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SMILES: CN1CCc2ccc(OCCCN3CCN(CC3)c3ccccc3Cl)cc2C1=O

InChI Key: InChIKey=QIMOBLHMKZLPIE-UHFFFAOYSA-N

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 6 hits for monomerid = 423312   
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
5-hydroxytryptamine receptor 1A


(Rattus norvegicus (rat))
BDBM423312
PNG
(US10501452, Compound 18)
Show SMILES CN1CCc2ccc(OCCCN3CCN(CC3)c3ccccc3Cl)cc2C1=O
Show InChI InChI=1S/C23H28ClN3O2/c1-25-11-9-18-7-8-19(17-20(18)23(25)28)29-16-4-10-26-12-14-27(15-13-26)22-6-3-2-5-21(22)24/h2-3,5-8,17H,4,9-16H2,1H3
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UniProtKB/SwissProt

GoogleScholar
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PC cid
PC sid
UniChem
Article
PubMed
89n/an/an/an/an/an/an/an/a


TBA

Assay Description
Displacement of [3H](+)8-OH-DPAT from rat cerebral cortex 5HT1A receptor measured after 30 mins by liquid scintillation counting method


Citation and Details

Article DOI: 10.1016/j.ejmech.2020.112709
BindingDB Entry DOI: 10.7270/Q2XK8K6M
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM423312
PNG
(US10501452, Compound 18)
Show SMILES CN1CCc2ccc(OCCCN3CCN(CC3)c3ccccc3Cl)cc2C1=O
Show InChI InChI=1S/C23H28ClN3O2/c1-25-11-9-18-7-8-19(17-20(18)23(25)28)29-16-4-10-26-12-14-27(15-13-26)22-6-3-2-5-21(22)24/h2-3,5-8,17H,4,9-16H2,1H3
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UniProtKB/SwissProt

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PC cid
PC sid
UniChem
Article
PubMed
179n/an/an/an/an/an/an/an/a


TBA

Assay Description
Displacement of [3H]ketanserin from rat cerebral cortex 5HT2A receptor measured after 15 mins by liquid scintillation counting method


Citation and Details

Article DOI: 10.1016/j.ejmech.2020.112709
BindingDB Entry DOI: 10.7270/Q2XK8K6M
More data for this
Ligand-Target Pair
D(2) dopamine receptor


(Rattus norvegicus (rat))
BDBM423312
PNG
(US10501452, Compound 18)
Show SMILES CN1CCc2ccc(OCCCN3CCN(CC3)c3ccccc3Cl)cc2C1=O
Show InChI InChI=1S/C23H28ClN3O2/c1-25-11-9-18-7-8-19(17-20(18)23(25)28)29-16-4-10-26-12-14-27(15-13-26)22-6-3-2-5-21(22)24/h2-3,5-8,17H,4,9-16H2,1H3
PDB

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PC cid
PC sid
UniChem
Article
PubMed
391n/an/an/an/an/an/an/an/a


TBA

Assay Description
Displacement of [3H]spiperone from D2 receptor in rat striatum measured after 15 mins by liquid scintillation counting method


Citation and Details

Article DOI: 10.1016/j.ejmech.2020.112709
BindingDB Entry DOI: 10.7270/Q2XK8K6M
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 1A


(Rattus norvegicus (rat))
BDBM423312
PNG
(US10501452, Compound 18)
Show SMILES CN1CCc2ccc(OCCCN3CCN(CC3)c3ccccc3Cl)cc2C1=O
Show InChI InChI=1S/C23H28ClN3O2/c1-25-11-9-18-7-8-19(17-20(18)23(25)28)29-16-4-10-26-12-14-27(15-13-26)22-6-3-2-5-21(22)24/h2-3,5-8,17H,4,9-16H2,1H3
PDB

KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
>2.00E+3n/an/an/an/an/an/an/an/a



NHWA PHARMA. CORPORATION

US Patent


Assay Description
5-HT1A: (1) The prepared membrane was applied with appropriate amount of buffer, and homogenizer was used for evenly dispersing. 15 tubes were mixed ...


US Patent US10501452 (2019)


BindingDB Entry DOI: 10.7270/Q2BK1FR6
More data for this
Ligand-Target Pair
D(2) dopamine receptor


(Homo sapiens (Human))
BDBM423312
PNG
(US10501452, Compound 18)
Show SMILES CN1CCc2ccc(OCCCN3CCN(CC3)c3ccccc3Cl)cc2C1=O
Show InChI InChI=1S/C23H28ClN3O2/c1-25-11-9-18-7-8-19(17-20(18)23(25)28)29-16-4-10-26-12-14-27(15-13-26)22-6-3-2-5-21(22)24/h2-3,5-8,17H,4,9-16H2,1H3
PDB

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DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
>2.00E+3n/an/an/an/an/an/an/an/a



NHWA PHARMA. CORPORATION

US Patent


Assay Description
D2:Procedures(1) The prepared membrane was applied with appropriate amount of buffer, and homogenizer was used for evenly dispersing. 15 tubes were m...


US Patent US10501452 (2019)


BindingDB Entry DOI: 10.7270/Q2BK1FR6
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Rattus norvegicus (rat))
BDBM423312
PNG
(US10501452, Compound 18)
Show SMILES CN1CCc2ccc(OCCCN3CCN(CC3)c3ccccc3Cl)cc2C1=O
Show InChI InChI=1S/C23H28ClN3O2/c1-25-11-9-18-7-8-19(17-20(18)23(25)28)29-16-4-10-26-12-14-27(15-13-26)22-6-3-2-5-21(22)24/h2-3,5-8,17H,4,9-16H2,1H3
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
>2.00E+3n/an/an/an/an/an/an/an/a



NHWA PHARMA. CORPORATION

US Patent


Assay Description
5-HT2A:(1) The prepared membrane was applied with buffer, and homogenizer was used for evenly dispersing. 15 tubes were mixed into a 100 ml container...


US Patent US10501452 (2019)


BindingDB Entry DOI: 10.7270/Q2BK1FR6
More data for this
Ligand-Target Pair