Structure–Activity Relationships of Herbicidal Aryltriazolinones

A series of substituted aryltriazolinones, known to inhibit protoporphyrinogen oxidase, were prepared and their structure–activity requirements at positions 4 and 5 of the aromatic ring investigated. A QSAR equation obtained for substituents at the 5 position identified the hydrophobicity term π and the Sterimol minimum width B₁ as the two parameters affecting in-vitro biological activity. Greenhouse pre-emergence activity correlated with in-vitro activity and the hydrophobicity term π of the substituent at that position. It was found that the phenoxy-4-oxyacetate group at aromatic position 5 was an outlier and had to be considered separately. SAR analysis of substituents at aromatic position 4 revealed that two different models were required to explain all observed substituent effects. In the first model, where the 5 position was occupied by hydrogen, the 4-chlorobenzyloxy group at aromatic position 4 gave the best compound. The second model, where the 5 position of the aromatic ring was occupied by a group other than hydrogen, resulted in a QSAR equation, previously derived, which links substituent effects at position 4 with π and with the electronic para inductive term F_p. In this model the chloro group provides optimum biological activity. The need to separate the aryltriazolinone herbicides into several different classes in order to explain their substituent effects at aromatic positions 4 and 5 could be rationalized if more than one binding conformation, within the same binding site, is possible. © 1997 SCI     

Synthesis and pesticidal activity of some quinazolin-4(3H)-one derivatives

A number of quinazolin-4(3H)-one carbothioamides, pyrazoles, pyrazolones and tetrazole derivatives have been synthesised by the reaction of 2-hydrazino-3-(4-substituted phenyl)-quinazolin-4(3H)-ones with the appropriate aryl isothiocyanate, acetyl acetone, ethylacetoacetate and nitrous acid. All the compounds were tested in vitro for antibacterial, insecticidal and antifungal activity and found to have some activity.     

Communication to the Editor Insecticide Resistance in a Strain of Aphis gossypii from Southern France

A strain (R) of Aphis gossypii from Southern France was found to be resistant to several insecticides, particularly to pirimicarb, as compared to a susceptible strain (S). Resistance levels were determined by biological tests, and the highest resistance factor (1350) was for pirimicarb. Resistance was mainly restricted to anticholinesterase inhibitors. Use of synergists, DEF and PB, suggested that resistance mechanisms based on detoxification were involved to a minor extent, since a good correlation was observed between I₅₀ values and k_i values of AChE and in-vivo bioassay data. The two strains differed in esterase activity, with a 27·7-fold increase in the R strain. Resolution of esterases by polyacrylamide gel electrophoresis showed different patterns in the S and R strains, and two isozymes were less sensitive to pirimicarb in the S strain; however, no in-vitro degradation of [¹⁴C]pirimicarb was observed. These data suggest that the main mechanism of resistance was through a decrease in the sensitivity of the target, AChE, to the insecticides. © 1997 SCI.     

Synthesis of six heterocyclic multifunctional alkylating agents and evaluation of their activity againstPyrenophora avenae andBlumeria graminis f.sp.hordei

Six heterocyclic alkylating agents were synthesized and examined for activity against the oat stripe pathogenPyrenophora avenae on agar plates and against the barley powdery mildew fungusBlumeria graminis f.sp.hordei on barley seedlings. Radial growth ofP. avenae was not significantly affected by any of the compounds, but four of them,α,α-bis[4,7-bis(2-chloroethyl)-1,4,7-triazacyclononane]-para-xylene[3], 1,4,8,11-tetra(2-chloroethyl)-1,4,8,11-tetraazacyclotetradecane[4], 8,11-bis(2-chloroethyl)-1,4,8,11-tetraaza-5,7-oxocyclotetradecane[5] and 7,16-bis(2-chloroethyl-1,4,10,13-tetraoxa-7,16-diazaoctadecane[6], gave significant reductions in biomass ofP. avenae grown in liquid culture and in powdery mildew infection on barley when used at 25μM. Polyamine biosynthesis was examined by following the incorporation of labeled ornithine into polyamines inP. avenae. The four compounds3–6 which reduced mildew infection all reduced the flux of label through to the polyamines inP. avenae. Whether the reductions in mildew infection caused by these compounds is related to reduced formation of polyamines is not known and awaits investigation. http://www.phytoparasitica.org posting May 22, 2005.     

