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Compile Data Set for Download or QSAR

Found 6366 hits with Last Name = 'mclean' and Initial = 'h'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM50194747
PNG
(((R)-4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)met...)
Show SMILES COc1cc(Br)c(OC)c2C[C@@H](CN)c12
Show InChI InChI=1S/C11H14BrNO2/c1-14-9-4-8(12)11(15-2)7-3-6(5-13)10(7)9/h4,6H,3,5,13H2,1-2H3/t6-/m0/s1
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0.260n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Homo sapiens (Human))
BDBM50194747
PNG
(((R)-4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)met...)
Show SMILES COc1cc(Br)c(OC)c2C[C@@H](CN)c12
Show InChI InChI=1S/C11H14BrNO2/c1-14-9-4-8(12)11(15-2)7-3-6(5-13)10(7)9/h4,6H,3,5,13H2,1-2H3/t6-/m0/s1
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0.350n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Homo sapiens (Human))
BDBM50005267
PNG
(2,5-dimethoxy-4-bromophenethylamine | 2-(4-Bromo-2...)
Show SMILES COc1cc(CCN)c(OC)cc1Br
Show InChI InChI=1S/C10H14BrNO2/c1-13-9-6-8(11)10(14-2)5-7(9)3-4-12/h5-6H,3-4,12H2,1-2H3
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0.660n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Homo sapiens (Human))
BDBM50194752
PNG
((+/-)-(4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)m...)
Show SMILES COc1cc(Br)c(OC)c2CC(CN)c12
Show InChI InChI=1S/C11H14BrNO2/c1-14-9-4-8(12)11(15-2)7-3-6(5-13)10(7)9/h4,6H,3,5,13H2,1-2H3
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0.730n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM50194752
PNG
((+/-)-(4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)m...)
Show SMILES COc1cc(Br)c(OC)c2CC(CN)c12
Show InChI InChI=1S/C11H14BrNO2/c1-14-9-4-8(12)11(15-2)7-3-6(5-13)10(7)9/h4,6H,3,5,13H2,1-2H3
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0.75n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM50005267
PNG
(2,5-dimethoxy-4-bromophenethylamine | 2-(4-Bromo-2...)
Show SMILES COc1cc(CCN)c(OC)cc1Br
Show InChI InChI=1S/C10H14BrNO2/c1-13-9-6-8(11)10(14-2)5-7(9)3-4-12/h5-6H,3-4,12H2,1-2H3
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0.880n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM21342
PNG
((4R,7R)-N,N-diethyl-6-methyl-6,11-diazatetracyclo[...)
Show SMILES [H][C@@]12Cc3c[nH]c4cccc(C1=C[C@H](CN2C)C(=O)N(CC)CC)c34 |c:12|
Show InChI InChI=1S/C20H25N3O/c1-4-23(5-2)20(24)14-9-16-15-7-6-8-17-19(15)13(11-21-17)10-18(16)22(3)12-14/h6-9,11,14,18,21H,4-5,10,12H2,1-3H3/t14-,18-/m1/s1
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3.5n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of [125I]DOI from rat 5HT2A receptor


J Med Chem 49: 4269-74 (2006)


Article DOI: 10.1021/jm060272y
BindingDB Entry DOI: 10.7270/Q2PC320K
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2C


(Rattus norvegicus (Rat))
BDBM21342
PNG
((4R,7R)-N,N-diethyl-6-methyl-6,11-diazatetracyclo[...)
Show SMILES [H][C@@]12Cc3c[nH]c4cccc(C1=C[C@H](CN2C)C(=O)N(CC)CC)c34 |c:12|
Show InChI InChI=1S/C20H25N3O/c1-4-23(5-2)20(24)14-9-16-15-7-6-8-17-19(15)13(11-21-17)10-18(16)22(3)12-14/h6-9,11,14,18,21H,4-5,10,12H2,1-3H3/t14-,18-/m1/s1
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5.5n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of [125I]DOI from rat 5HT2C receptor


J Med Chem 49: 4269-74 (2006)


