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Compile Data Set for Download or QSAR

Found 2 hits of ic50 for monomerid = 50029812   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Monoamine Oxidase Type B (MAO-B)


(Rattus norvegicus (rat))
BDBM50029812
PNG
(3-(5-Biphenyl-4-yl-tetrazol-2-yl)-propan-1-ol | CH...)
Show SMILES OCCCn1nnc(n1)-c1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C16H16N4O/c21-12-4-11-20-18-16(17-19-20)15-9-7-14(8-10-15)13-5-2-1-3-6-13/h1-3,5-10,21H,4,11-12H2
PDB
MMDB

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UniProtKB/SwissProt

GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.36E+3n/an/an/an/an/an/a



Université Paris 7

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against rat brain Monoamine oxidase B


J Med Chem 38: 4786-92 (1996)


Article DOI: 10.1021/jm00024a006
BindingDB Entry DOI: 10.7270/Q2T72GFV
More data for this
Ligand-Target Pair
Monoamine oxidase


(Rattus norvegicus (rat))
BDBM50029812
PNG
(3-(5-Biphenyl-4-yl-tetrazol-2-yl)-propan-1-ol | CH...)
Show SMILES OCCCn1nnc(n1)-c1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C16H16N4O/c21-12-4-11-20-18-16(17-19-20)15-9-7-14(8-10-15)13-5-2-1-3-6-13/h1-3,5-10,21H,4,11-12H2
PDB
MMDB

Reactome pathway

UniProtKB/SwissProt

DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 4.60E+3n/an/an/an/an/an/a



Université Paris 7

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against rat brain Monoamine oxidase A


J Med Chem 38: 4786-92 (1996)


Article DOI: 10.1021/jm00024a006
BindingDB Entry DOI: 10.7270/Q2T72GFV
More data for this
Ligand-Target Pair