• Title/Summary/Keyword: 제초 활성

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Synthesis and Herbicidal Activities of 5-Benzyloxymethyl-3-(thiophen-5-yl)-1,2-isoxazoline and Their Related Derivatives (5-Benzyloxymethyl-3-(thiophen-5-yl)-1,2-isoxazoline 유도체의 합성과 제초활성)

  • Jeon, Dong-Ju;Song, Jong-Hwan;Kim, Hyoung-Rae;Kim, Eun-Ju;Hwang, In-Taek
    • The Korean Journal of Pesticide Science
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    • v.11 no.2
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    • pp.67-71
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    • 2007
  • Nobel series of 5-benzyloxymethyl-3-(thiophen-5-yl)-1,2-isoxazoline derivatives were designed and synthesized. The herbicidal activities of these compounds to main dominant weeds to these compounds were evaluated in pot tests that simulated rice paddy conditions. Most of the compounds showed high herbicidal activity to main dominant weeds occurring in rice field without the serious rice injury.

Synthesis of new pyridylimidazolinones and their hubicidal effects (새로운 Pyridylimidazolinone 유도체의 합성과 제초활성)

  • Jeon, Dong-Ju;Chang, Hae-Sung;Hwang, In-Taek;Kim, Dae-Whang
    • The Korean Journal of Pesticide Science
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    • v.3 no.3
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    • pp.6-10
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    • 1999
  • New series of pyridylimidazolinorus substituted with N-(2-hydroxyethyl)-${\alpha}$-dicarbonylamide group, N-ethoxycarbonylthioamide and N-benzoylthioamide group in place of carboxyl group at 3-position of pyridine were prepared, and their herbicidal effects were tested(in vivo) in upland conditions. Most of pyridylimidazolinones substituted with hydroxydiketoamide and N-ethoxycarbonylthioamide group at 3-position of pyridine showed good herbicidal effects at a rate of 250 g/ha, while pyridylimidazolinone substituted with N-benzoylthioamide group showed no herbicidal effects.

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Herbicidal Activities of Phenylvinylsulfone Derivatives (Phenylvinylsulfone 유도체의 제초활성)

  • Yu, Seong-Jae;Jeon, Dong-Ju;Kim, Dae-Whang;Sung, Nack-Do
    • Applied Biological Chemistry
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    • v.38 no.1
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    • pp.90-94
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    • 1995
  • Post emergence herbicidal activities$(pI_{50})$ of X-substituted phenylvinylsulfone derivatives(S) in-vivo against rice(Oryza sativa L.), Barnyard grass(Echinochloa crus-galli) and Pickerelweed(Monochoria vaginalis Presl) were measured by the pot test under paddy conditions. The (S) showed herbicidal symptom rapidly with lower activity(average $pI_{50}=2.0$) as proherbicide, which was excellent tolerance to rice. The structure activity relationships(SAR) were analyzed using such a physicochemical parameters as hydrophobic$({\pi})$ and molecular orbital(MO) quantity by the multiple regression technique, and discussed with quantum pharmacology. The herbicidal activities were related to the hydrophobic$({\pi})$ effect of X-substituent and orbital(HOMO & LUMO) energy. In case of Pickerelweed, the effect was rationalized by parabolic function of ${\pi}$ constant, where the optimal value of ${\pi}$ was 1.10. An increase in hydrophobicity and negative orbital energy by the electron attracting X-substituent may contribute to the herbicidal activity. Based on results proposed from SAR analysis, the mode of herbicidal action could be assumed.

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Screening of Penicillium sp. Showing Herbicidal Activity on Trifolium repens L. (토끼풀(Trifolium repens L.)에 제초활성을 나타내는 Penicillium sp.의 탐색)

  • Kim, Pan-Kyung;Park, Dong-Jin;Choi, Soon-Yong;Kim, Chang-Jin
    • Applied Biological Chemistry
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    • v.39 no.6
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    • pp.455-459
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    • 1996
  • Nine hundred and eighty fungal strains were isolated from lesions of Trifolium repens L. and various weeds. Among them, F40362, F40496, F40497 strains were selected by the screening of herbicidal activity on Trifolium repens L. and Zoysia japonica. Selected three strains showed selective activity between Trifolium repens L. and Zoysia japonica, and were identified as Penicillium sp.

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Synthesis of new sulfonylureas and their herbicidal effects (새로운 Sulfonylurea 유도체의 합성과 제초활성)

  • Jeon, Dong-Ju;Koo, Dong-Wan;Ko, Young-Kwan;Hong, Kyung-Sik;Kim, Dae-Whang
    • The Korean Journal of Pesticide Science
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    • v.5 no.2
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    • pp.33-36
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    • 2001
  • New series of sulfonylureas containing substituted thiophene with 2-chloromethyl-1,3-dioxolane group were prepared, and their herbicidal effects were tested(in vivo) in the upland conditions and in the paddy submerged conditions. The sulfonylureas in which 4,6-dimethoxy- or 4-methyl-6-methoxy group in pyrimidine or triazine ring showed good herbicidal effects at a rate of 0.1 kg/ha. However, they showed weaker herbicidal effects than that of sulfonylureas containing substituted thiophene with 2-fluoromethyl-1,3-dioxolane group in general.