Article DOI: 10.1021/jm060272y
BindingDB Entry DOI: 10.7270/Q2PC320K
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Homo sapiens (Human))
BDBM50194750
PNG
(((S)-4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)met...)
Show SMILES COc1cc(Br)c(OC)c2C[C@H](CN)c12
Show InChI InChI=1S/C11H14BrNO2/c1-14-9-4-8(12)11(15-2)7-3-6(5-13)10(7)9/h4,6H,3,5,13H2,1-2H3/t6-/m1/s1
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15n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM50194750
PNG
(((S)-4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)met...)
Show SMILES COc1cc(Br)c(OC)c2C[C@H](CN)c12
Show InChI InChI=1S/C11H14BrNO2/c1-14-9-4-8(12)11(15-2)7-3-6(5-13)10(7)9/h4,6H,3,5,13H2,1-2H3/t6-/m1/s1
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42n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM50194751
PNG
(C-(5-bromo-4,7-dimethoxyindan-1-yl)methylamine | C...)
Show SMILES COc1cc(Br)c(OC)c2CCC(CN)c12
Show InChI InChI=1S/C12H16BrNO2/c1-15-10-5-9(13)12(16-2)8-4-3-7(6-14)11(8)10/h5,7H,3-4,6,14H2,1-2H3
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47n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Homo sapiens (Human))
BDBM50194751
PNG
(C-(5-bromo-4,7-dimethoxyindan-1-yl)methylamine | C...)
Show SMILES COc1cc(Br)c(OC)c2CCC(CN)c12
Show InChI InChI=1S/C12H16BrNO2/c1-15-10-5-9(13)12(16-2)8-4-3-7(6-14)11(8)10/h5,7H,3-4,6,14H2,1-2H3
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53n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2C


(Rattus norvegicus (Rat))
BDBM50190613
PNG
((+/-)-(2,3-dihydro-4,5,6-trimethoxy-1H-inden-1-yl)...)
Show SMILES COc1cc2C(CN)CCc2c(OC)c1OC
Show InChI InChI=1S/C13H19NO3/c1-15-11-6-10-8(7-14)4-5-9(10)12(16-2)13(11)17-3/h6,8H,4-5,7,14H2,1-3H3
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60n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of [125I]DOI from rat 5HT2C receptor


J Med Chem 49: 4269-74 (2006)


Article DOI: 10.1021/jm060272y
BindingDB Entry DOI: 10.7270/Q2PC320K
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM50190615
PNG
((R)-(+)-(4,5,6-trimethoxyindan-1-yl)methanamine | ...)
Show SMILES COc1cc2[C@H](CN)CCc2c(OC)c1OC
Show InChI InChI=1S/C13H19NO3/c1-15-11-6-10-8(7-14)4-5-9(10)12(16-2)13(11)17-3/h6,8H,4-5,7,14H2,1-3H3/t8-/m0/s1
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69n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of [125I]DOI from rat 5HT2A receptor


J Med Chem 49: 4269-74 (2006)


Article DOI: 10.1021/jm060272y
BindingDB Entry DOI: 10.7270/Q2PC320K
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM50194749
PNG
(C-(3-bromo-5-methoxy-1,6,7,8,9,9a-hexahydro-2-oxab...)
Show SMILES COc1cc(Br)c2OC[C@H]3CCC[C@H](CN)c1c23
Show InChI InChI=1S/C14H18BrNO2/c1-17-11-5-10(15)14-13-9(7-18-14)4-2-3-8(6-16)12(11)13/h5,8-9H,2-4,6-7,16H2,1H3/t8-,9-/m1/s1
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74n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM50190613
PNG
((+/-)-(2,3-dihydro-4,5,6-trimethoxy-1H-inden-1-yl)...)
Show SMILES COc1cc2C(CN)CCc2c(OC)c1OC
Show InChI InChI=1S/C13H19NO3/c1-15-11-6-10-8(7-14)4-5-9(10)12(16-2)13(11)17-3/h6,8H,4-5,7,14H2,1-3H3
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130n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of [125I]DOI from rat 5HT2A receptor


J Med Chem 49: 4269-74 (2006)


