Containing thiadiazole or oxadiazole derivatives and their application in the prevention and treatment of agricultural plant diseases
A technology of thiadiazole and oxadiazole, which is applied in the chemical, application, biocide and other directions for biological control, can solve problems such as unreported agricultural activity, and achieves simple structure, low production cost, and preparation process. simple effect
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Embodiment 1
[0044] Example 1: Determination of Indoor Inhibition of Bacterial Disease Pathogen Activity of Some Compounds
[0045] (1) Determination of the indoor activity of some compounds against rice bacterial blight
[0046] Put the rice bacterial blight pathogen in M210 (enzymatically hydrolyzed casein: 8g, sucrose: 5g, yeast extract: 4g, K 2 HPO 4 : 3g, MgSO 4 ·7H 2O: 0.3g, agar: 15g, secondary water: 1L, pH=7.0) Streak on the solid medium, culture at 28°C until a single colony grows. Pick a single colony of rice bacterial blight pathogen on M210 solid medium to M210 liquid medium (enzymatically hydrolyzed casein: 8g, sucrose: 5g, yeast extract: 4g, K 2 HPO 4 : 3g, MgSO 4 ·7H 2 O: 0.3g, secondary water: 1L, pH=7.0), cultured on a constant temperature shaker at 28°C and 180rpm until the logarithmic phase of growth was set aside.
[0047] The synthesized compound and the control drug were respectively configured at a concentration of 200 and 100 mu g / mL toxic M210 liquid medi...
Embodiment 2
[0061] Embodiment 2: Determination of the activity of some compounds inhibiting fungal pathogens of crops indoors
[0062] The antibacterial activity of the compounds was determined by the in vitro growth rate method. Heat potato dextrose agar medium (PDA medium: 200g potato, 20g agar, 20g glucose, 1000mL distilled water) to a molten state (40-60°C), pour 10mL of liquid medicine (10 times the final concentration of liquid medicine) into 90mL of PDA for culture Shake well, pour evenly into a petri dish with a diameter of 9cm, place it horizontally, and wait for it to cool and solidify. Use a puncher to punch a 4mm-diameter fungus dish at the edge of the fresh pathogenic bacteria colony that has been cultured for 4 days, put the fungus dish upside down in the center of the PDA plate containing the drug, and then place it in a constant temperature and humidity incubator at 27°C for upside-down culture, and wait for the blank control When the colony grows to nearly two-thirds of ...
Embodiment 3
[0067] Embodiment three: highly active compound toxicity regression equation and inhibitory medium concentration (EC 50 ) value determination
[0068] (1) Regression equation and EC of compound toxicity to rice bacterial blight pathogen 50 Determination of value
[0069] The synthetic compound and the control agent were respectively configured into 5 corresponding concentrations of toxic M210 liquid medium, 5 mL was taken in a test tube, and the OD value of the toxic sterile liquid medium was measured with a microplate reader (OD 595 ), adding 40 mu L contains the M210 liquid medium containing the pathogenic bacteria of Xanthomonas oryzae, then cultivated it on a constant temperature shaker at 28°C and 180rpm for 24~48h, and measured the OD values (OD 595 ). In addition, the OD value of the toxic and sterile M210 liquid medium containing the control drug and the OD value of the bacterial solution of each concentration after 24 to 48 hours were measured, and the OD value ...
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