SMB01340
Isoleucyl-Phenylalanine
Sinónimos:
L-Isoleucyl-L-phenylalanine, Ile-Phe, Isoleucylphenylalanine
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About This Item
Productos recomendados
assay
≥95% (HPLC)
Quality Level
form
solid
storage temp.
2-8°C
SMILES string
CC[C@H](C)[C@H](N)C(N[C@@H](CC1=CC=CC=C1)C(O)=O)=O
General description
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.
Application
Isoleucyl-Phenylalanine can be used in biochemical and metabolomics research applications
Features and Benefits
- Suitable for Metabolomics and Biochemical research
- High-quality compound suitable for multiple research applications
Other Notes
For additional information on our range of Biochemicals, please complete this form.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Certificados de análisis (COA)
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Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
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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