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Compile Data Set for Download or QSAR

Marvin 2D Structure

The following exact ligands are found in BindingDB

Wt: 1840.0
BDBM50197012

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

Found 4 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 2


(Homo sapiens (Human))
BDBM50197012
PNG
(CHEMBL429005)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](CCCN=C(N)N)NC(=O)OCC1c2ccccc2-c2ccccc12)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |wU:82.86,83.89,4.4,100.104,20.28,67.71,120.124,wD:75.79,8.17,30.39,89.93,59.63,109.113,(14.12,-12.75,;14.12,-14.29,;15.46,-15.06,;12.8,-15.06,;12.8,-16.6,;11.45,-17.36,;10.12,-16.59,;10.12,-15.05,;8.79,-17.36,;8.79,-18.9,;10.12,-19.67,;11.46,-18.9,;12.79,-19.67,;12.79,-21.21,;14.1,-21.97,;11.46,-21.98,;10.12,-21.21,;7.46,-16.59,;6.13,-17.38,;6.13,-18.92,;4.8,-16.61,;4.8,-15.07,;6.13,-14.3,;7.54,-14.93,;8.57,-13.78,;7.8,-12.45,;6.29,-12.77,;3.46,-17.37,;2.13,-16.6,;2.13,-15.06,;.8,-17.37,;.8,-18.91,;2.13,-19.68,;2.13,-21.22,;3.46,-21.99,;3.47,-23.53,;2.12,-24.29,;4.78,-24.29,;-.54,-16.6,;-1.86,-17.39,;-1.86,-18.93,;-3.2,-16.62,;-4.53,-17.39,;-5.86,-16.62,;-6.04,-15.1,;-5.01,-13.96,;-5.48,-12.5,;-6.99,-12.19,;-8.01,-13.32,;-7.54,-14.77,;-8.31,-16.11,;-9.8,-16.44,;-10.27,-17.9,;-9.23,-19.04,;-7.74,-18.71,;-7.27,-17.25,;14.12,-17.37,;14.12,-18.91,;15.45,-16.59,;16.78,-17.36,;16.78,-18.9,;18.11,-19.67,;19.44,-18.9,;18.11,-21.21,;18.11,-16.59,;18.11,-15.05,;19.45,-17.36,;20.79,-16.6,;20.79,-15.06,;22.11,-14.29,;22.11,-12.75,;23.45,-15.06,;22.11,-17.37,;22.11,-18.91,;23.44,-16.59,;24.78,-17.36,;24.78,-18.9,;26.11,-19.67,;23.44,-19.67,;26.11,-16.59,;26.11,-15.05,;27.44,-17.36,;28.78,-16.59,;28.78,-15.05,;27.44,-14.28,;30.1,-14.28,;30.11,-17.36,;30.11,-18.9,;31.44,-16.59,;32.77,-17.36,;32.77,-18.9,;34.09,-19.67,;34.09,-21.21,;35.43,-21.97,;35.43,-23.51,;34.1,-24.28,;36.77,-24.28,;34.09,-16.59,;34.09,-15.05,;35.43,-17.36,;36.77,-16.59,;36.77,-15.05,;38.1,-14.28,;38.1,-12.74,;36.77,-11.97,;39.43,-11.97,;38.1,-17.36,;38.1,-18.9,;39.43,-16.59,;40.76,-17.36,;40.76,-18.9,;42.09,-19.67,;42.09,-21.21,;43.43,-21.98,;43.43,-23.52,;42.09,-24.28,;44.76,-24.28,;42.09,-16.59,;42.09,-15.05,;43.43,-17.36,;44.76,-16.59,;44.76,-15.05,;46.09,-14.28,;47.43,-15.05,;48.76,-14.28,;48.76,-12.74,;50.09,-11.97,;47.43,-11.97,;46.09,-12.74,;46.09,-17.36,;47.43,-16.59,;46.09,-18.9,)|
Show InChI InChI=1S/C87H126N26O19/c1-44(2)35-63(106-78(125)65(38-49-24-28-52(116)29-25-49)108-79(126)66(39-50-41-97-43-101-50)109-75(122)60(21-14-34-100-86(95)96)111-87(131)132-42-57-55-17-10-8-15-53(55)54-16-9-11-18-56(54)57)77(124)110-67(40-69(89)118)80(127)107-64(36-45(3)4)81(128)112-70(46(5)6)82(129)113-71(47(7)114)83(130)104-59(20-13-33-99-85(93)94)73(120)103-61(30-31-68(88)117)76(123)102-58(19-12-32-98-84(91)92)74(121)105-62(72(90)119)37-48-22-26-51(115)27-23-48/h8-11,15-18,22-29,41,43-47,57-67,70-71,114-116H,12-14,19-21,30-40,42H2,1-7H3,(H2,88,117)(H2,89,118)(H2,90,119)(H,97,101)(H,102,123)(H,103,120)(H,104,130)(H,105,121)(H,106,125)(H,107,127)(H,108,126)(H,109,122)(H,110,124)(H,111,131)(H,112,128)(H,113,129)(H4,91,92,98)(H4,93,94,99)(H4,95,96,100)/t47-,58+,59+,60+,61+,62+,63+,64+,65+,66+,67+,70+,71+/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
95n/an/an/an/an/an/an/an/a



