Reaction Details |
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Target | Histamine N-methyltransferase |
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Ligand | BDBM50110291 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_87238 (CHEMBL696458) |
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IC50 | 310±n/a nM |
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Citation | Apelt, J; Ligneau, X; Pertz, HH; Arrang, JM; Ganellin, CR; Schwartz, JC; Schunack, W; Stark, H Development of a new class of nonimidazole histamine H(3) receptor ligands with combined inhibitory histamine N-methyltransferase activity. J Med Chem45:1128-41 (2002) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Histamine N-methyltransferase |
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Name: | Histamine N-methyltransferase |
Synonyms: | HNMT_RAT | Hnmt |
Type: | PROTEIN |
Mol. Mass.: | 33931.03 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_87236 |
Residue: | 295 |
Sequence: | MASFMRSLFSDHSRYVESFRRFLNNSTEHQCMQEFMDKKLPGIIARIGETKAEIKILSIG
GGAGEIDLQILSKVQAQYPGICINNEVVEPNAEQIVKYKELVAKTSNMENIKFAWHKETS
SEYQKRVVEEDEEPPKWDFIHMIQMLYYVKDIPATLKFFHGLLAANAKILIILVSGTSGW
EKLWKKYGFRLPRDDLCQYVTSSDLAQILDDLGIKYECYDLLSTMDITDCFIDGNENGDL
LWDFLTETCNFIKTAPLDLKEEIMKDLQEPEFSVKKEGKVLFNNNLSFIVVEANV
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BDBM50110291 |
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n/a |
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Name | BDBM50110291 |
Synonyms: | (7-Chloro-quinolin-4-yl)-[4-(3-piperidin-1-yl-propoxy)-phenyl]-amine; Oxalic acid | CHEMBL14364 |
Type | Small organic molecule |
Emp. Form. | C23H26ClN3O |
Mol. Mass. | 395.925 |
SMILES | Clc1ccc2c(Nc3ccc(OCCCN4CCCCC4)cc3)ccnc2c1 |
Structure |
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