Synthesis and Anthelmintic Activity of 7-Hydroxy- 5-oxo-5H-thieno[3,2-b]pyran-6-carboxanilides and -6-thiocarboxanilides

7-Hydroxy-5-oxo-5H-thieno[3,2-b]pyran-6-carboxanilides and -6-thio-carboxanilides represent a novel series of anthelmintic compounds, with broad-spectrum activity against important parasitic nematodes in sheep and dogs. In particular, an improved efficacy against Trichostrongylus colubriformis in sheep over the related 3-carbamoyl-4-hydroxycoumarins has been noted. New synthetic routes to the key intermediate, 7-hydroxythieno[3,2-b]pyran-5-one, have been developed.     

Fungitoxicity of 6H-pyrazolo[3,4-c][l,2,5]thiadiazine-2,2-dioxides

A base-promoted cyclisation of 4-nitroso-5-benzylsulphonamidopyrazoles (VII) afforded 6 H -pyrazolo[3,4-c][1,2,5]thiadiazine-2,2-dioxides (VIII). They were tested in vitro for antifungal activity against a series of phytopathogenic fungi of different taxonomic classes. Five of the compounds had noteworthy activity; in particular 6H-3-phenyl-5-methyl-7–(3,4-dichlorophenyl) pyrazolo[3,4-c][1,2,5]thiadiazine-2,2-dioxide (VIIIc) at the concentration of 200 mg litre^?1 completely inhibited the growth of Pythium ultimum, Corticium solani and Sclerotinia minor.     

Fungicidal activity of 2-(1-alkenyl)-3-hydroxy-1,4-naphthoquinones and related compounds

The fungicidal activity of a series of 2-(1-alkenyl)-3-hydroxy-1,4-naphthoquinones and their acetates has been assessed against various fungi in vitro and against others, notably powdery mildews, in vivo, and the activity compared with that of analogous compounds bearing saturated side chains. Several of the compounds demonstrated a broad spectrum of activity in vitro. Whereas the presence of α-unsaturation in the side chain is essential for the in-vitro activity against the non-obligate fungi tested, it is of virtually no importance for the curative effect against Erysiphe graminis on barley. Only the corresponding acetates had activity against the latter pathogen.     

Independent and joint biological activity of isomeric forms of synthetic pyrethroids

Various isomeric mixtures of pyrethroids were examined in topical application tests against houseflies, Musca domestica. On the basis of the activities of the separate isomers of 5-benzyl-3-furylmethyl (±)-cis,trans-chrysanthemate, it was shown that when combined in pairs to give the (±)-trans or (±)-cis or (+)-cis,trans mixtures the observed mortalities did not differ from those expected by simple additive action calculated by the harmonic mean. In contrast the (±)-cis,trans mixture showed considerable antagonism with a mortality only 60% of that expected. Similar evaluations using the separate and combined isomers of bioallethrin [(R,S)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (allethronyl) ( + )-trans-[(1R,3R)-chrysanthemate] and the corresponding (+)-cis-(1R,3S)-chrysanthemate indicate antagonism calculated to be correlated with the content of the (R)-isomer of the alcoholic moiety. Hence the activity of the most active isomer of the “allethrin” series, (S)-3-allyl-2-methyl-4-oxocyclopent-2-enyl ( + )-trans-(1R,3R)-chrysanthemate, (S)-bioallethrin, is not fully realised unless it is present in pure form and a substantial part of the value of bioresmethrin (5-benzyl-3-furylmethyl ( + )-trans-chrysanthemate] as a killing agent is lost when the racemic form is used. In racemic mixtures there is mutual antagonism between pairs of isomers so that considerable masking of activity occurs.     

