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Found 44 with Last Name = 'barrow' and Initial = 'cj'
TargetSubstance-K receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030096((R)-11-{Hydroxy-[4-methoxy-3-(3-methyl-but-2-enyl)...)
Affinity DataKi:  120nMAssay Description:Displacement of [125I]-NKA substance P binding to human urinary bladder membrane protein (NK2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030095((R)-11-{Hydroxy-[4-methoxy-3-(2-methyl-butyl)-phen...)
Affinity DataKi:  120nMAssay Description:Displacement of [125I]-NKA substance P binding to human urinary bladder membrane protein (NK2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030095((R)-11-{Hydroxy-[4-methoxy-3-(2-methyl-butyl)-phen...)
Affinity DataKi:  120nMAssay Description:Displacement of [125I]- substance P binding to human astrocytoma cells (NK1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030096((R)-11-{Hydroxy-[4-methoxy-3-(3-methyl-but-2-enyl)...)
Affinity DataKi:  120nMAssay Description:Displacement of [125I]- substance P binding to human astrocytoma cells (NK1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030099((R)-5-(1H-Indol-3-ylmethyl)-17-isopropyl-11-[4-met...)
Affinity DataKi:  2.50E+3nMAssay Description:Displacement of [125I]- substance P binding to human astrocytoma cells (NK1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030092((R)-11-{Hydroxy-[4-hydroxy-3-(3-methyl-but-2-enyl)...)
Affinity DataKi:  3.80E+3nMAssay Description:Displacement of [125I]-NKA substance P binding to human urinary bladder membrane protein (NK2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030092((R)-11-{Hydroxy-[4-hydroxy-3-(3-methyl-but-2-enyl)...)
Affinity DataKi:  3.80E+3nMAssay Description:Displacement of [125I]- substance P binding to human astrocytoma cells (NK1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030094((R)-11-[Hydroxy-(4-methoxy-phenyl)-methyl]-5-(1H-i...)
Affinity DataKi:  1.80E+4nMAssay Description:Displacement of [125I]-NKA substance P binding to human urinary bladder membrane protein (NK2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030094((R)-11-[Hydroxy-(4-methoxy-phenyl)-methyl]-5-(1H-i...)
Affinity DataKi:  1.80E+4nMAssay Description:Displacement of [125I]- substance P binding to human astrocytoma cells (NK1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50407271(CHEMBL2112592)
Affinity DataKi:  2.70E+4nMAssay Description:Displacement of [125I]-NKA substance P binding to human urinary bladder membrane protein (NK2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50407272(CHEMBL2111789)
Affinity DataKi:  3.10E+4nMAssay Description:Displacement of [125I]-NKA substance P binding to human urinary bladder membrane protein (NK2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50407271(CHEMBL2112592)
Affinity DataKi:  4.80E+4nMAssay Description:Displacement of [125I]- substance P binding to human astrocytoma cells (NK1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030091((R)-5-(1H-Indol-3-ylmethyl)-17-isopropyl-11-(4-met...)
Affinity DataKi:  7.20E+4nMAssay Description:Displacement of [125I]- substance P binding to human astrocytoma cells (NK1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030091((R)-5-(1H-Indol-3-ylmethyl)-17-isopropyl-11-(4-met...)
Affinity DataKi:  7.30E+4nMAssay Description:Displacement of [125I]-NKA substance P binding to human urinary bladder membrane protein (NK2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50407272(CHEMBL2111789)
Affinity DataKi:  9.30E+4nMAssay Description:Displacement of [125I]- substance P binding to human astrocytoma cells (NK1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50292436(CHEMBL515179 | spiroquinazoline)
Affinity DataKi:  9.50E+4nMAssay Description:Displacement of [3H]substance P from NK1 receptor in human astrocytoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030097((R)-11-[Hydroxy-(4-hydroxy-phenyl)-methyl]-5-(1H-i...)
Affinity DataKi: >1.00E+5nMAssay Description:Displacement of [125I]- substance P binding to human astrocytoma cells (NK1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030098((R)-11-(4-Hydroxy-benzyl)-5-(1H-indol-3-ylmethyl)-...)
Affinity DataKi: >1.00E+5nMAssay Description:Displacement of [125I]-NKA substance P binding to human urinary bladder membrane protein (NK2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030098((R)-11-(4-Hydroxy-benzyl)-5-(1H-indol-3-ylmethyl)-...)
Affinity DataKi: >1.00E+5nMAssay Description:Displacement of [125I]- substance P binding to human astrocytoma cells (NK1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030090((R)-11-(1H-Indol-5-ylmethyl)-5-(1H-indol-3-ylmethy...)
Affinity DataKi: >1.00E+5nMAssay Description:Displacement of [125I]- substance P binding to human astrocytoma cells (NK1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030090((R)-11-(1H-Indol-5-ylmethyl)-5-(1H-indol-3-ylmethy...)
Affinity DataKi: >1.00E+5nMAssay Description:Displacement of [125I]-NKA substance P binding to human urinary bladder membrane protein (NK2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50030097((R)-11-[Hydroxy-(4-hydroxy-phenyl)-methyl]-5-(1H-i...)
Affinity DataKi: >1.00E+5nMAssay Description:Displacement of [125I]-NKA substance P binding to human urinary bladder membrane protein (NK2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50292437(CHEMBL480101 | acyl aszonalenin)
Affinity DataKi:  1.70E+5nMAssay Description:Displacement of [3H]substance P from NK1 receptor in human astrocytoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin alpha-L(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50412085(CHEMBL455056)
Affinity DataIC50:  180nMAssay Description:Inhibition of LFA1 expressed in human JY cells interaction with ICAM1-IG expressed in human HeLa cell monolayer after 45 mins by cell adhesion assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50292417((3S,5aR,10bR,11aS,3'S,5'R,11'R)-3,3'-Dibenzyl-2,3,...)
