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Biological Role An essential amino acid for humans, meaning it must be obtained from the diet. Plays a role in protein structure (e.g., forming hydrogen bonds via its hydroxyl group) and functions as a precursor for biosynthesis of glycine, serine, and other compounds. Stereochemistry Exists in four stereoisomers due to two chiral centers (at α-carbon and β-carbon), but only L-threonine is naturally occurring and biologically active. Stability Stable under normal storage conditions when kept dry and away from light. Can be degraded by heat, strong acids, or bases, especially during prolonged exposure. These properties make L-threonine critical for nutritional supplements, food fortification, and pharmaceutical applications, while its chemical reactivity enables its use in peptide synthesis and biochemical research.
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L-proline |
The basic information of L-proline1. Chemical structureMolecular formula: C₅H₉NO₂Molecular weight: 115.13 g/molStructural features: The α -am... |
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L-Lysine monohydrochloride |
The most prominent performance advantage ofL-Lysine monohydrochloride is its optimized physical and chemical properties that eliminate the critical... |
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L-Methionine |
Industrial Biotechnology: Used as a precursor in the synthesis of bioactive molecules (e.g., S-adenosylmethionine, glutathione) for biopharmaceutic... |
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L-lysine monohydrochloride |
The free Cl⁻ ion in the hydrochloride salt form undergoes typical halide ion reactions, which are used for qualitative identification of L-lysine m... |
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L-Methionine |
Core Biological Functions of L-Methionine Protein Synthesis Precursor: As an essential amino acid, L-Methionine is a fundamental building block for... |
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