Target
Histamine H3 receptor
Ligand
BDBM50091395
Substrate
n/a
Meas. Tech.
ChEMBL_86898 (CHEMBL698408)
Ki
77±n/a nM
Citation
 Sasse, ASadek, BLigneau, XElz, SPertz, HHLuger, PGanellin, CRArrang, JMSchwartz, JCSchunack, WStark, H New histamine H(3)-receptor ligands of the proxifan series: imoproxifan and other selective antagonists with high oral in vivo potency. J Med Chem 43:3335-43 (2000) [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:
BDBM50091395
Synonyms:
4-[3-(1H-Imidazol-4-yl)-propoxy]-N,N-dimethyl-benzenesulfonamide with (0.85M) oxalic acid | CHEMBL112858
Type:
Small organic molecule
Emp. Form.:
C14H19N3O3S
Mol. Mass.:
309.384
SMILES:
CN(C)S(=O)(=O)c1ccc(OCCCc2cnc[nH]2)cc1
Structure:
Search PDB for entries with ligand similarity: