5'-THIODENOSINE DERIVATIVES AS POTENT AND SELECTIVE INHIBITORS OF HISTAMINE N-METHYL-TRANSFERASE
Author:
Publisher
Walter de Gruyter GmbH
Subject
Pharmacology (medical)
Link
https://www.degruyter.com/document/doi/10.1515/DMDI.1989.7.2-3.111/pdf
Reference13 articles.
1. Histamine catabolism in guinea pigs, rats and mice
2. Potential inhibitors of S-adenosylmethionine-dependent methyltransferases. 6. Structural modifications of S-adenosylmethionine
3. Potential inhibitors of S-adenosylmethionine-dependent methyltransferases. 4. Further modifications of the amino acid and base portions of S-adenosyl-L-homocysteine
4. Multisubstrate adducts as potential inhibitors of S-adenosylmethionine dependent methylases: inhibition of indole N-methyltransferase by (5H-deoxyadenosyl)[3-(3-indolyl)propyl-1-yl]methylsulfonium and (5'-deoxyadenosyl)[4-(3-indolyl)but-1-yl]methylsulfonium salts
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Structure-Based Drug Design of Bisubstrate Inhibitors of Phenylethanolamine N-Methyltransferase Possessing Low Nanomolar Affinity at Both Substrate Binding Domains1;Journal of Medicinal Chemistry;2020-11-04
2. Histamine N-methyltransferase;Enzyme Handbook 11;1996
3. Sulfur- and seleno-sugar modified nucleosides. Synthesis, chemical transformations and biological properties.;Tetrahedron;1993-01
4. Histamine N-methyltransferase;Springer Handbook of Enzymes
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