BindingDB logo
myBDB logout

BDBM176018 US10047103, 51::US9688695, 51

SMILES: COc1nn2cc(nc2s1)-c1cc2c(OCc3csc(n3)N3C[C@H](C)O[C@H](C)C3)cc(OC)cc2o1

InChI Key: InChIKey=XCRBATARHOSVCH-OKILXGFUSA-N

Data: 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 2 hits for monomerid = 176018   
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
Proteinase-activated receptor 4 (PAR4)


(Homo sapiens (Human))
BDBM176018
PNG
(US10047103, 51 | US9688695, 51)
Show SMILES COc1nn2cc(nc2s1)-c1cc2c(OCc3csc(n3)N3C[C@H](C)O[C@H](C)C3)cc(OC)cc2o1 |r|
Show InChI InChI=1S/C24H25N5O5S2/c1-13-8-28(9-14(2)33-13)22-25-15(12-35-22)11-32-19-5-16(30-3)6-20-17(19)7-21(34-20)18-10-29-23(26-18)36-24(27-29)31-4/h5-7,10,12-14H,8-9,11H2,1-4H3/t13-,14+
UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a 0.260n/an/an/a25



BRISTOL-MYERS SQUIBB COMPANY

US Patent


Assay Description
Briefly, HEK293 EBNA PAR4 clone 20664.1J cells were plated 24 hrs. prior to experiment in 384 well, Poly-D-Lysine coated, black, clear bottom plates ...


US Patent US9688695 (2017)


BindingDB Entry DOI: 10.7270/Q28K777N
More data for this
Ligand-Target Pair
Proteinase-activated receptor 4 (PAR4)


(Homo sapiens (Human))
BDBM176018
PNG
(US10047103, 51 | US9688695, 51)
Show SMILES COc1nn2cc(nc2s1)-c1cc2c(OCc3csc(n3)N3C[C@H](C)O[C@H](C)C3)cc(OC)cc2o1 |r|
Show InChI InChI=1S/C24H25N5O5S2/c1-13-8-28(9-14(2)33-13)22-25-15(12-35-22)11-32-19-5-16(30-3)6-20-17(19)7-21(34-20)18-10-29-23(26-18)36-24(27-29)31-4/h5-7,10,12-14H,8-9,11H2,1-4H3/t13-,14+
UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a 0.260n/an/an/a25



Bristol-Myers Squibb Company; Universite de Montreal

US Patent


Assay Description
The activity of the PAR4 antagonists of the present invention were tested in PAR4 expressing cells by monitoring H-Ala-Phe(4-F)-Pro-Gly-Trp-Leu-Val-L...


US Patent US10047103 (2018)


BindingDB Entry DOI: 10.7270/Q2QF8VWN
More data for this
Ligand-Target Pair