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重要文件

98956

Supelco

N-Cinnamoylglycine

analytical standard

同義詞:

N-(1-Oxo-3-phenyl-2-propen-1-yl)glycine, Cinnamoyl glycine

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About This Item

經驗公式(希爾表示法):
C11H11NO3
CAS號碼:
分子量::
205.21
MDL號碼:
分類程式碼代碼:
12352209
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

化驗

≥98.0% (HPLC)

儲存期限

limited shelf life, expiry date on the label

應用

clinical testing

格式

neat

儲存溫度

2-8°C

InChI

1S/C11H11NO3/c13-10(12-8-11(14)15)7-6-9-4-2-1-3-5-9/h1-7H,8H2,(H,12,13)(H,14,15)/b7-6+

InChI 密鑰

YAADMLWHGMUGQL-VOTSOKGWSA-N

生化/生理作用

Cinnamoylglycine is known as a urinary metabolite in man, although whether it is formed de novo from plant cinnamate or is a plant product excreted unchanged has not been conclusively demonstrated. When cinnamoylglycine occurs naturally it is probably a food constituent excreted unchanged. It is not found when small quantities (0.5-6 g) of cinnamic acid are fed to man, but by analogy with animal experiments may be produced when much larger quantities are given.

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象形圖

Exclamation mark

訊號詞

Warning

危險聲明

防範說明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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G K Brown et al.
Journal of chromatography, 145(2), 177-184 (1978-03-01)
The profile of high boiling point organic acids in urine samples from both normal subjects and patients suspected of having some form of metabolic disorder has been determined by combined gas chromatography-mass spectrometry. Fifteen different compounds eluting after hippuric acid
J A Hoskins et al.
Biomedical mass spectrometry, 11(6), 296-300 (1984-06-01)
The enzyme phenylalanine ammonia lyase taken orally has been found to reduce the rise in blood phenylalanine that normally occurs following a protein meal. Therefore the enzyme has a potential use in the management of the genetic disease phenylketonuria. The
Bejan J Saeedi et al.
Cell metabolism, 31(5), 956-968 (2020-03-28)
Many studies have suggested a role for gut-resident microbes (the "gut microbiome") in modulating host health; however, the mechanisms by which they impact systemic physiology remain largely unknown. In this study, metabolomic and transcriptional profiling of germ-free and conventionalized mouse

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