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98956

Supelco

N-Cinnamoylglycine

analytical standard

Synonyme(s) :

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

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About This Item

Formule empirique (notation de Hill):
C11H11NO3
Numéro CAS:
16534-24-0
Poids moléculaire :
205.21
Numéro MDL:
MFCD00136326
Code UNSPSC :
12352209
ID de substance PubChem :
329770559
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Pureté

≥98.0% (HPLC)

Durée de conservation

limited shelf life, expiry date on the label

Application(s)

clinical testing

Format

neat

Température de stockage

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+

Clé InChI

YAADMLWHGMUGQL-VOTSOKGWSA-N

Actions biochimiques/physiologiques

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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Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302

Conseils de prudence

P301 + P312 + P330

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number
BCCG4879
BCCB5973
BCBZ7851
BCBS3770

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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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