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BDBM50197021 (2S)-N-[(1S)-4-carbamimidamido-1-{[(1S)-1-carbamoyl-2-(4-hydroxyphenyl)ethyl]carbamoyl}butyl]-2-[(2S)-5-carbamimidamido-2-[(2S,3R)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-5-carbamimidamido-2-(phenylformamido)pentanamido]-3-(1H-imidazol-5-yl)propanamido]-3-(4-hydroxyphenyl)propanamido]-4-methylpentanamido]-3-carbamoylpropanamido]-4-methylpentanamido]-3-methylbutanamido]-3-hydroxybutanamido]pentanamido]pentanediamide::CHEMBL437290

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)c1ccccc1)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

InChI Key: InChIKey=JKFWONLWKVRWQV-FGYHNYNQSA-N

Data: 3 KI  1 EC50

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 4 hits for monomerid = 50197021   
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
Neuropeptide Y receptor type 2


(Homo sapiens (Human))
BDBM50197021
PNG
((2S)-N-[(1S)-4-carbamimidamido-1-{[(1S)-1-carbamoy...)
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)c1ccccc1)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:73.75,74.78,4.4,91.93,20.28,58.60,111.113,wD:66.68,8.17,30.39,80.82,50.52,100.102,(12.08,-14.52,;12.08,-16.06,;13.42,-16.83,;10.75,-16.83,;10.75,-18.37,;9.41,-19.13,;8.08,-18.36,;8.08,-16.82,;6.75,-19.13,;6.75,-20.67,;8.08,-21.44,;9.41,-20.67,;10.75,-21.44,;10.75,-22.98,;12.06,-23.74,;9.41,-23.75,;8.08,-22.98,;5.41,-18.36,;4.09,-19.14,;4.09,-20.68,;2.76,-18.37,;2.76,-16.83,;4.09,-16.06,;5.49,-16.69,;6.53,-15.54,;5.76,-14.21,;4.25,-14.53,;1.42,-19.13,;.08,-18.36,;.08,-16.82,;-1.25,-19.13,;-1.25,-20.67,;.08,-21.44,;.08,-22.98,;1.42,-23.75,;1.43,-25.29,;.08,-26.06,;2.74,-26.06,;-2.58,-18.37,;-3.91,-19.15,;-3.9,-20.69,;-5.24,-18.39,;-5.24,-16.85,;-6.57,-16.08,;-7.91,-16.85,;-7.9,-18.4,;-6.57,-19.16,;12.08,-19.14,;12.08,