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BDBM50197010 (2S)-2-[(2S)-2-[(2S,3R)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2S)-2-[(2-aminophenyl)formamido]-5-carbamimidamidopentanamido]-3-(1H-imidazol-5-yl)propanamido]-3-(4-hydroxyphenyl)propanamido]-4-methylpentanamido]-3-carbamoylpropanamido]-4-methylpentanamido]-3-methylbutanamido]-3-hydroxybutanamido]-5-carbamimidamidopentanamido]-N-[(1S)-4-carbamimidamido-1-{[(1S)-1-carbamoyl-2-(4-hydroxyphenyl)ethyl]carbamoyl}butyl]pentanediamide::CHEMBL227456

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)c1ccccc1N)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=WINDOIBEGFZUKU-DVERMALCSA-N

Data: 6 KI  2 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 8 hits for monomerid = 50197010   
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))
BDBM50197010
PNG
((2S)-2-[(2S)-2-[(2S,3R)-2-[(2S)-2-[(2S)-2-[(2S)-2-...)
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)c1ccccc1N)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:8.17,67.69,81.83,30.39,101.103,51.53,wD:74.76,75.79,4.4,20.28,92.94,112.114,59.61,(11.01,-29.89,;11.01,-28.35,;12.34,-27.58,;9.68,-27.58,;9.68,-26.04,;8.34,-25.27,;7.01,-26.04,;7.01,-27.58,;5.67,-25.27,;5.67,-23.73,;7.01,-22.96,;8.34,-23.73,;9.67,-22.96,;9.67,-21.42,;11.01,-20.65,;8.33,-20.65,;7,-21.42,;4.34,-26.04,;3.01,-25.27,;3.01,-23.73,;1.67,-26.04,;1.67,-27.58,;3.01,-28.35,;4.48,-27.88,;5.38,-29.14,;4.46,-30.37,;3,-29.88,;.34,-25.27,;-.99,-26.04,;-.99,-27.58,;-2.33,-25.27,;-2.33,-23.73,;-.99,-22.96,;-.99,-21.42,;.34,-20.65,;.34,-19.1,;1.67,-18.33,;-.99,-18.33,;-3.66,-26.04,;-5,-25.27,;-5,-23.73,;-6.33,-26.04,;-6.32,-27.56,;-7.65,-28.34,;-8.99,-27.57,;-8.99,-26.03,;-7.66,-25.26,;-7.66,-23.72,;11.01,-25.27,;11.01,-23.73,;12.34,-26.04,;13.66,-25.25,;13.64,-23.71,;14.97,-22.92,;16.31,-23.67,;14.94,-21.38,;15.01,-26,;15.03,-27.54,;16.33,-25.21,;17.67,-25.96,;17.7,-27.5,;19.04,-28.25,;19.06,-29.79,;20.36,-27.47,;19,-25.17,;18.98,-23.63,;20.34,-25.93,;21.66,-25.14,;21.64,-23.6,;22.97,-22.81,;20.3,-22.85,;23.01,-25.89,;23.03,-27.43,;24.33,-25.1,;25.68,-25.85,;25.7,-27.39,;24.37,-28.18,;27.04,-28.14,;27,-25.06,;26.98,-23.52,;28.34,-25.82,;29.67,-25.03,;29.65,-23.49,;30.97,-22.7,;30.95,-21.16,;32.27,-20.37,;32.25,-18.83,;33.57,-18.04,;30.9,-18.08,;31.01,-25.78,;31.03,-27.32,;32.33,-24.99,;33.68,-25.74,;33.7,-27.28,;35.04,-28.03,;35.06,-29.57,;33.74,-30.36,;36.41,-30.32,;35,-24.95,;34.98,-23.41,;36.34,-25.7,;37.67,-24.92,;37.65,-23.38,;38.97,-22.59,;38.95,-21.05,;40.27,-20.26,;40.25,-18.72,;41.57,-17.93,;38.91,-17.97,;39.01,-25.67,;39.03,-27.21,;40.34,-24.88,;41.68,-25.63,;41.7,-27.17,;43.04,-27.92,;43.06,-29.46,;44.4,-30.21,;45.73,-29.42,;47.07,-30.17,;45.7,-27.87,;44.36,-27.13,;43,-24.84,;44.35,-25.59,;42.98,-23.3,)|
Show InChI InChI=1S/C79H121N27O18/c1-39(2)31-55(100-71(119)57(34-44-20-24-47(109)25-21-44)102-72(120)58(35-45-37-90-38-94-45)103-68(116)50(15-10-28-91-77(84)85)95-65(113)48-13-8-9-14-49(48)80)70(118)104-59(36-61(82)111)73(121)101-56(32-40(3)4)74(122)105-62(41(5)6)75(123)106-63(42(7)107)76(124)98-52(17-12-30-93-79(88)89)66(114)97-53(26-27-60(81)110)69(117)96-51(16-11-29-92-78(86)87)67(115)99-54(64(83)112)33-43-18-22-46(108)23-19-43/h8-9,13-14,18-25,37-42,50-59,62-63,107-109H,10-12,15-17,26-36,80H2,1-7H3,(H2,81,110)(H2,82,111)(H2,83,112)(H,90,94)(H,95,113)(H,96,117)(H,97,114)(H,98,124)(H,99,115)(H,100,119)(H,101,121)(H,102,120)(H,103,116)(H,104,118)(H,105,122)(H,106,123)(H4,84,85,91)(H4,86,87,92)(H4,88,89,93)/t42-,50+,51+,52+,53+,54+,55+,56+,57+,58+,59+,62+,63+/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
4n/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 2


