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SMILES: Cn1c(SCCCN2CCOC(C2)c2ccc(cc2)C(F)(F)F)nnc1-c1ccc(cc1)-n1cnnc1

InChI Key: InChIKey=IHKSAHBRVXUIPJ-UHFFFAOYSA-N

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 5 hits for monomerid = 50139922   
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
D(3) dopamine receptor


(Homo sapiens (Human))
BDBM50139922
PNG
(CHEMBL3765072 | US10577361, E21)
Show SMILES Cn1c(SCCCN2CCOC(C2)c2ccc(cc2)C(F)(F)F)nnc1-c1ccc(cc1)-n1cnnc1
Show InChI InChI=1S/C25H26F3N7OS/c1-33-23(19-5-9-21(10-6-19)35-16-29-30-17-35)31-32-24(33)37-14-2-11-34-12-13-36-22(15-34)18-3-7-20(8-4-18)25(26,27)28/h3-10,16-17,22H,2,11-15H2,1H3
PDB

UniProtKB/SwissProt

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PC sid
UniChem
US Patent
126n/an/an/an/an/an/an/an/a



INDIVIOR UK LIMITED

US Patent


Assay Description
[3H]-Spiperone Binding Assay at hD3 and hD4 recombinant receptors CHO cells transiently transfected with human dopamine type 3 or 4 receptors (CHO-hD...


US Patent US10577361 (2020)


BindingDB Entry DOI: 10.7270/Q2GQ715H
More data for this
Ligand-Target Pair
D(3) dopamine receptor


(Rattus norvegicus (Rat))
BDBM50139922
PNG
(CHEMBL3765072 | US10577361, E21)
Show SMILES Cn1c(SCCCN2CCOC(C2)c2ccc(cc2)C(F)(F)F)nnc1-c1ccc(cc1)-n1cnnc1
Show InChI InChI=1S/C25H26F3N7OS/c1-33-23(19-5-9-21(10-6-19)35-16-29-30-17-35)31-32-24(33)37-14-2-11-34-12-13-36-22(15-34)18-3-7-20(8-4-18)25(26,27)28/h3-10,16-17,22H,2,11-15H2,1H3
KEGG

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126n/an/an/an/an/an/an/an/a



Aptuit s.r.l

Curated by ChEMBL


Assay Description
Displacement of [125I]-7-OH-PIPAT from rat brain dopamine D3 receptor after 45 mins by microplate scintillation counting analysis


Bioorg Med Chem Lett 26: 1329-32 (2016)


BindingDB Entry DOI: 10.7270/Q2HM5B83
More data for this
Ligand-Target Pair
D(2) dopamine receptor


(Homo sapiens (Human))
BDBM50139922
PNG
(CHEMBL3765072 | US10577361, E21)
Show SMILES Cn1c(SCCCN2CCOC(C2)c2ccc(cc2)C(F)(F)F)nnc1-c1ccc(cc1)-n1cnnc1
Show InChI InChI=1S/C25H26F3N7OS/c1-33-23(19-5-9-21(10-6-19)35-16-29-30-17-35)31-32-24(33)37-14-2-11-34-12-13-36-22(15-34)18-3-7-20(8-4-18)25(26,27)28/h3-10,16-17,22H,2,11-15H2,1H3
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9.12E+3n/an/an/an/an/an/an/an/a



INDIVIOR UK LIMITED

US Patent


Assay Description
CHO cells stably expressing human dopamine receptor type 2, long variant (hD2L), coupled to Gα16 protein (CHO-Gα16-hD2L) were re-suspended ...


US Patent US10577361 (2020)


BindingDB Entry DOI: 10.7270/Q2GQ715H
More data for this
Ligand-Target Pair
D(3) dopamine receptor


(Homo sapiens (Human))
BDBM50139922
PNG
(CHEMBL3765072 | US10577361, E21)
Show SMILES Cn1c(SCCCN2CCOC(C2)c2ccc(cc2)C(F)(F)F)nnc1-c1ccc(cc1)-n1cnnc1
Show InChI InChI=1S/C25H26F3N7OS/c1-33-23(19-5-9-21(10-6-19)35-16-29-30-17-35)31-32-24(33)37-14-2-11-34-12-13-36-22(15-34)18-3-7-20(8-4-18)25(26,27)28/h3-10,16-17,22H,2,11-15H2,1H3
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<1.00E+4n/an/an/an/an/an/an/an/a



Aptuit s.r.l

Curated by ChEMBL


Assay Description
Agonist activity at human dopamine D3 receptor expressed in CHO cells after 90 mins by [35S]-GTPgamma S assay


Bioorg Med Chem Lett 26: 1329-32 (2016)


BindingDB Entry DOI: 10.7270/Q2HM5B83
More data for this
Ligand-Target Pair
D(2) dopamine receptor


(Homo sapiens (Human))
BDBM50139922
PNG
(CHEMBL3765072 | US10577361, E21)
Show SMILES Cn1c(SCCCN2CCOC(C2)c2ccc(cc2)C(F)(F)F)nnc1-c1ccc(cc1)-n1cnnc1
Show InChI InChI=1S/C25H26F3N7OS/c1-33-23(19-5-9-21(10-6-19)35-16-29-30-17-35)31-32-24(33)37-14-2-11-34-12-13-36-22(15-34)18-3-7-20(8-4-18)25(26,27)28/h3-10,16-17,22H,2,11-15H2,1H3
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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antibodypedia
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PC cid
PC sid
UniChem
PubMed
1.00E+4n/an/an/an/an/an/an/an/a



Aptuit s.r.l

Curated by ChEMBL


Assay Description
Displacement of [125I]-7-OH-PIPAT from rat brain dopamine D2 receptor after 45 mins by microplate scintillation counting analysis


Bioorg Med Chem Lett 26: 1329-32 (2016)


BindingDB Entry DOI: 10.7270/Q2HM5B83
More data for this
Ligand-Target Pair