Fungicidal activity and chemical constitution. XX. The activity of substituted 1,4-naphthohydroquinone esters and substituted 1,4-naphthoquinones against powdery mildews

Eleven 2-n-alkyl-, ten 2-n-alkyl-3-hydroxy- and ten 2-n-alkyl-2,3-epoxy-3-hydro-1,4-naphthoquinones, together with eighteen 1,4-naphthohydroquinone esters were tested as protectant fungicides against the apple and cucumber powdery mildews (caused by Podosphaera leucotricha and Sphaerotheca fuliginea respectively). In.general the former pathogen was more susceptible to compounds from all four series, the lowest 10⁵ED⁵⁰(M) being 0.7 for 2-n-octyl-2,3-epoxy-3-hydro-1,4 naphthoquinone.     

Synthesis and insecticidal activity of novel 1,3,4-oxadiazolin-5-one and pyrazolin-5-one derivatives

A series of novel 2-(2,4,6-trisubstituted phenyl)-1,3,4-oxadiazolin-5-one derivatives and 3-(2,4,6-trichlorophenyl)pyrazolin-5-one derivatives were synthesized and evaluated for insecticidal activity. It was found that a moderately bulky alkyl group, such as a tert-butyl group, on the heterocyclic ring, and a trifluoromethyl group on the benzene ring were optimal substituents on the molecule. The oxygen atom in the oxadiazoline ring was essential for insecticidal activity. Of the compounds assayed, 4-tert-butyl-2-(2,6-dichloro-4-trifluoromethylphenyl)-1,3,4-oxadiazolin-5-one gave the highest activity against Nephtotettix cincticeps, with an LC₅₀ value of 0.51 mg litre⁻¹. © 1999 Society of Chemical Industry     

Isolation and biochemical diagnosis of cell lines of groundnut (Arachis hypogaea L) selected on glyphosate†

Three cell lines of groundnut (Arachis hypogaea L), an important oilseed legume, were selected on glyphosate using in-vitro culture techniques. The cell lines isolated through single as well as stepwise selection procedures showed c 20-fold increase in glyphosate tolerance as compared to the unselected control cell line. Studies on the biochemical mechanism of glyphosate tolerance in these cell lines showed a significant increase in the total extractable activity of the target enzyme, 5-enolpyruvyl shikimate-3-phosphate (EPSP) synthase (EC 2.5.1.19), which was further confirmed with immunological data. The over-expressed EPSP synthase activity was, however, subject to inhibition by glyphosate in vitro. Two other key regulated enzymes of the shikimic acid pathway, 3-deoxy-D -arabino heptulosonate 7-phosphate (DAHP) synthase (EC 4.1.2.15) and chorismate mutase (CM) (EC 5.4.99.5) did not show any change in specific activity in the selected cell lines. The enhanced activity of EPSP synthase in the tolerant cell lines was found to be stably inherited in the absence of selection pressure. © 1999 Society of Chemical Industry     

The toxicities of some analogues of dieldrin,endosulfan and isobenzan to bloodsucking diptera,especially tsetse flies

The dieldrin analogue, 1, 8, 9, 10, 11, 11-hexachloro-4, 5-exo-epoxy-2, 3-7, 6-endo-tricyclo-[6.2.1.0^{2, 7}]undec-9-ene (HEOM), and the isomeric 3, 4-exo-epoxy-and 3, 6-endo-epoxy compounds (HCE and ODA, respectively), incorporating structural modifications of the non-chlorinated ring system, were tested against adult mosquitoes (mainly Anopheles stephensi List.), tsetse flies (mainly Glossina austeni Newst.) and stable flies, Stomoxys calcitrans (L.). The order of toxicity was ODA > HCE > HEOM. In further tests of residual activity against A. stephensi, ODA was better than HCE but neither was sufficiently persistent to be a promising mosquito toxicant. Analogues of dieldrin (HEOD), endosulfan and isobenzan with reduced numbers of chlorine atoms were tested against G. austeni. In the pentachloro-analogues of dieldrin and α-endosulfan, the anti-bridge chlorine was more important than the syn-chlorine for toxicity. The general effect of reductive dechlorination was to reduce toxicity, but the effect was small for some endosulfan analogues and in one case there was an increase in toxicity. In the main, toxicities of the endosulfan analogues compared favourably with those of the dieldrin analogues. However, toxicity fell drastically following replacement of the second ethylenic chlorine in isobenzan. The effect of these structural changes on toxicity evidently varied from one series to another and was influenced in an unpredictable manner by the rest of the molecule.     

