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BDBM50060471 4-Chloro-5,6-dihydro-benzo[c]acridin-7-ylamine::CHEMBL333011

SMILES: Nc1c2CCc3c(Cl)cccc3-c2nc2ccccc12

InChI Key: InChIKey=WTSAZZJEZMYESQ-UHFFFAOYSA-N

Data: 4 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50060471   
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
Norepinephrine Monoamine transporters


(Rattus norvegicus)
BDBM50060471
PNG
(4-Chloro-5,6-dihydro-benzo[c]acridin-7-ylamine | C...)
Show SMILES Nc1c2CCc3c(Cl)cccc3-c2nc2ccccc12
Show InChI InChI=1S/C17H13ClN2/c18-14-6-3-5-11-10(14)8-9-13-16(19)12-4-1-2-7-15(12)20-17(11)13/h1-7H,8-9H2,(H2,19,20)
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UniProtKB/TrEMBL

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CHEMBL
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PC sid
UniChem

Similars

Article
PubMed
n/an/a 4.10E+4n/an/an/an/an/an/a



University of Strathclyde

Curated by ChEMBL


Assay Description
Inhibition of neuronal uptake of Noradrenaline in rat brain homogenate


J Med Chem 40: 3516-23 (1997)


Article DOI: 10.1021/jm970150t
BindingDB Entry DOI: 10.7270/Q25H7FC9
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Rattus norvegicus (rat))
BDBM50060471
PNG
(4-Chloro-5,6-dihydro-benzo[c]acridin-7-ylamine | C...)
Show SMILES Nc1c2CCc3c(Cl)cccc3-c2nc2ccccc12
Show InChI InChI=1S/C17H13ClN2/c18-14-6-3-5-11-10(14)8-9-13-16(19)12-4-1-2-7-15(12)20-17(11)13/h1-7H,8-9H2,(H2,19,20)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

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Article
PubMed
n/an/a 1.44E+5n/an/an/an/an/an/a



University of Strathclyde

Curated by ChEMBL


Assay Description
In vitro inhibition of acetylcholinesterase, isolated from rat brain.


J Med Chem 40: 3516-23 (1997)


Article DOI: 10.1021/jm970150t
BindingDB Entry DOI: 10.7270/Q25H7FC9
More data for this
Ligand-Target Pair
Sodium-dependent serotonin transporter


(Rattus norvegicus (rat))
BDBM50060471
PNG
(4-Chloro-5,6-dihydro-benzo[c]acridin-7-ylamine | C...)
Show SMILES Nc1c2CCc3c(Cl)cccc3-c2nc2ccccc12
Show InChI InChI=1S/C17H13ClN2/c18-14-6-3-5-11-10(14)8-9-13-16(19)12-4-1-2-7-15(12)20-17(11)13/h1-7H,8-9H2,(H2,19,20)
PDB

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UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.43E+4n/an/an/an/an/an/a



University of Strathclyde

Curated by ChEMBL


Assay Description
Inhibition of neuronal uptake of 5 - Hydroxytryptamine in rat brain homogenate


J Med Chem 40: 3516-23 (1997)


Article DOI: 10.1021/jm970150t
BindingDB Entry DOI: 10.7270/Q25H7FC9
More data for this
Ligand-Target Pair
Cholinesterases


(Homo sapiens (Human))
BDBM50060471
PNG
(4-Chloro-5,6-dihydro-benzo[c]acridin-7-ylamine | C...)
Show SMILES Nc1c2CCc3c(Cl)cccc3-c2nc2ccccc12
Show InChI InChI=1S/C17H13ClN2/c18-14-6-3-5-11-10(14)8-9-13-16(19)12-4-1-2-7-15(12)20-17(11)13/h1-7H,8-9H2,(H2,19,20)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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antibodypedia
GoogleScholar
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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.03E+4n/an/an/an/an/an/a



University of Strathclyde

Curated by ChEMBL


Assay Description
In vitro inhibition of Butyrylcholinesterase from human plasma.


J Med Chem 40: 3516-23 (1997)


Article DOI: 10.1021/jm970150t
BindingDB Entry DOI: 10.7270/Q25H7FC9
More data for this
Ligand-Target Pair