Pyridoxamine/ja: Difference between revisions

Pyridoxamine/ja
Created page with "{{Chembox | Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 464377112 | ImageFile_Ref = {{chemboximage|correct|??}} | ImageFile = Pyridoxamin.svg | ImageSize = 120px | PIN = 4-(Aminomethyl)-5-(hydroxymethyl)-2-methylpyridin-3-ol | OtherNames = |Section1={{Chembox Identifiers | KEGG_Ref = {{keggcite|correct|kegg}} | KEGG = C00534 | InChI = 1/C8H12N2O2/c1-5-8(12)7(2-9)6(4-11)3-10-5/h3,11-12H,2,4,9H2,1H3 | InChIKey = NHZMQXZHNVQTQA-UHFFFAOYAS | StdInCh..."
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Created page with "'''ピリドキサミン'''('''Pyridoxamine''')は、ビタミンB<sub>6</sub>の一形態である。化学的にはピリジン環構造を基本としており、ヒドロキシルメチルアミノメチルヒドロキシメチル置換基を持つ。ピリドキシンとは4位の置換基で異なる。その環の..."
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'''ピリドキサミン'''('''Pyridoxamine''')は、[[vitamin B6/ja|ビタミンB<sub>6</sub>]]の一形態である。化学的には[[pyridine/ja|ピリジン]]環構造を基本としており、[[hydroxyl/ja|ヒドロキシル]][[methyl/ja|メチル]][[aminomethyl/ja|アミノメチル]][[hydroxymethyl/ja|ヒドロキシメチル]][[subtituent/ja|置換基]]を持つ。[[pyridoxine/ja|ピリドキシン]]とは4位の置換基で異なる。その環の3位のヒドロキシルと4位のアミノメチル基は、ピリドキサミンに、糖や脂質の分解で形成される[[free radical/ja|フリーラジカル]]種やカルボニル種の[[scavenger (chemistry)/ja|スカベンジャー]]作用や、[[amadori rearrangement/ja|アマドリ反応]]を触媒する金属イオンの[[chelation/ja|キレート化]]作用など、様々な化学的性質を与える。
'''Pyridoxamine''' is one form of [[vitamin B6|vitamin B<sub>6</sub>]]. Chemically it is based on a [[pyridine]] ring structure, with [[hydroxyl]], [[methyl]], [[aminomethyl]], and [[hydroxymethyl]] [[substituent]]s. It differs from [[pyridoxine]] by the substituent at the 4-position. The hydroxyl at position 3 and aminomethyl group at position 4 of its ring endow pyridoxamine with a variety of chemical properties, including the [[Scavenger (chemistry)|scavenging]] of [[free radical]] species and carbonyl species formed in sugar and lipid degradation and [[chelation]] of metal ions that catalyze [[Amadori rearrangement|Amadori reactions]].
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