(Homo sapiens (Human))
BDBM50197010
PNG
((2S)-2-[(2S)-2-[(2S,3R)-2-[(2S)-2-[(2S)-2-[(2S)-2-...)
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)c1ccccc1N)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:8.17,67.69,81.83,30.39,101.103,51.53,wD:74.76,75.79,4.4,20.28,92.94,112.114,59.61,(11.01,-29.89,;11.01,-28.35,;12.34,-27.58,;9.68,-27.58,;9.68,-26.04,;8.34,-25.27,;7.01,-26.04,;7.01,-27.58,;5.67,-25.27,;5.67,-23.73,;7.01,-22.96,;8.34,-23.73,;9.67,-22.96,;9.67,-21.42,;11.01,-20.65,;8.33,-20.65,;7,-21.42,;4.34,-26.04,;3.01,-25.27,;3.01,-23.73,;1.67,-26.04,;1.67,-27.58,;3.01,-28.35,;4.48,-27.88,;5.38,-29.14,;4.46,-30.37,;3,-29.88,;.34,-25.27,;-.99,-26.04,;-.99,-27.58,;-2.33,-25.27,;-2.33,-23.73,;-.99,-22.96,;-.99,-21.42,;.34,-20.65,;.34,-19.1,;1.67,-18.33,;-.99,-18.33,;-3.66,-26.04,;-5,-25.27,;-5,-23.73,;-6.33,-26.04,;-6.32,-27.56,;-7.65,-28.34,;-8.99,-27.57,;-8.99,-26.03,;-7.66,-25.26,;-7.66,-23.72,;11.01,-25.27,;11.01,-23.73,;12.34,-26.04,;13.66,-25.25,;13.64,-23.71,;14.97,-22.92,;16.31,-23.67,;14.94,-21.38,;15.01,-26,;15.03,-27.54,;16.33,-25.21,;17.67,-25.96,;17.7,-27.5,;19.04,-28.25,;19.06,-29.79,;20.36,-27.47,;19,-25.17,;18.98,-23.63,;20.34,-25.93,;21.66,-25.14,;21.64,-23.6,;22.97,-22.81,;20.3,-22.85,;23.01,-25.89,;23.03,-27.43,;24.33,-25.1,;25.68,-25.85,;25.7,-27.39,;24.37,-28.18,;27.04,-28.14,;27,-25.06,;26.98,-23.52,;28.34,-25.82,;29.67,-25.03,;29.65,-23.49,;30.97,-22.7,;30.95,-21.16,;32.27,-20.37,;32.25,-18.83,;33.57,-18.04,;30.9,-18.08,;31.01,-25.78,;31.03,-27.32,;32.33,-24.99,;33.68,-25.74,;33.7,-27.28,;35.04,-28.03,;35.06,-29.57,;33.74,-30.36,;36.41,-30.32,;35,-24.95,;34.98,-23.41,;36.34,-25.7,;37.67,-24.92,;37.65,-23.38,;38.97,-22.59,;38.95,-21.05,;40.27,-20.26,;40.25,-18.72,;41.57,-17.93,;38.91,-17.97,;39.01,-25.67,;39.03,-27.21,;40.34,-24.88,;41.68,-25.63,;41.7,-27.17,;43.04,-27.92,;43.06,-29.46,;44.4,-30.21,;45.73,-29.42,;47.07,-30.17,;45.7,-27.87,;44.36,-27.13,;43,-24.84,;44.35,-25.59,;42.98,-23.3,)|
Show InChI InChI=1S/C79H121N27O18/c1-39(2)31-55(100-71(119)57(34-44-20-24-47(109)25-21-44)102-72(120)58(35-45-37-90-38-94-45)103-68(116)50(15-10-28-91-77(84)85)95-65(113)48-13-8-9-14-49(48)80)70(118)104-59(36-61(82)111)73(121)101-56(32-40(3)4)74(122)105-62(41(5)6)75(123)106-63(42(7)107)76(124)98-52(17-12-30-93-79(88)89)66(114)97-53(26-27-60(81)110)69(117)96-51(16-11-29-92-78(86)87)67(115)99-54(64(83)112)33-43-18-22-46(108)23-19-43/h8-9,13-14,18-25,37-42,50-59,62-63,107-109H,10-12,15-17,26-36,80H2,1-7H3,(H2,81,110)(H2,82,111)(H2,83,112)(H,90,94)(H,95,113)(H,96,117)(H,97,114)(H,98,124)(H,99,115)(H,100,119)(H,101,121)(H,102,120)(H,103,116)(H,104,118)(H,105,122)(H,106,123)(H4,84,85,91)(H4,86,87,92)(H4,88,89,93)/t42-,50+,51+,52+,53+,54+,55+,56+,57+,58+,59+,62+,63+/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
4n/an/an/an/an/an/an/an/a



Bayer Pharmaceuticals Corporation

Curated by ChEMBL


Assay Description
Displacement of [125I]PYY from human NPY2


J Med Chem 50: 2264-8 (2007)


Article DOI: 10.1021/jm061454v
BindingDB Entry DOI: 10.7270/Q2JS9Q3Z
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 5 ( NPY Y5)


(Homo sapiens (Human))
BDBM50197010
PNG
((2S)-2-[(2S)-2-[(2S,3R)-2-[(2S)-2-[(2S)-2-[(2S)-2-...)
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)c1ccccc1N)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:8.17,67.69,81.83,30.39,101.103,51.53,wD:74.76,75.79,4.4,20.28,92.94,112.114,59.61,(11.01,-29.89,;11.01,-28.35,;12.34,-27.58,;9.68,-27.58,;9.68,-26.04,;8.34,-25.27,;7.01,-26.04,;7.01,-27.58,;5.67,-25.27,;5.67,-23.73,;7.01,-22.96,;8.34,-23.73,;9.67,-22.96,;9.67,-21.42,;11.01,-20.65,;8.33,-20.65,;7,-21.42,;4.34,-26.04,;3.01,-25.27,;3.01,-23.73,;1.67,-26.04,;1.67,-27.58,;3.01,-28.35,;4.48,-27.88,;5.38,-29.14,;4.46,-30.37,;3,-29.88,;.34,-25.27,;-.99,-26.04,;-.99,-27.58,;-2.33,-25.27,;-2.33,-23.73,;-.99,-22.96,;-.99,-21.42,;.34,-20.65,;.34,-19.1,;1.67,-18.33,;-.99,-18.33,;-3.66,-26.04,;-5,-25.27,;-5,-23.73,;-6.33,-26.04,;-6.32,-27.56,;-7.65,-28.34,;-8.99,-27.57,;-8.99,-26.03,;-7.66,-25.26,;-7.66,-23.72,;11.01,-25.27,;11.01,-23.73,;12.34,-26.04,;13.66,-25.25,;13.64,-23.71,;14.97,-22.92,;16.31,-23.67,;14.94,-21.38,;15.01,-26,;15.03,-27.54,;16.33,-25.21,;17.67,-25.96,;17.7,-27.5,;19.04,-28.25,;19.06,-29.79,;20.36,-27.47,;19,-25.17,;18.98,-23.63,;20.34,-25.93,;21.66,-25.14,;21.64,-23.6,;22.97,-22.81,;20.3,-22.85,;23.01,-25.89,;23.03,-27.43,;24.33,-25.1,;25.68,-25.85,;25.7,-27.39,;24.37,-28.18,;27.04,-28.14,;27,-25.06,;26.98,-23.52,;28.34,-25.82,;29.67,-25.03,;29.65,-23.49,;30.97,-22.7,;30.95,-21.16,;32.27,-20.37,;32.25,-18.83,;33.57,-18.04,;30.9,-18.08,;31.01,-25.78,;31.03,-27.32,;32.33,-24.99,;33.68,-25.74,;33.7,-27.28,;35.04,-28.03,;35.06,-29.57,;33.74,-30.36,;36.41,-30.32,;35,-24.95,;34.98,-23.41,;36.34,-25.7,;37.67,-24.92,;37.65,-23.38,;38.97,-22.59,;38.95,-21.05,;40.27,-20.26,;40.25,-18.72,;41.57,-17.93,;38.91,-17.97,;39.01,-25.67,;39.03,-27.21,;40.34,-24.88,;41.68,-25.63,;41.7,-27.17,;43.04,-27.92,;43.06,-29.46,;44.4,-30.21,;45.73,-29.42,;47.07,-30.17,;45.7,-27.87,;44.36,-27.13,;43,-24.84,;44.35,-25.59,;42.98,-23.3,)|
Show InChI InChI=1S/C79H121N27O18/c1-39(2)31-55(100-71(119)57(34-44-20-24-47(109)25-21-44)102-72(120)58(35-45-37-90-38-94-45)103-68(116)50(15-10-28-91-77(84)85)95-65(113)48-13-8-9-14-49(48)80)70(118)104-59(36-61(82)111)73(121)101-56(32-40(3)4)74(122)105-62(41(5)6)75(123)106-63(42(7)107)76(124)98-52(17-12-30-93-79(88)89)66(114)97-53(26-27-60(81)110)69(117)96-51(16-11-29-92-78(86)87)67(115)99-54(64(83)112)33-43-18-22-46(108)23-19-43/h8-9,13-14,18-25,37-42,50-59,62-63,107-109H,10-12,15-17,26-36,80H2,1-7H3,(H2,81,110)(H2,82,111)(H2,83,112)(H,90,94)(H,95,113)(H,96,117)(H,97,114)(H,98,124)(H,99,115)(H,100,119)(H,101,121)(H,102,120)(H,103,116)(H,104,118)(H,105,122)(H,106,123)(H4,84,85,91)(H4,86,87,92)(H4,88,89,93)/t42-,50+,51+,52+,53+,54+,55+,56+,57+,58+,59+,62+,63+/m1/s1
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

