Continued from 3AA-22
References for Appendix
Continued in Addenda
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It is often helpful to use trivial names in order to avoid cumbersome systematic or semisystematic names, particularly if the substance has to be named frequently. Coining of trivial names is treated in 3AA-2.1, and a number of existing trivial names are listed in the appendices to the previous edition of recommendations on amino-acid nomenclature [6]; only the commoner are listed here.
Trivial name | Symbol | Structure of substance or of derived ion in the form predominating at neutral pH |
---|---|---|
β-Alanine | βAla | NH3+-CH2-CH2-COO- |
Allysine | - | HCO-[CH2]3-CH(NH3+)COO |
Citrulline | Cit | NH2-CO-NH-[CH2]3-CH(NH3+)COO- |
Cystathionine | ||
Cysteic acid | Cya | -O3S-CH2-CH(NH3+)COO- |
Cystine | ||
Dopa | - | |
Homocysteine | Hcy | HS-CH2-CH2-CH(NH3+)COO- |
Homoserine | Hse | HO-CH2-CH2-CH(NH3+)COO- |
Homoserine lactone | Hsl | |
Lanthionine | ||
Ornithine | NH3+-[CH2]3-CH(NH3+)COO- | |
5-Oxoproline | Glp | |
Sarcosine | Sar | CH3-NH2+-CH2-COO- |
Selenocysteine | Sec | HSe-CH2-CH(NH3+)COO- |
Thyronine | - | |
Thyroxine | Thx |
6. IUPAC Commission on the Nomenclature of Organic Chemistry (CNOC) and IUPAC-IUB Commission on Biochemical Nomenclature (CBN), Nomenclature of α-Amino Acids, Recommendations 1974, Biochem. J. 149, 1-16 (1975); Biochemistry, 14, 449-462 (1975); Eur. J. Biochem. 53, 1-14 (1975); also pp. 64-77 in [7].
7. International Union of Biochemistry (1978) Biochemical Nomenclature and Related Documents, The Biochemical Society, London.
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