Bayer Pharmaceuticals Corporation

Curated by ChEMBL


Assay Description
Displacement of human [125I]PYY from NPY2 receptor expressed in human KAN-TS cells


Bioorg Med Chem Lett 17: 538-41 (2007)


Article DOI: 10.1016/j.bmcl.2006.10.007
BindingDB Entry DOI: 10.7270/Q2959H6F
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 5


(Homo sapiens (Human))
BDBM50197012
PNG
(CHEMBL429005)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](CCCN=C(N)N)NC(=O)OCC1c2ccccc2-c2ccccc12)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |wU:82.86,83.89,4.4,100.104,20.28,67.71,120.124,wD:75.79,8.17,30.39,89.93,59.63,109.113,(14.12,-12.75,;14.12,-14.29,;15.46,-15.06,;12.8,-15.06,;12.8,-16.6,;11.45,-17.36,;10.12,-16.59,;10.12,-15.05,;8.79,-17.36,;8.79,-18.9,;10.12,-19.67,;11.46,-18.9,;12.79,-19.67,;12.79,-21.21,;14.1,-21.97,;11.46,-21.98,;10.12,-21.21,;7.46,-16.59,;6.13,-17.38,;6.13,-18.92,;4.8,-16.61,;4.8,-15.07,;6.13,-14.3,;7.54,-14.93,;8.57,-13.78,;7.8,-12.45,;6.29,-12.77,;3.46,-17.37,;2.13,-16.6,;2.13,-15.06,;.8,-17.37,;.8,-18.91,;2.13,-19.68,;2.13,-21.22,;3.46,-21.99,;3.47,-23.53,;2.12,-24.29,;4.78,-24.29,;-.54,-16.6,;-1.86,-17.39,;-1.86,-18.93,;-3.2,-16.62,;-4.53,-17.39,;-5.86,-16.62,;-6.04,-15.1,;-5.01,-13.96,;-5.48,-12.5,;-6.99,-12.19,;-8.01,-13.32,;-7.54,-14.77,;-8.31,-16.11,;-9.8,-16.44,;-10.27,-17.9,;-9.23,-19.04,;-7.74,-18.71,;-7.27,-17.25,;14.12,-17.37,;14.12,-18.91,;15.45,-16.59,;16.78,-17.36,;16.78,-18.9,;18.11,-19.67,;19.44,-18.9,;18.11,-21.21,;18.11,-16.59,;18.11,-15.05,;19.45,-17.36,;20.79,-16.6,;20.79,-15.06,;22.11,-14.29,;22.11,-12.75,;23.45,-15.06,;22.11,-17.37,;22.11,-18.91,;23.44,-16.59,;24.78,-17.36,;24.78,-18.9,;26.11,-19.67,;23.44,-19.67,;26.11,-16.59,;26.11,-15.05,;27.44,-17.36,;28.78,-16.59,;28.78,-15.05,;27.44,-14.28,;30.1,-14.28,;30.11,-17.36,;30.11,-18.9,;31.44,-16.59,;32.77,-17.36,;32.77,-18.9,;34.09,-19.67,;34.09,-21.21,;35.43,-21.97,;35.43,-23.51,;34.1,-24.28,;36.77,-24.28,;34.09,-16.59,;34.09,-15.05,;35.43,-17.36,;36.77,-16.59,;36.77,-15.05,;38.1,-14.28,;38.1,-12.74,;36.77,-11.97,;39.43,-11.97,;38.1,-17.36,;38.1,-18.9,;39.43,-16.59,;40.76,-17.36,;40.76,-18.9,;42.09,-19.67,;42.09,-21.21,;43.43,-21.98,;43.43,-23.52,;42.09,-24.28,;44.76,-24.28,;42.09,-16.59,;42.09,-15.05,;43.43,-17.36,;44.76,-16.59,;44.76,-15.05,;46.09,-14.28,;47.43,-15.05,;48.76,-14.28,;48.76,-12.74,;50.09,-11.97,;47.43,-11.97,;46.09,-12.74,;46.09,-17.36,;47.43,-16.59,;46.09,-18.9,)|
Show InChI InChI=1S/C87H126N26O19/c1-44(2)35-63(106-78(125)65(38-49-24-28-52(116)29-25-49)108-79(126)66(39-50-41-97-43-101-50)109-75(122)60(21-14-34-100-86(95)96)111-87(131)132-42-57-55-17-10-8-15-53(55)54-16-9-11-18-56(54)57)77(124)110-67(40-69(89)118)80(127)107-64(36-45(3)4)81(128)112-70(46(5)6)82(129)113-71(47(7)114)83(130)104-59(20-13-33-99-85(93)94)73(120)103-61(30-31-68(88)117)76(123)102-58(19-12-32-98-84(91)92)74(121)105-62(72(90)119)37-48-22-26-51(115)27-23-48/h8-11,15-18,22-29,41,43-47,57-67,70-71,114-116H,12-14,19-21,30-40,42H2,1-7H3,(H2,88,117)(H2,89,118)(H2,90,119)(H,97,101)(H,102,123)(H,103,120)(H,104,130)(H,105,121)(H,106,125)(H,107,127)(H,108,126)(H,109,122)(H,110,124)(H,111,131)(H,112,128)(H,113,129)(H4,91,92,98)(H4,93,94,99)(H4,95,96,100)/t47-,58+,59+,60+,61+,62+,63+,64+,65+,66+,67+,70+,71+/m1/s1
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
512n/an/an/an/an/an/an/an/a



