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TargetKiSS-1 receptor
LigandBDBM50203787
Substrate/Competitorn/a
Meas. Tech.ChEMBL_425686 (CHEMBL912002)
Ki 33.4±n/a nM
Citation Orsini, MJKlein, MABeavers, MPConnolly, PJMiddleton, SAMayo, KH Metastin (KiSS-1) mimetics identified from peptide structure-activity relationship-derived pharmacophores and directed small molecule database screening. J Med Chem50:462-71 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
KiSS-1 receptor
Name:KiSS-1 receptor
Synonyms:AXOR12 | G-protein Coupled Receptor 54 | G-protein coupled receptor 54 (GPR54) | GPR54 | Hypogonadotropin-1 | KISS1R | KISSR_HUMAN | KiSS-1R | Kisspeptins receptor | Metastin receptor | hOT7T175
Type:G Protein-Coupled Receptor (GPCR)
Mol. Mass.:42613.79
Organism:Homo sapiens (Human)
Description:Binding assay was performed using membranes from the CHO cell transfectants.
Residue:398
Sequence:
MHTVATSGPNASWGAPANASGCPGCGANASDGPVPSPRAVDAWLVPLFFAALMLLGLVGN
SLVIYVICRHKPMRTVTNFYIANLAATDVTFLLCCVPFTALLYPLPGWVLGDFMCKFVNY
IQQVSVQATCATLTAMSVDRWYVTVFPLRALHRRTPRLALAVSLSIWVGSAAVSAPVLAL
HRLSPGPRAYCSEAFPSRALERAFALYNLLALYLLPLLATCACYAAMLRHLGRVAVRPAP
ADSALQGQVLAERAGAVRAKVSRLVAAVVLLFAACWGPIQLFLVLQALGPAGSWHPRSYA
AYALKTWAHCMSYSNSALNPLLYAFLGSHFRQAFRRVCPCAPRRPRRPRRPGPSDPAAPH
AELLRLGSHPAPARAQKPGSSGLAARGLCVLGEDNAPL
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  Blast E-value cutoff:
BDBM50203787
n/a
NameBDBM50203787
Synonyms:(2S)-2-{[(2S)-1-[(2S)-2-amino-4-methylpentanoyl]pyrrolidin-2-yl]formamido}-N-[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-[({[(1S)-1-{[(1S)-4-carbamimidamido-1-{[(1S)-1-carbamoyl-2-phenylethyl]carbamoyl}butyl]carbamoyl}-3-methylbutyl]carbamoyl}methyl)carbamoyl]-2-phenylethyl]carbamoyl}-2-hydroxyethyl]carbamoyl}ethyl]carbamoyl}-2-(1H-indol-3-yl)ethyl]carbamoyl}-2-carbamoylethyl]carbamoyl}-2-(4-hydroxyphenyl)ethyl]butanediamide | CHEMBL373676
TypeSmall organic molecule
Emp. Form.C77H106N20O17
Mol. Mass.1583.7893
SMILESCC(C)C[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccccc1)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1ccccc1)C(N)=O |wU:4.4,58.62,69.72,84.88,36.37,12.13,103.107,wD:63.66,24.24,92.96,16.16,44.45,(-9.93,-20.42,;-9.9,-21.96,;-11.22,-22.75,;-8.55,-22.7,;-8.55,-24.26,;-9.88,-25.03,;-7.21,-25.03,;-7.21,-26.57,;-5.88,-24.27,;-5.4,-22.81,;-3.86,-22.81,;-3.39,-24.27,;-4.64,-25.18,;-4.64,-26.72,;-5.98,-27.49,;-3.31,-27.49,;-3.31,-29.03,;-4.65,-29.8,;-4.65,-31.34,;-3.32,-32.11,;-5.98,-32.11,;-1.98,-29.8,;-1.98,-31.34,;-.64,-29.03,;.69,-29.8,;.69,-31.34,;2.02,-32.12,;2.01,-33.65,;3.34,-34.42,;4.68,-33.65,;6.01,-34.42,;4.68,-32.11,;3.35,-31.35,;2.02,-29.04,;2.02,-27.5,;3.36,-29.81,;4.69,-29.04,;4.69,-27.5,;6.03,-26.73,;7.36,-27.5,;6.03,-25.19,;6.02,-29.81,;6.02,-31.35,;7.36,-29.04,;8.69,-29.81,;8.69,-31.35,;10.02,-32.12,;11.27,-31.13,;12.51,-32.12,;12.03,-33.59,;12.79,-34.91,;12.03,-36.23,;10.49,-36.23,;9.73,-34.9,;10.5,-33.58,;10.03,-29.04,;10.03,-27.5,;11.36,-29.82,;12.69,-29.05,;12.69,-27.51,;14.03,-29.82,;14.02,-31.36,;15.36,-29.05,;16.69,-29.82,;16.69,-31.36,;18.02,-32.13,;18.03,-29.05,;18.03,-27.51,;19.36,-29.82,;20.69,-29.06,;20.7,-27.52,;22.03,-26.75,;23.36,-27.52,;24.7,-26.76,;24.7,-25.21,;23.36,-24.44,;22.03,-25.21,;22.03,-29.83,;22.03,-31.37,;23.36,-29.06,;24.7,-29.83,;26.03,-29.06,;26.03,-27.52,;27.36,-29.83,;28.7,-29.06,;28.7,-27.52,;30.03,-26.76,;30.03,-25.22,;31.37,-27.53,;30.03,-29.84,;30.03,-31.38,;31.36,-29.07,;32.7,-29.84,;32.7,-31.38,;34.03,-32.15,;34.03,-33.69,;35.36,-34.46,;35.36,-36,;36.69,-36.77,;34.02,-36.77,;34.03,-29.07,;34.03,-27.53,;35.36,-29.84,;36.7,-29.07,;36.7,-27.53,;38.04,-26.76,;39.36,-27.54,;40.7,-26.78,;40.7,-25.24,;39.36,-24.46,;38.03,-25.24,;38.03,-29.84,;39.37,-29.08,;38.03,-31.38,)|
Structure
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