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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 1


(Homo sapiens (Human))
BDBM50197010
PNG
((2S)-2-[(2S)-2-[(2S,3R)-2-[(2S)-2-[(2S)-2-[(2S)-2-...)
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)c1ccccc1N)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:8.17,67.69,81.83,30.39,101.103,51.53,wD:74.76,75.79,4.4,20.28,92.94,112.114,59.61,(11.01,-29.89,;11.01,-28.35,;12.34,-27.58,;9.68,-27.58,;9.68,-26.04,;8.34,-25.27,;7.01,-26.04,;7.01,-27.58,;5.67,-25.27,;5.67,-23.73,;7.01,-22.96,;8.34,-23.73,;9.67,-22.96,;9.67,-21.42,;11.01,-20.65,;8.33,-20.65,;7,-21.42,;4.34,-26.04,;3.01,-25.27,;3.01,-23.73,;1.67,-26.04,;1.67,-27.58,;3.01,-28.35,;4.48,-27.88,;5.38,-29.14,;4.46,-30.37,;3,-29.88,;.34,-25.27,;-.99,-26.04,;-.99,-27.58,;-2.33,-25.27,;-2.33,-23.73,;-.99,-22.96,;-.99,-21.42,;.34,-20.65,;.34,-19.1,;1.67,-18.33,;-.99,-18.33,;-3.66,-26.04,;-5,-25.27,;-5,-23.73,;-6.33,-26.04,;-6.32,-27.56,;-7.65,-28.34,;-8.99,-27.57,;-8.99,-26.03,;-7.66,-25.26,;-7.66,-23.72,;11.01,-25.27,;11.01,-23.73,;12.34,-26.04,;13.66,-25.25,;13.64,-23.71,;14.97,-22.92,;16.31,-23.67,;14.94,-21.38,;15.01,-26,;15.03,-27.54,;16.33,-25.21,;17.67,-25.96,;17.7,-27.5,;19.04,-28.25,;19.06,-29.79,;20.36,-27.47,;19,-25.17,;18.98,-23.63,;20.34,-25.93,;21.66,-25.14,;21.64,-23.6,;22.97,-22.81,;20.3,-22.85,;23.01,-25.89,;23.03,-27.43,;24.33,-25.1,;25.68,-25.85,;25.7,-27.39,;24.37,-28.18,;27.04,-28.14,;27,-25.06,;26.98,-23.52,;28.34,-25.82,;29.67,-25.03,;29.65,-23.49,;30.97,-22.7,;30.95,-21.16,;32.27,-20.37,;32.25,-18.83,;33.57,-18.04,;30.9,-18.08,;31.01,-25.78,;31.03,-27.32,;32.33,-24.99,;33.68,-25.74,;33.7,-27.28,;35.04,-28.03,;35.06,-29.57,;33.74,-30.36,;36.41,-30.32,;35,-24.95,;34.98,-23.41,;36.34,-25.7,;37.67,-24.92,;37.65,-23.38,;38.97,-22.59,;38.95,-21.05,;40.27,-20.26,;40.25,-18.72,;41.57,-17.93,;38.91,-17.97,;39.01,-25.67,;39.03,-27.21,;40.34,-24.88,;41.68,-25.63,;41.7,-27.17,;43.04,-27.92,;43.06,-29.46,;44.4,-30.21,;45.73,-29.42,;47.07,-30.17,;45.7,-27.87,;44.36,-27.13,;43,-24.84,;44.35,-25.59,;42.98,-23.3,)|
Show InChI InChI=1S/C79H121N27O18/c1-39(2)31-55(100-71(119)57(34-44-20-24-47(109)25-21-44)102-72(120)58(35-45-37-90-38-94-45)103-68(116)50(15-10-28-91-77(84)85)95-65(113)48-13-8-9-14-49(48)80)70(118)104-59(36-61(82)111)73(121)101-56(32-40(3)4)74(122)105-62(41(5)6)75(123)106-63(42(7)107)76(124)98-52(17-12-30-93-79(88)89)66(114)97-53(26-27-60(81)110)69(117)96-51(16-11-29-92-78(86)87)67(115)99-54(64(83)112)33-43-18-22-46(108)23-19-43/h8-9,13-14,18-25,37-42,50-59,62-63,107-109H,10-12,15-17,26-36,80H2,1-7H3,(H2,81,110)(H2,82,111)(H2,83,112)(H,90,94)(H,95,113)(H,96,117)(H,97,114)(H,98,124)(H,99,115)(H,100,119)(H,101,121)(H,102,120)(H,103,116)(H,104,118)(H,105,122)(H,106,123)(H4,84,85,91)(H4,86,87,92)(H4,88,89,93)/t42-,50+,51+,52+,53+,54+,55+,56+,57+,58+,59+,62+,63+/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 1