Article DOI: 10.1021/jm060272y
BindingDB Entry DOI: 10.7270/Q2PC320K
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Homo sapiens (Human))
BDBM50194749
PNG
(C-(3-bromo-5-methoxy-1,6,7,8,9,9a-hexahydro-2-oxab...)
Show SMILES COc1cc(Br)c2OC[C@H]3CCC[C@H](CN)c1c23
Show InChI InChI=1S/C14H18BrNO2/c1-17-11-5-10(15)14-13-9(7-18-14)4-2-3-8(6-16)12(11)13/h5,8-9H,2-4,6-7,16H2,1H3/t8-,9-/m1/s1
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170n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM50194748
PNG
(C-(3-bromo-5-methoxy-1,6,7,8,9,9a-hexahydro-2-oxab...)
Show SMILES COc1cc(Br)c2OC[C@H]3CCC[C@@H](CN)c1c23
Show InChI InChI=1S/C14H18BrNO2/c1-17-11-5-10(15)14-13-9(7-18-14)4-2-3-8(6-16)12(11)13/h5,8-9H,2-4,6-7,16H2,1H3/t8-,9+/m0/s1
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170n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Homo sapiens (Human))
BDBM50194748
PNG
(C-(3-bromo-5-methoxy-1,6,7,8,9,9a-hexahydro-2-oxab...)
Show SMILES COc1cc(Br)c2OC[C@H]3CCC[C@@H](CN)c1c23
Show InChI InChI=1S/C14H18BrNO2/c1-17-11-5-10(15)14-13-9(7-18-14)4-2-3-8(6-16)12(11)13/h5,8-9H,2-4,6-7,16H2,1H3/t8-,9+/m0/s1
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200n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptor


J Med Chem 49: 5794-803 (2006)


Article DOI: 10.1021/jm060656o
BindingDB Entry DOI: 10.7270/Q2NS0TH3
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM50059891
PNG
(1-amino-2-(3,4,5-trimethoxyphenyl)ethane | 2-(3,4,...)
Show SMILES COc1cc(CCN)cc(OC)c1OC
Show InChI InChI=1S/C11H17NO3/c1-13-9-6-8(4-5-12)7-10(14-2)11(9)15-3/h6-7H,4-5,12H2,1-3H3
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360n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of [125I]DOI from rat 5HT2A receptor


J Med Chem 49: 4269-74 (2006)


Article DOI: 10.1021/jm060272y
BindingDB Entry DOI: 10.7270/Q2PC320K
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2C


(Rattus norvegicus (Rat))
BDBM50059891
PNG
(1-amino-2-(3,4,5-trimethoxyphenyl)ethane | 2-(3,4,...)
Show SMILES COc1cc(CCN)cc(OC)c1OC
Show InChI InChI=1S/C11H17NO3/c1-13-9-6-8(4-5-12)7-10(14-2)11(9)15-3/h6-7H,4-5,12H2,1-3H3
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380n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of [125I]DOI from rat 5HT2C receptor


J Med Chem 49: 4269-74 (2006)


Article DOI: 10.1021/jm060272y
BindingDB Entry DOI: 10.7270/Q2PC320K
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM50190614
PNG
((S)-(-)-(4,5,6-trimethoxyindan-1-yl)methanamine | ...)
Show SMILES COc1cc2[C@@H](CN)CCc2c(OC)c1OC
Show InChI InChI=1S/C13H19NO3/c1-15-11-6-10-8(7-14)4-5-9(10)12(16-2)13(11)17-3/h6,8H,4-5,7,14H2,1-3H3/t8-/m1/s1
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1.12E+3n/an/an/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Displacement of [125I]DOI from rat 5HT2A receptor


J Med Chem 49: 4269-74 (2006)


Article DOI: 10.1021/jm060272y
BindingDB Entry DOI: 10.7270/Q2PC320K
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50467024
PNG
(CHEMBL4280697)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(C(=O)OC)c(Cl)c2)C(=O)N1c1ccccc1C
Show InChI InChI=1S/C22H21ClN2O3S/c1-4-11-24-22-25(18-8-6-5-7-14(18)2)20(26)19(29-22)13-15-9-10-16(17(23)12-15)21(27)28-3/h5-10,12-13H,4,11H2,1-3H3/b19-13-,24-22-
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n/an/a 2.5n/an/an/an/an/an/a



University of Dundee

Curated by ChEMBL


Assay Description
Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assay


Bioorg Med Chem Lett 28: 3255-3259 (2018)


