Found 4 hits for monomerid = 50269971 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)) | BDBM50269971
(Ala-Val-Ala-Glu-lle-Gln-Leu-Met-His-Gln-Har-Ala-Ly...)Show SMILES CC[C@H](C)[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(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)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(N)=O |r,wU:26.27,96.96,17.17,4.4,44.43,60.59,79.79,wD:70.70,8.13,105.105,2.2,35.34,52.51,91.92,22.22,(5.02,-.01,;5.03,-1.56,;6.37,-2.33,;7.7,-1.56,;6.37,-3.87,;5.16,-4.77,;3.8,-4.05,;3.81,-2.5,;2.53,-4.91,;2.53,-6.45,;3.86,-7.22,;3.86,-8.75,;2.53,-9.53,;5.19,-9.53,;1.32,-4.02,;-.03,-4.74,;-.03,-6.29,;-1.3,-3.88,;-1.3,-2.34,;-2.53,-4.76,;-3.88,-4.03,;-3.87,-2.49,;-5.16,-4.9,;-6.37,-4.01,;-7.72,-4.74,;-7.72,-6.28,;-9,-3.87,;-9,-2.33,;-10.21,-4.76,;-5.16,-6.45,;-3.83,-7.21,;-6.49,-7.21,;7.64,-4.74,;7.65,-6.28,;9.01,-4,;10.21,-4.89,;10.22,-6.43,;11.55,-7.21,;11.55,-8.74,;10.22,-9.51,;12.87,-9.51,;11.49,-4.03,;11.49,-2.48,;12.85,-4.75,;14.06,-3.85,;14.06,-2.31,;15.4,-1.54,;15.4,-0,;16.72,-2.31,;15.33,-4.72,;15.34,-6.26,;16.7,-4,;17.9,-4.88,;17.9,-6.42,;19.23,-7.2,;19.23,-8.73,;20.56,-9.5,;19.18,-4.02,;19.19,-2.47,;20.54,-4.75,;21.76,-3.86,;21.76,-2.32,;23.09,-1.54,;24.56,-2.04,;25.47,-.8,;24.58,.46,;23.1,-0,;23.03,-4.72,;23.04,-6.27,;24.39,-4,;25.61,-4.89,;25.61,-6.43,;26.93,-7.2,;26.93,-8.73,;25.61,-9.5,;28.27,-9.5,;26.88,-4.02,;26.89,-2.48,;28.25,-4.75,;29.46,-3.86,;29.47,-2.32,;30.8,-1.55,;30.8,-.01,;32.12,.76,;32.12,2.28,;33.45,3.05,;33.45,4.58,;34.77,2.28,;30.74,-4.73,;30.74,-6.27,;32.1,-4,;33.3,-4.89,;33.3,-6.43,;34.58,-4.03,;34.59,-2.48,;35.95,-4.76,;37.16,-3.86,;37.16,-2.32,;38.5,-1.55,;38.5,-.01,;39.82,.75,;39.82,2.29,;38.44,-4.73,;38.45,-6.28,;39.79,-3.99,;41.02,-4.88,;41.02,-6.42,;42.34,-7.2,;43.84,-6.86,;44.63,-8.17,;43.61,-9.33,;43.81,-10.86,;42.58,-11.78,;41.16,-11.17,;40.98,-9.66,;42.21,-8.73,;42.29,-4.02,;43.64,-4.74,;42.29,-2.47,)| Show InChI InChI=1S/C76H124N24O18S/c1-11-40(6)61(100-71(114)52(24-27-59(103)104)91-65(108)43(9)89-74(117)60(39(4)5)99-63(106)41(7)78)75(118)95-51(23-26-58(80)102)69(112)97-55(32-38(2)3)72(115)94-53(28-31-119-10)70(113)98-56(34-45-36-84-37-87-45)73(116)93-50(22-25-57(79)101)68(111)92-48(21-15-17-30-85-76(82)83)66(109)88-42(8)64(107)90-49(20-14-16-29-77)67(110)96-54(62(81)105)33-44-35-86-47-19-13-12-18-46(44)47/h12-13,18-19,35-43,48-56,60-61,86H,11,14-17,20-34,77-78H2,1-10H3,(H2,79,101)(H2,80,102)(H2,81,105)(H,84,87)(H,88,109)(H,89,117)(H,90,107)(H,91,108)(H,92,111)(H,93,116)(H,94,115)(H,95,118)(H,96,110)(H,97,112)(H,98,113)(H,99,106)(H,100,114)(H,103,104)(H4,82,83,85)/t40-,41-,42-,43-,48-,49-,50-,51-,52-,53-,54-,55-,56-,60-,61-/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 | 32 | 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 receptor
(Homo sapiens (Human)) | BDBM50269971
(Ala-Val-Ala-Glu-lle-Gln-Leu-Met-His-Gln-Har-Ala-Ly...)Show SMILES CC[C@H](C)[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(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)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(N)=O |r,wU:26.27,96.96,17.17,4.4,44.43,60.59,79.79,wD:70.70,8.13,105.105,2.2,35.34,52.51,91.92,22.22,(5.02,-.01,;5.03,-1.56,;6.37,-2.33,;7.7,-1.56,;6.37,-3.87,;5.16,-4.77,;3.8,-4.05,;3.81,-2.5,;2.53,-4.91,;2.53,-6.45,;3.86,-7.22,;3.86,-8.75,;2.53,-9.53,;5.19,-9.53,;1.32,-4.02,;-.03,-4.74,;-.03,-6.29,;-1.3,-3.88,;-1.3,-2.34,;-2.53,-4.76,;-3.88,-4.03,;-3.87,-2.49,;-5.16,-4.9,;-6.37,-4.01,;-7.72,-4.74,;-7.72,-6.28,;-9,-3.87,;-9,-2.33,;-10.21,-4.76,;-5.16,-6.45,;-3.83,-7.21,;-6.49,-7.21,;7.64,-4.74,;7.65,-6.28,;9.01,-4,;10.21,-4.89,;10.22,-6.43,;11.55,-7.21,;11.55,-8.74,;10.22,-9.51,;12.87,-9.51,;11.49,-4.03,;11.49,-2.48,;12.85,-4.75,;14.06,-3.85,;14.06,-2.31,;15.4,-1.54,;15.4,-0,;16.72,-2.31,;15.33,-4.72,;15.34,-6.26,;16.7,-4,;17.9,-4.88,;17.9,-6.42,;19.23,-7.2,;19.23,-8.73,;20.56,-9.5,;19.18,-4.02,;19.19,-2.47,;20.54,-4.75,;21.76,-3.86,;21.76,-2.32,;23.09,-1.54,;24.56,-2.04,;25.47,-.8,;24.58,.46,;23.1,-0,;23.03,-4.72,;23.04,-6.27,;24.39,-4,;25.61,-4.89,;25.61,-6.43,;26.93,-7.2,;26.93,-8.73,;25.61,-9.5,;28.27,-9.5,;26.88,-4.02,;26.89,-2.48,;28.25,-4.75,;29.46,-3.86,;29.47,-2.32,;30.8,-1.55,;30.8,-.01,;32.12,.76,;32.12,2.28,;33.45,3.05,;33.45,4.58,;34.77,2.28,;30.74,-4.73,;30.74,-6.27,;32.1,-4,;33.3,-4.89,;33.3,-6.43,;34.58,-4.03,;34.59,-2.48,;35.95,-4.76,;37.16,-3.86,;37.16,-2.32,;38.5,-1.55,;38.5,-.01,;39.82,.75,;39.82,2.29,;38.44,-4.73,;38.45,-6.28,;39.79,-3.99,;41.02,-4.88,;41.02,-6.42,;42.34,-7.2,;43.84,-6.86,;44.63,-8.17,;43.61,-9.33,;43.81,-10.86,;42.58,-11.78,;41.16,-11.17,;40.98,-9.66,;42.21,-8.73,;42.29,-4.02,;43.64,-4.74,;42.29,-2.47,)| Show InChI InChI=1S/C76H124N24O18S/c1-11-40(6)61(100-71(114)52(24-27-59(103)104)91-65(108)43(9)89-74(117)60(39(4)5)99-63(106)41(7)78)75(118)95-51(23-26-58(80)102)69(112)97-55(32-38(2)3)72(115)94-53(28-31-119-10)70(113)98-56(34-45-36-84-37-87-45)73(116)93-50(22-25-57(79)101)68(111)92-48(21-15-17-30-85-76(82)83)66(109)88-42(8)64(107)90-49(20-14-16-29-77)67(110)96-54(62(81)105)33-44-35-86-47-19-13-12-18-46(44)47/h12-13,18-19,35-43,48-56,60-61,86H,11,14-17,20-34,77-78H2,1-10H3,(H2,79,101)(H2,80,102)(H2,81,105)(H,84,87)(H,88,109)(H,89,117)(H,90,107)(H,91,108)(H,92,111)(H,93,116)(H,94,115)(H,95,118)(H,96,110)(H,97,112)(H,98,113)(H,99,106)(H,100,114)(H,103,104)(H4,82,83,85)/t40-,41-,42-,43-,48-,49-,50-,51-,52-,53-,54-,55-,56-,60-,61-/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 | 1.05E+4 | 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 1 receptor (PTH1R)