Bayer Pharmaceuticals Corporation

Curated by ChEMBL


Assay Description
Displacement of [125I]PYY from NPY5 receptor expressed in human HEK293 cells


Bioorg Med Chem Lett 17: 538-41 (2007)


Article DOI: 10.1016/j.bmcl.2006.10.007
BindingDB Entry DOI: 10.7270/Q2959H6F
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 1


(Homo sapiens (Human))
BDBM50197012
PNG
(CHEMBL429005)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](CCCN=C(N)N)NC(=O)OCC1c2ccccc2-c2ccccc12)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |wU:82.86,83.89,4.4,100.104,20.28,67.71,120.124,wD:75.79,8.17,30.39,89.93,59.63,109.113,(14.12,-12.75,;14.12,-14.29,;15.46,-15.06,;12.8,-15.06,;12.8,-16.6,;11.45,-17.36,;10.12,-16.59,;10.12,-15.05,;8.79,-17.36,;8.79,-18.9,;10.12,-19.67,;11.46,-18.9,;12.79,-19.67,;12.79,-21.21,;14.1,-21.97,;11.46,-21.98,;10.12,-21.21,;7.46,-16.59,;6.13,-17.38,;6.13,-18.92,;4.8,-16.61,;4.8,-15.07,;6.13,-14.3,;7.54,-14.93,;8.57,-13.78,;7.8,-12.45,;6.29,-12.77,;3.46,-17.37,;2.13,-16.6,;2.13,-15.06,;.8,-17.37,;.8,-18.91,;2.13,-19.68,;2.13,-21.22,;3.46,-21.99,;3.47,-23.53,;2.12,-24.29,;4.78,-24.29,;-.54,-16.6,;-1.86,-17.39,;-1.86,-18.93,;-3.2,-16.62,;-4.53,-17.39,;-5.86,-16.62,;-6.04,-15.1,;-5.01,-13.96,;-5.48,-12.5,;-6.99,-12.19,;-8.01,-13.32,;-7.54,-14.77,;-8.31,-16.11,;-9.8,-16.44,;-10.27,-17.9,;-9.23,-19.04,;-7.74,-18.71,;-7.27,-17.25,;14.12,-17.37,;14.12,-18.91,;15.45,-16.59,;16.78,-17.36,;16.78,-18.9,;18.11,-19.67,;19.44,-18.9,;18.11,-21.21,;18.11,-16.59,;18.11,-15.05,;19.45,-17.36,;20.79,-16.6,;20.79,-15.06,;22.11,-14.29,;22.11,-12.75,;23.45,-15.06,;22.11,-17.37,;22.11,-18.91,;23.44,-16.59,;24.78,-17.36,;24.78,-18.9,;26.11,-19.67,;23.44,-19.67,;26.11,-16.59,;26.11,-15.05,;27.44,-17.36,;28.78,-16.59,;28.78,-15.05,;27.44,-14.28,;30.1,-14.28,;30.11,-17.36,;30.11,-18.9,;31.44,-16.59,;32.77,-17