Article DOI: 10.1016/j.bmcl.2018.07.044
BindingDB Entry DOI: 10.7270/Q2BG2RPC
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50316768
PNG
((Z,Z)-5-[3-Chloro-4-((2S)-2,3-dihydroxy-propoxy)-b...)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(OC[C@H](O)CO)c(Cl)c2)C(=O)N1c1ccccc1C |r|
Show InChI InChI=1S/C23H25ClN2O4S/c1-3-10-25-23-26(19-7-5-4-6-15(19)2)22(29)21(31-23)12-16-8-9-20(18(24)11-16)30-14-17(28)13-27/h4-9,11-12,17,27-28H,3,10,13-14H2,1-2H3/b21-12-,25-23-/t17-/m1/s1
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n/an/a 13n/an/an/an/an/an/a



University of Dundee

Curated by ChEMBL


Assay Description
Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assay


Bioorg Med Chem Lett 28: 3255-3259 (2018)


Article DOI: 10.1016/j.bmcl.2018.07.044
BindingDB Entry DOI: 10.7270/Q2BG2RPC
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50553299
PNG
(CHEMBL4790404)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(O)c(Br)c2)C(=O)N1c1ccccc1C
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TBA

Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50553304
PNG
(CHEMBL4748743)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(O)c(C)c2)C(=O)N1c1ccccc1C
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TBA

Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50553297
PNG
(CHEMBL4747234)
Show SMILES Cc1ccccc1N1C(=O)\C(S\C1=N/CCCF)=C\c1ccc(O)c(Cl)c1
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TBA

Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50553300
PNG
(CHEMBL4796729)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(O)c(c2)C(F)(F)F)C(=O)N1c1ccccc1C
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TBA

Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50553289
PNG
(CHEMBL4763318)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(O)c(Cl)c2)C(=O)N1C1CCOCC1
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TBA

Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50316771
PNG
((Z,Z)-5-(3-Chloro-4-hydroxy-benzylidene)-2-propyli...)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(O)c(Cl)c2)C(=O)N1c1ccccc1C
Show InChI InChI=1S/C20H19ClN2O2S/c1-3-10-22-20-23(16-7-5-4-6-13(16)2)19(25)18(26-20)12-14-8-9-17(24)15(21)11-14/h4-9,11-12,24H,3,10H2,1-2H3/b18-12-,22-20-
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TBA

Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50553294
PNG
(CHEMBL4759157)
Show SMILES Cc1ccccc1N1C(=O)\C(S\C1=N/C1COC1)=C\c1ccc(O)c(Cl)c1
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TBA

Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50553287
PNG
(CHEMBL4745979)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(O)c(Cl)c2)C(=O)N1c1ccccc1OC
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TBA

Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Amine oxidase [flavin-containing] A


(Rattus norvegicus (rat))
BDBM50164336
PNG
(2-(2-Chloro-4,6-dimethoxy-phenyl)-1-methyl-ethylam...)
Show SMILES COc1cc(Cl)c(CC(C)N)c(OC)c1
Show InChI InChI=1S/C11H16ClNO2/c1-7(13)4-9-10(12)5-8(14-2)6-11(9)15-3/h5-7H,4,13H2,1-3H3
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n/an/a 70n/an/an/an/an/an/a



Universidad de Chile

Curated by ChEMBL


Assay Description
Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspension


J Med Chem 48: 2407-19 (2005)


Article DOI: 10.1021/jm0493109
BindingDB Entry DOI: 10.7270/Q27080XX
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50553303
PNG
(CHEMBL4748038)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(O)cc2)C(=O)N1c1ccccc1C
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TBA

Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Amine oxidase [flavin-containing] A


(Rattus norvegicus (rat))
BDBM50164326
PNG
(2-(4-Ethylsulfanyl-2,6-dimethoxy-phenyl)-1-methyl-...)
Show SMILES CCSc1cc(OC)c(CC(C)N)c(OC)c1
Show InChI InChI=1S/C13H21NO2S/c1-5-17-10-7-12(15-3)11(6-9(2)14)13(8-10)16-4/h7-9H,5-6,14H2,1-4H3
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Universidad de Chile

Curated by ChEMBL


Assay Description
Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspension


J Med Chem 48: 2407-19 (2005)


Article DOI: 10.1021/jm0493109
BindingDB Entry DOI: 10.7270/Q27080XX
More data for this
Ligand-Target Pair
Amine oxidase [flavin-containing] A