(Rattus norvegicus (Rat)) | BDBM50269971
(Ala-Val-Ala-Glu-lle-Gln-Leu-Met-His-Gln-Har-Ala-Ly...)Show SMILES CC[C@H](C)[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(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)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(N)=O |r,wU:26.27,96.96,17.17,4.4,44.43,60.59,79.79,wD:70.70,8.13,105.105,2.2,35.34,52.51,91.92,22.22,(5.02,-.01,;5.03,-1.56,;6.37,-2.33,;7.7,-1.56,;6.37,-3.87,;5.16,-4.77,;3.8,-4.05,;3.81,-2.5,;2.53,-4.91,;2.53,-6.45,;3.86,-7.22,;3.86,-8.75,;2.53,-9.53,;5.19,-9.53,;1.32,-4.02,;-.03,-4.74,;-.03,-6.29,;-1.3,-3.88,;-1.3,-2.34,;-2.53,-4.76,;-3.88,-4.03,;-3.87,-2.49,;-5.16,-4.9,;-6.37,-4.01,;-7.72,-4.74,;-7.72,-6.28,;-9,-3.87,;-9,-2.33,;-10.21,-4.76,;-5.16,-6.45,;-3.83,-7.21,;-6.49,-7.21,;7.64,-4.74,;7.65,-6.28,;9.01,-4,;10.21,-4.89,;10.22,-6.43,;11.55,-7.21,;11.55,-8.74,;10.22,-9.51,;12.87,-9.51,;11.49,-4.03,;11.49,-2.48,;12.85,-4.75,;14.06,-3.85,;14.06,-2.31,;15.4,-1.54,;15.4,-0,;16.72,-2.31,;15.33,-4.72,;15.34,-6.26,;16.7,-4,;17.9,-4.88,;17.9,-6.42,;19.23,-7.2,;19.23,-8.73,;20.56,-9.5,;19.18,-4.02,;19.19,-2.47,;20.54,-4.75,;21.76,-3.86,;21.76,-2.32,;23.09,-1.54,;24.56,-2.04,;25.47,-.8,;24.58,.46,;23.1,-0,;23.03,-4.72,;23.04,-6.27,;24.39,-4,;25.61,-4.89,;25.61,-6.43,;26.93,-7.2,;26.93,-8.73,;25.61,-9.5,;28.27,-9.5,;26.88,-4.02,;26.89,-2.48,;28.25,-4.75,;29.46,-3.86,;29.47,-2.32,;30.8,-1.55,;30.8,-.01,;32.12,.76,;32.12,2.28,;33.45,3.05,;33.45,4.58,;34.77,2.28,;30.74,-4.73,;30.74,-6.27,;32.1,-4,;33.3,-4.89,;33.3,-6.43,;34.58,-4.03,;34.59,-2.48,;35.95,-4.76,;37.16,-3.86,;37.16,-2.32,;38.5,-1.55,;38.5,-.01,;39.82,.75,;39.82,2.29,;38.44,-4.73,;38.45,-6.28,;39.79,-3.99,;41.02,-4.88,;41.02,-6.42,;42.34,-7.2,;43.84,-6.86,;44.63,-8.17,;43.61,-9.33,;43.81,-10.86,;42.58,-11.78,;41.16,-11.17,;40.98,-9.66,;42.21,-8.73,;42.29,-4.02,;43.64,-4.74,;42.29,-2.47,)| Show InChI InChI=1S/C76H124N24O18S/c1-11-40(6)61(100-71(114)52(24-27-59(103)104)91-65(108)43(9)89-74(117)60(39(4)5)99-63(106)41(7)78)75(118)95-51(23-26-58(80)102)69(112)97-55(32-38(2)3)72(115)94-53(28-31-119-10)70(113)98-56(34-45-36-84-37-87-45)73(116)93-50(22-25-57(79)101)68(111)92-48(21-15-17-30-85-76(82)83)66(109)88-42(8)64(107)90-49(20-14-16-29-77)67(110)96-54(62(81)105)33-44-35-86-47-19-13-12-18-46(44)47/h12-13,18-19,35-43,48-56,60-61,86H,11,14-17,20-34,77-78H2,1-10H3,(H2,79,101)(H2,80,102)(H2,81,105)(H,84,87)(H,88,109)(H,89,117)(H,90,107)(H,91,108)(H,92,111)(H,93,116)(H,94,115)(H,95,118)(H,96,110)(H,97,112)(H,98,113)(H,99,106)(H,100,114)(H,103,104)(H4,82,83,85)/t40-,41-,42-,43-,48-,49-,50-,51-,52-,53-,54-,55-,56-,60-,61-/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 | 155 | 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)) | BDBM50269971
