Found 4 hits for monomerid = 50269973 Target/Host
(Institution) | Ligand | Target/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 | pH | Temp
°C |
|---|
Parathyroid hormone receptor
(Homo sapiens (Human)) | BDBM50269973
(Ala-Val-Ala-Glu-lle-Gln-Leu-Nle-His-Gln-Har-Ala-Ly...)Show SMILES CCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@H](C)N)C(C)C)[C@@H](C)CC)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN=C(N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r,wU:96.96,47.48,25.25,79.79,8.12,60.59,38.38,119.121,wD:16.21,91.92,53.53,43.43,70.70,4.4,105.105,29.34,(16.87,-8.93,;15.54,-8.19,;15.51,-6.66,;14.17,-5.91,;14.15,-4.38,;12.85,-3.57,;11.49,-4.29,;11.5,-5.84,;10.22,-3.42,;10.22,-1.88,;11.55,-1.11,;11.56,.43,;12.88,-1.88,;9,-4.32,;7.64,-3.6,;7.64,-2.05,;6.36,-4.47,;6.37,-6.01,;7.7,-6.78,;7.7,-8.31,;6.37,-9.09,;9.03,-9.09,;5.16,-3.57,;3.79,-4.31,;3.8,-5.86,;2.51,-3.44,;1.3,-4.34,;-.05,-3.62,;-.05,-2.07,;-1.33,-4.48,;-1.33,-6.02,;0,-6.8,;0,-8.33,;-1.32,-9.11,;1.34,-9.11,;-2.54,-3.59,;-3.9,-4.32,;-3.89,-5.86,;-5.17,-3.45,;-5.17,-1.91,;-6.39,-4.33,;-7.74,-3.6,;-7.74,-2.06,;-9.03,-4.47,;-10.24,-3.58,;-11.6,-4.31,;-11.59,-5.85,;-12.89,-3.44,;-12.89,-1.9,;-14.09,-4.33,;-9.03,-6.02,;-7.7,-6.79,;-10.36,-6.79,;2.51,-1.9,;3.85,-1.13,;1.18,-1.12,;1.16,.42,;15.34,-3.59,;15.35,-2.04,;16.7,-4.32,;17.92,-3.43,;17.92,-1.89,;19.25,-1.11,;20.72,-1.6,;21.63,-.37,;20.75,.89,;19.27,.43,;19.2,-4.3,;19.21,-5.84,;20.56,-3.57,;21.77,-4.46,;21.77,-6,;23.1,-6.78,;23.1,-8.31,;21.78,-9.08,;24.45,-9.08,;23.05,-3.59,;23.06,-2.05,;24.42,-4.32,;25.64,-3.43,;25.64,-1.89,;26.97,-1.11,;26.97,.43,;28.3,1.19,;28.3,2.72,;29.63,3.49,;29.63,5.02,;30.95,2.72,;26.91,-4.3,;26.92,-5.84,;28.27,-3.57,;29.48,-4.47,;29.48,-6.01,;30.76,-3.6,;30.77,-2.05,;32.13,-4.33,;33.34,-3.44,;33.34,-1.89,;34.68,-1.12,;34.68,.42,;36.01,1.18,;36.01,2.72,;34.62,-4.3,;34.63,-5.85,;35.98,-3.57,;37.2,-4.46,;37.21,-6,;38.53,-6.78,;40.03,-6.44,;40.82,-7.75,;39.8,-8.91,;40,-10.44,;38.76,-11.36,;37.35,-10.75,;37.16,-9.24,;38.4,-8.3,;38.48,-3.59,;38.48,-2.04,;39.83,-4.31,;41.13,-3.51,;41.08,-1.97,;42.38,-1.17,;43.73,-1.9,;45.03,-1.09,;44.98,.44,;46.28,1.25,;43.62,1.16,;42.33,.35,;42.48,-4.23,;43.79,-3.42,;42.53,-5.76,)| Show InChI InChI=1S/C86H135N25O20/c1-11-13-21-56(103-81(127)63(37-44(3)4)107-79(125)60(30-33-67(90)114)105-85(131)70(46(7)12-2)111-80(126)61(31-34-68(115)116)101-74(120)49(10)99-84(130)69(45(5)6)110-72(118)47(8)88)76(122)109-65(40-52-42-94-43-97-52)83(129)104-59(29-32-66(89)113)78(124)102-57(24-17-19-36-95-86(92)93)75(121)98-48(9)73(119)100-58(23-16-18-35-87)77(123)108-64(39-51-41-96-55-22-15-14-20-54(51)55)82(128)106-62(71(91)117)38-50-25-27-53(112)28-26-50/h14-15,20,22,25-28,41-49,56-65,69-70,96,112H,11-13,16-19,21,23-24,29-40,87-88H2,1-10H3,(H2,89,113)(H2,90,114)(H2,91,117)(H,94,97)(H,98,121)(H,99,130)(H,100,119)(H,101,120)(H,102,124)(H,103,127)(H,104,129)(H,105,131)(H,106,128)(H,107,125)(H,108,123)(H,109,122)(H,110,118)(H,111,126)(H,115,116)(H4,92,93,95)/t46-,47-,48-,49-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65-,69-,70-/m0/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