Toxicity of some pyrethroids to the adult desert locust,Schistocerca gregaria forsk

The toxicity of a number of topically applied pyrethroids has been tested against adult male desert locusts, Schistocerca gregaria: the most potent proved to be 5-benzyl-3-furylmethyl (+)-trans-chrysanthemate (bioresmethrin) with a weighted mean LD₅₀ of 4.0 μg/g. The remaining compounds may be ranked in order of toxicity as follows: 5-benzyl-3-furylmethyl (±)-cis-trans-chrysanthemate (resmethrin) > 4-allyl-2,6-dimethyl-benzyl(+)-trans-chrysanthemate > 4-allylbenzyl (+)-trans-chrysanthemate > 2,4,6-trimethylbenzyl (+)-cis-trans-chrysanthemate > 2,3,4-trimethylbenzyl (+)-cis-trans-chrysanthemate > 2,4-dimethylbenzyl (±)-cis-trans-chrysanthemate; 2-methylbenzyl (±)-cis-trans-chrysanthemate. A small factor of synergism (4.2) was obtained with bioresmethrin following pre-treatment with sesamex, but with resmethrin the synergistic ratio (1.6) was of little practical significance.     

The activity of some pyrethroids against Periplaneta americana and Blattella germanica

The knockdown and contact killing actions of various pyrethroids were compared using Blattella germanica and Periplaneta americana. A wide range of knockdown activity was found; 5-benzyl-3-furylmethyl (1R)-cis-3-(dihydro-2-oxo-3-thienylidenemethyl)-2,2-dimethylcyclopropanecarboxylate (RU 15525) acted fastest, more rapidly than pyrethrins, against B. germanica as well as having a low LD₅₀ value. Topical application and direct spray tests showed that (S)-α-cyano-3-phenoxybenzyl (1R)-cir-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate (NRDC 161) was more active as a killing agent, by an order of magnitude, than cismethrin, the next most active compound, and also had considerable knockdown activity. Piperonyl butoxide generally had little synergist effect. Female P. americana were over three times more tolerant than males to a range of insecticides applied topically. Residual knockdown action in the WHO resistance test was observed to provide baseline data. There was little overlap in speed of action between pyrethroids and other insecticides among the compounds tested.     

2-吡啶酰氨基环己烷基磺酰胺的合成与杀菌活性

为了进一步研究环烷基磺酰胺类化合物的杀菌活性与构效关系,在前期工作基础上,对先导化合物进一步展开研究,合成了15个未见文献报道的2-吡啶酰氨基环己烷基磺酰胺类化合物。首先以2-氧代环己烷基磺酰胺为原料,经过还原胺化后得到2-氨基环己烷基磺酰胺;再与取代吡啶甲酰氯反应,得到目标化合物。分别通过菌丝生长速率法与黄瓜活体叶片法测定了目标化合物对番茄灰霉病菌Botrytis cinerea及其他5种植物病原菌的杀菌活性。结果表明:目标化合物对番茄灰霉病菌表现出较好的抑制活性,其中化合物V-8在离体条件下对番茄灰霉病菌的EC50值为1.41 mg/L,在500 mg/L下的活体防效为79.17%;此外,部分目标化合物在50 mg/L下,对水稻纹枯病菌、水稻稻瘟病菌、大豆根腐病菌、黄瓜绵腐病菌和辣椒疫霉的抑制率高于60%,其中,化合物V-7对黄瓜绵腐病菌的EC50值为2.7 mg/L,其活性高于对照药剂多菌灵（EC50值为4.4 mg/L）,有进一步研究的价值。     

