Reaction Details |
| Report a problem with these data |
Target | Histamine H2 receptor |
---|
Ligand | BDBM22566 |
---|
Substrate/Competitor | BDBM22568 |
---|
Meas. Tech. | Radioligand Binding Assay |
---|
pH | 7.5±n/a |
---|
Temperature | 298.15±n/a K |
---|
Ki | >1000±n/a nM |
---|
Citation | Thurmond, RL; Desai, PJ; Dunford, PJ; Fung-Leung, WP; Hofstra, CL; Jiang, W; Nguyen, S; Riley, JP; Sun, S; Williams, KN; Edwards, JP; Karlsson, L A potent and selective histamine H4 receptor antagonist with anti-inflammatory properties. J Pharmacol Exp Ther309:404-13 (2004) [PubMed] Article |
---|
More Info.: | Get all data from this article, Solution Info, Assay Method |
---|
|
Histamine H2 receptor |
---|
Name: | Histamine H2 receptor |
Synonyms: | Gastric receptor I | H2R | HISTAMINE H2 | HRH2 | HRH2_CAVPO | Histamine H2-Gs alpha S |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 40567.22 |
Organism: | Cavia porcellus (domestic guinea pig) |
Description: | For the H2 receptor-binding assays, guinea pig striatum was used. |
Residue: | 359 |
Sequence: | MAFNGTVPSFCMDFTVYKVTISVILIILILVTVAGNVVVCLAVGLNRRLRSLTNCFIVSL
AVTDLLLGLLVLPFSAIYQLSCKWSFSKVFCNIYTSLDVMLCTASILNLFMISLDRYCAV
TDPLRYPVLITPARVAISLVFIWVISITLSFLSIHLGWNSRNETSKDNDTIVKCKVQVNE
VYGLVDGLVTFYLPLLIMCITYFRIFKIAREQARRINHIGSWKAATIREHKATVTLAAVM
GAFIICWFPYFTVFVYRGLKGDDAVNEVFEDVVLWLGYANSALNPILYAALNRDFRTAYH
QLFCCRLASHNSHETSLRLNNSQLNRSQCQEPRWQEDKPLNLQVWSGTEVTAPQGATNR
|
|
|
BDBM22566 |
---|
BDBM22568 |
---|
Name | BDBM22566 |
Synonyms: | 5-chloro-2-[(4-methylpiperazin-1-yl)carbonyl]-1H-indole | CHEMBL129198 | JNJ 7777120 |
Type | Small organic molecule |
Emp. Form. | C14H16ClN3O |
Mol. Mass. | 277.749 |
SMILES | CN1CCN(CC1)C(=O)c1cc2cc(Cl)ccc2[nH]1 |
Structure |
|