(Homo sapiens (Human))
BDBM50197010
PNG
((2S)-2-[(2S)-2-[(2S,3R)-2-[(2S)-2-[(2S)-2-[(2S)-2-...)
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)c1ccccc1N)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:8.17,67.69,81.83,30.39,101.103,51.53,wD:74.76,75.79,4.4,20.28,92.94,112.114,59.61,(11.01,-29.89,;11.01,-28.35,;12.34,-27.58,;9.68,-27.58,;9.68,-26.04,;8.34,-25.27,;7.01,-26.04,;7.01,-27.58,;5.67,-25.27,;5.67,-23.73,;7.01,-22.96,;8.34,-23.73,;9.67,-22.96,;9.67,-21.42,;11.01,-20.65,;8.33,-20.65,;7,-21.42,;4.34,-26.04,;3.01,-25.27,;3.01,-23.73,;1.67,-26.04,;1.67,-27.58,;3.01,-28.35,;4.48,-27.88,;5.38,-29.14,;4.46,-30.37,;3,-29.88,;.34,-25.27,;-.99,-26.04,;-.99,-27.58,;-2.33,-25.27,;-2.33,-23.73,;-.99,-22.96,;-.99,-21.42,;.34,-20.65,;.34,-19.1,;1.67,-18.33,;-.99,-18.33,;-3.66,-26.04,;-5,-25.27,;-5,-23.73,;-6.33,-26.04,;-6.32,-27.56,;-7.65,-28.34,;-8.99,-27.57,;-8.99,-26.03,;-7.66,-25.26,;-7.66,-23.72,;11.01,-25.27,;11.01,-23.73,;12.34,-26.04,;13.66,-25.25,;13.64,-23.71,;14.97,-22.92,;16.31,-23.67,;14.94,-21.38,;15.01,-26,;15.03,-27.54,;16.33,-25.21,;17.67,-25.96,;17.7,-27.5,;19.04,-28.25,;19.06,-29.79,;20.36,-27.47,;19,-25.17,;18.98,-23.63,;20.34,-25.93,;21.66,-25.14,;21.64,-23.6,;22.97,-22.81,;20.3,-22.85,;23.01,-25.89,;23.03,-27.43,;24.33,-25.1,;25.68,-25.85,;25.7,-27.39,;24.37,-28.18,;27.04,-28.14,;27,-25.06,;26.98,-23.52,;28.34,-25.82,;29.67,-25.03,;29.65,-23.49,;30.97,-22.7,;30.95,-21.16,;32.27,-20.37,;32.25,-18.83,;33.57,-18.04,;30.9,-18.08,;31.01,-25.78,;31.03,-27.32,;32.33,-24.99,;33.68,-25.74,;33.7,-27.28,;35.04,-28.03,;35.06,-29.57,;33.74,-30.36,;36.41,-30.32,;35,-24.95,;34.98,-23.41,;36.34,-25.7,;37.67,-24.92,;37.65,-23.38,;38.97,-22.59,;38.95,-21.05,;40.27,-20.26,;40.25,-18.72,;41.57,-17.93,;38.91,-17.97,;39.01,-25.67,;39.03,-27.21,;40.34,-24.88,;41.68,-25.63,;41.7,-27.17,;43.04,-27.92,;43.06,-29.46,;44.4,-30.21,;45.73,-29.42,;47.07,-30.17,;45.7,-27.87,;44.36,-27.13,;43,-24.84,;44.35,-25.59,;42.98,-23.3,)|
Show InChI InChI=1S/C79H121N27O18/c1-39(2)31-55(100-71(119)57(34-44-20-24-47(109)25-21-44)102-72(120)58(35-45-37-90-38-94-45)103-68(116)50(15-10-28-91-77(84)85)95-65(113)48-13-8-9-14-49(48)80)70(118)104-59(36-61(82)111)73(121)101-56(32-40(3)4)74(122)105-62(41(5)6)75(123)106-63(42(7)107)76(124)98-52(17-12-30-93-79(88)89)66(114)97-53(26-27-60(81)110)69(117)96-51(16-11-29-92-78(86)87)67(115)99-54(64(83)112)33-43-18-22-46(108)23-19-43/h8-9,13-14,18-25,37-42,50-59,62-63,107-109H,10-12,15-17,26-36,80H2,1-7H3,(H2,81,110)(H2,82,111)(H2,83,112)(H,90,94)(H,95,113)(H,96,117)(H,97,114)(H,98,124)(H,99,115)(H,100,119)(H,101,121)(H,102,120)(H,103,116)(H,104,118)(H,105,122)(H,106,123)(H4,84,85,91)(H4,86,87,92)(H4,88,89,93)/t42-,50+,51+,52+,53+,54+,55+,56+,57+,58+,59+,62+,63+/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 human NPY1


J Med Chem 50: 2264-8 (2007)


