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BDBM258571 US10633384, Example 12.33::US9493486, 12.33

SMILES: Fc1cc(COC(=O)N2CC3(C2)CCN(CC3)C(=O)C2CCc3[nH]nnc3C2)ccc1OC(F)(F)F

InChI Key:

Data: 2 IC50

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 2 hits for monomerid = 258571   
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
Ataxin-2


(Homo sapiens (Human))
BDBM258571
PNG
(US10633384, Example 12.33 | US9493486, 12.33)
Show SMILES Fc1cc(COC(=O)N2CC3(C2)CCN(CC3)C(=O)C2CCc3[nH]nnc3C2)ccc1OC(F)(F)F
UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 13n/an/an/an/an/an/a



Hoffmann-La Roche Inc.

US Patent


Assay Description
ATX inhibition was measured by a fluorescence quenching assay using a specifically labeled substrate analogue (MR121 substrate). To obtain this MR121...


US Patent US10633384 (2020)

More data for this
Ligand-Target Pair
Ectonucleotide pyrophosphatase/phosphodiesterase family member 2


(Homo sapiens (Human))
BDBM258571
PNG
(US10633384, Example 12.33 | US9493486, 12.33)
Show SMILES Fc1cc(COC(=O)N2CC3(C2)CCN(CC3)C(=O)C2CCc3[nH]nnc3C2)ccc1OC(F)(F)F
PDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 13n/an/an/an/a8.030



Hoffmann-La Roches Inc.

US Patent


Assay Description
ATX inhibition was measured by a fluorescence quenching assay using a specifically labeled substrate analogue (MR121 substrate). To obtain this MR121...


US Patent US9493486 (2016)


BindingDB Entry DOI: 10.7270/Q2VT1R1K
More data for this
Ligand-Target Pair