BindingDB logo
myBDB logout

BDBM50492435 HWA-285::PROPENTOFYLLINE::Propentofylline

SMILES: CCCn1cnc2n(C)c(=O)n(CCCCC(C)=O)c(=O)c12

InChI Key: InChIKey=RBQOQRRFDPXAGN-UHFFFAOYSA-N

Data: 2 IC50

PDB links: 2 PDB IDs match this monomer.

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 2 hits for monomerid = 50492435   
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
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50492435
PNG
(HWA-285 | PROPENTOFYLLINE | Propentofylline)
Show SMILES CCCn1cnc2n(C)c(=O)n(CCCCC(C)=O)c(=O)c12
Show InChI InChI=1S/C15H22N4O3/c1-4-8-18-10-16-13-12(18)14(21)19(15(22)17(13)3)9-6-5-7-11(2)20/h10H,4-9H2,1-3H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
PDB
UniChem
Article
PubMed
n/an/a 6.40E+3n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human AChE using acetylthiocholine iodide as substrate treated 5 mins before substrate addition measured up to 4 mins by Ellman's metho...


Bioorg Med Chem Lett 23: 4336-41 (2013)


Article DOI: 10.1016/j.bmcl.2013.05.092
BindingDB Entry DOI: 10.7270/Q2JD50Q1
More data for this
Ligand-Target Pair
Cholinesterases; ACHE & BCHE


(Homo sapiens (Human))
BDBM50492435
PNG
(HWA-285 | PROPENTOFYLLINE | Propentofylline)
Show SMILES CCCn1cnc2n(C)c(=O)n(CCCCC(C)=O)c(=O)c12
Show InChI InChI=1S/C15H22N4O3/c1-4-8-18-10-16-13-12(18)14(21)19(15(22)17(13)3)9-6-5-7-11(2)20/h10H,4-9H2,1-3H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
PDB
UniChem
Article
PubMed
n/an/a>5.00E+4n/an/an/an/an/an/a



University of Waterloo

Curated by ChEMBL


Assay Description
Inhibition of human BuChE using S-butyrylthiocholine iodide as substrate treated 5 mins before substrate addition measured up to 4 mins by Ellman's m...


Bioorg Med Chem Lett 23: 4336-41 (2013)


Article DOI: 10.1016/j.bmcl.2013.05.092
BindingDB Entry DOI: 10.7270/Q2JD50Q1
More data for this
Ligand-Target Pair