.36,;32.77,-18.9,;34.09,-19.67,;34.09,-21.21,;35.43,-21.97,;35.43,-23.51,;34.1,-24.28,;36.77,-24.28,;34.09,-16.59,;34.09,-15.05,;35.43,-17.36,;36.77,-16.59,;36.77,-15.05,;38.1,-14.28,;38.1,-12.74,;36.77,-11.97,;39.43,-11.97,;38.1,-17.36,;38.1,-18.9,;39.43,-16.59,;40.76,-17.36,;40.76,-18.9,;42.09,-19.67,;42.09,-21.21,;43.43,-21.98,;43.43,-23.52,;42.09,-24.28,;44.76,-24.28,;42.09,-16.59,;42.09,-15.05,;43.43,-17.36,;44.76,-16.59,;44.76,-15.05,;46.09,-14.28,;47.43,-15.05,;48.76,-14.28,;48.76,-12.74,;50.09,-11.97,;47.43,-11.97,;46.09,-12.74,;46.09,-17.36,;47.43,-16.59,;46.09,-18.9,)|
Show InChI InChI=1S/C87H126N26O19/c1-44(2)35-63(106-78(125)65(38-49-24-28-52(116)29-25-49)108-79(126)66(39-50-41-97-43-101-50)109-75(122)60(21-14-34-100-86(95)96)111-87(131)132-42-57-55-17-10-8-15-53(55)54-16-9-11-18-56(54)57)77(124)110-67(40-69(89)118)80(127)107-64(36-45(3)4)81(128)112-70(46(5)6)82(129)113-71(47(7)114)83(130)104-59(20-13-33-99-85(93)94)73(120)103-61(30-31-68(88)117)76(123)102-58(19-12-32-98-84(91)92)74(121)105-62(72(90)119)37-48-22-26-51(115)27-23-48/h8-11,15-18,22-29,41,43-47,57-67,70-71,114-116H,12-14,19-21,30-40,42H2,1-7H3,(H2,88,117)(H2,89,118)(H2,90,119)(H,97,101)(H,102,123)(H,103,120)(H,104,130)(H,105,121)(H,106,125)(H,107,127)(H,108,126)(H,109,122)(H,110,124)(H,111,131)(H,112,128)(H,113,129)(H4,91,92,98)(H4,93,94,99)(H4,95,96,100)/t47-,58+,59+,60+,61+,62+,63+,64+,65+,66+,67+,70+,71+/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
>1.00E+3n/an/an/an/an/an/an/an/a



Bayer Pharmaceuticals Corporation

Curated by ChEMBL


Assay Description
Displacement of [125I]PYY from NPY1 receptor expressed in human SK-N-MC cells


Bioorg Med Chem Lett 17: 538-41 (2007)


Article DOI: 10.1016/j.bmcl.2006.10.007
BindingDB Entry DOI: 10.7270/Q2959H6F
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 2


