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BDBM50426960 CHEMBL2325072

SMILES: Cc1cc2oc(nc2cc1Cl)N1CCC(CC1)C(=O)N[C@H]1CC[C@H](CC1)C(C)(C)O

InChI Key: InChIKey=TVJHIGHWTRUKJB-CALCHBBNSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50426960   
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
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50426960
PNG
(CHEMBL2325072)
Show SMILES Cc1cc2oc(nc2cc1Cl)N1CCC(CC1)C(=O)N[C@H]1CC[C@H](CC1)C(C)(C)O |r,wU:20.22,23.29,(3.97,-46.23,;5.31,-45.46,;6.64,-46.23,;7.97,-45.46,;9.45,-45.94,;10.36,-44.69,;9.45,-43.43,;7.97,-43.91,;6.64,-43.15,;5.31,-43.92,;3.98,-43.15,;11.9,-44.69,;12.66,-46.03,;14.19,-46.03,;14.97,-44.7,;14.2,-43.37,;12.66,-43.36,;16.51,-44.71,;17.28,-43.38,;17.27,-46.04,;18.81,-46.05,;19.58,-44.73,;21.13,-44.74,;21.89,-46.08,;21.11,-47.41,;19.57,-47.4,;23.43,-46.09,;24.21,-44.77,;24.97,-46.09,;24.19,-47.43,)|
Show InChI InChI=1S/C23H32ClN3O3/c1-14-12-20-19(13-18(14)24)26-22(30-20)27-10-8-15(9-11-27)21(28)25-17-6-4-16(5-7-17)23(2,3)29/h12-13,15-17,29H,4-11H2,1-3H3,(H,25,28)/t16-,17+
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PC cid
PC sid
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Similars

Article
PubMed
n/an/a 34n/an/an/an/an/an/a



Pfizer Inc.

Curated by ChEMBL


Assay Description
Inhibition of human mPGES1 by ELISA


Bioorg Med Chem Lett 23: 1120-6 (2013)


Article DOI: 10.1016/j.bmcl.2012.11.107
BindingDB Entry DOI: 10.7270/Q26W9CDS
More data for this
Ligand-Target Pair
Prostaglandin E synthase


(Homo sapiens (Human))
BDBM50426960
PNG
(CHEMBL2325072)
Show SMILES Cc1cc2oc(nc2cc1Cl)N1CCC(CC1)C(=O)N[C@H]1CC[C@H](CC1)C(C)(C)O |r,wU:20.22,23.29,(3.97,-46.23,;5.31,-45.46,;6.64,-46.23,;7.97,-45.46,;9.45,-45.94,;10.36,-44.69,;9.45,-43.43,;7.97,-43.91,;6.64,-43.15,;5.31,-43.92,;3.98,-43.15,;11.9,-44.69,;12.66,-46.03,;14.19,-46.03,;14.97,-44.7,;14.2,-43.37,;12.66,-43.36,;16.51,-44.71,;17.28,-43.38,;17.27,-46.04,;18.81,-46.05,;19.58,-44.73,;21.13,-44.74,;21.89,-46.08,;21.11,-47.41,;19.57,-47.4,;23.43,-46.09,;24.21,-44.77,;24.97,-46.09,;24.19,-47.43,)|
Show InChI InChI=1S/C23H32ClN3O3/c1-14-12-20-19(13-18(14)24)26-22(30-20)27-10-8-15(9-11-27)21(28)25-17-6-4-16(5-7-17)23(2,3)29/h12-13,15-17,29H,4-11H2,1-3H3,(H,25,28)/t16-,17+
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 570n/an/an/an/an/an/a



Pfizer Inc.

Curated by ChEMBL


Assay Description
Inhibition of mPGES1 mediated PGE2 production in LPS-stimulated human whole blood by ELISA


Bioorg Med Chem Lett 23: 1120-6 (2013)


Article DOI: 10.1016/j.bmcl.2012.11.107
BindingDB Entry DOI: 10.7270/Q26W9CDS
More data for this
Ligand-Target Pair