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BDBM50432917 CHEMBL2376858

SMILES: CN(CCCCc1ccccc1)C(=O)n1nnnc1Cc1ccc(cc1)-c1ccccc1

InChI Key: InChIKey=SGPVVHIANGEMSB-UHFFFAOYSA-N

Data: 4 IC50  2 EC50

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 6 hits for monomerid = 50432917   
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
Monoglyceride lipase


(Homo sapiens (Human))
BDBM50432917
PNG
(CHEMBL2376858)
Show SMILES CN(CCCCc1ccccc1)C(=O)n1nnnc1Cc1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C26H27N5O/c1-30(19-9-8-12-21-10-4-2-5-11-21)26(32)31-25(27-28-29-31)20-22-15-17-24(18-16-22)23-13-6-3-7-14-23/h2-7,10-11,13-18H,8-9,12,19-20H2,1H3
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n/an/a>1.00E+3n/an/an/an/an/an/a



Sapienza Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of MAGL (unknown origin) expressed in African green monkey COS7 cell cytosolic fraction assessed as [3H]2-AG hydrolysis to [3H]arachidonic...


Eur J Med Chem 63: 118-32 (2013)


Article DOI: 10.1016/j.ejmech.2013.02.005
BindingDB Entry DOI: 10.7270/Q2K64KFB
More data for this
Ligand-Target Pair
Fatty-acid amide hydrolase 1 (aa 30-579)


(Rattus norvegicus (rat))
BDBM50432917
PNG
(CHEMBL2376858)
Show SMILES CN(CCCCc1ccccc1)C(=O)n1nnnc1Cc1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C26H27N5O/c1-30(19-9-8-12-21-10-4-2-5-11-21)26(32)31-25(27-28-29-31)20-22-15-17-24(18-16-22)23-13-6-3-7-14-23/h2-7,10-11,13-18H,8-9,12,19-20H2,1H3
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n/an/a 21n/an/an/an/an/an/a



Sapienza Universit£ di Roma

Curated by ChEMBL


Assay Description
Inhibition of FAAH in rat brain membranes assessed as [14C]AEA hydrolysis to [14C]Ethanolamine after 30 mins by scintillation counting analysis


Eur J Med Chem 63: 118-32 (2013)


Article DOI: 10.1016/j.ejmech.2013.02.005
BindingDB Entry DOI: 10.7270/Q2K64KFB
More data for this
Ligand-Target Pair
Transient receptor potential cation channel subfamily V member 1


(Homo sapiens (Human))
BDBM50432917
PNG
(CHEMBL2376858)
Show SMILES CN(CCCCc1ccccc1)C(=O)n1nnnc1Cc1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C26H27N5O/c1-30(19-9-8-12-21-10-4-2-5-11-21)26(32)31-25(27-28-29-31)20-22-15-17-24(18-16-22)23-13-6-3-7-14-23/h2-7,10-11,13-18H,8-9,12,19-20H2,1H3
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n/an/an/an/a 1.50E+3n/an/an/an/a



Sapienza Universit£ di Roma

Curated by ChEMBL


Assay Description
Agonist activity at human TRPV1 receptor expressed in HEK293 cells assessed as increase in intracellular Ca2+ concentration by spectrofluorimetric an...


Eur J Med Chem 63: 118-32 (2013)


Article DOI: 10.1016/j.ejmech.2013.02.005
BindingDB Entry DOI: 10.7270/Q2K64KFB
More data for this
Ligand-Target Pair
Transient receptor potential cation channel subfamily A member 1


(Rattus norvegicus)
BDBM50432917
PNG
(CHEMBL2376858)
Show SMILES CN(CCCCc1ccccc1)C(=O)n1nnnc1Cc1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C26H27N5O/c1-30(19-9-8-12-21-10-4-2-5-11-21)26(32)31-25(27-28-29-31)20-22-15-17-24(18-16-22)23-13-6-3-7-14-23/h2-7,10-11,13-18H,8-9,12,19-20H2,1H3
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n/an/an/an/a 2.01E+4n/an/an/an/a



Sapienza Universit£ di Roma

Curated by ChEMBL


Assay Description
Agonist activity at rat TRPA1 receptor expressed in HEK293 cells assessed as increase in intracellular Ca2+ concentration by spectrofluorimetric anal...


Eur J Med Chem 63: 118-32 (2013)


Article DOI: 10.1016/j.ejmech.2013.02.005
BindingDB Entry DOI: 10.7270/Q2K64KFB
More data for this
Ligand-Target Pair
Transient receptor potential cation channel subfamily V member 1


(Homo sapiens (Human))
BDBM50432917
PNG
(CHEMBL2376858)
Show SMILES CN(CCCCc1ccccc1)C(=O)n1nnnc1Cc1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C26H27N5O/c1-30(19-9-8-12-21-10-4-2-5-11-21)26(32)31-25(27-28-29-31)20-22-15-17-24(18-16-22)23-13-6-3-7-14-23/h2-7,10-11,13-18H,8-9,12,19-20H2,1H3
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n/an/a 7.10E+3n/an/an/an/an/an/a



Sapienza Universit£ di Roma

Curated by ChEMBL


Assay Description
Antagonist activity at human TRPV1 receptor expressed in HEK293 cells assessed as inhibition of capsaicin-induced intracellular Ca2+ elevation incuba...


Eur J Med Chem 63: 118-32 (2013)


Article DOI: 10.1016/j.ejmech.2013.02.005
BindingDB Entry DOI: 10.7270/Q2K64KFB
More data for this
Ligand-Target Pair
Transient receptor potential cation channel subfamily A member 1


(Rattus norvegicus)
BDBM50432917
PNG
(CHEMBL2376858)
Show SMILES CN(CCCCc1ccccc1)C(=O)n1nnnc1Cc1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C26H27N5O/c1-30(19-9-8-12-21-10-4-2-5-11-21)26(32)31-25(27-28-29-31)20-22-15-17-24(18-16-22)23-13-6-3-7-14-23/h2-7,10-11,13-18H,8-9,12,19-20H2,1H3
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PC sid
UniChem

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Article
PubMed
n/an/a 8.37E+4n/an/an/an/an/an/a



Sapienza Universit£ di Roma

Curated by ChEMBL


Assay Description
Antagonist activity at rat TRPA1 receptor expressed in HEK293 cells assessed as inhibition of allyl isothiocyanate-induced intracellular Ca2+ elevati...


Eur J Med Chem 63: 118-32 (2013)


Article DOI: 10.1016/j.ejmech.2013.02.005
BindingDB Entry DOI: 10.7270/Q2K64KFB
More data for this
Ligand-Target Pair