UniProtKB/TrEMBL
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| CHEMBL
KEGG
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.19E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Pharmaceutical Research Institute
Curated by ChEMBL
| Assay Description
Displacement of [125I]DPC-AJ1951 from PTH/PTH-related peptide receptor (unknown origin) expressed in HKRK-B28 cells |
Proc Natl Acad Sci U S A 104: 6846-51 (2007)
Article DOI: 10.1073/pnas.0605125104
BindingDB Entry DOI: 10.7270/Q28P608V |
More data for this
Ligand-Target Pair | |
Parathyroid hormone receptor
(Homo sapiens (Human)) | BDBM50269973
(Ala-Val-Ala-Glu-lle-Gln-Leu-Nle-His-Gln-Har-Ala-Ly...)Show SMILES CCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@H](C)N)C(C)C)[C@@H](C)CC)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN=C(N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r,wU:96.96,47.48,25.25,79.79,8.12,60.59,38.38,119.121,wD:16.21,91.92,53.53,43.43,70.70,4.4,105.105,29.34,(16.87,-8.93,;15.54,-8.19,;15.51,-6.66,;14.17,-5.91,;14.15,-4.38,;12.85,-3.57,;11.49,-4.29,;11.5,-5.84,;10.22,-3.42,;10.22,-1.88,;11.55,-1.11,;11.56,.43,;12.88,-1.88,;9,-4.32,;7.64,-3.6,;7.64,-2.05,;6.36,-4.47,;6.37,-6.01,;7.7,-6.78,;7.7,-8.31,;6.37,-9.09,;9.03,-9.09,;5.16,-3.57,;3.79,-4.31,;3.8,-5.86,;2.51,-3.44,;1.3,-4.34,;-.05,-3.62,;-.05,-2.07,;-1.33,-4.48,;-1.33,-6.02,;0,-6.8,;0,-8.33,;-1.32,-9.11,;1.34,-9.11,;-2.54,-3.59,;-3.9,-4.32,;-3.89,-5.86,;-5.17,-3.45,;-5.17,-1.91,;-6.39,-4.33,;-7.74,-3.6,;-7.74,-2.06,;-9.03,-4.47,;-10.24,-3.58,;-11.6,-4.31,;-11.59,-5.85,;-12.89,-3.44,;-12.89,-1.9,;-14.09,-4.33,;-9.03,-6.02,;-7.7,-6.79,;-10.36,-6.79,;2.51,-1.9,;3.85,-1.13,;1.18,-1.12,;1.16,.42,;15.34,-3.59,;15.35,-2.04,;16.7,-4.32,;17.92,-3.43,;17.92,-1.89,;19.25,-1.11,;20.72,-1.6,;21.63,-.37,;20.75,.89,;19.27,.43,;19.2,-4.3,;19.21,-5.84,;20.56,-3.57,;21.77,-4.46,;21.77,-6,;23.1,-6.78,;23.1,-8.31,;21.78,-9.08,;24.45,-9.08,;23.05,-3.59,;23.06,-2.05,;24.42,-4.32,;25.64,-3.43,;25.64,-1.89,;26.97,-1.11,;26.97,.43,;28.3,1.19,;28.3,2.72,;29.63,3.49,;29.63,5.02,;30.95,2.72,;26.91,-4.3,;26.92,-5.84,;28.27,-3.57,;29.48,-4.47,;29.48,-6.01,;30.76,-3.6,;30.77,-2.05,;32.13,-4.33,;33.34,-3.44,;33.34,-1.89,;34.68,-1.12,;34.68,.42,;36.01,1.18,;36.01,2.72,;34.62,-4.3,;34.63,-5.85,;35.98,-3.57,;37.2,-4.46,;37.21,-6,;38.53,-6.78,;40.03,-6.44,;40.82,-7.75,;39.8,-8.91,;40,-10.44,;38.76,-11.36,;37.35,-10.75,;37.16,-9.24,;38.4,-8.3,;38.48,-3.59,;38.48,-2.04,;39.83,-4.31,;41.13,-3.51,;41.08,-1.97,;42.38,-1.17,;43.73,-1.9,;45.03,-1.09,;44.98,.44,;46.28,1.25,;43.62,1.16,;42.33,.35,;42.48,-4.23,;43.79,-3.42,;42.53,-5.76,)| Show