-20.68,;13.41,-18.36,;14.74,-19.13,;14.74,-20.67,;16.07,-21.44,;17.4,-20.66,;16.07,-22.98,;16.07,-18.36,;16.07,-16.82,;17.4,-19.13,;18.74,-18.36,;18.74,-16.82,;20.07,-16.05,;20.07,-14.51,;21.41,-16.82,;20.07,-19.13,;20.07,-20.67,;21.4,-18.36,;22.73,-19.13,;22.73,-20.67,;24.06,-21.44,;21.4,-21.44,;24.06,-18.36,;24.06,-16.82,;25.4,-19.13,;26.73,-18.36,;26.73,-16.82,;25.4,-16.05,;28.06,-16.04,;28.06,-19.13,;28.06,-20.67,;29.39,-18.35,;30.72,-19.13,;30.72,-20.67,;32.05,-21.44,;32.05,-22.98,;33.39,-23.74,;33.39,-25.28,;32.05,-26.04,;34.73,-26.04,;32.05,-18.36,;32.05,-16.82,;33.39,-19.12,;34.73,-18.36,;34.73,-16.82,;36.05,-16.05,;36.05,-14.51,;34.72,-13.73,;37.39,-13.74,;36.05,-19.13,;36.05,-20.67,;37.39,-18.36,;38.72,-19.13,;38.72,-20.67,;40.05,-21.44,;40.05,-22.98,;41.38,-23.74,;41.38,-25.28,;40.05,-26.05,;42.72,-26.05,;40.05,-18.36,;40.05,-16.82,;41.38,-19.13,;42.72,-18.36,;42.72,-16.82,;44.05,-16.05,;45.38,-16.82,;46.72,-16.05,;46.72,-14.51,;48.05,-13.74,;45.38,-13.74,;44.05,-14.51,;44.05,-19.13,;45.38,-18.36,;44.05,-20.67,)|
Show InChI InChI=1S/C79H120N26O18/c1-40(2)32-55(99-71(118)57(35-45-21-25-49(108)26-22-45)101-72(119)58(36-47-38-89-39-93-47)102-68(115)50(16-11-29-90-77(83)84)94-65(112)46-14-9-8-10-15-46)70(117)103-59(37-61(81)110)73(120)100-56(33-41(3)4)74(121)104-62(42(5)6)75(122)105-63(43(7)106)76(123)97-52(18-13-31-92-79(87)88)66(113)96-53(27-28-60(80)109)69(116)95-51(17-12-30-91-78(85)86)67(114)98-54(64(82)111)34-44-19-23-48(107)24-20-44/h8-10,14-15,19-26,38-43,50-59,62-63,106-108H,11-13,16-18,27-37H2,1-7H3,(H2,80,109)(H2,81,110)(H2,82,111)(H,89,93)(H,94,112)(H,95,116)(H,96,113)(H,97,123)(H,98,114)(H,99,118)(H,100,120)(H,101,119)(H,102,115)(H,103,117)(H,104,121)(H,105,122)(H4,83,84,90)(H4,85,86,91)(H4,87,88,92)/t43-,50+,51+,52+,53+,54+,55+,56+,57+,58+,59+,62+,63+/m1/s1
PDB