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Herbicidal Efficacy Affected by Different Formulation of Benzobicyclon-Mixtures Herbicides in Paddy Rice Field (Benzobicyclon 혼합제의 제형에 따른 제초활성 특성)

  • Song, Jae-Eun;Park, Mae-Sol;Jeong, Jong-Hee;Park, Eun-Hee;Jeong, Chang-Kuk
    • Korean Journal of Weed Science
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    • v.31 no.4
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    • pp.384-393
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    • 2011
  • Sulfonylurea herbicide-resistant weeds are spreading widely and distributed about 106,951 hectare in paddy rice fields in Korea. Morever all biotype of Scirpus juncoides which were collected at 69 spots all over paddy rice fields in 2008 were identified biotype of sulfonylurea herbicide-resistant. Benzobicyclon is a p-hydroxyphenylpyruvate dioxygenase (HPPD) inhibitor, which is absorbed through root and basal stem of weeds so cause bleaching of newly developing leaves. Benzobicyclon was very effective to control Scirpus juncoides, Monochoria vaginalis, sedges and broadleaves weeds, so it have been developed various formulation like a suspension concentrate (SC), a water dispersible granule (WG), a granule (GR) and a DT (tablet for Direct application). During recently 6 years, benzobicyclon-mixtures herbicides have been registered over than 54 products in paddy fields. Herbicidal efficacy by formulations of benzobicyclon and its mixture herbicides were highest in DT, followed by SC and GR. Herbicidal efficacy of the kaolin and $CaCO_3$ carrier of GR was better and stable than that of talc and bentonite carrier. Growth and yield of rice were not affected much by formulations, application rates and rice cultivation methods.

Isolation of Herbicidal Compounds from Pulsatilla koreana Roots (백두옹(Pulsatilia koreana Nakai) 뿌리로부터 제초활성물질의 분리)

  • 정형진
    • Korean Journal of Plant Resources
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    • v.9 no.1
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    • pp.47-54
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    • 1996
  • To search herbicidal compounds in Pulsatilla koreana Nakai, methanol extract of P. koreana roots was purified by sequences of XAD-7 column chromatography, silica gel adsorption column chromatography, silica gel flash column chromatography, preparative layer chromatography and preparative high performance liquid chromatography(Prep, HPLC).The final Prep. HPLC gave two herbicidally-active fractions. These fractions treatment at 100ppm inhibited the root length of Echinochloa crus-galli seedlings by 48% and 60% as compared with the control, respectively. Components in the two active fractions were analyzed by GC-MS Spectrometry. These compounds, which were isolated from P. koreana roots, were identified as several fatty esters, hydrocarbons, squalene, evidonol, and a diazepin analogue.

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2D-QSAR and HQSAR Analysis on the Herbicidal Activity of New Cyclohexanedione Derivatives (새로운 Cyclohexanedione계 유도체의 제초활성에 관한 2D-QSAR 및 HQSAR 분석)

  • Kim, Yong-Chul; Hwang, Tae-Yeon;Sung, Nack-Do
    • The Korean Journal of Pesticide Science
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    • v.12 no.1
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    • pp.9-17
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    • 2008
  • QSARs (Quantitative structure-activity relationships) between a series of new cyclohexanedione derivatives (5-benzofuryl-2-[1-(alkoxyimino)-alkyl]-3-hydroxycyclohex-2-en-1-ones) and their herbicidal activity against Rice plant (Oryza sativa L.) and Barnyard grass (Echinochloa crus-galli.) were discussed quantitatively using 2D-QSAR and holographic (H) QSAR methods. Generally, the HQSAR models have better predictability and fitness than the 2D-QSAR models. The herbicidal activities against Barnyard grass with 2D-QSAR II model were dependent upon Balaban indice (BI) of molecule and hydrophobicity of $R_1$ and $R_3$ group. And also, the $R_3=ethyl$ group, according to the information of the optimized HQSAR IV model, was more contribute to the herbicidal activities against Rice plant, while the 5-(cyclohex-3-enyl)-2,3-dihydrobenzofuran ring part was not contribute to the herbicidal activities against two plants.

Synthesis and Herbicidal Activities of 5-benzyloxymethyl-3-(thiophen-4-yl)-1,2-isoxazoline derivatives (5-Benzyloxymethyl-3-(thiophen-4-yl)-1,2-isoxazoline 유도체의 합성과 제초활성)

  • Song, Jong-Hwan;Jeon, Dong-Ju
    • The Korean Journal of Pesticide Science
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    • v.12 no.2
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    • pp.197-200
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    • 2008
  • Novel series of 5-benzyloxymethyl-3-(thiophen-5-yl)-1,2-isoxazoline derivatives were designed and synthesized, and their herbicidal activities to diverse weeds were tested under flooded paddy conditions in a greenhouse. Among them, some compounds (3d-f) showed good activities to dominant weeds such as Echinocloa orizycola and Monochoria vaginalis presl. at a rate of 0.063 kg/ha without the serious injury toward rice.

제초제 사용 40년, 수도용 제초제 생산과 잡초발생 양상(2) - 저성분.고활성 제초제 보급 계열 다른 약제 바꾸어 사용해야

  • O, Se-Mun
    • Life and Agrochemicals
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    • s.248
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    • pp.50-53
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    • 2009
  • 제초제가 보급되면서 분명 벼 재배의 생력화는 누구도 부인할 수 없을 것이다. 농업인들은 저항성 잡초가 발생하지 않도록 계열이 다른 약제를 바꾸어 가며 사용하고, 이미 발생된 포장에는 빠른 기간 내에 제거될 수 있도록 제초제를 체계적으로 잘 사용하여야 한다.

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