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98956

Supelco

N-Cinnamoylglycine

analytical standard

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C11H11NO3
Numero CAS:
16534-24-0
Peso molecolare:
205.21
Numero MDL:
MFCD00136326
Codice UNSPSC:
12352209
ID PubChem:
329770559
NACRES:
NA.24

Grado

analytical standard

Saggio

≥98.0% (HPLC)

Durata

limited shelf life, expiry date on the label

applicazioni

clinical testing

Formato

neat

Temperatura di conservazione

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+
YAADMLWHGMUGQL-VOTSOKGWSA-N

Azioni biochim/fisiol

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.

Prodotti consigliati

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

Consigli di prudenza

P301 + P312 + P330

Classi di pericolo

Acute Tox. 4 Oral

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (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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