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Target
Melanin-concentrating hormone receptor 1
Ligand
BDBM50173454
Substrate
n/a
Meas. Tech.
ChEMBL_321503 (CHEMBL880563)
IC50
3±n/a nM
Citation
 Kym, PR; Iyengar, R; Souers, AJ; Lynch, JK; Judd, AS; Gao, J; Freeman, J; Mulhern, M; Zhao, G; Vasudevan, A; Wodka, D; Blackburn, C; Brown, J; Che, JL; Cullis, C; Lai, SJ; LaMarche, MJ; Marsilje, T; Roses, J; Sells, T; Geddes, B; Govek, E; Patane, M; Fry, D; Dayton, BD; Brodjian, S; Falls, D; Brune, M; Bush, E; Shapiro, R; Knourek-Segel, V; Fey, T; McDowell, C; Reinhart, GA; Preusser, LC; Marsh, K; Hernandez, L; Sham, HL; Collins, CA Discovery and characterization of aminopiperidinecoumarin melanin concentrating hormone receptor 1 antagonists. J Med Chem 48:5888-91 (2005) [PubMed]  Article 
Target
Name:
Melanin-concentrating hormone receptor 1
Synonyms:
G-protein coupled receptor 24 | GPR24 | MCH receptor 1 | MCH-1R | MCH-R1 | MCHR | MCHR-1 | MCHR1 | MCHR1_HUMAN | Melanin Concentrating Hormone 1 | Melanin-Concentrating Hormone Receptor 1 (MCH1R) | Melanin-concentrating hormone receptor | Melanin-concentrating hormone receptor 1 (MCH-1) | Melanin-concentrating hormone receptor 1 (MCH1) | Melanin-concentrating hormone receptor 1 (MCHR-1) | Melanin-concentrating hormone receptor 1 (MCHR1) | SLC-1 | SLC1 | Somatostatin receptor-like protein
Type:
G Protein-Coupled Receptor (GPCR)
Mol. Mass.:
45976.27
Organism:
Homo sapiens (Human)
Description:
Membranes from CHO-K1 cells stably expressing human MCH1R were used in assays.
Residue:
422
Sequence:
MSVGAMKKGVGRAVGLGGGSGCQATEEDPLPNCGACAPGQGGRRWRLPQPAWVEGSSARLWEQATGTGWMDLEASLLPTGPNASNTSDGPDNLTSAGSPPRTGSISYINIIMPSVFGTICLLGIIGNSTVIFAVVKKSKLHWCNNVPDIFIINLSVVDLLFLLGMPFMIHQLMGNGVWHFGETMCTLITAMDANSQFTSTYILTAMAIDRYLATVHPISSTKFRKPSVATLVICLLWALSFISITPVWLYARLIPFPGGAVGCGIRLPNPDTDLYWFTLYQFFLAFALPFVVITAAYVRILQRMTSSVAPASQRSIRLRTKRVTRTAIAICLVFFVCWAPYYVLQLTQLSISRPTLTFVYLYNAAISLGYANSCLNPFVYIVLCETFRKRLVLSVKPAAQGQLRAVSNAQTADEERTESKGT
  
Inhibitor
Name:
BDBM50173454
Synonyms:
4-(1-Benzooxazol-5-ylmethyl-piperidin-4-ylamino)-6-chloro-chromen-2-one | CHEMBL196350
Type:
Small organic molecule
Emp. Form.:
C22H20ClN3O3
Mol. Mass.:
409.866
SMILES:
Clc1ccc2oc(=O)cc(NC3CCN(Cc4ccc5ocnc5c4)CC3)c2c1
Structure:
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