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Compile Data Set for Download or QSAR

Marvin 2D Structure

The following exact ligands are found in BindingDB

Wt: 1025.1
BDBM50542847

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

Found 14 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
Neuropeptide Y receptor type 4


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
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4n/an/an/an/an/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Displacement of [3H]UR-KK200 from human Y4 receptor expressed in CHO cells co-expressing Gqi5-mtAEQ measured after 90 mins by scintillation counting ...


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 4


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
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4n/an/an/an/an/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Displacement of [3H]UR-KK200 from human Y4 receptor expressed in CHO cells co-expressing Gqi5-mtAEQ measured after 90 mins by scintillation counting ...


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 1


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
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>300n/an/an/an/an/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Displacement of [3H]UR-MK299 from Y1 receptor in human SK-N-MC cells


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 1


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
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<316n/an/an/an/an/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Displacement of [3H]UR-MK299 from Y1 receptor in human SK-N-MC cells


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 2


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
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>3.00E+3n/an/an/an/an/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Displacement of [3H]propionyl-pNPY from human Y2 receptor expressed in CHO cells measured after 2 hrs by microbeta liquid scintillation counting anal...


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 2


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
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<3.16E+3n/an/an/an/an/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Displacement of [3H]propionyl-pNPY from human Y2 receptor expressed in CHO cells measured after 2 hrs by microbeta liquid scintillation counting anal...


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 5


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
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<1.00E+4n/an/an/an/an/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Displacement of [3H]propionyl-pNPY from human Y5 receptor expressed in human HEC1B cells


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 5


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
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>1.00E+4n/an/an/an/an/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Displacement of [3H]propionyl-pNPY from human Y5 receptor expressed in human HEC1B cells


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 4


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
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n/an/an/an/a 457n/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Agonist activity at human Y4R expressed in HEK293T cells co-expressing ARRB1 assessed as induction of beta-arrestin1 recruitment measured for 40 mins...


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 4


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
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n/an/an/an/a 460n/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Agonist activity at human Y4R expressed in HEK293T cells co-expressing ARRB1 assessed as induction of beta-arrestin1 recruitment measured for 40 mins...


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 4


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
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n/an/an/an/a 427n/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Agonist activity at human Y4R expressed in HEK293T cells co-expressing ARRB2 assessed as induction of beta-arrestin2 recruitment measured for 40 mins...


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 4


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
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n/an/an/an/a 430n/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Agonist activity at human Y4R expressed in HEK293T cells co-expressing ARRB2 assessed as induction of beta-arrestin2 recruitment measured for 40 mins...


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 4


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
PDB

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UniChem
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n/an/an/an/a 617n/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Agonist activity at human Y4 receptor expressed in CHO cells co-expressing Gqi5-mtAEQ assessed as intracellular calcium mobilization measured for 43 ...


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 4


(Homo sapiens (Human))
BDBM50542847
PNG
(CHEMBL4637617)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C46H72N16O11/c1-25(2)22-34(42(72)58-31(7-4-20-55-45(50)51)40(70)60-33(38(47)68)23-26-9-13-28(63)14-10-26)61-41(71)32(8-5-21-56-46(52)53)59-43(73)35(24-27-11-15-29(64)16-12-27)62-39(69)30(6-3-19-54-44(48)49)57-36(65)17-18-37(66)67/h9-16,25,30-35,63-64H,3-8,17-24H2,1-2H3,(H2,47,68)(H,57,65)(H,58,72)(H,59,73)(H,60,70)(H,61,71)(H,62,69)(H,66,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t30-,31-,32-,33-,34-,35-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 620n/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Agonist activity at human Y4 receptor expressed in CHO cells co-expressing Gqi5-mtAEQ assessed as intracellular calcium mobilization measured for 43 ...


J Med Chem 63: 8198-8215 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00426
BindingDB Entry DOI: 10.7270/Q22R3W7V
More data for this
Ligand-Target Pair