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BDBM50327485 (R)-8-(1-isopropylpiperidin-4-yloxy)-4-methyl-3,4-dihydropyrazino[1,2-a]indol-1(2H)-one::CHEMBL1257851

SMILES: CC(C)N1CCC(CC1)Oc1ccc2n3[C@H](C)CNC(=O)c3cc2c1

InChI Key: InChIKey=JGXUYJUQTMMZNX-CQSZACIVSA-N

Data: 1 KI  3 IC50  1 EC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50327485   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Histamine receptor (H3)


(Homo sapiens (Human))
BDBM50327485
PNG
((R)-8-(1-isopropylpiperidin-4-yloxy)-4-methyl-3,4-...)
Show SMILES CC(C)N1CCC(CC1)Oc1ccc2n3[C@H](C)CNC(=O)c3cc2c1 |r|
Show InChI InChI=1S/C20H27N3O2/c1-13(2)22-8-6-16(7-9-22)25-17-4-5-18-15(10-17)11-19-20(24)21-12-14(3)23(18)19/h4-5,10-11,13-14,16H,6-9,12H2,1-3H3,(H,21,24)/t14-/m1/s1
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PC sid
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26n/an/an/an/an/an/an/an/a



F Hoffmann-La Roche Ltd

Curated by ChEMBL


Assay Description
Displacement of [3H]-RAMH from human histamine H3 receptor


Bioorg Med Chem Lett 20: 5713-7 (2010)


Article DOI: 10.1016/j.bmcl.2010.08.009
BindingDB Entry DOI: 10.7270/Q2571C7N
More data for this
Ligand-Target Pair
Cytochrome P450 3A


(Homo sapiens (Human))
BDBM50327485
PNG
((R)-8-(1-isopropylpiperidin-4-yloxy)-4-methyl-3,4-...)
Show SMILES CC(C)N1CCC(CC1)Oc1ccc2n3[C@H](C)CNC(=O)c3cc2c1 |r|
Show InChI InChI=1S/C20H27N3O2/c1-13(2)22-8-6-16(7-9-22)25-17-4-5-18-15(10-17)11-19-20(24)21-12-14(3)23(18)19/h4-5,10-11,13-14,16H,6-9,12H2,1-3H3,(H,21,24)/t14-/m1/s1
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n/an/a>5.00E+4n/an/an/an/an/an/a



F Hoffmann-La Roche Ltd

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4


Bioorg Med Chem Lett 20: 5713-7 (2010)


Article DOI: 10.1016/j.bmcl.2010.08.009
BindingDB Entry DOI: 10.7270/Q2571C7N
More data for this
Ligand-Target Pair
Histamine receptor (H3)


(Homo sapiens (Human))
BDBM50327485
PNG
((R)-8-(1-isopropylpiperidin-4-yloxy)-4-methyl-3,4-...)
Show SMILES CC(C)N1CCC(CC1)Oc1ccc2n3[C@H](C)CNC(=O)c3cc2c1 |r|
Show InChI InChI=1S/C20H27N3O2/c1-13(2)22-8-6-16(7-9-22)25-17-4-5-18-15(10-17)11-19-20(24)21-12-14(3)23(18)19/h4-5,10-11,13-14,16H,6-9,12H2,1-3H3,(H,21,24)/t14-/m1/s1
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n/an/an/an/a 29n/an/an/an/a



F Hoffmann-La Roche Ltd

Curated by ChEMBL


Assay Description
Inverse agonist activity at human recombinant histamine H3 receptor assessed as effect on [35S]GTPgammaS binding


Bioorg Med Chem Lett 20: 5713-7 (2010)


Article DOI: 10.1016/j.bmcl.2010.08.009
BindingDB Entry DOI: 10.7270/Q2571C7N
More data for this
Ligand-Target Pair
Cytochrome P450 2C9


(Homo sapiens (Human))
BDBM50327485
PNG
((R)-8-(1-isopropylpiperidin-4-yloxy)-4-methyl-3,4-...)
Show SMILES CC(C)N1CCC(CC1)Oc1ccc2n3[C@H](C)CNC(=O)c3cc2c1 |r|
Show InChI InChI=1S/C20H27N3O2/c1-13(2)22-8-6-16(7-9-22)25-17-4-5-18-15(10-17)11-19-20(24)21-12-14(3)23(18)19/h4-5,10-11,13-14,16H,6-9,12H2,1-3H3,(H,21,24)/t14-/m1/s1
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n/an/a>5.00E+4n/an/an/an/an/an/a



F Hoffmann-La Roche Ltd

Curated by ChEMBL


Assay Description
Inhibition of CYP2C9


Bioorg Med Chem Lett 20: 5713-7 (2010)


Article DOI: 10.1016/j.bmcl.2010.08.009
BindingDB Entry DOI: 10.7270/Q2571C7N
More data for this
Ligand-Target Pair
Cytochrome P450 2D6 (2D6)


(Homo sapiens (Human))
BDBM50327485
PNG
((R)-8-(1-isopropylpiperidin-4-yloxy)-4-methyl-3,4-...)
Show SMILES CC(C)N1CCC(CC1)Oc1ccc2n3[C@H](C)CNC(=O)c3cc2c1 |r|
Show InChI InChI=1S/C20H27N3O2/c1-13(2)22-8-6-16(7-9-22)25-17-4-5-18-15(10-17)11-19-20(24)21-12-14(3)23(18)19/h4-5,10-11,13-14,16H,6-9,12H2,1-3H3,(H,21,24)/t14-/m1/s1
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PC sid
UniChem
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n/an/a 2.20E+4n/an/an/an/an/an/a



F Hoffmann-La Roche Ltd

Curated by ChEMBL


Assay Description
Inhibition of CYP2D6


Bioorg Med Chem Lett 20: 5713-7 (2010)


Article DOI: 10.1016/j.bmcl.2010.08.009
BindingDB Entry DOI: 10.7270/Q2571C7N
More data for this
Ligand-Target Pair