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Compile Data Set for Download or QSAR

Marvin 2D Structure

The following exact ligands are found in BindingDB

Wt: 990.1
BDBM50542844

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))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
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1.40n/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))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
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1.40n/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 2


(Homo sapiens (Human))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
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<1.00E+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))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
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>1.00E+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 1


(Homo sapiens (Human))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
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>1.00E+3n/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))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
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<1.00E+3n/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 5


(Homo sapiens (Human))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
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<1.00E+3n/an/an/an/an/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Displacement of [3H]propionyl-pNPY from human 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))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
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>1.00E+3n/an/an/an/an/an/an/an/a



University of Regensburg

Curated by ChEMBL


Assay Description
Displacement of [3H]propionyl-pNPY from human 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))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
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n/an/an/an/a 68n/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))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
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n/an/an/an/a 67n/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))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
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n/an/an/an/a 35n/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))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
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n/an/an/an/a 35n/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))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
PDB

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UniChem
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n/an/an/an/a 117n/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))
BDBM50542844
PNG
(CHEMBL4646391)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCCNC(N)=N)NC(C)=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/C46H71N17O8/c1-25(2)21-36(42(70)59-33(12-7-19-55-45(50)51)40(68)61-35(38(47)66)22-27-14-16-29(65)17-15-27)62-41(69)34(13-8-20-56-46(52)53)60-43(71)37(23-28-24-57-31-10-5-4-9-30(28)31)63-39(67)32(58-26(3)64)11-6-18-54-44(48)49/h4-5,9-10,14-17,24-25,32-37,57,65H,6-8,11-13,18-23H2,1-3H3,(H2,47,66)(H,58,64)(H,59,70)(H,60,71)(H,61,68)(H,62,69)(H,63,67)(H4,48,49,54)(H4,50,51,55)(H4,52,53,56)/t32-,33-,34-,35-,36-,37-/m0/s1
PDB

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UniProtKB/SwissProt

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GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 120n/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