In:
Zeitschrift für Naturforschung C, Walter de Gruyter GmbH, Vol. 45, No. 11-12 ( 1990-12-1), p. 1127-1132
Kurzfassung:
3-Acyl-5-(1-aminoalkylidene)-4-hydroxy-2 H- pyran-2,6(3 H)-dione derivatives carrying lipophilic amino groups were found to be highly potent inhibitors of photosynthetic electron transport, and both the acyl and the aminoalkylidene groups on the pyran ring appeared to be indispensable for high activity. The structural features needed for activity in the 3-acyl-5- (l-am inoalkylidene)-4-hydroxy -2 H-pyran -2 ,6 (3 H)-dione derivatives were very similar to those for 3 -(l-aminoalkylidene)-2H-pyran-2,4(3H)-diones, except for the acyl group in the former compounds. Thermoluminescence measurements indicated that the 3-acyl-5- (1-aminoalkylidene)-4 -hydroxy -2H-pyran -2 ,6 (3 H )-dione derivatives bind to the D 1 protein in a manner similar to that of DCMU .
Materialart:
Online-Ressource
ISSN:
1865-7125
,
0939-5075
DOI:
10.1515/znc-1990-11-1208
Sprache:
Englisch
Verlag:
Walter de Gruyter GmbH
Publikationsdatum:
1990
ZDB Id:
2078107-6
SSG:
12
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