Reaction Details Report a problem with these data
Target
KiSS-1 receptor
Ligand
BDBM50203797
Substrate
n/a
Meas. Tech.
ChEMBL_425686 (CHEMBL912002)
Ki
80.8±n/a nM
Citation
 Orsini, MJ; Klein, MA; Beavers, MP; Connolly, PJ; Middleton, SA; Mayo, KH Metastin (KiSS-1) mimetics identified from peptide structure-activity relationship-derived pharmacophores and directed small molecule database screening. J Med Chem 50:462-71 (2007) [PubMed]  Article 
Target
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:
MHTVATSGPNASWGAPANASGCPGCGANASDGPVPSPRAVDAWLVPLFFAALMLLGLVGNSLVIYVICRHKPMRTVTNFYIANLAATDVTFLLCCVPFTALLYPLPGWVLGDFMCKFVNYIQQVSVQATCATLTAMSVDRWYVTVFPLRALHRRTPRLALAVSLSIWVGSAAVSAPVLALHRLSPGPRAYCSEAFPSRALERAFALYNLLALYLLPLLATCACYAAMLRHLGRVAVRPAPADSALQGQVLAERAGAVRAKVSRLVAAVVLLFAACWGPIQLFLVLQALGPAGSWHPRSYAAYALKTWAHCMSYSNSALNPLLYAFLGSHFRQAFRRVCPCAPRRPRRPRRPGPSDPAAPHAELLRLGSHPAPARAQKPGSSGLAARGLCVLGEDNAPL
  
Inhibitor
Name:
BDBM50203797
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-(4-hydroxyphenyl)ethyl]carbamoyl}butyl]carbamoyl}-3-methylbutyl]carbamoyl}methyl)carbamoyl]-2-phenylethyl]carbamoyl}-2-hydroxyethyl]carbamoyl}-2-carbamoylethyl]carbamoyl}-2-(1H-indol-3-yl)ethyl]carbamoyl}-2-carbamoylethyl]carbamoyl}-2-(4-hydroxyphenyl)ethyl]butanediamide | CHEMBL414073
Type:
Small organic molecule
Emp. Form.:
C78H107N21O19
Mol. Mass.:
1642.8135
SMILES:
CC(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](CC(N)=O)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](Cc1ccc(O)cc1)C(N)=O |wU:72.75,87.91,36.37,12.13,106.110,58.61,4.4,wD:66.69,24.24,95.99,16.16,44.45,(-4.64,-18.24,;-4.61,-19.78,;-5.93,-20.57,;-3.26,-20.52,;-3.26,-22.09,;-4.59,-22.86,;-1.92,-22.86,;-1.92,-24.4,;-.59,-22.09,;-.11,-20.63,;1.42,-20.63,;1.9,-22.09,;.65,-23,;.65,-24.54,;-.69,-25.31,;1.98,-25.31,;1.98,-26.85,;.65,-27.62,;.65,-29.16,;1.98,-29.93,;-.69,-29.93,;3.31,-27.62,;3.31,-29.16,;4.65,-26.85,;5.98,-27.62,;5.98,-29.16,;7.31,-29.94,;7.31,-31.47,;8.63,-32.24,;9.98,-31.47,;11.31,-32.24,;9.97,-29.93,;8.65,-29.17,;7.32,-26.86,;7.32,-25.32,;8.65,-27.63,;9.98,-26.86,;9.98,-25.32,;11.32,-24.55,;12.65,-25.32,;11.32,-23.01,;11.32,-27.63,;11.31,-29.17,;12.65,-26.86,;13.98,-27.63,;13.98,-29.17,;15.31,-29.94,;16.57,-28.95,;17.8,-29.94,;17.32,-31.41,;18.08,-32.72,;17.32,-34.05,;15.78,-34.05,;15.02,-32.72,;15.79,-31.4,;15.32,-26.86,;15.32,-25.32,;16.65,-27.64,;17.98,-26.87,;17.99,-25.33,;19.32,-24.56,;20.66,-25.33,;19.32,-23.02,;19.31,-27.64,;19.31,-29.18,;20.65,-26.87,;21.98,-27.64,;21.98,-29.18,;23.32,-29.95,;23.32,-26.87,;23.32,-25.33,;24.65,-27.65,;25.98,-26.88,;25.98,-25.34,;27.32,-24.57,;28.65,-25.34,;29.99,-24.57,;29.99,-23.03,;28.64,-22.26,;27.32,-23.03,;27.32,-27.65,;27.32,-29.19,;28.65,-26.88,;29.99,-27.64,;31.32,-26.87,;31.32,-25.33,;32.65,-27.65,;33.99,-26.88,;33.99,-25.34,;35.32,-24.57,;35.32,-23.03,;36.66,-25.34,;35.32,-27.65,;35.32,-29.19,;36.66,-26.88,;37.99,-27.65,;37.99,-29.19,;39.32,-29.96,;39.32,-31.5,;40.65,-32.28,;40.65,-33.82,;41.98,-34.59,;39.32,-34.58,;39.33,-26.88,;39.33,-25.34,;40.66,-27.66,;41.99,-26.89,;41.99,-25.35,;43.32,-24.58,;44.65,-25.35,;45.98,-24.58,;45.99,-23.04,;47.32,-22.27,;44.65,-22.27,;43.32,-23.04,;43.33,-27.66,;44.66,-26.89,;43.32,-29.2,)|
Structure:
Search PDB for entries with ligand similarity: