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Target
Histamine H3 receptor
Ligand
BDBM22888
Substrate
n/a
Meas. Tech.
ChEMBL_86913 (CHEMBL699051)
Ki
70±n/a nM
Citation
 Ganellin, CR; Hosseini, SK; Khalaf, YS; Tertiuk, W; Arrang, JM; Garbarg, M; Ligneau, X; Schwartz, JC Design of potent non-thiourea H3-receptor histamine antagonists. J Med Chem 38:3342-50 (1995) [PubMed]  Article 
Target
Name:
Histamine H3 receptor
Synonyms:
HH3R | HRH3_RAT | Hrh3
Type:
G Protein-Coupled Receptor (GPCR)
Mol. Mass.:
48607.98
Organism:
Rattus norvegicus (rat)
Description:
n/a
Residue:
445
Sequence:
MERAPPDGLMNASGTLAGEAAAAGGARGFSAAWTAVLAALMALLIVATVLGNALVMLAFVADSSLRTQNNFFLLNLAISDFLVGAFCIPLYVPYVLTGRWTFGRGLCKLWLVVDYLLCASSVFNIVLISYDRFLSVTRAVSYRAQQGDTRRAVRKMALVWVLAFLLYGPAILSWEYLSGGSSIPEGHCYAEFFYNWYFLITASTLEFFTPFLSVTFFNLSIYLNIQRRTRLRLDGGREAGPEPPPDAQPSPPPAPPSCWGCWPKGHGEAMPLHRYGVGEAGPGVEAGEAALGGGSGGGAAASPTSSSGSSSRGTERPRSLKRGSKPSASSASLEKRMKMVSQSITQRFRLSRDKKVAKSLAIIVSIFGLCWAPYTLLMIIRAACHGRCIPDYWYETSFWLLWANSAVNPVLYPLCHYSFRRAFTKLLCPQKLKVQPHGSLEQCWK
  
Inhibitor
Name:
BDBM22888
Synonyms:
1-[4-(1H-imidazol-5-yl)butyl]-3-methylthiourea | Burimamide | CHEMBL12160
Type:
Small organic molecule
Emp. Form.:
C9H16N4S
Mol. Mass.:
212.315
SMILES:
CNC(=S)NCCCCc1cnc[nH]1
Structure:
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