Article DOI: 10.1021/jm061454v
BindingDB Entry DOI: 10.7270/Q2JS9Q3Z
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 5 ( NPY Y5)


(Homo sapiens (Human))
BDBM50197010
PNG
((2S)-2-[(2S)-2-[(2S,3R)-2-[(2S)-2-[(2S)-2-[(2S)-2-...)
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)c1ccccc1N)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:8.17,67.69,81.83,30.39,101.103,51.53,wD:74.76,75.79,4.4,20.28,92.94,112.114,59.61,(11.01,-29.89,;11.01,-28.35,;12.34,-27.58,;9.68,-27.58,;9.68,-26.04,;8.34,-25.27,;7.01,-26.04,;7.01,-27.58,;5.67,-25.27,;5.67,-23.73,;7.01,-22.96,;8.34,-23.73,;9.67,-22.96,;9.67,-21.42,;11.01,-20.65,;8.33,-20.65,;7,-21.42,;4.34,-26.04,;3.01,-25.27,;3.01,-23.73,;1.67,-26.04,;1.67,-27.58,;3.01,-28.35,;4.48,-27.88,;5.38,-29.14,;4.46,-30.37,;3,-29.88,;.34,-25.27,;-.99,-26.04,;-.99,-27.58,;-2.33,-25.27,;-2.33,-23.73,;-.99,-22.96,;-.99,-21.42,;.34,-20.65,;.34,-19.1,;1.67,-18.33,;-.99,-18.33,;-3.66,-26.04,;-5,-25.27,;-5,-23.73,;-6.33,-26.04,;-6.32,-27.56,;-7.65,-28.34,;-8.99,-27.57,;-8.99,-26.03,;-7.66,-25.26,;-7.66,-23.72,;11.01,-25.27,;11.01,-23.73,;12.34,-26.04,;13.66,-25.25,;13.64,-23.71,;14.97,-22.92,;16.31,-23.67,;14.94,-21.38,;15.01,-26,;15.03,-27.54,;16.33,-25.21,;17.67,-25.96,;17.7,-27.5,;19.04,-28.25,;19.06,-29.79,;20.36,-27.47,;19,-25.17,;18.98,-23.63,;20.34,-25.93,;21.66,-25.14,;21.64,-23.6,;22.97,-22.81,;20.3,-22.85,;23.01,-25.89,;23.03,-27.43,;24.33,-25.1,;25.68,-25.85,;25.7,-27.39,;24.37,-28.18,;27.04,-28.14,;27,-25.06,;26.98,-23.52,;28.34,-25.82,;29.67,-25.03,;29.65,-23.49,;30.97,-22.7,;30.95,-21.16,;32.27,-20.37,;32.25,-18.83,;33.57,-18.04,;30.9,-18.08,;31.01,-25.78,;31.03,-27.32,;32.33,-24.99,;33.68,-25.74,;33.7,-27.28,;35.04,-28.03,;35.06,-29.57,;33.74,-30.36,;36.41,-30.32,;35,-24.95,;34.98,-23.41,;36.34,-25.7,;37.67,-24.92,;37.65,-23.38,;38.97,-22.59,;38.95,-21.05,;40.27,-20.26,;40.25,-18.72,;41.57,-17.93,;38.91,-17.97,;39.01,-25.67,;39.03,-27.21,;40.34,-24.88,;41.68,-25.63,;41.7,-27.17,;43.04,-27.92,;43.06,-29.46,;44.4,-30.21,;45.73,-29.42,;47.07,-30.17,;45.7,-27.87,;44.36,-27.13,;43,-24.84,;44.35,-25.59,;42.98,-23.3,)|
Show InChI InChI=1S/C79H121N27O18/c1-39(2)31-55(100-71(119)57(34-44-20-24-47(109)25-21-44)102-72(120)58(35-45-37-90-38-94-45)103-68(116)50(15-10-28-91-77(84)85)95-65(113)48-13-8-9-14-49(48)80)70(118)104-59(36-61(82)111)73(121)101-56(32-40(3)4)74(122)105-62(41(5)6)75(123)106-63(42(7)107)76(124)98-52(17-12-30-93-79(88)89)66(114)97-53(26-27-60(81)110)69(117)96-51(16-11-29-92-78(86)87)67(115)99-54(64(83)112)33-43-18-22-46(108)23-19-43/h8-9,13-14,18-25,37-42,50-59,62-63,107-109H,10-12,15-17,26-36,80H2,1-7H3,(H2,81,110)(H2,82,111)(H2,83,112)(H,90,94)(H,95,113)(H,96,117)(H,97,114)(H,98,124)(H,99,115)(H,100,119)(H,101,121)(H,102,120)(H,103,116)(H,104,118)(H,105,122)(H,106,123)(H4,84,85,91)(H4,86,87,92)(H4,88,89,93)/t42-,50+,51+,52+,53+,54+,55+,56+,57+,58+,59+,62+,63+/m1/s1
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 human NPY5


J Med Chem 50: 2264-8 (2007)


