SMB01340
Isoleucyl-Phenylalanine
Sinonimo/i:
L-Isoleucyl-L-phenylalanine, Ile-Phe, Isoleucylphenylalanine
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About This Item
Prodotti consigliati
Saggio
≥95% (HPLC)
Livello qualitativo
Forma fisica
solid
Temperatura di conservazione
2-8°C
Stringa SMILE
CC[C@H](C)[C@H](N)C(N[C@@H](CC1=CC=CC=C1)C(O)=O)=O
Descrizione generale
Isoleucyl-Phenylalanine is a dipeptide derived from the incomplete breakdown of protein digestion or protein catabolism. It has not yet been identified in human tissues or biofluids and so it is classified as an ′Expected′ metabolite.
Applicazioni
Isoleucyl-Phenylalanine can be used in biochemical and metabolomics research applications
Caratteristiche e vantaggi
- Suitable for Metabolomics and Biochemical research
- High-quality compound suitable for multiple research applications
Altre note
For additional information on our range of Biochemicals, please complete this form.
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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I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
PloS one, 11(3), e0152126-e0152126 (2016-03-26)
Investigation of microbe-metabolite relationships in the gut is needed to understand and potentially reduce colorectal cancer (CRC) risk. Microbiota and metabolomics profiling were performed on lyophilized feces from 42 CRC cases and 89 matched controls. Multivariable logistic regression was used
Carcinogenesis, 35(9), 2089-2096 (2014-07-20)
Metabolomic analysis of feces may provide insights on colorectal cancer (CRC) if assay performance is satisfactory. In lyophilized feces from 48 CRC cases, 102 matched controls, and 48 masked quality control specimens, 1043 small molecules were detected with a commercial
Cancer & metabolism, 4, 11-11 (2016-06-09)
Colorectal cancers (CRC) are associated with perturbations in cellular amino acids, nucleotides, pentose-phosphate pathway carbohydrates, and glycolytic, gluconeogenic, and tricarboxylic acid intermediates. A non-targeted global metabolome approach was utilized for exploring human CRC, adjacent mucosa, and stool. In this pilot
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