Histidine and derivatives
Histidine and its derivatives are a class of amino acids widely used in various applications due to their unique properties and biological activities. Histidine, with the chemical formula C6H9N3O2, is an essential amino acid that plays a crucial role in protein synthesis. Its derivatives include histidine analogs such as 4-hydroxyhistidine (4-OHHis), N-methylhistidine, and other modified forms.
These compounds are utilized in pharmaceuticals for their potential in treating certain diseases, particularly those related to inflammation and neurological conditions. In the food industry, they serve as flavor enhancers and preservatives due to histidine's ability to interact with amino acids and peptides, enhancing taste profiles. Additionally, in biochemical research, derivatives of histidine are used as labeling agents for proteins and nucleic acids, facilitating their detection and analysis.
The versatility of histidine and its derivatives makes them indispensable in multiple sectors, including drug development, food science, and biotechnology.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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L-Histidine | 71-00-1 | C6H9N3O2 |
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N-Acetyl-L-histidine | 2497-02-1 | C8H11N3O3 |
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L-Histidine,5-mercapto-N,3-dimethyl- | 108418-14-0 | C8H13N3O2S |
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L-Histidine Base | 7006-35-1 | C6H9N3O2 |
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BDS 391 | 1282041-72-8 | C16H15BrN4O3 |
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L-Histidine,N-[2-[[(1S)-4-[(aminoiminomethyl)amino]-1-carboxybutyl]amino]ethyl]- | 93361-66-1 | C14H25N7O4 |
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(2S)-2-(dimethylamino)-3-(1H-imidazol-5-yl)propanoic acid | 24940-57-6 | C8H13N3O2 |
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2-Amino-3-(4-mercapto-1-methyl-1H-imidazol-5-yl)propanoic acid | 122174-26-9 | C7H11N3O2S |
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DL-HISTIDINE (Ring-2-13C, 99%) | 2483735-59-5 | C6H9N3O2 |
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(2S)-3-(2-{[(2S,3S)-3-amino-3-carboxy-2-hydroxypropyl]sulfanyl}-1H-imidazol-5-yl)-2-(trimethylammonio)propanoate | 78873-51-5 | C13H22N4O5S |
Related Literature
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Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
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