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The Diaminobutyric (DABA), Delta Aminopentanoic, and Epsilon Aminohexanoic Acids

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Molecular Orbital Calculations for Amino Acids and Peptides
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Abstract

The L isomer of DABA, 2,4-diaminobutyric acid, is a major component of the polymixin group of antibiotics and a component of bacterial cell walls and of certain Lathyrus and related seeds (1–2). It was found to be neurotoxic in rats and mice (3), though it may not be neurotoxic in humans. L-DABA is widely distributed in nature (4).

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References

  1. Ressler, C., Restone, P.A., and Ehrenberg, R.H. Science 134, 188, 1961.

    Article  PubMed  CAS  Google Scholar 

  2. Bell, E.A., and Tirimana, A.S.L. Biochem. J. 97, 104, 1965.

    PubMed  CAS  Google Scholar 

  3. Kessel, D. Fed. Proc. Fed. Amer. Chem. Soc. Exp. Biol. 18, 258, 1959.

    Google Scholar 

  4. Chen, C.H., Flory, W., and Koeppe, R.E. Tox. and Appl. Pharmacology23, 334, 1972.

    Article  CAS  Google Scholar 

  5. Erecinska, M., Troeger, M.B., and Alston, T.A. J. Neurochem. 46, 1452, 1986.

    Article  PubMed  CAS  Google Scholar 

  6. Iversen, L.L., and Johnston, G.A.R. J. Neurochem. 18, 1939, 1971.

    Article  PubMed  CAS  Google Scholar 

  7. Roskoski, R. J. Neurochem. 36, 1236, 1981.

    Article  Google Scholar 

  8. Simon, J.R., Martin, D.L., and Kroll, M. J. Neurochem. 23, 981, 1974.

    Article  PubMed  CAS  Google Scholar 

  9. Radian, R., and Kanner, B.I. Biochemistry. 26, 1236, 1983.

    Article  Google Scholar 

  10. O’Neal, R.M., Chen, C.H., Reynolds, C.S., Meghal, S.K., and Koeppe, R.E. Biochem. J. 106, 699, 1968.

    PubMed  Google Scholar 

  11. Horton, R.W., Collins, J.F., Anlezark, G.M., and Meldrum, B.S. Eur. J. Pharmacol. 59, 75, 1979.

    Article  PubMed  CAS  Google Scholar 

  12. Bichard, A.R., and Little, H.J. Br. J. Pharmacol. 76, 447, 1982.

    Article  PubMed  CAS  Google Scholar 

  13. Rostain, J.C., Wardley-Smith, B., Forni, C., and Halsey, M.J. Neuropharmacol. 25, 5, 545, 1986.

    Article  CAS  Google Scholar 

  14. Meldrum, B.S., Croucher, M.J., and Krogsgaard-Larsen, R. Excerpta Medica, 182, 1982.

    Google Scholar 

  15. Hinazumi, H., and Mitsui, T. Acta Cryst. B27, 2152, 1971.

    Google Scholar 

  16. Fugler-Domenico, L., Russell, C.S., and Sapse, A.M. Struct. Chem. 1, 379, 1990.

    Article  CAS  Google Scholar 

  17. Schlegel, H.B. J. Comp. Chem.3, 214, 1982.

    Article  CAS  Google Scholar 

  18. Iverson, L.L., and Kelly, J.S. Biochem. Pharmacol. 24, 933, 1975.

    Article  Google Scholar 

  19. Krogsgaard-Larsen, R.J. Med. Chem. 24, 1377, 1981.

    Article  CAS  Google Scholar 

  20. Debler, E.A., and Lajtha, A. J. Neurochem. 48, 1851, 1987.

    Article  PubMed  CAS  Google Scholar 

  21. Ramek, M. Int. J. Quantum Chem. Quantum Biol. Symp. 17, 45, 1990.

    Article  CAS  Google Scholar 

  22. Ramek, M. Structural Chem. 6, 1, 15, 1995.

    Article  CAS  Google Scholar 

  23. Ramek, M. Int. J. Quantum Chem. Quantum Biol. Symp. 21, 79, 1994.

    Article  CAS  Google Scholar 

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Sapse, AM. (2000). The Diaminobutyric (DABA), Delta Aminopentanoic, and Epsilon Aminohexanoic Acids. In: Molecular Orbital Calculations for Amino Acids and Peptides. Birkhäuser, Boston, MA. https://doi.org/10.1007/978-1-4612-1354-3_4

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  • DOI: https://doi.org/10.1007/978-1-4612-1354-3_4

  • Publisher Name: Birkhäuser, Boston, MA

  • Print ISBN: 978-1-4612-7109-3

  • Online ISBN: 978-1-4612-1354-3

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