Development of a fluorogenic small substrate for dipeptidyl peptidase-4
2017 ◽
Vol 13
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pp. 2690-2697
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Keyword(s):
A series of aniline and m-phenylenediamine derivatives with electron-withdrawing 3,3,3-trifluoropropenyl substituents were synthesized as small and chemically stable fluorescent organic compounds. Their fluorescence performances were evaluated by converting 2,4-disubstituted aniline 1 to the non-fluorescent dipeptide analogue H-Gly-Pro-1 for the use as a fluorogenic substrate for dipeptidyl peptidase-4 (DPP-4). The progress of the enzymatic hydrolysis of H-Gly-Pro-1 with DPP-4 was monitored by fluorometric determination of 1 released into the reaction medium. The results suggest that 1 could be used as fluorophore in OFF–ON-type fluorogenic probes.
2018 ◽
Vol 14
(5)
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pp. 483-490
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2014 ◽
Vol 64
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pp. 799-809
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Keyword(s):
Keyword(s):
2005 ◽
Vol 22
(1)
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pp. 19-29
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2011 ◽
Vol 102
(20)
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pp. 9646-9652
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Keyword(s):
2016 ◽
Vol 22
(3)
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pp. 421-433
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2012 ◽
Vol 36
(3)
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pp. 162-170
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Keyword(s):