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  Home > JCE Print > Journal of Chemical Education > Issues > 2003  > May  >
Chemical Education Today
Letters
Trivial, Common, and Systematic Chemical Names
Giovanni Lentini
Dipartimento Farmaco Chimico, Facoltà di Farmacia, 70125 Bari, Italy

Cover
May 2003
Vol. 80 No. 5
p. 487

Full Text
In the “Anniversaries: 2001” by Paul F. Schatz (1), my first-choice reading in the January issue of this Journal each year, it was reported that just 100 years ago adrenaline was isolated by Jokichi Takamine from animal adrenal glands, and that “the chemical name for adrenaline is epinephrine”.

I do not agree with the frequent misuse of ‘chemical name’ for ‘common (generic, nonproprietary) name’ (2). The name epinephrine, from Greek epi-, upon or close upon, and nephros, kidney (3), was given by Abel to a substance he isolated in 1897 from the adrenal gland in the form of the corresponding dibenzoyl derivative. He erroneously thought it was an indole derivative. A few years later, Furth and Takamine independently isolated the same substance in the free base form and gave it the name suprarenine (from Latin supra-, upon, and ren, kidney) and adrenaline (from Latin ad-, near, and ren, kidney), respectively. These three names—epinephrine, suprarenine, and adrenaline—may be referred to as ‘traditional’ or ‘trivial’ chemical names (4) in their origin. However, ‘epinephrine’ was later chosen as the international nonproprietary name (INN) for this substance by the international panel of experts engaged in the international nomenclature program for pharmaceutical substances, started by the World Health Organization in 1959.

Of course the generic name epinephrine has nothing to do with a systematic (rational) chemical name, which has to be constructed observing the rules codified by the International Union of Pure and Applied Chemistry (IUPAC). Thus, the unspecified use of ‘chemical name’ should be discouraged as misleading, in that it may indicate both a trivial and a systematic chemical name. In this case ‘epinephrine’ is neither the former nor the latter—it is an INN.

Literature Cited

  1. Schatz, P. F. J. Chem. Educ. 2001, 78, 10–13.
  2. Kopp-Kubel, S. E. In The Practice of Medicinal Chemistry; Wermuth, C. -G., Ed.; Academic Press: London, 1996; Chapter 40.
  3. Atkins, P. W. Molecules; W. H. Freeman: New York, 1987; Chapter 6.
  4. International Union of Pure and Applied Chemistry. Commission on Nomenclature of Organic Chemistry. Revised Section F: Natural Products and Related Compounds (Recommendations 1999); (accessed Mar 2003).
More Information
*  Citation
Lentini, Giovanni. J. Chem. Educ. 2003 80 487.
*  Keywords
Nomenclature / Units / Symbols; Public Understanding
*  History
Created:
Last Updated:
March 28, 2003
February 28, 2005
  Home > JCE Print > Journal of Chemical Education > Issues > 2003  > May  > Page 487


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