Found 32 with Last Name = 'zhang' and Initial = 'xl' 
3D Structure (crystal)
TargetReverse transcriptase(Human immunodeficiency virus 1)
Wuhan Institute of Technology
Curated by ChEMBL
Wuhan Institute of Technology
Curated by ChEMBL
Affinity DataIC50: 5.86E+3nMAssay Description:Inhibition of recombinant wild type HIV-1 reverse transcriptase p66/p51 using poly(rA)/oligo(dT)16 as template/primer after 40 mins by ELISAMore data for this Ligand-Target Pair
TargetReverse transcriptase(Human immunodeficiency virus 1)
Wuhan Institute of Technology
Curated by ChEMBL
Wuhan Institute of Technology
Curated by ChEMBL
Affinity DataIC50: 5.93E+3nMAssay Description:Inhibition of recombinant wild type HIV-1 reverse transcriptase p66/p51 using poly(rA)/oligo(dT)16 as template/primer after 40 mins by ELISAMore data for this Ligand-Target Pair
TargetReverse transcriptase(Human immunodeficiency virus 1)
Wuhan Institute of Technology
Curated by ChEMBL
Wuhan Institute of Technology
Curated by ChEMBL
Affinity DataIC50: 6.06E+3nMAssay Description:Inhibition of recombinant wild type HIV-1 reverse transcriptase p66/p51 using poly(rA)/oligo(dT)16 as template/primer after 40 mins by ELISAMore data for this Ligand-Target Pair
Affinity DataIC50: 9.90E+3nMAssay Description:The compound was evaluated for the antagonistic activity against beta-1 adrenergic receptorMore data for this Ligand-Target Pair
In DepthDetails
TargetReverse transcriptase(Human immunodeficiency virus 1)
Wuhan Institute of Technology
Curated by ChEMBL
Wuhan Institute of Technology
Curated by ChEMBL
Affinity DataIC50: 2.52E+4nMAssay Description:Inhibition of recombinant wild type HIV-1 reverse transcriptase p66/p51 using poly(rA)/oligo(dT)16 as template/primer after 40 mins by ELISAMore data for this Ligand-Target Pair
Affinity DataIC50: 3.02E+4nMAssay Description:In vitro concentration required to inhibit partially purified dihydropteroate synthase of Escherichia coli by 50%More data for this Ligand-Target Pair
In DepthDetails
Affinity DataIC50: 3.54E+4nMAssay Description:In vitro inhibitory activity against beta-2 adrenergic receptor was measured by the inhibition of isoproterenol-induced relaxation of PGF2-alpha cont...More data for this Ligand-Target Pair
In DepthDetails
Affinity DataIC50: 4.53E+4nMAssay Description:In vitro concentration required to inhibit partially purified dihydropteroate synthase of Escherichia coli by 50%More data for this Ligand-Target Pair
In DepthDetails
Affinity DataIC50: 6.34E+4nMAssay Description:In vitro inhibitory activity against beta-2 adrenergic receptor was measured by the inhibition of isoproterenol-induced relaxation of PGF2-alpha cont...More data for this Ligand-Target Pair
In DepthDetails
Affinity DataIC50: 6.41E+4nMAssay Description:The compound was evaluated for the antagonistic activity against beta-2 adrenergic receptor.More data for this Ligand-Target Pair
In DepthDetails
Affinity DataIC50: 8.25E+4nMAssay Description:In vitro concentration required to inhibit partially purified dihydropteroate synthase of Escherichia coli by 50%More data for this Ligand-Target Pair
In DepthDetails
Affinity DataIC50: 8.76E+4nMAssay Description:In vitro concentration required to inhibit partially purified dihydropteroate synthase of Escherichia coli by 50%More data for this Ligand-Target Pair
In DepthDetails
Affinity DataIC50: 8.78E+4nMAssay Description:The compound was evaluated for the antagonistic activity against beta-2 adrenergic receptor.More data for this Ligand-Target Pair
In DepthDetails
Affinity DataIC50: 9.36E+4nMAssay Description:In vitro concentration required to inhibit partially purified dihydropteroate synthase of Escherichia coli by 50%More data for this Ligand-Target Pair
In DepthDetails
TargetReverse transcriptase(Human immunodeficiency virus 1)
Wuhan Institute of Technology
Curated by ChEMBL
Wuhan Institute of Technology
Curated by ChEMBL
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant wild type HIV-1 reverse transcriptase p66/p51 using poly(rA)/oligo(dT)16 as template/primer after 40 mins by ELISAMore data for this Ligand-Target Pair
Affinity DataIC50: 1.54E+5nMAssay Description:In vitro inhibitory activity against beta-2 adrenergic receptor was measured by the inhibition of isoproterenol-induced relaxation of PGF2-alpha cont...More data for this Ligand-Target Pair
Affinity DataIC50: 2.59E+5nMAssay Description:In vitro inhibitory activity against beta-2 adrenergic receptor was measured by the inhibition of isoproterenol-induced relaxation of PGF2-alpha cont...More data for this Ligand-Target Pair
Affinity DataIC50: 5.07E+5nMAssay Description:The compound was evaluated for the antagonistic activity against beta-2 adrenergic receptor.More data for this Ligand-Target Pair
In DepthDetails
