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SMB01340

Sigma-Aldrich

Isoleucyl-Phenylalanine

别名:

L-Isoleucyl-L-phenylalanine, Ile-Phe, Isoleucylphenylalanine

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About This Item

经验公式（希尔记法）:
C15H22N2O3
CAS号:
22951-98-0
分子量:
278.35
MDL编号:
MFCD00037253
UNSPSC代码:
12352209
NACRES:
NA.26
价格与库存信息目前不能提供

方案

≥95% (HPLC)

质量水平

200

表单

solid

储存温度

2-8°C

SMILES字符串

CC[C@H](C)[C@H](N)C(N[C@@H](CC1=CC=CC=C1)C(O)=O)=O

InChI key

WMDZARSFSMZOQO-DRZSPHRISA-N

一般描述

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.

应用

Isoleucyl-Phenylalanine can be used in biochemical and metabolomics research applications

特点和优势

  • Suitable for Metabolomics and Biochemical research
  • High-quality compound suitable for multiple research applications

其他说明

For additional information on our range of Biochemicals, please complete this form.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

历史批次信息供参考:

分析证书(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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