A Practical Synthetic Method for Furylacryloyl-Gly-Leu-NH2

Shan Shan Gong; Guo Dong Liu; Qing Kun Yang; Qi Sun

doi:10.4028/www.scientific.net/AMR.848.207

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A Practical Synthetic Method for Furylacryloyl-Gly-Leu-NH₂
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HomeAdvanced Materials ResearchAdvanced Materials Research Vol. 848A Practical Synthetic Method for...

A Practical Synthetic Method for Furylacryloyl-Gly-Leu-NH₂

Abstract:

A novel and efficient strategy has been developed for the synthesis of FA-Gly-Leu-NH₂ (FAGLA), a furylacryloyl dipeptide substrate for the thermolysin from Bacillus thermoproteolyticus.

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Periodical:

Advanced Materials Research (Volume 848)

Pages:

207-210

DOI:

https://doi.org/10.4028/www.scientific.net/AMR.848.207

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Online since:

November 2013

Authors:

Shan Shan Gong, Guo Dong Liu, Qing Kun Yang, Qi Sun*

Keywords:

Component, Dipeptide Substrate, Fmoc, Furylacrylic Acid, HATU, Thermolysin

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* - Corresponding Author

References

[1] A.A. Olayiwola, S. Ingebrigt, Chem. Biol. Drug. Des, Vol. 73 (2009), p.7.

Google Scholar

[2] K. Chih-Min, N. Norikazu, C.P. James, Biochemistry, Vol. 18 (1979), p.3032.

Google Scholar

[3] S. Endo, J. Fermentation Tech. Vol. 40 (1962), p.346.

Google Scholar

[4] S.A. Bernhard, S.J. Lou, H.F. Noller, Biochemistry, Vol. 4 (1965), p.1108.

Google Scholar

[5] J. Feder, Biochemistry, Vol. 6 (1967), p. (2088).

Google Scholar

[6] H. Matsubara, Biochem. Biophys. Res. Commun. Vol. 24 (1966), p.427.

Google Scholar

[7] L.H. Weaver, W.R. Kestre, B.W. Matthews, J. Mol. Biol. Vol. 114 (1977), p.119.

Google Scholar

[8] K. Shigeru, T. Kazuo, Y. Kouji, M. Yoshio, I. Takanoby, Bulletin of the Chemical Society of Jupan, Vol. 62 (1989), p.514.

Google Scholar

[9] J. Feder, J.M. Schuck, Biochemistry, Vol. 9 (1970), p.2784.

Google Scholar

[10] J. Kováč, J. Štetionvá, J. Surá, F. Špaček, R. Brežny, Collect. Czech. Chem. Commun. Vol. 42 (1977), p.1871.

Google Scholar

[11] G. Arsequell, R.A. Dwek, S.Y. Wong, Anal. Biochem, Vol. 216 (1994), p.165.

Google Scholar

[12] R.W. Chambers, F.H. Carpenter, J. Am. Chem. Soc. Vol. 77 (1955), p.1522.

Google Scholar

[13] L.A. Carpino, H. Tmazumi, B.M. Foxman, M.J. Vela, P. Henklein, A. El-Faham, J. Klose, M. Bienger, Org. Lett. Vol. 2 (2000), p.2253.

Google Scholar