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SMILES: NC(=O)c1cccc([C@@H]2CCC[C@@H]2Nc2ncc(cc2F)C(F)(F)F)c1-n1nccn1

InChI Key: InChIKey=WMEIDAZZXGGFNY-LRDDRELGSA-N

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   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 402146   
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
Orexin receptor type 2


(Homo sapiens (Human))
BDBM402146
PNG
(US10011588, Example 105 | [(1S,2S)-2-{[3-Fluoro-5-...)
Show SMILES NC(=O)c1cccc([C@@H]2CCC[C@@H]2Nc2ncc(cc2F)C(F)(F)F)c1-n1nccn1
Show InChI InChI=1S/C20H18F4N6O/c21-15-9-11(20(22,23)24)10-26-19(15)29-16-6-2-3-12(16)13-4-1-5-14(18(25)31)17(13)30-27-7-8-28-30/h1,4-5,7-10,12,16H,2-3,6H2,(H2,25,31)(H,26,29)/t12-,16-/m0/s1
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PC sid
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n/an/a>1.00E+4n/an/an/an/an/an/a



Vertex



Assay Description
Orexin antagonist activity was determined by measuring changes in intracellular calcium levels using a Ca2+ sensitive fluorescent dye. The changes in...


J Med Chem 52: 6362-8 (2009)


BindingDB Entry DOI: 10.7270/Q2891871
More data for this
Ligand-Target Pair
Orexin/Hypocretin receptor type 1


(Homo sapiens (Human))
BDBM402146
PNG
(US10011588, Example 105 | [(1S,2S)-2-{[3-Fluoro-5-...)
Show SMILES NC(=O)c1cccc([C@@H]2CCC[C@@H]2Nc2ncc(cc2F)C(F)(F)F)c1-n1nccn1
Show InChI InChI=1S/C20H18F4N6O/c21-15-9-11(20(22,23)24)10-26-19(15)29-16-6-2-3-12(16)13-4-1-5-14(18(25)31)17(13)30-27-7-8-28-30/h1,4-5,7-10,12,16H,2-3,6H2,(H2,25,31)(H,26,29)/t12-,16-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 39n/an/an/an/an/an/a



Vertex



Assay Description
Orexin antagonist activity was determined by measuring changes in intracellular calcium levels using a Ca2+ sensitive fluorescent dye. The changes in...


J Med Chem 52: 6362-8 (2009)


BindingDB Entry DOI: 10.7270/Q2891871
More data for this
Ligand-Target Pair