L-Phenylglycine
2935-35-5N[C@H](C(=O)O)c1ccccc1ZGUNAGUHMKGQNY-ZETCQYMHSA-NL-alpha-phenylglycine is the S stereoisomer of alpha-phenylglycine. It is an enantiomer of a D-alpha-phenylglycine. It is a tautomer of a L-alpha-phenylglycine zwitterion.
2935-35-5DTXSID801022916CHEMBL378605CHEBI:439819安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
This chemical does not meet GHS hazard criteria for 33.3% (1 of 3) of reports.
Warning
H315 (66.7%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 3 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
解説L-フェニルグリシンは抗生物質の構成成分,D-フェニルグリシンの誘導体はアヤメ属Iris tingitana,ゴウダソウ属Lunaria annua,モクセイ属Reseda luteolaに見いだされている.α-アミノベンゾニトリルの加水分解により合成できる.DL-フェニルグリシンは光輝ある小板状結晶.255 ℃(昇華).酸,アルカリに易溶,有機溶媒に不溶.L-フェニルグリシンは融点305~310 ℃.[α]20D-157.8°(希塩酸).セファロスポリン,セファレキシン,ペニシリンなどの合成原料.(b)はアニリノ酢酸,N-フェニルグリシンにあたる.インジゴの合成中間体として,モノクロロ酢酸とアニリンから合成される.融点127~128 ℃.水に可溶.
説明L-Phenylglycine is an amide that belongs to the group of pyridoxal phosphate analogues. It has been shown to be a response element for enzymes and natural compounds in Escherichia coli and Saccharomyces cerevisiae. It inhibits aminotransferase activity, dopamine synthesis, and microbial metabolism in these organisms. This compound also has a structural analysis that includes x-ray diffraction data, which can be used to identify its three-dimensional structure.
使用L-(+)-2-Phenylglycine is a derivative of Glycine (G615990), the smallest of all the amino acids, and is also used to treat schizophrenia, stroke, and benign prostatic hyperplasia. L-(+)-2-Phenylglycine is also used as an N-linked side chain of an SMTP (Stachybotrys microspora tripenyl phenols) congener, which was potent in enhancing plasminogen activation in S. microspora.
純化方法Crystallise it from EtOH. [Kaneko J Chem Soc Jpn 60 538 1939, Rudman et al. J Am Chem Soc 74 551 1952, Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 3 pp 2694-2697 1961, Beilstein 14 III 1187, 14 IV 1317.]
読み込み中…
化学的特性White crystalline powder
定義ChEBI: The S stereoisomer of alpha-phenylglycine.