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Found 77 from The First Affiliated Hospital of Dalian Medical University
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115974(CHEMBL3612170)
Affinity DataKi:  120nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115973(CHEMBL3612151)
Affinity DataKi:  120nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115978(CHEMBL3612172)
Affinity DataKi:  220nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115977(CHEMBL3612153)
Affinity DataKi:  220nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115971(CHEMBL3612150)
Affinity DataKi:  320nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115972(CHEMBL3612169)
Affinity DataKi:  320nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115976(CHEMBL3612171)
Affinity DataKi:  470nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115975(CHEMBL3612152)
Affinity DataKi:  470nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116014(CHEMBL3612160)
Affinity DataKi:  480nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116013(CHEMBL3612141)
Affinity DataKi:  480nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115962(CHEMBL3612149)
Affinity DataKi:  730nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115968(CHEMBL3612168)
Affinity DataKi:  730nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116015(CHEMBL3612142)
Affinity DataKi:  940nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116016(CHEMBL3612161)
Affinity DataKi:  940nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115960(CHEMBL3612148)
Affinity DataKi:  1.01E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115961(CHEMBL3612167)
Affinity DataKi:  1.01E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115979(CHEMBL3612154)
Affinity DataKi:  1.34E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115980(CHEMBL3612173)
Affinity DataKi:  1.34E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115958(CHEMBL3612158)
Affinity DataKi:  1.71E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115829(CHEMBL3612139)
Affinity DataKi:  1.71E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116021(CHEMBL3612145)
Affinity DataKi:  1.78E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116022(CHEMBL3612164)
Affinity DataKi:  1.78E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116020(CHEMBL3612163)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116019(CHEMBL3612144)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116018(CHEMBL3612162)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116017(CHEMBL3612143)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116011(CHEMBL3612159)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115986(CHEMBL3612236)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115985(CHEMBL3612157)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115984(CHEMBL3612175)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115983(CHEMBL3612156)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115982(CHEMBL3612174)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115981(CHEMBL3612155)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50115987(CHEMBL3612140)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116079(CHEMBL3612166)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116069(CHEMBL3612147)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116060(CHEMBL3612165)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50116023(CHEMBL3612146)
Affinity DataKi: >2.23E+3nMAssay Description:Inhibition of P-glycoprotein in human drug-resistant K562/ADR cells assessed as reduction in P-gp mediated rhodamine 123 efflux by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50357312(IBRUTINIB | PCI-32765 | US10124003, Ref. Ex. Compo...)
Affinity DataIC50:  0.300nMAssay Description:Inhibition of recombinant full-length N-terminal His-tagged human BTK expressed in baculovirus infected Sf9 insect cells using Poly(4:1 Glu,Tyr) pept...More data for this Ligand-Target Pair
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50464517(CHEMBL4294772)
Affinity DataIC50:  0.5nMAssay Description:Inhibition of recombinant full-length N-terminal His-tagged human BTK expressed in baculovirus infected Sf9 insect cells using Poly(4:1 Glu,Tyr) pept...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50464516(CHEMBL4290692)
Affinity DataIC50:  0.600nMAssay Description:Inhibition of recombinant full-length N-terminal His-tagged human BTK expressed in baculovirus infected Sf9 insect cells using Poly(4:1 Glu,Tyr) pept...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50161162(AVL-292 | CC-292 | Spebrutinib | US10596172, Compo...)
Affinity DataIC50:  0.600nMAssay Description:Inhibition of recombinant full-length N-terminal His-tagged human BTK expressed in baculovirus infected Sf9 insect cells using Poly(4:1 Glu,Tyr) pept...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50464521(CHEMBL4289281)
Affinity DataIC50:  0.690nMAssay Description:Inhibition of recombinant N-terminal GST-tagged human JAK3 (781 to end residues) expressed in baculovirus infected Sf9 insect cells using Poly(4:1 Gl...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50464526(CHEMBL4284156)
Affinity DataIC50:  0.700nMAssay Description:Inhibition of recombinant full-length N-terminal His-tagged human BTK expressed in baculovirus infected Sf9 insect cells using Poly(4:1 Glu,Tyr) pept...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50464524(CHEMBL4290449)
Affinity DataIC50:  0.700nMAssay Description:Inhibition of recombinant full-length N-terminal His-tagged human BTK expressed in baculovirus infected Sf9 insect cells using Poly(4:1 Glu,Tyr) pept...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50464513(CHEMBL4286900)
Affinity DataIC50:  0.800nMAssay Description:Inhibition of recombinant full-length N-terminal His-tagged human BTK expressed in baculovirus infected Sf9 insect cells using Poly(4:1 Glu,Tyr) pept...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50464521(CHEMBL4289281)
Affinity DataIC50:  0.800nMAssay Description:Inhibition of recombinant full-length N-terminal His-tagged human BTK expressed in baculovirus infected Sf9 insect cells using Poly(4:1 Glu,Tyr) pept...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50464516(CHEMBL4290692)
Affinity DataIC50:  0.830nMAssay Description:Inhibition of recombinant N-terminal GST-tagged human JAK3 (781 to end residues) expressed in baculovirus infected Sf9 insect cells using Poly(4:1 Gl...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50464517(CHEMBL4294772)
Affinity DataIC50:  0.910nMAssay Description:Inhibition of recombinant N-terminal GST-tagged human JAK3 (781 to end residues) expressed in baculovirus infected Sf9 insect cells using Poly(4:1 Gl...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
The First Affiliated Hospital Of Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50464524(CHEMBL4290449)
Affinity DataIC50:  0.950nMAssay Description:Inhibition of recombinant N-terminal GST-tagged human JAK3 (781 to end residues) expressed in baculovirus infected Sf9 insect cells using Poly(4:1 Gl...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
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