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UniChem

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Article
PubMed
6n/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 1


(Homo sapiens (Human))
BDBM50197021
PNG
((2S)-N-[(1S)-4-carbamimidamido-1-{[(1S)-1-carbamoy...)
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)c1ccccc1)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:73.75,74.78,4.4,91.93,20.28,58.60,111.113,wD:66.68,8.17,30.39,80.82,50.52,100.102,(12.08,-14.52,;12.08,-16.06,;13.42,-16.83,;10.75,-16.83,;10.75,-18.37,;9.41,-19.13,;8.08,-18.36,;8.08,-16.82,;6.75,-19.13,;6.75,-20.67,;8.08,-21.44,;9.41,-20.67,;10.75,-21.44,;10.75,-22.98,;12.06,-23.74,;9.41,-23.75,;8.08,-22.98,;5.41,-18.36,;4.09,-19.14,;4.09,-20.68,;2.76,-18.37,;2.76,-16.83,;4.09,-16.06,;5.49,-16.69,;6.53,-15.54,;5.76,-14.21,;4.25,-14.53,;1.42,-19.13,;.08,-18.36,;.08,-16.82,;-1.25,-19.13,;-1.25,-20.67,;.08,-21.44,;.08,-22.98,;1.42,-23.75,;1.43,-25.29,;.08,-26.06,;2.74,-26.06,;-2.58,-18.37,;-3.91,-19.15,;-3.9,-20.69,;-5.24,-18.39,;-5.24,-16.85,;-6.57,-16.08,;-7.91,-16.85,;-7.9,-18.4,;-6.57,-19.16,;12.08,-19.14,;12.08,-20.68,;13.41,-18.36,;14.74,-19.13,;14.74,-20.67,;16.07,-21.44,;17.4,-20.66,;16.07,-22.98,;16.07,-18.36,;16.07,-16.82,;17.4,-19.13,;18.74,-18.36,;18.74,-16.82,;20.07,-16.05,;20.07,-14.51,;21.41,-16.82,;20.07,-19.13,;20.07,-20.67,;21.4,-18.36,;22.73,-19.13,;22.73,-20.67,;24.06,-21.44,;21.4,-21.44,;24.06,-18.36,;24.06,-16.82,;25.4,-19.13,;26.73,-18.36,;26.73,-16.82,;25.4,-16.05,;28.06,-16.04,;28.06,-19.13,;28.06,-20.67,;29.39,-18.35,;30.72,-19.13,;30.72,-20.67,;32.05,-21.44,;32.05,-22.98,;33.39,-23.74,;33.39,-25.28,;32.05,-26.04,;34.73,-26.04,;32.05,-18.36,;32.05,-16.82,;33.39,-19.12,;34.73,-18.36,;34.73,-16.82,;36.05,-16.05,;36.05,-14.51,;34.72,-13.73,;37.39,-13.74,;36.05,-19.13,;36.05,-20.67,;37.39,-18.36,;38.72,-19.13,;38.72,-20.67,;40.05,-21.44,;40.05,-22.98,;41.38,-23.74,;41.38,-25.28,;40.05,-26.05,;42.72,-26.05,;40.05,-18.36,;40.05,-16.82,;41.38,-19.13,;42.72,-18.36,;42.72,-16.82,;44.05,-16.05,;45.38,-16.82,;46.72,-16.05,;46.72,-14.51,;48.05,-13.74,;45.38,-13.74,;44.05,-14.51,;44.05,-19.13,;45.38,-18.36,;44.05,-20.67,)|
Show InChI InChI=1S/C79H120N26O18/c1-40(2)32-55(99-71(118)57(35-45-21-25-49(108)26-22-45)101-72(119)58(36-47-38-89-39-93-47)102-68(115)50(16-11-29-90-77(83)84)94-65(112)46-14-9-8-10-15-46)70(117)103-59(37-61(81)110)73(120)100-56(33-41(3)4)74(121)104-62(42(5)6)75(122)105-63(43(7)106)76(123)97-52(18-13-31-92-79(87)88)66(113)96-53(27-28-60(80)109)69(116)95-51(17-12-30-91-78(85)86)67(114)98-54(64(82)111)34-44-19-23-48(107)24-20-44/h8-10,14-15,19-26,38-43,50-59,62-63,106-108H,11-13,16-18,27-37H2,1-7H3,(H2,80,109)(H2,81,110)(H2,82,111)(H,89,93)(H,94,112)(H,95,116)(H,96,113)(H,97,123)(H,98,114)(H,99,118)(H,100,120)(H,101,119)(H,102,115)(H,103,117)(H,104,121)(H,105,122)(H4,83,84,90)(H4,85,86,91)(H4,87,88,92)/t43-,50+,51+,52+,53+,54+,55+,56+,57+,58+,59+,62+,63+/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
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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 5


