Literature summary extracted from

Chen, H.; Han, X.; Qin, N.; Wei, L.; Yang, Y.; Rao, L.; Chi, B.; Feng, L.; Ren, Y.; Wan, J.
Synthesis and biological evaluation of novel inhibitors against 1,3,8-trihydroxynaphthalene reductase from Magnaporthe grisea (2016), Bioorg. Med. Chem., 24, 1225-1230.

Inhibitors

EC Number	Inhibitors	Comment	Organism	Structure
1.1.1.252	1-[(Z)-2-bromo-2-nitroethenyl]-3-fluorobenzene	high in vivo activities against Magnaporthe oryzae, EC50 9.5 ppm	Pyricularia oryzae
1.1.1.252	1-[(Z)-2-bromo-2-nitroethenyl]-4-ethylbenzene	beta-nitrostyrene compound highest inhibitory activity among compounds analyzed	Pyricularia oryzae
1.1.1.252	Tricyclazole	-	Pyricularia oryzae

Organism

EC Number	Organism	UniProt	Comment	Textmining
1.1.1.252	Pyricularia oryzae	Q12634	-	-
1.1.1.252	Pyricularia oryzae ATCC MYA-4617	Q12634	-	-

Synonyms

EC Number	Synonyms	Comment	Organism
1.1.1.252	MGG_02252	-	Pyricularia oryzae

IC50 Value

EC Number	IC50 Value	IC50 Value Maximum	Comment	Organism	Inhibitor	Structure
1.1.1.252	0.00023	-	pH 7.0, 30°C	Pyricularia oryzae	Tricyclazole
1.1.1.252	0.00029	-	pH 7.0, 30°C	Pyricularia oryzae	1-[(Z)-2-bromo-2-nitroethenyl]-4-ethylbenzene
1.1.1.252	0.00058	-	pH 7.0, 30°C	Pyricularia oryzae	1-[(Z)-2-bromo-2-nitroethenyl]-3-fluorobenzene

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Release 2023.1 (January 2023)