![N-[3-(N-L-Alanyl)-amino-3-carboxypropyl]-D-histidine Trihydrochloride - chemical structure image](https://media.scbt.com/product/n-3-n-l-alanyl-amino-3-carboxypropyl-d-histidine-structure_36_72_b_367261.jpg)
![Molecular structure of N-[3-(N-L-Alanyl)-amino-3-carboxypropyl]-D-histidine Trihydrochloride N-[3-(N-L-Alanyl)-amino-3-carboxypropyl]-D-histidine Trihydrochloride - chemical structure image](https://media.scbt.com/product/n-3-n-l-alanyl-amino-3-carboxypropyl-d-histidine-structure_36_72_t_367261.jpg)
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N-[3-(N-L-Alanyl)-amino-3-carboxypropyl]-D-histidine Trihydrochloride functions as a substrate for enzymes involved in the synthesis of peptides and proteins. It plays a role in the regulation of cellular processes by serving as a precursor for the production of specific amino acids. The mechanism of action involves the interaction of the compound with specific enzymes, leading to the formation of peptide bonds and the incorporation of amino acids into growing peptide chains. N-[3-(N-L-Alanyl)-amino-3-carboxypropyl]-D-histidine Trihydrochloride facilitates the transfer of amino acids to the ribosome during protein synthesis, contributing to the accurate assembly of polypeptides. It is involved in the modulation of gene expression and the regulation of cellular signaling pathways through its interaction with various enzymes and proteins. The compound′s function in the experiment is to provide a substrate for enzymatic reactions and to support the accurate and efficient synthesis of peptides and proteins within biological systems.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
N-[3-(N-L-Alanyl)-amino-3-carboxypropyl]-D-histidine Trihydrochloride, 0.5 mg | sc-480645 | 0.5 mg | $622.00 |