Quinclorac

Quinclorac (18.75-600 g a.i. ha^-1; 3 weeks) inhibits the growth of Echinochloa crusgalli var. zelayensis in a dose-dependent manner^[1].
Quinclorac (600 g a.i. ha^-1; 24-72 h) significantly increases ethylene production, abscisic acid content and indole-3-acetic acid content in barnyard grass seedlings, and all three hormones reach their peak levels at 24 h after treatment^[1].
Quinclorac (active ingredient at 600 g/ha; 24-120 h post-treatment) reduces carotenoid content in the leaves of barnyard grass^[1].
Quinclorac (0.2-5 μM; 10 min) weakly inhibits the activity of recombinant Arabidopsis HPPD in vitro, with an inhibition rate of 20.3% at high doses^[1].
Strain J5, isolated from the rhizosphere soil of a rice-tobacco rotation field, degrades 23.7% of quinclorac (5 µg/mL; 5 d) in MSM^[2].
Quinclorac (5 µg/mL; 48 h) upregulates the expression of 4-hydroxyphenylacetate 3-monooxygenase (HPMO) in the J5 bacterial isolate^[2].
Quinclorac (10-30 μM; 30 days) reduces the relative growth rate of callus culture cells from non-acclimated common bean (Phaseolus vulgaris L.) while increasing lipid peroxidation (MDA); Q30 cells acclimated to 30 μM exhibit milder growth inhibition over the same 30-day period^[3].

Quinclorac (600 g a.i. ha^-1; 24-72 h) induces lipid peroxidation in the aboveground parts of barnyard grass, resulting in a significant increase in malondialdehyde content after treatment^[1].
Quinclorac (10-30 μM; 30 days) increases the level of lipid peroxidation in untamed Phaseolus vulgaris callus culture cells by more than 3-fold; in contrast, the lipid peroxidation level in acclimated cells decreases significantly^[3].
Exposure to Quinclorac (10-30 μM; 30 days) increases the activity of class III peroxidase in unadapted callus culture cells of common bean; in contrast, constitutive glutathione reductase activity is significantly elevated in Quinclorac-adapted cells, and cells adapted to 30 μM also exhibit increased superoxide dismutase and class III peroxidase activities. These enhanced antioxidant activities are retained in de-adapted cells^[3].
Acclimation with Quinclorac (10-30 μM; 30 days) alters the peroxidase isoenzyme profile in cultured callus cells of common bean. Specifically, the staining intensity of two detected peroxidase isoenzymes increases in cells acclimated with 30 μM Quinclorac and in cells treated with 30 μM quinclorac after acclimation at a low concentration, and this enhanced staining effect remains in de-acclimated cells^[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.