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BDBM50163166 7-Phenyl-1-(5-thiophen-2-yl-oxazol-2-yl)-heptan-1-one::7-phenyl-1-(5-(thiophen-2-yl)oxazol-2-yl)heptan-1-one::CHEMBL178071

SMILES: O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cccs1

InChI Key: InChIKey=CFBRVIBLBRUALR-UHFFFAOYSA-N

Data: 4 KI  3 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 7 hits for monomerid = 50163166   
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
Fatty-acid amide hydrolase 1


(Homo sapiens (Human))
BDBM50163166
PNG
(7-Phenyl-1-(5-thiophen-2-yl-oxazol-2-yl)-heptan-1-...)
Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cccs1
Show InChI InChI=1S/C20H21NO2S/c22-17(20-21-15-18(23-20)19-13-8-14-24-19)12-7-2-1-4-9-16-10-5-3-6-11-16/h3,5-6,8,10-11,13-15H,1-2,4,7,9,12H2
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Article
PubMed
55n/an/an/an/an/an/an/an/a



The Scripps Research Institute

Curated by ChEMBL


Assay Description
Inhibition of FAAH


Bioorg Med Chem Lett 21: 4674-85 (2011)


Article DOI: 10.1016/j.bmcl.2011.06.096
BindingDB Entry DOI: 10.7270/Q2W959JK
More data for this
Ligand-Target Pair
Fatty-acid amide hydrolase 1 (aa 30-579)


(Rattus norvegicus (rat))
BDBM50163166
PNG
(7-Phenyl-1-(5-thiophen-2-yl-oxazol-2-yl)-heptan-1-...)
Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cccs1
Show InChI InChI=1S/C20H21NO2S/c22-17(20-21-15-18(23-20)19-13-8-14-24-19)12-7-2-1-4-9-16-10-5-3-6-11-16/h3,5-6,8,10-11,13-15H,1-2,4,7,9,12H2
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55n/an/an/an/an/an/an/an/a



The Scripps Research Institute

Curated by ChEMBL


Assay Description
Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coli


J Med Chem 48: 1849-56 (2005)


Article DOI: 10.1021/jm049614v
BindingDB Entry DOI: 10.7270/Q2Q52P54
More data for this
Ligand-Target Pair
Fatty-acid amide hydrolase 1 (aa 30-579)


(Rattus norvegicus (rat))
BDBM50163166
PNG
(7-Phenyl-1-(5-thiophen-2-yl-oxazol-2-yl)-heptan-1-...)
Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cccs1
Show InChI InChI=1S/C20H21NO2S/c22-17(20-21-15-18(23-20)19-13-8-14-24-19)12-7-2-1-4-9-16-10-5-3-6-11-16/h3,5-6,8,10-11,13-15H,1-2,4,7,9,12H2
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55n/an/an/an/an/an/a9.0n/a



Institute for Chemical Biology

Curated by ChEMBL


Assay Description
Inhibition of rat FAAH expressed in Escherichia coli at pH 9.0


J Med Chem 51: 4392-403 (2008)


Article DOI: 10.1021/jm800136b
BindingDB Entry DOI: 10.7270/Q26D5TW3
More data for this
Ligand-Target Pair
Fatty-acid amide hydrolase 1


(Homo sapiens (Human))
BDBM50163166
PNG
(7-Phenyl-1-(5-thiophen-2-yl-oxazol-2-yl)-heptan-1-...)
Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cccs1
Show InChI InChI=1S/C20H21NO2S/c22-17(20-21-15-18(23-20)19-13-8-14-24-19)12-7-2-1-4-9-16-10-5-3-6-11-16/h3,5-6,8,10-11,13-15H,1-2,4,7,9,12H2
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55n/an/an/an/an/an/an/an/a



The Scripps Research Institute

Curated by ChEMBL


Assay Description
Inhibition of rat recombinant FAAH expressed in Escherichia coli by [14C]oleamide breakdown


J Med Chem 50: 1058-68 (2007)


Article DOI: 10.1021/jm0611509
BindingDB Entry DOI: 10.7270/Q26H4J6G
More data for this
Ligand-Target Pair
Acyl-CoA: cholesterol acyltransferase (ACAT)


(Homo sapiens (Human))
BDBM50163166
PNG
(7-Phenyl-1-(5-thiophen-2-yl-oxazol-2-yl)-heptan-1-...)
Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cccs1
Show InChI InChI=1S/C20H21NO2S/c22-17(20-21-15-18(23-20)19-13-8-14-24-19)12-7-2-1-4-9-16-10-5-3-6-11-16/h3,5-6,8,10-11,13-15H,1-2,4,7,9,12H2
PDB

KEGG

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PubMed
n/an/a 200n/an/an/an/an/an/a



Institute for Chemical Biology

Curated by ChEMBL


Assay Description
Inhibition of TGH


J Med Chem 51: 4392-403 (2008)


Article DOI: 10.1021/jm800136b
BindingDB Entry DOI: 10.7270/Q26D5TW3
More data for this
Ligand-Target Pair
Neutral cholesterol ester hydrolase 1


(Homo sapiens (Human))
BDBM50163166
PNG
(7-Phenyl-1-(5-thiophen-2-yl-oxazol-2-yl)-heptan-1-...)
Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cccs1
Show InChI InChI=1S/C20H21NO2S/c22-17(20-21-15-18(23-20)19-13-8-14-24-19)12-7-2-1-4-9-16-10-5-3-6-11-16/h3,5-6,8,10-11,13-15H,1-2,4,7,9,12H2
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n/an/a>1.00E+5n/an/an/an/an/an/a



Institute for Chemical Biology

Curated by ChEMBL


Assay Description
Inhibition of KIAA1363 hydrolase


J Med Chem 51: 4392-403 (2008)


Article DOI: 10.1021/jm800136b
BindingDB Entry DOI: 10.7270/Q26D5TW3
More data for this
Ligand-Target Pair
Fatty-acid amide hydrolase 1 (aa 30-579)


(Rattus norvegicus (rat))
BDBM50163166
PNG
(7-Phenyl-1-(5-thiophen-2-yl-oxazol-2-yl)-heptan-1-...)
Show SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cccs1
Show InChI InChI=1S/C20H21NO2S/c22-17(20-21-15-18(23-20)19-13-8-14-24-19)12-7-2-1-4-9-16-10-5-3-6-11-16/h3,5-6,8,10-11,13-15H,1-2,4,7,9,12H2
PDB
MMDB

UniProtKB/SwissProt

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PubMed
n/an/a 55n/an/an/an/an/an/a



Institute for Chemical Biology

Curated by ChEMBL


Assay Description
Inhibition of rat FAAH expressed in Escherichia coli


J Med Chem 51: 4392-403 (2008)


Article DOI: 10.1021/jm800136b
BindingDB Entry DOI: 10.7270/Q26D5TW3
More data for this
Ligand-Target Pair