(Homo sapiens (Human))
BDBM50197021
PNG
((2S)-N-[(1S)-4-carbamimidamido-1-{[(1S)-1-carbamoy...)
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)c1ccccc1)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:73.75,74.78,4.4,91.93,20.28,58.60,111.113,wD:66.68,8.17,30.39,80.82,50.52,100.102,(12.08,-14.52,;12.08,-16.06,;13.42,-16.83,;10.75,-16.83,;10.75,-18.37,;9.41,-19.13,;8.08,-18.36,;8.08,-16.82,;6.75,-19.13,;6.75,-20.67,;8.08,-21.44,;9.41,-20.67,;10.75,-21.44,;10.75,-22.98,;12.06,-23.74,;9.41,-23.75,;8.08,-22.98,;5.41,-18.36,;4.09,-19.14,;4.09,-20.68,;2.76,-18.37,;2.76,-16.83,;4.09,-16.06,;5.49,-16.69,;6.53,-15.54,;5.76,-14.21,;4.25,-14.53,;1.42,-19.13,;.08,-18.36,;.08,-16.82,;-1.25,-19.13,;-1.25,-20.67,;.08,-21.44,;.08,-22.98,;1.42,-23.75,;1.43,-25.29,;.08,-26.06,;2.74,-26.06,;-2.58,-18.37,;-3.91,-19.15,;-3.9,-20.69,;-5.24,-18.39,;-5.24,-16.85,;-6.57,-16.08,;-7.91,-16.85,;-7.9,-18.4,;-6.57,-19.16,;12.08,-19.14,;12.08,-20.68,;13.41,-18.36,;14.74,-19.13,;14.74,-20.67,;16.07,-21.44,;17.4,-20.66,;16.07,-22.98,;16.07,-18.36,;16.07,-16.82,;17.4,-19.13,;18.74,-18.36,;18.74,-16.82,;20.07,-16.05,;20.07,-14.51,;21.41,-16.82,;20.07,-19.13,;20.07,-20.67,;21.4,-18.36,;22.73,-19.13,;22.73,-20.67,;24.06,-21.44,;21.4,-21.44,;24.06,-18.36,;24.06,-16.82,;25.4,-19.13,;26.73,-18.36,;26.73,-16.82,;25.4,-16.05,;28.06,-16.04,;28.06,-19.13,;28.06,-20.67,;29.39,-18.35,;30.72,-19.13,;30.72,-20.67,;32.05,-21.44,;32.05,-22.98,;33.39,-23.74,;33.39,-25.28,;32.05,-26.04,;34.73,-26.04,;32.05,-18.36,;32.05,-16.82,;33.39,-19.12,;34.73,-18.36,;34.73,-16.82,;36.05,-16.05,;36.05,-14.51,;34.72,-13.73,;37.39,-13.74,;36.05,-19.13,;36.05,-20.67,;37.39,-18.36,;38.72,-19.13,;38.72,-20.67,;40.05,-21.44,;40.05,-22.98,;41.38,-23.74,;41.38,-25.28,;40.05,-26.05,;42.72,-26.05,;40.05,-18.36,;40.05,-16.82,;41.38,-19.13,;42.72,-18.36,;42.72,-16.82,;44.05,-16.05,;45.38,-16.82,;46.72,-16.05,;46.72,-14.51,;48.05,-13.74,;45.38,-13.74,;44.05,-14.51,;44.05,-19.13,;45.38,-18.36,;44.05,-20.67,)|
Show InChI InChI=1S/C79H120N26O18/c1-40(2)32-55(99-71(118)57(35-45-21-25-49(108)26-22-45)101-72(119)58(36-47-38-89-39-93-47)102-68(115)50(16-11-29-90-77(83)84)94-65(112)46-14-9-8-10-15-46)70(117)103-59(37-61(81)110)73(120)100-56(33-41(3)4)74(121)104-62(42(5)6)75(122)105-63(43(7)106)76(123)97-52(18-13-31-92-79(87)88)66(113)96-53(27-28-60(80)109)69(116)95-51(17-12-30-91-78(85)86)67(114)98-54(64(82)111)34-44-19-23-48(107)24-20-44/h8-10,14-15,19-26,38-43,50-59,62-63,106-108H,11-13,16-18,27-37H2,1-7H3,(H2,80,109)(H2,81,110)(H2,82,111)(H,89,93)(H,94,112)(H,95,116)(H,96,113)(H,97,123)(H,98,114)(H,99,118)(H,100,120)(H,101,119)(H,102,115)(H,103,117)(H,104,121)(H,105,122)(H4,83,84,90)(H4,85,86,91)(H4,87,88,92)/t43-,50+,51+,52+,53+,54+,55+,56+,57+,58+,59+,62+,63+/m1/s1
KEGG

UniProtKB/SwissProt

antibodypedia
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CHEMBL
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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 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 2


