Reaction Details |
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Target | Histamine N-methyltransferase |
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Ligand | BDBM50026331 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_87234 |
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Ki | 10400±n/a nM |
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Citation | Houston, DM; Matuszewska, B; Borchardt, RT Potential inhibitors of S-adenosylmethionine-dependent methyltransferases. 10. Base- and amino acid modified analogues of S-aristeromycinyl-L-homocysteine. J Med Chem28:478-82 (1985) [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: | HMT | HNMT | HNMT_HUMAN |
Type: | PROTEIN |
Mol. Mass.: | 33287.63 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_87234 |
Residue: | 292 |
Sequence: | MASSMRSLFSDHGKYVESFRRFLNHSTEHQCMQEFMDKKLPGIIGRIGDTKSEIKILSIG
GGAGEIDLQILSKVQAQYPGVCINNEVVEPSAEQIAKYKELVAKTSNLENVKFAWHKETS
SEYQSRMLEKKELQKWDFIHMIQMLYYVKDIPATLKFFHSLLGTNAKMLIIVVSGSSGWD
KLWKKYGSRFPQDDLCQYITSDDLTQMLDNLGLKYECYDLLSTMDISDCFIDGNENGDLL
WDFLTETCNFNATAPPDLRAELGKDLQEPEFSAKKEGKVLFNNTLSFIVIEA
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BDBM50026331 |
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n/a |
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Name | BDBM50026331 |
Synonyms: | 2-Amino-4-[4-(6-amino-purin-9-yl)-2,3-dihydroxy-cyclopentylmethylsulfanyl]-butyric acid | CHEMBL342283 | L-2-Amino-4-[5-(6-amino-purin-9-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethylsulfanyl]-butyric acid |
Type | Small organic molecule |
Emp. Form. | C15H22N6O4S |
Mol. Mass. | 382.438 |
SMILES | NC(CCSCC1CC(C(O)C1O)n1cnc2c(N)ncnc12)C(O)=O |
Structure |
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