Article DOI: 10.1021/jm061454v
BindingDB Entry DOI: 10.7270/Q2JS9Q3Z
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 2


(Homo sapiens (Human))
BDBM50197010
PNG
((2S)-2-[(2S)-2-[(2S,3R)-2-[(2S)-2-[(2S)-2-[(2S)-2-...)
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)c1ccccc1N)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:8.17,67.69,81.83,30.39,101.103,51.53,wD:74.76,75.79,4.4,20.28,92.94,112.114,59.61,(11.01,-29.89,;11.01,-28.35,;12.34,-27.58,;9.68,-27.58,;9.68,-26.04,;8.34,-25.27,;7.01,-26.04,;7.01,-27.58,;5.67,-25.27,;5.67,-23.73,;7.01,-22.96,;8.34,-23.73,;9.67,-22.96,;9.67,-21.42,;11.01,-20.65,;8.33,-20.65,;7,-21.42,;4.34,-26.04,;3.01,-25.27,;3.01,-23.73,;1.67,-26.04,;1.67,-27.58,;3.01,-28.35,;4.48,-27.88,;5.38,-29.14,;4.46,-30.37,;3,-29.88,;.34,-25.27,;-.99,-26.04,;-.99,-27.58,;-2.33,-25.27,;-2.33,-23.73,;-.99,-22.96,;-.99,-21.42,;.34,-20.65,;.34,-19.1,;1.67,-18.33,;-.99,-18.33,;-3.66,-26.04,;-5,-25.27,;-5,-23.73,;-6.33,-26.04,;-6.32,-27.56,;-7.65,-28.34,;-8.99,-27.57,;-8.99,-26.03,;-7.66,-25.26,;-7.66,-23.72,;11.01,-25.27,;11.01,-23.73,;12.34,-26.04,;13.66,-25.25,;13.64,-23.71,;14.97,-22.92,;16.31,-23.67,;14.94,-21.38,;15.01,-26,;15.03,-27.54,;16.33,-25.21,;17.67,-25.96,;17.7,-27.5,;19.04,-28.25,;19.06,-29.79,;20.36,-27.47,;19,-25.17,;18.98,-23.63,;20.34,-25.93,;21.66,-25.14,;21.64,-23.6,;22.97,-22.81,;20.3,-22.85,;23.01,-25.89,;23.03,-27.43,;24.33,-25.1,;25.68,-25.85,;25.7,-27.39,;24.37,-28.18,;27.04,-28.14,;27,-25.06,;26.98,-23.52,;28.34,-25.82,;29.67,-25.03,;29.65,-23.49,;30.97,-22.7,;30.95,-21.16,;32.27,-20.37,;32.25,-18.83,;33.57,-18.04,;30.9,-18.08,;31.01,-25.78,;31.03,-27.32,;32.33,-24.99,;33.68,-25.74,;33.7,-27.28,;35.04,-28.03,;35.06,-29.57,;33.74,-30.36,;36.41,-30.32,;35,-24.95,;34.98,-23.41,;36.34,-25.7,;37.67,-24.92,;37.65,-23.38,;38.97,-22.59,;38.95,-21.05,;40.27,-20.26,;40.25,-18.72,;41.57,-17.93,;38.91,-17.97,;39.01,-25.67,;39.03,-27.21,;40.34,-24.88,;41.68,-25.63,;41.7,-27.17,;43.04,-27.92,;43.06,-29.46,;44.4,-30.21,;45.73,-29.42,;47.07,-30.17,;45.7,-27.87,;44.36,-27.13,;43,-24.84,;44.35,-25.59,;42.98,-23.3,)|
Show InChI InChI=1S/C79H121N27O18/c1-39(2)31-55(100-71(119)57(34-44-20-24-47(109)25-21-44)102-72(120)58(35-45-37-90-38-94-45)103-68(116)50(15-10-28-91-77(84)85)95-65(113)48-13-8-9-14-49(48)80)70(118)104-59(36-61(82)111)73(121)101-56(32-40(3)4)74(122)105-62(41(5)6)75(123)106-63(42(7)107)76(124)98-52(17-12-30-93-79(88)89)66(114)97-53(26-27-60(81)110)69(117)96-51(16-11-29-92-78(86)87)67(115)99-54(64(83)112)33-43-18-22-46(108)23-19-43/h8-9,13-14,18-25,37-42,50-59,62-63,107-109H,10-12,15-17,26-36,80H2,1-7H3,(H2,81,110)(H2,82,111)(H2,83,112)(H,90,94)(H,95,113)(H,96,117)(H,97,114)(H,98,124)(H,99,115)(H,100,119)(H,101,121)(H,102,120)(H,103,116)(H,104,118)(H,105,122)(H,106,123)(H4,84,85,91)(H4,86,87,92)(H4,88,89,93)/t42-,50+,51+,52+,53+,54+,55+,56+,57+,58+,59+,62+,63+/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 3n/an/an/an/a



Bayer Pharmaceuticals Corporation

Curated by ChEMBL


Assay Description
Agonist activity at human NPY2 by [35S]GTPgammaS cAMP accumulation assay