(Homo sapiens (Human))
BDBM50197021
PNG
((2S)-N-[(1S)-4-carbamimidamido-1-{[(1S)-1-carbamoy...)
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)c1ccccc1)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:73.75,74.78,4.4,91.93,20.28,58.60,111.113,wD:66.68,8.17,30.39,80.82,50.52,100.102,(12.08,-14.52,;12.08,-16.06,;13.42,-16.83,;10.75,-16.83,;10.75,-18.37,;9.41,-19.13,;8.08,-18.36,;8.08,-16.82,;6.75,-19.13,;6.75,-20.67,;8.08,-21.44,;9.41,-20.67,;10.75,-21.44,;10.75,-22.98,;12.06,-23.74,;9.41,-23.75,;8.08,-22.98,;5.41,-18.36,;4.09,-19.14,;4.09,-20.68,;2.76,-18.37,;2.76,-16.83,;4.09,-16.06,;5.49,-16.69,;6.53,-15.54,;5.76,-14.21,;4.25,-14.53,;1.42,-19.13,;.08,-18.36,;.08,-16.82,;-1.25,-19.13,;-1.25,-20.67,;.08,-21.44,;.08,-22.98,;1.42,-23.75,;1.43,-25.29,;.08,-26.06,;2.74,-26.06,;-2.58,-18.37,;-3.91,-19.15,;-3.9,-20.69,;-5.24,-18.39,;-5.24,-16.85,;-6.57,-16.08,;-7.91,-16.85,;-7.9,-18.4,;-6.57,-19.16,;12.08,-19.14,;12.08,-20.68,;13.41,-18.36,;14.74,-19.13,;14.74,-20.67,;16.07,-21.44,;17.4,-20.66,;16.07,-22.98,;16.07,-18.36,;16.07,-16.82,;17.4,-19.13,;18.74,-18.36,;18.74,-16.82,;20.07,-16.05,;20.07,-14.51,;21.41,-16.82,;20.07,-19.13,;20.07,-20.67,;21.4,-18.36,;22.73,-19.13,;22.73,-20.67,;24.06,-21.44,;21.4,-21.44,;24.06,-18.36,;24.06,-16.82,;25.4,-19.13,;26.73,-18.36,;26.73,-16.82,;25.4,-16.05,;28.06,-16.04,;28.06,-19.13,;28.06,-20.67,;29.39,-18.35,;30.72,-19.13,;30.72,-20.67,;32.05,-21.44,;32.05,-22.98,;33.39,-23.74,;33.39,-25.28,;32.05,-26.04,;34.73,-26.04,;32.05,-18.36,;32.05,-16.82,;33.39,-19.12,;34.73,-18.36,;34.73,-16.82,;36.05,-16.05,;36.05,-14.51,;34.72,-13.73,;37.39,-13.74,;36.05,-19.13,;36.05,-20.67,;37.39,-18.36,;38.72,-19.13,;38.72,-20.67,;40.05,-21.44,;40.05,-22.98,;41.38,-23.74,;41.38,-25.28,;40.05,-26.05,;42.72,-26.05,;40.05,-18.36,;40.05,-16.82,;41.38,-19.13,;42.72,-18.36,;42.72,-16.82,;44.05,-16.05,;45.38,-16.82,;46.72,-16.05,;46.72,-14.51,;48.05,-13.74,;45.38,-13.74,;44.05,-14.51,;44.05,-19.13,;45.38,-18.36,;44.05,-20.67,)|
Show InChI InChI=1S/C79H120N26O18/c1-40(2)32-55(99-71(118)57(35-45-21-25-49(108)26-22-45)101-72(119)58(36-47-38-89-39-93-47)102-68(115)50(16-11-29-90-77(83)84)94-65(112)46-14-9-8-10-15-46)70(117)103-59(37-61(81)110)73(120)100-56(33-41(3)4)74(121)104-62(42(5)6)75(122)105-63(43(7)106)76(123)97-52(18-13-31-92-79(87)88)66(113)96-53(27-28-60(80)109)69(116)95-51(17-12-30-91-78(85)86)67(114)98-54(64(82)111)34-44-19-23-48(107)24-20-44/h8-10,14-15,19-26,38-43,50-59,62-63,106-108H,11-13,16-18,27-37H2,1-7H3,(H2,80,109)(H2,81,110)(H2,82,111)(H,89,93)(H,94,112)(H,95,116)(H,96,113)(H,97,123)(H,98,114)(H,99,118)(H,100,120)(H,101,119)(H,102,115)(H,103,117)(H,104,121)(H,105,122)(H4,83,84,90)(H4,85,86,91)(H4,87,88,92)/t43-,50+,51+,52+,53+,54+,55+,56+,57+,58+,59+,62+,63+/m1/s1
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n/an/an/an/a 6n/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