BDBM39664 (6-bromo-1-butyl-2,3-dihydropyrrolo[2,3-b]quinolin-4-yl)amine;hydrochloride::6-bromanyl-1-butyl-2,3-dihydropyrrolo[2,3-b]quinolin-4-amine;hydrochloride::6-bromo-1-butyl-2,3-dihydro-1H-pyrrolo[2,3-b]quinolin-4-amine hydrochloride::6-bromo-1-butyl-2,3-dihydropyrrolo[2,3-b]quinolin-4-amine;hydrochloride::MLS000532161::SMR000137102::cid_2831789

SMILES CCCCN1CCc2c1nc1ccc(Br)cc1c2N

InChI Key InChIKey=XHNLICSHYXRRRU-UHFFFAOYSA-N

Data  3 IC50  2 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 39664   

TargetAcetylcholinesterase(Electric eel)
Nanjing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM39664(MLS000532161 | SMR000137102 | 6-bromo-1-butyl-2,3-...)
Affinity DataIC50: 300nMAssay Description:Inhibition of Electrophorus electricus AChE pre-incubated for 5 mins before acetylthiocholine iodide substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2016
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Nanjing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM39664(MLS000532161 | SMR000137102 | 6-bromo-1-butyl-2,3-...)
Affinity DataIC50: 8.92E+3nMAssay Description:Inhibition of equine serum BChE pre-incubated for 5 mins before butyrylthiocholineiodide substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/17/2016
Entry Details Article
PubMed
TargetAlkaline phosphatase, germ cell type(Human)
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM39664(MLS000532161 | SMR000137102 | 6-bromo-1-butyl-2,3-...)
Affinity DataEC50:  7.72E+4nMAssay Description:Sanford-Burnham Center for Chemical Genomics (SBCCG) Sanford-Burnham Medical Research Institute (SBMRI, San Diego, CA) NIH Molecular Libraries Screen...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/8/2011
Entry Details
PCBioAssay
TargetXylosyl- and glucuronyltransferase LARGE1(Human)
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM39664(MLS000532161 | SMR000137102 | 6-bromo-1-butyl-2,3-...)
Affinity DataEC50: >8.00E+4nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2013
Entry Details
PCBioAssay
TargetAlkaline phosphatase, germ cell type(Human)
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM39664(MLS000532161 | SMR000137102 | 6-bromo-1-butyl-2,3-...)
Affinity DataIC50: 9.99E+5nMAssay Description:Sanford-Burnham Center for Chemical Genomics (SBCCG) Sanford-Burnham Medical Research Institute (SBMRI, San Diego, CA) NIH Molecular Libraries Screen...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/30/2011
Entry Details
PCBioAssay