InChI InChI=1S/C86H135N25O20/c1-11-13-21-56(103-81(127)63(37-44(3)4)107-79(125)60(30-33-67(90)114)105-85(131)70(46(7)12-2)111-80(126)61(31-34-68(115)116)101-74(120)49(10)99-84(130)69(45(5)6)110-72(118)47(8)88)76(122)109-65(40-52-42-94-43-97-52)83(129)104-59(29-32-66(89)113)78(124)102-57(24-17-19-36-95-86(92)93)75(121)98-48(9)73(119)100-58(23-16-18-35-87)77(123)108-64(39-51-41-96-55-22-15-14-20-54(51)55)82(128)106-62(71(91)117)38-50-25-27-53(112)28-26-50/h14-15,20,22,25-28,41-49,56-65,69-70,96,112H,11-13,16-19,21,23-24,29-40,87-88H2,1-10H3,(H2,89,113)(H2,90,114)(H2,91,117)(H,94,97)(H,98,121)(H,99,130)(H,100,119)(H,101,120)(H,102,124)(H,103,127)(H,104,129)(H,105,131)(H,106,128)(H,107,125)(H,108,123)(H,109,122)(H,110,118)(H,111,126)(H,115,116)(H4,92,93,95)/t46-,47-,48-,49-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65-,69-,70-/m0/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
UniProtKB/TrEMBL
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
KEGG
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 26 | n/a | n/a | n/a | n/a |
Pharmaceutical Research Institute
Curated by ChEMBL
| Assay Description
Activity at human PTH/PTH-related peptide receptor expressed in HEK293 cells assessed as induction of luciferase activity by CRE-luciferase reporter ... |
Proc Natl Acad Sci U S A 104: 6846-51 (2007)
Article DOI: 10.1073/pnas.0605125104
BindingDB Entry DOI: 10.7270/Q28P608V |
More data for this
Ligand-Target Pair | |
Parathyroid hormone 1 receptor (PTH1R)
(Rattus norvegicus (Rat)) | BDBM50269973
(Ala-Val-Ala-Glu-lle-Gln-Leu-Nle-His-Gln-Har-Ala-Ly...)Show SMILES CCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@H](C)N)C(C)C)[C@@H](C)CC)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN=C(N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r,wU:96.96,47.48,25.25,79.79,8.12,60.59,38.38,119.121,wD:16.21,91.92,53.53,43.43,70.70,4.4,105.105,29.34,(16.87,-8.93,;15.54,-8.19,;15.51,-6.66,;14.17,-5.91,;14.15,-4.38,;12.85,-3.57,;11.49,-4.29,;11.5,-5.84,;10.22,-3.42,;10.22,-1.88,;11.55,-1.11,;11.56,.43,;12.88,-1.88,;9,-4.32,;7.64,-3.6,;7.64,-2.05,;6.36,-4.47,;6.37,-6.01,;7.7,-6.78,;7.7,-8.31,;6.37,-9.09,;9.03,-9.09,;5.16,-3.57,;3.79,-4.31,;3.8,-5.86,;2.51,-3.44,;1.3,-4.34,;-.05,-3.62,;-.05,-2.07,;-1.33,-4.48,;-1.33,-6.02,;0,-6.8,;0,-8.33,;-1.32,-9.11,;1.34,-9.11,;-2.54,-3.59,;-3.9,-4.32,;-3.89,-5.86,;-5.17,-3.45,;-5.17,-1.91,;-6.39,-4.33,;-7.74,-3.6,;-7.74,-2.06,;-9.03,-4.47,;-10.24,-3.58,;-11.6,-4.31,;-11.59,-5.85,;-12.89,-3.44,;-12.89,-1.9,;-14.09,-4.33,;-9.03,-6.02,;-7.7,-6.79,;-10.36,-6.79,;2.51,-1.9,;3.85,-1.13,;1.18,-1.12,;1.16,.42,;15.34,-3.59,;15.35,-2.04,;16.7,-4.32,;17.92,-3.43,;17.92,-1.89,;19.25,-1.11,;20.72,-1.6,;21.63,-.37,;20.75,.89,;19.27,.43,;19.2,-4.3,;19.21,-5