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Compile Data Set for Download or QSAR

Marvin 2D Structure

The following exact ligands are found in BindingDB

Wt: 486.5
BDBM208679

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB (change energy unit to kcal/mol)

Found 5 hits in this display   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
C-X-C chemokine receptor type 3/Guanine nucleotide-binding protein subunit alpha-15


(Homo sapiens (Human))
BDBM208679
PNG
(US9266876, 146)
Show SMILES CCc1nc(-c2nc3ccccc3[nH]2)c(s1)N1CCN([C@H](C)C1)C(=O)Cn1cnc2cccnc12
Show InChI InChI=1S/C25H26N8OS/c1-3-20-30-22(23-28-17-7-4-5-8-18(17)29-23)25(35-20)31-11-12-33(16(2)13-31)21(34)14-32-15-27-19-9-6-10-26-24(19)32/h4-10,15-16H,3,11-14H2,1-2H3,(H,28,29)/t16-/m1/s1
PDB

UniProtKB/SwissProt

antibodypedia
antibodypedia
GoogleScholar
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PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/a7.437



Actelion Pharmaceuticals Ltd.

US Patent


Assay Description
The bioactivity of compounds is tested in a fluorometric imaging plate reader (FLIPR: Molecular Devices) using engineered CHO-K1 cells expressing the...


US Patent US9266876 (2016)


BindingDB Entry DOI: 10.7270/Q2DB80NB
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 3


(Homo sapiens (Human))
BDBM208679
PNG
(US9266876, 146)
Show SMILES CCc1nc(-c2nc3ccccc3[nH]2)c(s1)N1CCN([C@H](C)C1)C(=O)Cn1cnc2cccnc12
Show InChI InChI=1S/C25H26N8OS/c1-3-20-30-22(23-28-17-7-4-5-8-18(17)29-23)25(35-20)31-11-12-33(16(2)13-31)21(34)14-32-15-27-19-9-6-10-26-24(19)32/h4-10,15-16H,3,11-14H2,1-2H3,(H,28,29)/t16-/m1/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 1.80n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00675
BindingDB Entry DOI: 10.7270/Q29K4G85
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 3


(Homo sapiens (Human))
BDBM208679
PNG
(US9266876, 146)
Show SMILES CCc1nc(-c2nc3ccccc3[nH]2)c(s1)N1CCN([C@H](C)C1)C(=O)Cn1cnc2cccnc12
Show InChI InChI=1S/C25H26N8OS/c1-3-20-30-22(23-28-17-7-4-5-8-18(17)29-23)25(35-20)31-11-12-33(16(2)13-31)21(34)14-32-15-27-19-9-6-10-26-24(19)32/h4-10,15-16H,3,11-14H2,1-2H3,(H,28,29)/t16-/m1/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 561n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00675
BindingDB Entry DOI: 10.7270/Q29K4G85
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 3


(Homo sapiens (Human))
BDBM208679
PNG
(US9266876, 146)
Show SMILES CCc1nc(-c2nc3ccccc3[nH]2)c(s1)N1CCN([C@H](C)C1)C(=O)Cn1cnc2cccnc12
Show InChI InChI=1S/C25H26N8OS/c1-3-20-30-22(23-28-17-7-4-5-8-18(17)29-23)25(35-20)31-11-12-33(16(2)13-31)21(34)14-32-15-27-19-9-6-10-26-24(19)32/h4-10,15-16H,3,11-14H2,1-2H3,(H,28,29)/t16-/m1/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 862n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00675
BindingDB Entry DOI: 10.7270/Q29K4G85
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM208679
PNG
(US9266876, 146)
Show SMILES CCc1nc(-c2nc3ccccc3[nH]2)c(s1)N1CCN([C@H](C)C1)C(=O)Cn1cnc2cccnc12
Show InChI InChI=1S/C25H26N8OS/c1-3-20-30-22(23-28-17-7-4-5-8-18(17)29-23)25(35-20)31-11-12-33(16(2)13-31)21(34)14-32-15-27-19-9-6-10-26-24(19)32/h4-10,15-16H,3,11-14H2,1-2H3,(H,28,29)/t16-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 960n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00675
BindingDB Entry DOI: 10.7270/Q29K4G85
More data for this
Ligand-Target Pair