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BDBM388491 US9944618, Compound ID No. 25

SMILES: CNCC([C@H](CO)c1ccccc1)c1ccc2ccccc2c1

InChI Key: InChIKey=CUSKZMGSNSWKJU-BPGUCPLFSA-N

Data: 3 KI  2 IC50

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 = 388491   
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
Sodium-dependent noradrenaline transporter


(Homo sapiens (Human))
BDBM388491
PNG
(US9944618, Compound ID No. 25)
Show SMILES CNCC([C@H](CO)c1ccccc1)c1ccc2ccccc2c1 |r|
Show InChI InChI=1S/C21H23NO/c1-22-14-20(21(15-23)17-8-3-2-4-9-17)19-12-11-16-7-5-6-10-18(16)13-19/h2-13,20-23H,14-15H2,1H3/t20?,21-/m1/s1
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2.20n/an/an/an/an/an/an/an/a



Schering-Plough Research Institute



Assay Description
NET: This protocol was designed to measure inhibition of uptake by the human norepinephrine transporter. The reagents were human NET (HEK293F) cells,...


Bioorg Med Chem Lett 19: 1164-7 (2009)


BindingDB Entry DOI: 10.7270/Q26D5WBR
More data for this
Ligand-Target Pair
Sodium-dependent serotonin transporter


(Homo sapiens (Human))
BDBM388491
PNG
(US9944618, Compound ID No. 25)
Show SMILES CNCC([C@H](CO)c1ccccc1)c1ccc2ccccc2c1 |r|
Show InChI InChI=1S/C21H23NO/c1-22-14-20(21(15-23)17-8-3-2-4-9-17)19-12-11-16-7-5-6-10-18(16)13-19/h2-13,20-23H,14-15H2,1H3/t20?,21-/m1/s1
PDB

KEGG

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antibodypedia
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PC cid
PC sid
UniChem
US Patent
22.7n/an/an/an/an/an/an/an/a



Schering-Plough Research Institute



Assay Description
SERT: This protocol was designed to measure inhibition of uptake by the human serotonin transporter. The reagents were human SERT (HEK293F) cells, fl...


Bioorg Med Chem Lett 19: 1164-7 (2009)


BindingDB Entry DOI: 10.7270/Q26D5WBR
More data for this
Ligand-Target Pair
Sodium-dependent dopamine transporter


(Homo sapiens (Human))
BDBM388491
PNG
(US9944618, Compound ID No. 25)
Show SMILES CNCC([C@H](CO)c1ccccc1)c1ccc2ccccc2c1 |r|
Show InChI InChI=1S/C21H23NO/c1-22-14-20(21(15-23)17-8-3-2-4-9-17)19-12-11-16-7-5-6-10-18(16)13-19/h2-13,20-23H,14-15H2,1H3/t20?,21-/m1/s1
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106n/an/an/an/an/an/an/an/a



Schering-Plough Research Institute



Assay Description
DAT: This protocol was designed to measure inhibition of uptake by the human dopamine transporter. The reagents were human DAT (HEK293F) cells, GBR 1...


Bioorg Med Chem Lett 19: 1164-7 (2009)


BindingDB Entry DOI: 10.7270/Q26D5WBR
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))
BDBM388491
PNG
(US9944618, Compound ID No. 25)
Show SMILES CNCC([C@H](CO)c1ccccc1)c1ccc2ccccc2c1 |r|
Show InChI InChI=1S/C21H23NO/c1-22-14-20(21(15-23)17-8-3-2-4-9-17)19-12-11-16-7-5-6-10-18(16)13-19/h2-13,20-23H,14-15H2,1H3/t20?,21-/m1/s1
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 320n/an/an/an/an/an/a



Schering-Plough Research Institute



Assay Description
Cytochrome P450 3A4 and 2D6:Recombinant enzymes, 3A4 and 2D6, generated using the ABL yeast expression system were used. For CYP3A4, the enzyme amou...


Bioorg Med Chem Lett 19: 1164-7 (2009)


BindingDB Entry DOI: 10.7270/Q26D5WBR
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM388491
PNG
(US9944618, Compound ID No. 25)
Show SMILES CNCC([C@H](CO)c1ccccc1)c1ccc2ccccc2c1 |r|
Show InChI InChI=1S/C21H23NO/c1-22-14-20(21(15-23)17-8-3-2-4-9-17)19-12-11-16-7-5-6-10-18(16)13-19/h2-13,20-23H,14-15H2,1H3/t20?,21-/m1/s1
PDB
MMDB

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n/an/a 3.30E+4n/an/an/an/an/an/a



Schering-Plough Research Institute



Assay Description
HERG: The pre- and post-compound hERG current was evoked by a single voltage pulse consisting of a 20 s period holding at −70 mV, a 160 ms step...


Bioorg Med Chem Lett 19: 1164-7 (2009)


BindingDB Entry DOI: 10.7270/Q26D5WBR
More data for this
Ligand-Target Pair