.84,;20.56,-3.57,;21.77,-4.46,;21.77,-6,;23.1,-6.78,;23.1,-8.31,;21.78,-9.08,;24.45,-9.08,;23.05,-3.59,;23.06,-2.05,;24.42,-4.32,;25.64,-3.43,;25.64,-1.89,;26.97,-1.11,;26.97,.43,;28.3,1.19,;28.3,2.72,;29.63,3.49,;29.63,5.02,;30.95,2.72,;26.91,-4.3,;26.92,-5.84,;28.27,-3.57,;29.48,-4.47,;29.48,-6.01,;30.76,-3.6,;30.77,-2.05,;32.13,-4.33,;33.34,-3.44,;33.34,-1.89,;34.68,-1.12,;34.68,.42,;36.01,1.18,;36.01,2.72,;34.62,-4.3,;34.63,-5.85,;35.98,-3.57,;37.2,-4.46,;37.21,-6,;38.53,-6.78,;40.03,-6.44,;40.82,-7.75,;39.8,-8.91,;40,-10.44,;38.76,-11.36,;37.35,-10.75,;37.16,-9.24,;38.4,-8.3,;38.48,-3.59,;38.48,-2.04,;39.83,-4.31,;41.13,-3.51,;41.08,-1.97,;42.38,-1.17,;43.73,-1.9,;45.03,-1.09,;44.98,.44,;46.28,1.25,;43.62,1.16,;42.33,.35,;42.48,-4.23,;43.79,-3.42,;42.53,-5.76,)| Show InChI InChI=1S/C86H135N25O20/c1-11-13-21-56(103-81(127)63(37-44(3)4)107-79(125)60(30-33-67(90)114)105-85(131)70(46(7)12-2)111-80(126)61(31-34-68(115)116)101-74(120)49(10)99-84(130)69(45(5)6)110-72(118)47(8)88)76(122)109-65(40-52-42-94-43-97-52)83(129)104-59(29-32-66(89)113)78(124)102-57(24-17-19-36-95-86(92)93)75(121)98-48(9)73(119)100-58(23-16-18-35-87)77(123)108-64(39-51-41-96-55-22-15-14-20-54(51)55)82(128)106-62(71(91)117)38-50-25-27-53(112)28-26-50/h14-15,20,22,25-28,41-49,56-65,69-70,96,112H,11-13,16-19,21,23-24,29-40,87-88H2,1-10H3,(H2,89,113)(H2,90,114)(H2,91,117)(H,94,97)(H,98,121)(H,99,130)(H,100,119)(H,101,120)(H,102,124)(H,103,127)(H,104,129)(H,105,131)(H,106,128)(H,107,125)(H,108,123)(H,109,122)(H,110,118)(H,111,126)(H,115,116)(H4,92,93,95)/t46-,47-,48-,49-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65-,69-,70-/m0/s1 | PDB
UniProtKB/SwissProt
GoogleScholar
AffyNet
| CHEMBL
KEGG
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 129 | n/a | n/a | n/a | n/a |
Pharmaceutical Research Institute
Curated by ChEMBL
| Assay Description
Activity at rat PTH/PTH-related peptide receptor expressed in rat UMR106 cells assessed as cAMP formation |
Proc Natl Acad Sci U S A 104: 6846-51 (2007)
Article DOI: 10.1073/pnas.0605125104
BindingDB Entry DOI: 10.7270/Q28P608V |
More data for this
Ligand-Target Pair | |
Parathyroid hormone receptor
(Homo sapiens (Human)) | BDBM50269973
(Ala-Val-Ala-Glu-lle-Gln-Leu-Nle-His-Gln-Har-Ala-Ly...)Show SMILES CCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@H](C)N)C(C)C)[C@@H](C)CC)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN=C(N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r,wU:96.96,47.48,25.25,79.79,8.12,60.59,38.38,119.121,wD:16.21,91.92,53.53,43.43,70.70,4.4,105.105,29.34,(16.87,-8.93,;15.54,-8.19,;15.51,-6.66,;14.17,-5.91,;14.15,-4.38,;12.85,-3.57,;11.49,-4.29,;11.5,-5.84,;10.22,-3.42,;10.22,-1.88,;11.55,-1.11,;11.56,.43,;12.88,-1.88,;9,-4.32,;7.64,-3.6,;7.64,-2.05,;6.36,-4.47,;6.37,-6.01,;7.7,-6.78,;7.7,-8.31,;6.37,-9.09,;9.03,-9.