 reverse transcriptase.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DZ06W4
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM93119(3-Hydroxy-2-oxo-3-trifluoromethylindole, 16)copy SMILEScopy InChI
Affinity DataIC50: 6.07E+3nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM93120(3-Hydroxy-2-oxo-3-trifluoromethylindole, 18)copy SMILEScopy InChI
Affinity DataIC50: 7.10E+3nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM93120(3-Hydroxy-2-oxo-3-trifluoromethylindole, 18)copy SMILEScopy InChI
Affinity DataIC50: 7.10E+3nMAssay Description:Biological assay using HIV-1 reverse transcriptase.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DZ06W4
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM93123(3-Hydroxy-2-oxo-3-trifluoromethylindole, 26)copy SMILEScopy InChI
Affinity DataIC50: 8.37E+3nMAssay Description:Biological assay using HIV-1 reverse transcriptase.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DZ06W4
TargetReverse transcriptase(Human immunodeficiency virus 1)
Instituto de Tecnologia em F£rmacos

Curated by ChEMBL
LigandPNGBDBM93123(3-Hydroxy-2-oxo-3-trifluoromethylindole, 26)copy SMILEScopy InChI
Affinity DataIC50: 8.37E+3nMAssay Description:Inhibition of HIV1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G162NXPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50510709(CHEMBL4571367)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli using L-arginine as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6HJQPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50521944(CHEMBL4204512)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli assessed as reduction in urea production using L-arginine as ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2ZJFPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50521942(CHEMBL4216180)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli assessed as reduction in urea production using L-arginine as ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2ZJFPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50510706(CHEMBL4515068)copy SMILEScopy InChI
Affinity DataIC50: 1.65E+4nMAssay Description:Non-competitive inhibition of Leishmania amazonensis arginase using L-arginine as substrate incubated for 15 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6HJQPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50510706(CHEMBL4515068)copy SMILEScopy InChI
Affinity DataIC50: 1.65E+4nMAssay Description:Inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli using L-arginine as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6HJQPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50521947(CHEMBL4530523)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+4nMAssay Description:Inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli assessed as reduction in urea production using L-arginine as ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2ZJFPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50521943(CHEMBL4574177)copy SMILEScopy InChI
Affinity DataIC50: 3.80E+4nMAssay Description:Inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli assessed as reduction in urea production using L-arginine as ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2ZJFPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50510711(CHEMBL4467463)copy SMILEScopy InChI
Affinity DataIC50: 4.70E+4nMAssay Description:Inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli using L-arginine as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6HJQPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50521945(CHEMBL4216693)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli assessed as reduction in urea production using L-arginine as ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2ZJFPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50521946(CHEMBL4211729)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli assessed as reduction in urea production using L-arginine as ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2ZJFPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50510710(CHEMBL4438412)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli using L-arginine as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6HJQPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50510707(CHEMBL4541649)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli using L-arginine as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6HJQPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50510708(CHEMBL4456185)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli using L-arginine as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6HJQPubMed
TargetArginase(Leishmania amazonensis)
Universidade Federal do Rio de Janeiro

Curated by ChEMBL
LigandPNGBDBM50510712(CHEMBL4570250)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant Leishmania amazonensis arginase expressed in Escherichia coli using L-arginine as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SX6HJQPubMed