J Med Chem 50: 2264-8 (2007)


Article DOI: 10.1021/jm061454v
BindingDB Entry DOI: 10.7270/Q2JS9Q3Z
More data for this
Ligand-Target Pair
Neuropeptide Y receptor type 2


(Homo sapiens (Human))
BDBM50197010
PNG
((2S)-2-[(2S)-2-[(2S,3R)-2-[(2S)-2-[(2S)-2-[(2S)-2-...)
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)c1ccccc1N)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:8.17,67.69,81.83,30.39,101.103,51.53,wD:74.76,75.79,4.4,20.28,92.94,112.114,59.61,(11.01,-29.89,;11.01,-28.35,;12.34,-27.58,;9.68,-27.58,;9.68,-26.04,;8.34,-25.27,;7.01,-26.04,;7.01,-27.58,;5.67,-25.27,;5.67,-23.73,;7.01,-22.96,;8.34,-23.73,;9.67,-22.96,;9.67,-21.42,;11.01,-20.65,;8.33,-20.65,;7,-21.42,;4.34,-26.04,;3.01,-25.27,;3.01,-23.73,;1.67,-26.04,;1.67,-27.58,;3.01,-28.35,;4.48,-27.88,;5.38,-29.14,;4.46,-30.37,;3,-29.88,;.34,-25.27,;-.99,-26.04,;-.99,-27.58,;-2.33,-25.27,;-2.33,-23.73,;-.99,-22.96,;-.99,-21.42,;.34,-20.65,;.34,-19.1,;1.67,-18.33,;-.99,-18.33,;-3.66,-26.04,;-5,-25.27,;-5,-23.73,;-6.33,-26.04,;-6.32,-27.56,;-7.65,-28.34,;-8.99,-27.57,;-8.99,-26.03,;-7.66,-25.26,;-7.66,-23.72,;11.01,-25.27,;11.01,-23.73,;12.34,-26.04,;13.66,-25.25,;13.64,-23.71,;14.97,-22.92,;16.31,-23.67,;14.94,-21.38,;15.01,-26,;15.03,-27.54,;16.33,-25.21,;17.67,-25.96,;17.7,-27.5,;19.04,-28.25,;19.06,-29.79,;20.36,-27.47,;19,-25.17,;18.98,-23.63,;20.34,-25.93,;21.66,-25.14,;21.64,-23.6,;22.97,-22.81,;20.3,-22.85,;23.01,-25.89,;23.03,-27.43,;24.33,-25.1,;25.68,-25.85,;25.7,-27.39,;24.37,-28.18,;27.04,-28.14,;27,-25.06,;26.98,-23.52,;28.34,-25.82,;29.67,-25.03,;29.65,-23.49,;30.97,-22.7,;30.95,-21.16,;32.27,-20.37,;32.25,-18.83,;33.57,-18.04,;30.9,-18.08,;31.01,-25.78,;31.03,-27.32,;32.33,-24.99,;33.68,-25.74,;33.7,-27.28,;35.04,-28.03,;35.06,-29.57,;33.74,-30.36,;36.41,-30.32,;35,-24.95,;34.98,-23.41,;36.34,-25.7,;37.67,-24.92,;37.65,-23.38,;38.97,-22.59,;38.95,-21.05,;40.27,-20.26,;40.25,-18.72,;41.57,-17.93,;38.91,-17.97,;39.01,-25.67,;39.03,-27.21,;40.34,-24.88,;41.68,-25.63,;41.7,-27.17,;43.04,-27.92,;43.06,-29.46,;44.4,-30.21,;45.73,-29.42,;47.07,-30.17,;45.7,-27.87,;44.36,-27.13,;43,-24.84,;44.35,-25.59,;42.98,-23.3,)|
Show InChI InChI=1S/C79H121N27O18/c1-39(2)31-55(100-71(119)57(34-44-20-24-47(109)25-21-44)102-72(120)58(35-45-37-90-38-94-45)103-68(116)50(15-10-28-91-77(84)85)95-65(113)48-13-8-9-14-49(48)80)70(118)104-59(36-61(82)111)73(121)101-56(32-40(3)4)74(122)105-62(41(5)6)75(123)106-63(42(7)107)76(124)98-52(17-12-30-93-79(88)89)66(114)97-53(26-27-60(81)110)69(117)96-51(16-11-29-92-78(86)87)67(115)99-54(64(83)112)33-43-18-22-46(108)23-19-43/h8-9,13-14,18-25,37-42,50-59,62-63,107-109H,10-12,15-17,26-36,80H2,1-7H3,(H2,81,110)(H2,82,111)(H2,83,112)(H,90,94)(H,95,113)(H,96,117)(H,97,114)(H,98,124)(H,99,115)(H,100,119)(H,101,121)(H,102,120)(H,103,116)(H,104,118)(H,105,122)(H,106,123)(H4,84,85,91)(H4,86,87,92)(H4,88,89,93)/t42-,50+,51+,52+,53+,54+,55+,56+,57+,58+,59+,62+,63+/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 3n/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