Reaction Details |
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Target | Histamine H2 receptor |
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Ligand | BDBM50404821 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_84894 |
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Ki | 4±n/a nM |
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Citation | Lumma, WC; Anderson, PS; Baldwin, JJ; Bolhofer, WA; Habecker, CN; Hirshfield, JM; Pietruszkiewicz, AM; Randall, WC; Torchiana, ML; Britcher, SF; Clineschmidt, BV; Denny, GH; Hirschmann, R; Hoffman, MJ; Phillips, BT; Streeter, KB Inhibitors of gastric acid secretion: 3,4-diamino-1,2,5-thiadiazole 1-oxides and 1,1-dioxides as urea equivalents in a series of histamine H2-receptor antagonists. J Med Chem25:207-10 (1982) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Histamine H2 receptor |
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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
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BDBM50404821 |
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n/a |
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Name | BDBM50404821 |
Synonyms: | CHEMBL306465 |
Type | Small organic molecule |
Emp. Form. | C17H25N5O2S |
Mol. Mass. | 363.478 |
SMILES | Nc1ns(=O)nc1NCCCOc1cccc(CN2CCCCC2)c1 |
Structure |
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