SMB01340
Isoleucyl-Phenylalanine
Synonym(e):
L-Isoleucyl-L-phenylalanine, Ile-Phe, Isoleucylphenylalanine
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Alle Fotos(1)
About This Item
Empirische Formel (Hill-System):
C15H22N2O3
CAS-Nummer:
Molekulargewicht:
278.35
MDL-Nummer:
UNSPSC-Code:
12352209
NACRES:
NA.26
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Assay
≥95% (HPLC)
Qualitätsniveau
Form
solid
Lagertemp.
2-8°C
SMILES String
CC[C@H](C)[C@H](N)C(N[C@@H](CC1=CC=CC=C1)C(O)=O)=O
Allgemeine Beschreibung
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.
Anwendung
Isoleucyl-Phenylalanine can be used in biochemical and metabolomics research applications
Leistungsmerkmale und Vorteile
- Suitable for Metabolomics and Biochemical research
- High-quality compound suitable for multiple research applications
Sonstige Hinweise
For additional information on our range of Biochemicals, please complete this form.
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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Analysenzertifikate (COA)
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Rashmi Sinha et al.
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
James J Goedert et al.
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
Dustin G Brown et al.
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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