(Ala-Val-Ala-Glu-lle-Gln-Leu-Met-His-Gln-Har-Ala-Ly...)Show SMILES CC[C@H](C)[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(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)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(N)=O |r,wU:26.27,96.96,17.17,4.4,44.43,60.59,79.79,wD:70.70,8.13,105.105,2.2,35.34,52.51,91.92,22.22,(5.02,-.01,;5.03,-1.56,;6.37,-2.33,;7.7,-1.56,;6.37,-3.87,;5.16,-4.77,;3.8,-4.05,;3.81,-2.5,;2.53,-4.91,;2.53,-6.45,;3.86,-7.22,;3.86,-8.75,;2.53,-9.53,;5.19,-9.53,;1.32,-4.02,;-.03,-4.74,;-.03,-6.29,;-1.3,-3.88,;-1.3,-2.34,;-2.53,-4.76,;-3.88,-4.03,;-3.87,-2.49,;-5.16,-4.9,;-6.37,-4.01,;-7.72,-4.74,;-7.72,-6.28,;-9,-3.87,;-9,-2.33,;-10.21,-4.76,;-5.16,-6.45,;-3.83,-7.21,;-6.49,-7.21,;7.64,-4.74,;7.65,-6.28,;9.01,-4,;10.21,-4.89,;10.22,-6.43,;11.55,-7.21,;11.55,-8.74,;10.22,-9.51,;12.87,-9.51,;11.49,-4.03,;11.49,-2.48,;12.85,-4.75,;14.06,-3.85,;14.06,-2.31,;15.4,-1.54,;15.4,-0,;16.72,-2.31,;15.33,-4.72,;15.34,-6.26,;16.7,-4,;17.9,-4.88,;17.9,-6.42,;19.23,-7.2,;19.23,-8.73,;20.56,-9.5,;19.18,-4.02,;19.19,-2.47,;20.54,-4.75,;21.76,-3.86,;21.76,-2.32,;23.09,-1.54,;24.56,-2.04,;25.47,-.8,;24.58,.46,;23.1,-0,;23.03,-4.72,;23.04,-6.27,;24.39,-4,;25.61,-4.89,;25.61,-6.43,;26.93,-7.2,;26.93,-8.73,;25.61,-9.5,;28.27,-9.5,;26.88,-4.02,;26.89,-2.48,;28.25,-4.75,;29.46,-3.86,;29.47,-2.32,;30.8,-1.55,;30.8,-.01,;32.12,.76,;32.12,2.28,;33.45,3.05,;33.45,4.58,;34.77,2.28,;30.74,-4.73,;30.74,-6.27,;32.1,-4,;33.3,-4.89,;33.3,-6.43,;34.58,-4.03,;34.59,-2.48,;35.95,-4.76,;37.16,-3.86,;37.16,-2.32,;38.5,-1.55,;38.5,-.01,;39.82,.75,;39.82,2.29,;38.44,-4.73,;38.45,-6.28,;39.79,-3.99,;41.02,-4.88,;41.02,-6.42,;42.34,-7.2,;43.84,-6.86,;44.63,-8.17,;43.61,-9.33,;43.81,-10.86,;42.58,-11.78,;41.16,-11.17,;40.98,-9.66,;42.21,-8.73,;42.29,-4.02,;43.64,-4.74,;42.29,-2.47,)| Show InChI InChI=1S/C76H124N24O18S/c1-11-40(6)61(100-71(114)52(24-27-59(103)104)91-65(108)43(9)89-74(117)60(39(4)5)99-63(106)41(7)78)75(118)95-51(23-26-58(80)102)69(112)97-55(32-38(2)3)72(115)94-53(28-31-119-10)70(113)98-56(34-45-36-84-37-87-45)73(116)93-50(22-25-57(79)101)68(111)92-48(21-15-17-30-85-76(82)83)66(109)88-42(8)64(107)90-49(20-14-16-29-77)67(110)96-54(62(81)105)33-44-35-86-47-19-13-12-18-46(44)47/h12-13,18-19,35-43,48-56,60-61,86H,11,14-17,20-34,77-78H2,1-10H3,(H2,79,101)(H2,80,102)(H2,81,105)(H,84,87)(H,88,109)(H,89,117)(H,90,107)(H,91,108)(H,92,111)(H,93,116)(H,94,115)(H,95,118)(H,96,110)(H,97,112)(H,98,113)(H,99,106)(H,100,114)(H,103,104)(H4,82,83,85)/t40-,41-,42-,43-,48-,49-,50-,51-,52-,53-,54-,55-,56-,60-,61-/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 | 800 | 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 | |