Affinity DataIC50:  230nMAssay Description:Inhibition of substance P receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50286412((3S,5aR,11aS,3'S,5'aR,11'aS)-3,3'-Dibenzyl-2,3,5a,...)
Affinity DataIC50:  240nMAssay Description:Antagonistic activity against Tachykinin receptor 1More data for this Ligand-Target Pair
In DepthDetails Article
TargetIntegrin alpha-L(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50378060(CUCURBITACIN B)
Affinity DataIC50:  300nMAssay Description:Inhibition of LFA1 expressed in human JY cells interaction with ICAM1-IG expressed in human HeLa cell monolayer after 45 mins by cell adhesion assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50286416((3S,5aR,11aS,3'S,5'aR,11'aS)-3,3'-Dibenzyl-10-meth...)
Affinity DataIC50:  440nMAssay Description:Antagonistic activity against Tachykinin receptor 1More data for this Ligand-Target Pair
In DepthDetails Article
TargetIntegrin alpha-L(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50412087(CUCURBITACIN I | NSC-521777)
Affinity DataIC50:  950nMAssay Description:Inhibition of LFA1 expressed in human JY cells interaction with ICAM1-IG expressed in human HeLa cell monolayer after 45 mins by cell adhesion assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin alpha-L(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50412086(CHEMBL492404)
Affinity DataIC50:  1.36E+3nMAssay Description:Inhibition of LFA1 expressed in human JY cells interaction with ICAM1-IG expressed in human HeLa cell monolayer after 45 mins by cell adhesion assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50286409((3S,5aR,11aS,3'S,5'aR,11'aS)-3,3'-Dibenzyl-10,10'-...)
Affinity DataIC50:  5.70E+3nMAssay Description:Antagonistic activity against Tachykinin receptor 1More data for this Ligand-Target Pair
In DepthDetails Article
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50292416(CHEMBL501675 | Ditryptophenaline)
Affinity DataIC50:  1.20E+4nMAssay Description:Inhibition of substance P receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50286418((3S,5aR,10bR,11aS)-10b-(5-Amino-2-methoxy-benzyl)-...)
Affinity DataIC50:  2.60E+4nMAssay Description:Antagonistic activity against Tachykinin receptor 1More data for this Ligand-Target Pair
In DepthDetails Article
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50286410((3S,5aS,10bS,11aS)-10b-(5-Amino-2-methoxy-benzyl)-...)
Affinity DataIC50:  3.80E+4nMAssay Description:Antagonistic activity against Tachykinin receptor 1More data for this Ligand-Target Pair
In DepthDetails Article
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50286411((3S,5aR,10bR,11aS)-3-Benzyl-10b-(2-hydroxy-5-nitro...)
Affinity DataIC50:  4.80E+4nMAssay Description:Antagonistic activity against Tachykinin receptor 1More data for this Ligand-Target Pair
In DepthDetails Article
TargetIntegrin alpha-L(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292420(CHEMBL480112 | Cucurbitacin R)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of LFA1 expressed in human JY cells interaction with ICAM1-IG expressed in human HeLa cell monolayer after 45 mins by cell adhesion assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin alpha-L(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292421(CHEMBL480111 | Cucurbitacin L)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of LFA1 expressed in human JY cells interaction with ICAM1-IG expressed in human HeLa cell monolayer after 45 mins by cell adhesion assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50286406((3S,5aR,10bR,11aS)-3-Benzyl-10b-(2-methoxy-5-nitro...)
Affinity DataIC50:  5.40E+4nMAssay Description:Antagonistic activity against Tachykinin receptor 1More data for this Ligand-Target Pair
In DepthDetails Article
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50286417((3S,5aS,10bS,11aS)-3-Benzyl-10b-(2-methoxy-5-nitro...)
Affinity DataIC50:  8.80E+4nMAssay Description:Antagonistic activity against Tachykinin receptor 1More data for this Ligand-Target Pair
In DepthDetails Article
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50286413((3S,5aS,10bS,11aS)-3-Benzyl-10b-(2-hydroxy-5-nitro...)
Affinity DataIC50:  9.80E+4nMAssay Description:Antagonistic activity against Tachykinin receptor 1More data for this Ligand-Target Pair
In DepthDetails Article
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50286408((3S,5aR,10bR,11aS)-3-Benzyl-2,10b-bis-(2-hydroxy-5...)
Affinity DataIC50: >1.00E+5nMAssay Description:Antagonistic activity against Tachykinin receptor 1More data for this Ligand-Target Pair
In DepthDetails Article
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50286407((3S,5aR,10bS,11aS)-3-Benzyl-10b-hydroxy-2,3,6,10b,...)
Affinity DataIC50: >1.00E+5nMAssay Description:Antagonistic activity against Tachykinin receptor 1More data for this Ligand-Target Pair
In DepthDetails Article
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50286415((3S,5aS,10bR,11aS)-3-Benzyl-10b-hydroxy-2,3,6,10b,...)
Affinity DataIC50: >1.00E+5nMAssay Description:Antagonistic activity against Tachykinin receptor 1More data for this Ligand-Target Pair
In DepthDetails Article
TargetSubstance-P receptor(Homo sapiens (Human))
Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL
LigandPNGBDBM50286414((3S,5aS,10bS,11aS)-3-Benzyl-2,10b-bis-(2-hydroxy-5...)
Affinity DataIC50: >1.00E+5nMAssay Description:Antagonistic activity against Tachykinin receptor 1More data for this Ligand-Target Pair
In DepthDetails Article