Reaction Details |
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Target | Histamine N-methyltransferase |
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Ligand | BDBM50110298 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_87238 (CHEMBL696458) |
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IC50 | 49±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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BDBM50110298 |
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n/a |
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Name | BDBM50110298 |
Synonyms: | CHEMBL277113 | Ethyl-(3-piperidin-1-yl-propyl)-quinolin-4-yl-amine; Oxalic acid |
Type | Small organic molecule |
Emp. Form. | C19H27N3 |
Mol. Mass. | 297.4378 |
SMILES | CCN(CCCN1CCCCC1)c1ccnc2ccccc12 |
Structure |
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