• 제목/요약/키워드: Selective insecticidal activity

검색결과 3건 처리시간 0.016초

2-(n-Octyl)-3-(n-propyl)isothiourea 유도체의 살충활성에 미치는 N-치환 Amino group의 영향 (Influence of N-substituted Amino Group on the Insecticidal Activity of 2-(n-Octyl)-3-(n-propyl)isothiourea Derivatives)

  • 정경채;전동주;김대황;성낙도
    • Applied Biological Chemistry
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    • 제38권2호
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    • pp.163-167
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    • 1995
  • 살충성Buprofezine분자의 구조를 변형한 20종의 새로운 isothiourea유도체(S)를 합성하고 N-치환(Z)amino기의 변화에 따르는 6종의 해충에 대한 살충활성을 검토한 바, 배추 좀나방(Plutella Xylostella Linnaeus)에 대하여 현저하게 선택적인 살충성을 나타내었다. N-치환(Z) amino기의 치환기(Z)가 변화함에 따른 물리-화학적 파라미터와 배추 좀나방에 대한 살충활성값 (Obs. $pI_{50}$)과의 구조-활성 관계(SAR)식으로부터 살충활성에 미치는 물리-화학적 파라미터의 영향은 MR>${\pi}$>$L_1$의 순이었으며, 이들 파라미터의 적정값(optimal value)은 각각 $L_1=5.22{{\AA}}$, $MR=15.70(Cm^3/mol)$${\pi}=1.60$이었다. 이 값을 만족하는 치환기(Z)로는 탄소 원자수가 3개로 구성된 iso-propyl 치환체(5)로써 가장 큰 살충성(Obs. $pI_{50}=3.00$)을 나타내었다.

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Synthesis, Spectroscopic Studies and Biological Applications of Organotin(IV) Derivatives of 3-[N-(4-Nitrophenyl)-amido]propenoic Acid and 3-[N-(4-Nitrophenyl)-amido]propanoic Acid

  • Shahid, Khadija;Shahzadi, Saira;Ali, Saqib;Mazhar, M.
    • Bulletin of the Korean Chemical Society
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    • 제27권1호
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    • pp.44-52
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    • 2006
  • New organotin(IV) derivatives with general formulae R_2SnL_2 and R_3SnL, where R = methyl, n-butyl, n-octyl and phenyl and HL is either 3-[N-(4-nitrophenyl)amido]-propenoic acid or 3-[N-(4-nitrophenyl)amido] propanoic acid have been synthesized in 1 : 2 and 1 : 1 molar ratio by different methods. The FTIR spectra clearly demonstrated that the organotin(IV) moieties react with [O,O] atoms of the ligands. The bonding and coordination behavior in these complexes are discussed on the basis of multinuclear (^1H,\,^{13}C,\,^{119}Sn) NMR and mass spectrometric studies. Antibacterial, and antifungal screening tests were performed for these compounds and reported here. These values were compared to those of the precursors and it was found that diorganotin(IV) complexes exhibit less activity as compared to triorganotin(IV) complexes . LD_{50} data were obtained by Brine Shrimp assay method. Insecticidal activity was performed for selective compounds by contact toxicity method.

A Genetically Engineered Pseudomonas fluorescens Strain Possesses Dual Activity Against Phytopathogenic Fungi and Insects

  • Lu, Wenwei;Zhang, Weiqiong;Bai, Yan;Fu, Yingying;Chen, Jun;Geng, Xiaolu;Wang, Yujing;Xiao, Ming
    • Journal of Microbiology and Biotechnology
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    • 제20권2호
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    • pp.281-286
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    • 2010
  • A Pseudomonas fluorescens strain was isolated and found to show antagonistic activity against phytopathogenic fungi and to possess a gene responsible for production of antibiotic 2,4-diacetylphloroglucinol. For the extension of biocontrol range, a gene for an Androetonus australis Hector insect toxin 1 (AaHIT1), one of the most known toxic insect-selective peptides, was designed and synthesized according to the preferred codon usage of Pseudomonas fluorescens, cloned, and transformed into the strain by pSUP106 vector, a broad-host-range plasmid. Bioassays indicated that the engineered strain was able to produce AaHIT1 with insecticidal activity, and at the same time retain the activity against plant pathogen. The experiments for nonplanted soil and rhizosphere colonization showed that, similar to the population of the wild-type strain, that of the engineered strain remained relatively constant in the first 10 days, and the subsequent 50 days, suggesting that AaHIT1 expression in the bacterial cell does not substantially impair its long-term colonization. It is first reported that a Pseudomonas fluorescens strain expressing an active scorpion neurotoxin has dual activity against phytopathogenic fungi and insects, making at attractive for agronomic applications.