Insect kinin analogues and application thereof in pest control
A technology of insect kinin and analogues, which is applied in the field of insect kinin analogues and their application in pest control, can solve the problems of kinin analogues with not very prominent biological activity and large molecular weight, and achieve obvious insecticidal activity , good anti-efficiency effect
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[0022] The preparation of compound shown in embodiment 1, I-A-1 (Raa comes from 2-chlorophenylalanine)
[0023] The compound shown in I-A-1 is prepared by the polypeptide solid-phase synthesis method, and the specific steps are as follows:
[0024] After checking the air tightness of the peptide synthesizer, take Rink Amide-Am resin (0.3mmol) and place it in 5mL DCM for activation for 2h, then wash it with DMF for 5 times, add 5mL of 20% piperidine in DMF and react for 20min to remove the resin Add Fmoc protecting group; prepare 5mL of DMF solution containing Fmoc-Gly-OH (1.2mmol), HBTU (1.2mmol), HOBt (1.2mmol), DIEA (1.2mmol), and react with the resin for 2h at room temperature after activation for 5min Get Fmoc-Gly with Rink Amide-Amresin. Continue to remove the Fmoc group, and insert Fmoc-Trp(Boc)-OH, Fmoc-β-Ala-OH, Fmoc-L-2-Cl-Phe-OH and cinnamic acid sequentially in the same way. Finally, a mixed solution of trifluoroacetic acid: phenol: sulfide anisole: water = 90:5:2...
Embodiment 32、I-C-10
[0087] Preparation of the compound shown in Example 32, I-C-10 (Raa comes from hydroxyproline)
[0088] The compound shown in I-C-10 was prepared according to the same steps as in Example 23, except that Fmoc-Glu-OH was replaced by Fmoc-Hyp-OH. The structural identification data are shown in Table 1, and the structure is verified to be correct.
[0089] Preparation of the compound shown in Example 33, I-C-11 (Raa comes from valine)
[0090] The compound shown in I-C-11 was prepared according to the same steps as in Example 23, except that Fmoc-Glu-OH was replaced by Fmoc-Val-OH. The structural identification data are shown in Table 1, and the structure is verified to be correct.
[0091] Preparation of the compound shown in Example 34, I-C-12 (Raa comes from isoleucine)
[0092] The compound shown in I-C-12 was prepared according to the same steps as in Example 23, except that Fmoc-Glu-OH was replaced by Fmoc-Ile-OH. The structural identification data are shown in Table 1,...
Embodiment 37
[0099] Example 37, the biological activity of the compounds of the present invention on aphids
[0100] The insecticidal activity of the compounds of the present invention against aphids is determined by the leaf-dipping method to measure the biological activity of the compounds against soybean aphids (Aphis glycines). The samples were prepared into solutions with different concentration gradients with an aqueous solution containing 0.05% Triton X-100. Soybean leaves cultivated indoors that have not been exposed to any pesticides and insects are punched out with a diameter of 15mm to punch out leaves of suitable size, immersed in the diluted medicinal solution, taken out after 15s to dry, and placed in a bioassay plate. The back of the leaf faces upwards, 1% agar is added to the bottom to keep it moist, and 20±3 soybean aphids are inserted into each well. Place them in an artificial climate box at a temperature of (25±1)°C, and check the number of aphid deaths after 48 hours....
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