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Found 6366 with Last Name = 'mclean' and Initial = 'h'
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50194747(((R)-4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)met...)
Affinity DataKi:  0.260nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50194747(((R)-4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)met...)
Affinity DataKi:  0.350nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50005267(2,5-dimethoxy-4-bromophenethylamine | 2-(4-Bromo-2...)
Affinity DataKi:  0.660nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50194752((+/-)-(4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)m...)
Affinity DataKi:  0.730nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50194752((+/-)-(4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)m...)
Affinity DataKi:  0.75nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50005267(2,5-dimethoxy-4-bromophenethylamine | 2-(4-Bromo-2...)
Affinity DataKi:  0.880nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM21342((4R,7R)-N,N-diethyl-6-methyl-6,11-diazatetracyclo[...)
Affinity DataKi:  3.5nMAssay Description:Displacement of [125I]DOI from rat 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2C(Rattus norvegicus (Rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM21342((4R,7R)-N,N-diethyl-6-methyl-6,11-diazatetracyclo[...)
Affinity DataKi:  5.5nMAssay Description:Displacement of [125I]DOI from rat 5HT2C receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50194750(((S)-4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)met...)
Affinity DataKi:  15nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50194750(((S)-4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)met...)
Affinity DataKi:  42nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50194751(C-(5-bromo-4,7-dimethoxyindan-1-yl)methylamine | C...)
Affinity DataKi:  47nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50194751(C-(5-bromo-4,7-dimethoxyindan-1-yl)methylamine | C...)
Affinity DataKi:  53nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2C(Rattus norvegicus (Rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50190613((+/-)-(2,3-dihydro-4,5,6-trimethoxy-1H-inden-1-yl)...)
Affinity DataKi:  60nMAssay Description:Displacement of [125I]DOI from rat 5HT2C receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50190615((R)-(+)-(4,5,6-trimethoxyindan-1-yl)methanamine | ...)
Affinity DataKi:  69nMAssay Description:Displacement of [125I]DOI from rat 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50194749(C-(3-bromo-5-methoxy-1,6,7,8,9,9a-hexahydro-2-oxab...)
Affinity DataKi:  74nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50190613((+/-)-(2,3-dihydro-4,5,6-trimethoxy-1H-inden-1-yl)...)
Affinity DataKi:  130nMAssay Description:Displacement of [125I]DOI from rat 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50194749(C-(3-bromo-5-methoxy-1,6,7,8,9,9a-hexahydro-2-oxab...)
Affinity DataKi:  170nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50194748(C-(3-bromo-5-methoxy-1,6,7,8,9,9a-hexahydro-2-oxab...)
Affinity DataKi:  170nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50194748(C-(3-bromo-5-methoxy-1,6,7,8,9,9a-hexahydro-2-oxab...)
Affinity DataKi:  200nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50059891(1-amino-2-(3,4,5-trimethoxyphenyl)ethane | 2-(3,4,...)
Affinity DataKi:  360nMAssay Description:Displacement of [125I]DOI from rat 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2C(Rattus norvegicus (Rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50059891(1-amino-2-(3,4,5-trimethoxyphenyl)ethane | 2-(3,4,...)
Affinity DataKi:  380nMAssay Description:Displacement of [125I]DOI from rat 5HT2C receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50190614((S)-(-)-(4,5,6-trimethoxyindan-1-yl)methanamine | ...)
Affinity DataKi:  1.12E+3nMAssay Description:Displacement of [125I]DOI from rat 5HT2A receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50467024(CHEMBL4280697)
Affinity DataIC50:  2.5nMAssay Description:Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50316768((Z,Z)-5-[3-Chloro-4-((2S)-2,3-dihydroxy-propoxy)-b...)
Affinity DataIC50:  13nMAssay Description:Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50553299(CHEMBL4790404)
Affinity DataIC50:  20nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50553304(CHEMBL4748743)
Affinity DataIC50:  25nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50553297(CHEMBL4747234)
Affinity DataIC50:  25nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50553300(CHEMBL4796729)
Affinity DataIC50:  32nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50553289(CHEMBL4763318)
Affinity DataIC50:  40nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50316771((Z,Z)-5-(3-Chloro-4-hydroxy-benzylidene)-2-propyli...)
Affinity DataIC50:  40nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50553294(CHEMBL4759157)
Affinity DataIC50:  50nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50553287(CHEMBL4745979)
Affinity DataIC50:  63nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile

Curated by ChEMBL
LigandPNGBDBM50164336(2-(2-Chloro-4,6-dimethoxy-phenyl)-1-methyl-ethylam...)
Affinity DataIC50:  70nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50553303(CHEMBL4748038)
Affinity DataIC50:  79nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile

Curated by ChEMBL
LigandPNGBDBM50164326(2-(4-Ethylsulfanyl-2,6-dimethoxy-phenyl)-1-methyl-...)
Affinity DataIC50:  80nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile

Curated by ChEMBL
LigandPNGBDBM50164327(2-(4-Ethylsulfanyl-phenyl)-1-methyl-ethylamine | 2...)
Affinity DataIC50:  100nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50553302(CHEMBL4751870)
Affinity DataIC50:  100nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50467023(CHEMBL4287514)
Affinity DataIC50:  100nMAssay Description:Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assayMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50467022(CHEMBL4292022)
Affinity DataIC50:  126nMAssay Description:Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50553288(CHEMBL4755800)
Affinity DataIC50:  158nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50553290(CHEMBL4740803)
Affinity DataIC50:  200nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile

Curated by ChEMBL
LigandPNGBDBM50005270(1-(4-ethoxyphenyl)propan-2-amine | 2-(4-Ethoxy-phe...)
Affinity DataIC50:  200nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile

Curated by ChEMBL
LigandPNGBDBM50063544(1-(6-(methylthio)naphthalen-2-yl)propan-2-amine | ...)
Affinity DataIC50:  200nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50553295(CHEMBL4758919)
Affinity DataIC50:  200nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50553293(CHEMBL4757599)
Affinity DataIC50:  251nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile

Curated by ChEMBL
LigandPNGBDBM50164324(2-(2,6-Dimethoxy-4-methylsulfanyl-phenyl)-1-methyl...)
Affinity DataIC50:  300nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile

Curated by ChEMBL
LigandPNGBDBM50164325(CHEMBL189630 | [2-(2,5-Dimethoxy-4-propylsulfanyl-...)
Affinity DataIC50:  300nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile

Curated by ChEMBL
LigandPNGBDBM50024209((+/-)2-(4-Methoxy-phenyl)-1-methyl-ethylamine | (-...)
Affinity DataIC50:  300nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSphingosine 1-phosphate receptor 1(Homo sapiens (Human))
University Of Dundee

Curated by ChEMBL
LigandPNGBDBM50467025(CHEMBL4288608)
Affinity DataIC50:  316nMAssay Description:Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile

Curated by ChEMBL
LigandPNGBDBM50164320(2-(4-Isobutylsulfanyl-phenyl)-1-methyl-ethylamine ...)
Affinity DataIC50:  400nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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