(Homo sapiens (Human))
BDBM50197012
PNG
(CHEMBL429005)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](CCCN=C(N)N)NC(=O)OCC1c2ccccc2-c2ccccc12)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |wU:82.86,83.89,4.4,100.104,20.28,67.71,120.124,wD:75.79,8.17,30.39,89.93,59.63,109.113,(14.12,-12.75,;14.12,-14.29,;15.46,-15.06,;12.8,-15.06,;12.8,-16.6,;11.45,-17.36,;10.12,-16.59,;10.12,-15.05,;8.79,-17.36,;8.79,-18.9,;10.12,-19.67,;11.46,-18.9,;12.79,-19.67,;12.79,-21.21,;14.1,-21.97,;11.46,-21.98,;10.12,-21.21,;7.46,-16.59,;6.13,-17.38,;6.13,-18.92,;4.8,-16.61,;4.8,-15.07,;6.13,-14.3,;7.54,-14.93,;8.57,-13.78,;7.8,-12.45,;6.29,-12.77,;3.46,-17.37,;2.13,-16.6,;2.13,-15.06,;.8,-17.37,;.8,-18.91,;2.13,-19.68,;2.13,-21.22,;3.46,-21.99,;3.47,-23.53,;2.12,-24.29,;4.78,-24.29,;-.54,-16.6,;-1.86,-17.39,;-1.86,-18.93,;-3.2,-16.62,;-4.53,-17.39,;-5.86,-16.62,;-6.04,-15.1,;-5.01,-13.96,;-5.48,-12.5,;-6.99,-12.19,;-8.01,-13.32,;-7.54,-14.77,;-8.31,-16.11,;-9.8,-16.44,;-10.27,-17.9,;-9.23,-19.04,;-7.74,-18.71,;-7.27,-17.25,;14.12,-17.37,;14.12,-18.91,;15.45,-16.59,;16.78,-17.36,;16.78,-18.9,;18.11,-19.67,;19.44,-18.9,;18.11,-21.21,;18.11,-16.59,;18.11,-15.05,;19.45,-17.36,;20.79,-16.6,;20.79,-15.06,;22.11,-14.29,;22.11,-12.75,;23.45,-15.06,;22.11,-17.37,;22.11,-18.91,;23.44,-16.59,;24.78,-17.36,;24.78,-18.9,;26.11,-19.67,;23.44,-19.67,;26.11,-16.59,;26.11,-15.05,;27.44,-17.36,;28.78,-16.59,;28.78,-15.05,;27.44,-14.28,;30.1,-14.28,;30.11,-17.36,;30.11,-18.9,;31.44,-16.59,;32.77,-17.36,;32.77,-18.9,;34.09,-19.67,;34.09,-21.21,;35.43,-21.97,;35.43,-23.51,;34.1,-24.28,;36.77,-24.28,;34.09,-16.59,;34.09,-15.05,;35.43,-17.36,;36.77,-16.59,;36.77,-15.05,;38.1,-14.28,;38.1,-12.74,;36.77,-11.97,;39.43,-11.97,;38.1,-17.36,;38.1,-18.9,;39.43,-16.59,;40.76,-17.36,;40.76,-18.9,;42.09,-19.67,;42.09,-21.21,;43.43,-21.98,;43.43,-23.52,;42.09,-24.28,;44.76,-24.28,;42.09,-16.59,;42.09,-15.05,;43.43,-17.36,;44.76,-16.59,;44.76,-15.05,;46.09,-14.28,;47.43,-15.05,;48.76,-14.28,;48.76,-12.74,;50.09,-11.97,;47.43,-11.97,;46.09,-12.74,;46.09,-17.36,;47.43,-16.59,;46.09,-18.9,)|
Show InChI InChI=1S/C87H126N26O19/c1-44(2)35-63(106-78(125)65(38-49-24-28-52(116)29-25-49)108-79(126)66(39-50-41-97-43-101-50)109-75(122)60(21-14-34-100-86(95)96)111-87(131)132-42-57-55-17-10-8-15-53(55)54-16-9-11-18-56(54)57)77(124)110-67(40-69(89)118)80(127)107-64(36-45(3)4)81(128)112-70(46(5)6)82(129)113-71(47(7)114)83(130)104-59(20-13-33-99-85(93)94)73(120)103-61(30-31-68(88)117)76(123)102-58(19-12-32-98-84(91)92)74(121)105-62(72(90)119)37-48-22-26-51(115)27-23-48/h8-11,15-18,22-29,41,43-47,57-67,70-71,114-116H,12-14,19-21,30-40,42H2,1-7H3,(H2,88,117)(H2,89,118)(H2,90,119)(H,97,101)(H,102,123)(H,103,120)(H,104,130)(H,105,121)(H,106,125)(H,107,127)(H,108,126)(H,109,122)(H,110,124)(H,111,131)(H,112,128)(H,113,129)(H4,91,92,98)(H4,93,94,99)(H4,95,96,100)/t47-,58+,59+,60+,61+,62+,63+,64+,65+,66+,67+,70+,71+/m1/s1
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n/an/an/an/a 106n/an/an/an/a



Bayer Pharmaceuticals Corporation

Curated by ChEMBL


Assay Description
Agonist activity at human NPY2 receptor expressed in human KAN-TS cells by [35S]GTPgammaS incorporation assay


Bioorg Med Chem Lett 17: 538-41 (2007)


Article DOI: 10.1016/j.bmcl.2006.10.007
BindingDB Entry DOI: 10.7270/Q2959H6F
More data for this
Ligand-Target Pair