(Rattus norvegicus (rat))
BDBM50164327
PNG
(2-(4-Ethylsulfanyl-phenyl)-1-methyl-ethylamine | 2...)
Show SMILES CCSc1ccc(CC(C)N)cc1
Show InChI InChI=1S/C11H17NS/c1-3-13-11-6-4-10(5-7-11)8-9(2)12/h4-7,9H,3,8,12H2,1-2H3
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Universidad de Chile

Curated by ChEMBL


Assay Description
Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspension


J Med Chem 48: 2407-19 (2005)


Article DOI: 10.1021/jm0493109
BindingDB Entry DOI: 10.7270/Q27080XX
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50553302
PNG
(CHEMBL4751870)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(O)cn2)C(=O)N1c1ccccc1C
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TBA

Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50467023
PNG
(CHEMBL4287514)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(cc2)C(=O)NCCO)C(=O)N1c1ccccc1C
Show InChI InChI=1S/C23H25N3O3S/c1-3-12-25-23-26(19-7-5-4-6-16(19)2)22(29)20(30-23)15-17-8-10-18(11-9-17)21(28)24-13-14-27/h4-11,15,27H,3,12-14H2,1-2H3,(H,24,28)/b20-15-,25-23-
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University of Dundee

Curated by ChEMBL


Assay Description
Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assay


Bioorg Med Chem Lett 28: 3255-3259 (2018)


Article DOI: 10.1016/j.bmcl.2018.07.044
BindingDB Entry DOI: 10.7270/Q2BG2RPC
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50467022
PNG
(CHEMBL4292022)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(cc2)C(=O)OCCO)C(=O)N1c1ccccc1C
Show InChI InChI=1S/C23H24N2O4S/c1-3-12-24-23-25(19-7-5-4-6-16(19)2)21(27)20(30-23)15-17-8-10-18(11-9-17)22(28)29-14-13-26/h4-11,15,26H,3,12-14H2,1-2H3/b20-15-,24-23-
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n/an/a 126n/an/an/an/an/an/a



University of Dundee

Curated by ChEMBL


Assay Description
Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assay


Bioorg Med Chem Lett 28: 3255-3259 (2018)


Article DOI: 10.1016/j.bmcl.2018.07.044
BindingDB Entry DOI: 10.7270/Q2BG2RPC
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50553288
PNG
(CHEMBL4755800)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(O)c(Cl)c2)C(=O)N1C(C)C
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TBA

Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50553290
PNG
(CHEMBL4740803)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(O)c(Cl)c2)C(=O)N1C1CCS(=O)(=O)CC1
PDB

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Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Amine oxidase [flavin-containing] A


(Rattus norvegicus (rat))
BDBM50005270
PNG
(1-(4-ethoxyphenyl)propan-2-amine | 2-(4-Ethoxy-phe...)
Show SMILES CCOc1ccc(CC(C)N)cc1
Show InChI InChI=1S/C11H17NO/c1-3-13-11-6-4-10(5-7-11)8-9(2)12/h4-7,9H,3,8,12H2,1-2H3
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Universidad de Chile

Curated by ChEMBL


Assay Description
Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspension


J Med Chem 48: 2407-19 (2005)


Article DOI: 10.1021/jm0493109
BindingDB Entry DOI: 10.7270/Q27080XX
More data for this
Ligand-Target Pair
Amine oxidase [flavin-containing] A


(Rattus norvegicus (rat))
BDBM50063544
PNG
(1-(6-(methylthio)naphthalen-2-yl)propan-2-amine | ...)
Show SMILES CSc1ccc(CC(C)N)cc1
Show InChI InChI=1S/C10H15NS/c1-8(11)7-9-3-5-10(12-2)6-4-9/h3-6,8H,7,11H2,1-2H3
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Universidad de Chile

Curated by ChEMBL


Assay Description
Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspension


J Med Chem 48: 2407-19 (2005)


Article DOI: 10.1021/jm0493109
BindingDB Entry DOI: 10.7270/Q27080XX
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50553295
PNG
(CHEMBL4758919)
Show SMILES Cc1ccccc1N1C(=O)\C(S\C1=N/C1CC(F)(F)C1)=C\c1ccc(O)c(Cl)c1
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TBA

Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50553293
PNG
(CHEMBL4757599)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(O)c(Cl)c2)C(=O)N1c1ccccc1O
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Assay Description
Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.8b00616
BindingDB Entry DOI: 10.7270/Q20868ZH
More data for this
Ligand-Target Pair
Amine oxidase [flavin-containing] A


(Rattus norvegicus (rat))
BDBM50164324
PNG
(2-(2,6-Dimethoxy-4-methylsulfanyl-phenyl)-1-methyl...)
Show SMILES COc1cc(SC)cc(OC)c1CC(C)N
Show InChI InChI=1S/C12H19NO2S/c1-8(13)5-10-11(14-2)6-9(16-4)7-12(10)15-3/h6-8H,5,13H2,1-4H3
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Universidad de Chile

Curated by ChEMBL


Assay Description
Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspension


J Med Chem 48: 2407-19 (2005)


Article DOI: 10.1021/jm0493109
BindingDB Entry DOI: 10.7270/Q27080XX
More data for this
Ligand-Target Pair
Amine oxidase [flavin-containing] A


(Rattus norvegicus (rat))
BDBM50164325
PNG
(CHEMBL189630 | [2-(2,5-Dimethoxy-4-propylsulfanyl-...)
Show SMILES CCCSc1cc(OC)c(CC(C)NC)cc1OC
Show InChI InChI=1S/C15H25NO2S/c1-6-7-19-15-10-13(17-4)12(8-11(2)16-3)9-14(15)18-5/h9-11,16H,6-8H2,1-5H3
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PubMed
n/an/a 300n/an/an/an/an/an/a



Universidad de Chile

Curated by ChEMBL


Assay Description
Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspension


J Med Chem 48: 2407-19 (2005)


Article DOI: 10.1021/jm0493109
BindingDB Entry DOI: 10.7270/Q27080XX
More data for this
Ligand-Target Pair
Amine oxidase [flavin-containing] A


(Rattus norvegicus (rat))
BDBM50024209
PNG
((+/-)2-(4-Methoxy-phenyl)-1-methyl-ethylamine | (-...)
Show SMILES COc1ccc(CC(C)N)cc1
Show InChI InChI=1S/C10H15NO/c1-8(11)7-9-3-5-10(12-2)6-4-9/h3-6,8H,7,11H2,1-2H3
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Article
PubMed
n/an/a 300n/an/an/an/an/an/a



Universidad de Chile

Curated by ChEMBL


Assay Description
Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspension


J Med Chem 48: 2407-19 (2005)


Article DOI: 10.1021/jm0493109
BindingDB Entry DOI: 10.7270/Q27080XX
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50467025
PNG
(CHEMBL4288608)
Show SMILES CCC\N=C1/S\C(=C/c2ccc(cc2)C(=O)OC)C(=O)N1c1ccccc1C
Show InChI InChI=1S/C22H22N2O3S/c1-4-13-23-22-24(18-8-6-5-7-15(18)2)20(25)19(28-22)14-16-9-11-17(12-10-16)21(26)27-3/h5-12,14H,4,13H2,1-3H3/b19-14-,23-22-
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antibodypedia
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Article
PubMed
n/an/a 316n/an/an/an/an/an/a



University of Dundee

Curated by ChEMBL


Assay Description
Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assay


Bioorg Med Chem Lett 28: 3255-3259 (2018)


Article DOI: 10.1016/j.bmcl.2018.07.044
BindingDB Entry DOI: 10.7270/Q2BG2RPC
More data for this
Ligand-Target Pair
Amine oxidase [flavin-containing] A


(Rattus norvegicus (rat))
BDBM50164320
PNG
(2-(4-Isobutylsulfanyl-phenyl)-1-methyl-ethylamine ...)
Show SMILES CC(C)CSc1ccc(CC(C)N)cc1
Show InChI InChI=1S/C13H21NS/c1-10(2)9-15-13-6-4-12(5-7-13)8-11(3)14/h4-7,10-11H,8-9,14H2,1-3H3
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
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GoogleScholar
AffyNet 
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PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 400n/an/an/an/an/an/a



Universidad de Chile

Curated by ChEMBL


Assay Description
Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspension


J Med Chem 48: 2407-19 (2005)


Article DOI: 10.1021/jm0493109
BindingDB Entry DOI: 10.7270/Q27080XX
More data for this
Ligand-Target Pair
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