| Name | protoporphyrinogen oxidase |
|---|---|
| Synonyms | Mutant protoporphyrinogen oxidase; VP; PPO; PPOX; Protoporphyrinogen oxidase; V290M; Protoporphyrinogen oxidases |
| Name | sulfentrazone |
|---|---|
| CAS |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 18943113 | Daugrois JH, Hoy JW, Griffin JL: Protoporphyrinogen oxidase inhibitor herbicide effects on pythium root rot of sugarcane, pythium species, and the soil microbial community. Phytopathology. 2005 Mar;95(3):220-6. ABSTRACT The effects of three protoporphyrinogen oxidase inhibitor herbicides, azafenidin, flumioxazin, and sulfentrazone, on Pythium root rot of sugarcane and the soil microbial community were evaluated in greenhouse experiments. |
32(0,1,1,2) | Details |
| 10432190 | Carre J, Eleouet S, Rousset N, Vonarx V, Heyman D, Lajat Y, Patrice T: fluorescence kinetics in C6 glioblastoma cells after incubation: effect of a protoporphyrinogen oxidase inhibitor. Cell Mol Biol (Noisy-le-grand). 1999 Jun;45(4):433-44. To perform this experiment we used confocal microspectrofluorometry to analyse the effects of a highly purified form of sulfentrazone (FP846) on the kinetics of synthesis after ALA administration to living C6 cells. |
1(0,0,0,1) | Details |
| 18298068 | Luo YP, Jiang LL, Wang GD, Chen Q, Yang GF: Syntheses and herbicidal activities of novel triazolinone derivatives. . J Agric Food Chem. 2008 Mar 26;56(6):2118-24. Epub 2008 Feb 26. Protoporphyrinogen oxidase (Protox, EC 1.3.3.4) has been identified as one of the most important action targets of herbicides. Most fortunately, compound 3, methyl 2-[3-methyl-(2--4-chloro-5-ethylsulfonamidephenyl)-4,5-dihydro-5-oxo -1 H-1,2,4-triazol-4-yl] methylenephenyl-2-( E)-methoxyiminoacetate, was found to be the most promising candidate due to its comparable herbicidal activity at 75-150 g of active ingredient/ha with the commercial product sulfentrazone. |
1(0,0,0,1) | Details |