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TargetHistamine H3 receptor
LigandBDBM50051195
Substrate/Competitorn/a
Meas. Tech.ChEMBL_86902 (CHEMBL698412)
Ki 5.8±n/a nM
Citation Stark, HPurand, KLigneau, XRouleau, AArrang, JMGarbarg, MSchwartz, JCSchunack, W Novel carbamates as potent histamine H3 receptor antagonists with high in vitro and oral in vivo activity. J Med Chem39:1157-63 (1996) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Histamine H3 receptor
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:
MERAPPDGLMNASGTLAGEAAAAGGARGFSAAWTAVLAALMALLIVATVLGNALVMLAFV
ADSSLRTQNNFFLLNLAISDFLVGAFCIPLYVPYVLTGRWTFGRGLCKLWLVVDYLLCAS
SVFNIVLISYDRFLSVTRAVSYRAQQGDTRRAVRKMALVWVLAFLLYGPAILSWEYLSGG
SSIPEGHCYAEFFYNWYFLITASTLEFFTPFLSVTFFNLSIYLNIQRRTRLRLDGGREAG
PEPPPDAQPSPPPAPPSCWGCWPKGHGEAMPLHRYGVGEAGPGVEAGEAALGGGSGGGAA
ASPTSSSGSSSRGTERPRSLKRGSKPSASSASLEKRMKMVSQSITQRFRLSRDKKVAKSL
AIIVSIFGLCWAPYTLLMIIRAACHGRCIPDYWYETSFWLLWANSAVNPVLYPLCHYSFR
RAFTKLLCPQKLKVQPHGSLEQCWK
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50051195
n/a
NameBDBM50051195
Synonyms:(2-ferrocenyl)-carbamic acid 3-(1H-imidazol-4-yl)-propylester: C4H4O40.25H2O | CHEMBL280249
TypeSmall organic molecule
Emp. Form.C18H21FeN3O2
Mol. Mass.367.222
SMILESO=C(NCC1=CC=CC1[Fe++]C1C=CC=C1)OCCCc1cnc[nH]1 |c:6,12,14,t:4|
Structure
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