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Found 284 with Last Name = 'robbins' and Initial = 'm'
TargetSmoothened homolog(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50385635(CHEMBL2043437)
Affinity DataIC50:  5nMAssay Description:Inhibition of Smo in mouse C3H10T1/2 cells using human recombinant SHH assessed as effect on SMO/SHH transient transcriptional activation after 20 hr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSmoothened homolog(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50385642(CHEMBL2043435)
Affinity DataIC50:  5nMAssay Description:Inhibition of Smo in mouse C3H10T1/2 cells using human recombinant SHH assessed as effect on SMO/SHH transient transcriptional activation after 20 hr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSmoothened homolog(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50249522(2-chloro-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(me...)
Affinity DataIC50:  5nMAssay Description:Inhibition of Smo in mouse C3H10T1/2 cells using human recombinant SHH assessed as effect on SMO/SHH transient transcriptional activation after 20 hr...More data for this Ligand-Target Pair
TargetSmoothened homolog(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50385637(CHEMBL2043430)
Affinity DataIC50:  5nMAssay Description:Inhibition of Smo in mouse C3H10T1/2 cells using human recombinant SHH assessed as effect on SMO/SHH transient transcriptional activation after 20 hr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216194(CHEMBL391935 | N-(2-chlorophenethyl)-N-(pyrrolidin...)
Affinity DataIC50:  8nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium- and chloride-dependent glycine transporter 1(Homo sapiens (Human))
Vanderbilt University Medical Center

Curated by ChEMBL
LigandPNGBDBM50448013(CHEMBL3115220)
Affinity DataIC50:  15nMAssay Description:Inhibition of GlyT1 (unknown origin) assessed as [14C]-glycine transportMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSmoothened homolog(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50385643(CHEMBL2043436)
Affinity DataIC50:  20nMAssay Description:Inhibition of Smo in mouse C3H10T1/2 cells using human recombinant SHH assessed as effect on SMO/SHH transient transcriptional activation after 20 hr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium- and chloride-dependent glycine transporter 1(Homo sapiens (Human))
Vanderbilt University Medical Center

Curated by ChEMBL
LigandPNGBDBM50448014(CHEMBL3115219)
Affinity DataIC50:  25nMAssay Description:Inhibition of GlyT1 (unknown origin) assessed as [14C]-glycine transportMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216201(CHEMBL233987 | N-(2-methoxyphenethyl)-4-(6-aza-bic...)
Affinity DataIC50:  29nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSmoothened homolog(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50385641(CHEMBL2043434)
Affinity DataIC50:  35nMAssay Description:Inhibition of Smo in mouse C3H10T1/2 cells using human recombinant SHH assessed as effect on SMO/SHH transient transcriptional activation after 20 hr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216180(CHEMBL233799 | N-(2-methoxyphenethyl)-N-(pyrrolidi...)
Affinity DataIC50:  37nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium- and chloride-dependent glycine transporter 1(Homo sapiens (Human))
Vanderbilt University Medical Center

Curated by ChEMBL
LigandPNGBDBM50448001(CHEMBL3115206)
Affinity DataIC50:  39nMAssay Description:Inhibition of GlyT1 (unknown origin) assessed as [14C]-glycine transportMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSmoothened homolog(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50385638(CHEMBL2043432)
Affinity DataIC50:  43nMAssay Description:Inhibition of Smo in mouse C3H10T1/2 cells using human recombinant SHH assessed as effect on SMO/SHH transient transcriptional activation after 20 hr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSmoothened homolog(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50385640(CHEMBL2043433)
Affinity DataIC50:  45nMAssay Description:Inhibition of Smo in mouse C3H10T1/2 cells using human recombinant SHH assessed as effect on SMO/SHH transient transcriptional activation after 20 hr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313959((R)-N-(4-(2-(2-hydroxy-2-(pyridin-3-yl)ethylamino)...)
Affinity DataIC50:  60nMAssay Description:Displacement of [125I]cyanopindolol from human beta 2 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSmoothened homolog(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50385644(CHEMBL2043438)
Affinity DataIC50:  72nMAssay Description:Inhibition of Smo in mouse C3H10T1/2 cells using human recombinant SHH assessed as effect on SMO/SHH transient transcriptional activation after 20 hr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSmoothened homolog(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50385639(CHEMBL2043431)
Affinity DataIC50:  88nMAssay Description:Inhibition of Smo in mouse C3H10T1/2 cells using human recombinant SHH assessed as effect on SMO/SHH transient transcriptional activation after 20 hr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216199(4-(2-aza-bicyclo[2.2.1]heptan-2-ylmethyl)-N-(2-met...)
Affinity DataIC50:  95nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313973((R)-N-(4-(2-(2-hydroxy-2-(pyridin-3-yl)ethylamino)...)
Affinity DataIC50:  100nMAssay Description:Displacement of [125I]cyanopindolol from human beta 2 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216188(CHEMBL233422 | N-(2-methoxyphenethyl)-4-(((1S,2S)-...)
Affinity DataIC50:  100nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSmoothened homolog(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50385636(CHEMBL2043429)
Affinity DataIC50:  103nMAssay Description:Inhibition of Smo in mouse C3H10T1/2 cells using human recombinant SHH assessed as effect on SMO/SHH transient transcriptional activation after 20 hr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216193(CHEMBL233609 | N-(2-methoxyphenethyl)-4-(((S)-2-(m...)
Affinity DataIC50:  140nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216197(CHEMBL233610 | N-(2-methoxyphenethyl)-4-(((S)-2-(m...)
Affinity DataIC50:  160nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216181((R)-N-(2-methoxyphenethyl)-4-((diethylamino)methyl...)
Affinity DataIC50:  170nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSmoothened homolog(Mus musculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50385645(CHEMBL2043439)
Affinity DataIC50:  191nMAssay Description:Inhibition of Smo in mouse C3H10T1/2 cells using human recombinant SHH assessed as effect on SMO/SHH transient transcriptional activation after 20 hr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216204(CHEMBL394028 | N-(2-methoxyphenethyl)-4-(piperidin...)
Affinity DataIC50:  250nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216206(CHEMBL393989 | N-(2-methoxyphenethyl)-4-(benzyloxy...)
Affinity DataIC50:  310nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313971((R)-N-(4-(2-(2-hydroxy-2-(pyridin-3-yl)ethylamino)...)
Affinity DataIC50:  400nMAssay Description:Displacement of [125I]cyanopindolol from human beta 2 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313972((R)-N-(4-(2-(2-hydroxy-2-(pyridin-3-yl)ethylamino)...)
Affinity DataIC50:  400nMAssay Description:Displacement of [125I]cyanopindolol from human beta 2 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313958((R)-N-(4-(2-(2-hydroxy-2-(pyridin-3-yl)ethylamino)...)
Affinity DataIC50:  400nMAssay Description:Displacement of [125I]cyanopindolol from human beta 2 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216191(CHEMBL232587 | N-(2,6-dichlorophenethyl)-4-((dieth...)
Affinity DataIC50:  430nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium- and chloride-dependent glycine transporter 1(Homo sapiens (Human))
Vanderbilt University Medical Center

Curated by ChEMBL
LigandPNGBDBM50448022(CHEMBL3115231)
Affinity DataIC50:  433nMAssay Description:Inhibition of GlyT1 (unknown origin) assessed as [14C]-glycine transportMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216187(CHEMBL232777 | N-(3-chlorophenethyl)-4-(benzyloxy)...)
Affinity DataIC50:  510nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216196(CHEMBL231776 | N-(2-methoxyphenethyl)-4-((diethyla...)
Affinity DataIC50:  540nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216183(CHEMBL233573 | N-(2-chlorophenethyl)-4-(benzyloxy)...)
Affinity DataIC50:  590nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313945((R)-N-(4-(2-(2-hydroxy-2-(pyridin-3-yl)ethylamino)...)
Affinity DataIC50:  600nMAssay Description:Displacement of [125I]cyanopindolol from human beta 2 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313970((R)-3-(2-(1H-pyrrol-1-yl)ethyl)-N-(4-(2-(2-hydroxy...)
Affinity DataIC50:  600nMAssay Description:Displacement of [125I]cyanopindolol from human beta 2 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313931((R)-2-(benzo[d]oxazol-2-yl)-N-(4-(2-(2-hydroxy-2-(...)
Affinity DataIC50:  600nMAssay Description:Displacement of [125I]cyanopindolol from human beta 1 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313955((R)-N-(4-(2-(2-hydroxy-2-(pyridin-3-yl)ethylamino)...)
Affinity DataIC50:  700nMAssay Description:Displacement of [125I]cyanopindolol from human beta 1 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216207(CHEMBL233572 | N-(2-chlorophenethyl)-4-((diethylam...)
Affinity DataIC50:  840nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313943((R)-(1H-benzo[d]imidazol-2-yl)methyl 4-(2-(2-hydro...)
Affinity DataIC50:  840nMAssay Description:Displacement of [125I]cyanopindolol from human beta 1 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium- and chloride-dependent glycine transporter 1(Homo sapiens (Human))
Vanderbilt University Medical Center

Curated by ChEMBL
LigandPNGBDBM50448000(CHEMBL3115207)
Affinity DataIC50:  900nMAssay Description:Inhibition of GlyT1 (unknown origin) assessed as [14C]-glycine transportMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216208((S)-N-(2-methoxyphenethyl)-4-((diethylamino)methyl...)
Affinity DataIC50:  970nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313931((R)-2-(benzo[d]oxazol-2-yl)-N-(4-(2-(2-hydroxy-2-(...)
Affinity DataIC50:  1.10E+3nMAssay Description:Displacement of [125I]cyanopindolol from human beta 2 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313938((R)-N-(4-(2-(2-hydroxy-2-(pyridin-3-yl)ethylamino)...)
Affinity DataIC50:  1.10E+3nMAssay Description:Displacement of [125I]cyanopindolol from human beta 1 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-2 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313941((R)-N-(4-(2-(2-hydroxy-2-(pyridin-3-yl)ethylamino)...)
Affinity DataIC50:  1.10E+3nMAssay Description:Displacement of [125I]cyanopindolol from human beta 2 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313920(CHEMBL1085444 | N-(4-(2-((R)-2-hydroxy-2-(pyridin-...)
Affinity DataIC50:  1.40E+3nMAssay Description:Displacement of [125I]cyanopindolol from human beta 1 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216186(CHEMBL232577 | N-(2-chlorophenethyl)-4-isopropoxy-...)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-1 adrenergic receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50313936((R)-N-(4-(2-(2-hydroxy-2-(pyridin-3-yl)ethylamino)...)
Affinity DataIC50:  1.50E+3nMAssay Description:Displacement of [125I]cyanopindolol from human beta 1 adrenergic receptor expressed in CHO cells at 10 uM after 3 to 4 hrs by scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMembrane-bound transcription factor site-1 protease(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50216203(4-diethylaminomethyl-N-pyrrolidin-3-yl-N-(2-o-toly...)
Affinity DataIC50:  1.60E+3nMAssay Description:Inhibition of human S1P expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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