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BDBM50009746 2-(10,10-Dioxo-10H-10lambda*6*-phenoxathiin-1-yl)-ethanol::CHEMBL66677

SMILES: OCCc1cccc2Oc3ccccc3S(=O)(=O)c12

InChI Key: InChIKey=WIDLMPSIFONHNH-UHFFFAOYSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50009746   
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
Monoamine oxidase


(Rattus norvegicus (rat))
BDBM50009746
PNG
(2-(10,10-Dioxo-10H-10lambda*6*-phenoxathiin-1-yl)-...)
Show SMILES OCCc1cccc2Oc3ccccc3S(=O)(=O)c12
Show InChI InChI=1S/C14H12O4S/c15-9-8-10-4-3-6-12-14(10)19(16,17)13-7-2-1-5-11(13)18-12/h1-7,15H,8-9H2
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 20n/an/an/an/an/an/a



The Wellcome Research Laboratories

Curated by ChEMBL


Assay Description
Inhibitory concentration against monoamine oxidase A.


J Med Chem 41: 2118-25 (1998)


Article DOI: 10.1021/jm970862j
BindingDB Entry DOI: 10.7270/Q25T3JM8
More data for this
Ligand-Target Pair
Monoamine oxidase


(Rattus norvegicus (rat))
BDBM50009746
PNG
(2-(10,10-Dioxo-10H-10lambda*6*-phenoxathiin-1-yl)-...)
Show SMILES OCCc1cccc2Oc3ccccc3S(=O)(=O)c12
Show InChI InChI=1S/C14H12O4S/c15-9-8-10-4-3-6-12-14(10)19(16,17)13-7-2-1-5-11(13)18-12/h1-7,15H,8-9H2
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 20n/an/an/an/an/an/a



Burroughs Wellcome Co.

Curated by ChEMBL


Assay Description
The compound was tested in vitro for inhibition of Monoamine Oxidase A from rat brain


J Med Chem 34: 2931-3 (1991)


BindingDB Entry DOI: 10.7270/Q28S4NW2
More data for this
Ligand-Target Pair