09,;5.16,-3.57,;3.79,-4.31,;3.8,-5.86,;2.51,-3.44,;1.3,-4.34,;-.05,-3.62,;-.05,-2.07,;-1.33,-4.48,;-1.33,-6.02,;0,-6.8,;0,-8.33,;-1.32,-9.11,;1.34,-9.11,;-2.54,-3.59,;-3.9,-4.32,;-3.89,-5.86,;-5.17,-3.45,;-5.17,-1.91,;-6.39,-4.33,;-7.74,-3.6,;-7.74,-2.06,;-9.03,-4.47,;-10.24,-3.58,;-11.6,-4.31,;-11.59,-5.85,;-12.89,-3.44,;-12.89,-1.9,;-14.09,-4.33,;-9.03,-6.02,;-7.7,-6.79,;-10.36,-6.79,;2.51,-1.9,;3.85,-1.13,;1.18,-1.12,;1.16,.42,;15.34,-3.59,;15.35,-2.04,;16.7,-4.32,;17.92,-3.43,;17.92,-1.89,;19.25,-1.11,;20.72,-1.6,;21.63,-.37,;20.75,.89,;19.27,.43,;19.2,-4.3,;19.21,-5.84,;20.56,-3.57,;21.77,-4.46,;21.77,-6,;23.1,-6.78,;23.1,-8.31,;21.78,-9.08,;24.45,-9.08,;23.05,-3.59,;23.06,-2.05,;24.42,-4.32,;25.64,-3.43,;25.64,-1.89,;26.97,-1.11,;26.97,.43,;28.3,1.19,;28.3,2.72,;29.63,3.49,;29.63,5.02,;30.95,2.72,;26.91,-4.3,;26.92,-5.84,;28.27,-3.57,;29.48,-4.47,;29.48,-6.01,;30.76,-3.6,;30.77,-2.05,;32.13,-4.33,;33.34,-3.44,;33.34,-1.89,;34.68,-1.12,;34.68,.42,;36.01,1.18,;36.01,2.72,;34.62,-4.3,;34.63,-5.85,;35.98,-3.57,;37.2,-4.46,;37.21,-6,;38.53,-6.78,;40.03,-6.44,;40.82,-7.75,;39.8,-8.91,;40,-10.44,;38.76,-11.36,;37.35,-10.75,;37.16,-9.24,;38.4,-8.3,;38.48,-3.59,;38.48,-2.04,;39.83,-4.31,;41.13,-3.51,;41.08,-1.97,;42.38,-1.17,;43.73,-1.9,;45.03,-1.09,;44.98,.44,;46.28,1.25,;43.62,1.16,;42.33,.35,;42.48,-4.23,;43.79,-3.42,;42.53,-5.76,)| Show InChI InChI=1S/C86H135N25O20/c1-11-13-21-56(103-81(127)63(37-44(3)4)107-79(125)60(30-33-67(90)114)105-85(131)70(46(7)12-2)111-80(126)61(31-34-68(115)116)101-74(120)49(10)99-84(130)69(45(5)6)110-72(118)47(8)88)76(122)109-65(40-52-42-94-43-97-52)83(129)104-59(29-32-66(89)113)78(124)102-57(24-17-19-36-95-86(92)93)75(121)98-48(9)73(119)100-58(23-16-18-35-87)77(123)108-64(39-51-41-96-55-22-15-14-20-54(51)55)82(128)106-62(71(91)117)38-50-25-27-53(112)28-26-50/h14-15,20,22,25-28,41-49,56-65,69-70,96,112H,11-13,16-19,21,23-24,29-40,87-88H2,1-10H3,(H2,89,113)(H2,90,114)(H2,91,117)(H,94,97)(H,98,121)(H,99,130)(H,100,119)(H,101,120)(H,102,124)(H,103,127)(H,104,129)(H,105,131)(H,106,128)(H,107,125)(H,108,123)(H,109,122)(H,110,118)(H,111,126)(H,115,116)(H4,92,93,95)/t46-,47-,48-,49-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65-,69-,70-/m0/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
UniProtKB/TrEMBL
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
KEGG
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 1.46E+3 | n/a | n/a | n/a | n/a |
Pharmaceutical Research Institute
Curated by ChEMBL
| Assay Description
Activity at human PTH/PTH-related peptide receptor expressed in SAOS2 cells assessed as cAMP formation |
Proc Natl Acad Sci U S A 104: 6846-51 (2007)
Article DOI: 10.1073/pnas.0605125104
BindingDB Entry DOI: 10.7270/Q28P608V |
More data for this
Ligand-Target Pair | |
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