嘧啶联吡唑甲酰胺类化合物的合成及除草活性

设计合成了一系列结构新颖的嘧啶联吡唑甲酰胺类化合物5a~5o,其结构均经过1H NM R和MS分析确证。初步生物活性测试结果表明:在有效成分150 g/hm2剂量下苗后茎叶喷雾处理时,化合物(R)-N-[1-(4-氯苯基)乙基]-3-二氟甲基-1-(4,6-二甲氧基嘧啶-2-基)-1H-吡唑-4-甲酰胺(5c)、N-[1-(4-氯苯基)乙基]-1-(4,6-二甲氧基嘧啶-2-基)-N-甲基-3-三氟甲基-1H-吡唑-4-甲酰胺(5i)和N-[1-(4-氯苯基)乙基]-1-(4,6-二甲氧基嘧啶-2-基)-3-三氟甲基-1H-吡唑-4-甲酰胺(5k)对繁缕Stellaria media的抑制率高达90%以上;而同样剂量下苗前土壤喷雾处理时,化合物N-[1-(4-氯苯基)乙基]-3-二氟甲基-1-(4,6-二甲氧基嘧啶-2-基)-1H-吡唑-4-甲酰胺(5b)和5c对繁缕的抑制率达100%。该类结构化合物有望作为除草先导化合物进行开发。     

A new pyrethroid of high insecticidal activity

New pyrethroids containing heterocyclic rings in the alcohol moieties were synthesised and their insecticidal activities were studied. Of these new pyrethroids, 3-benzylpyrrol-1-ylmethyl (1RS-cis, trans-3(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate was found to be the most effective, having higher activity than permethrin against Musca domestica by a topical application method. In addition, para-substituted analogues of the 3-benzylpyrrol-1-ylmethyl ester were also synthesised to study the substituent effects on insecticidal activities; the residual effects of these compounds against Blattella germanica were also examined.     

Preparation and biocidal activity of alkyl phenyl (dichloromethyl)phosphonates

Seventeen new alkyl (or phenacyl) phenyl (dichloromethyl)phosphonates were synthesised; seven of these showed poor fungicidal activity when tested in vitro against Pyricularia oryzae but some possessed high insecticidal activity against Culex fatigans and Drosophila melanogaster.     

山蒟中脂肪链酰胺类化合物的分离及杀虫活性

采用提取、萃取及柱层析等方法,从山蒟Piper hancei Maxim甲醇提取物的石油醚和氯仿萃取相中分离到6个脂肪链酰胺类化合物,通过核磁共振、质谱并结合相关文献比对,其结构被分别鉴定为已知化合物chingchengenamide A( C1 )、N-异丁基-反-2-反-4-癸二烯酰胺( C2 )、假荜拨酰胺A( C3 )、荜茇宁( C4 )、N-p-香豆酰酪胺( C5 )和N-反式-阿魏酰酪胺( C6 ),其中 C1 为首次从山蒟中获得。利用幼虫浸液法测试了各化合物对白纹伊蚊Aedes albopictus和致倦库蚊Culex pipiens quinquefasciatus幼虫的12 h杀虫活性。结果表明:在20 mg/L下,化合物 C1 对白纹伊蚊的杀虫活性较高,其校正死亡率为100%,LC₅₀值为5.37 mg/L;化合物 C1 、 C2 、 C3 和 C4 对致倦库蚊的杀虫活性较高,20 mg/L下的校正死亡率分别为100%、88.5%、100%和100%,LC₅₀值分别为1.03、9.68、3.08和2.87 mg/L。     

Phytotoxic activity of norbornane and nortricyclene lactones

A series of bromo-, hydroxy- and keto-derivatives of norbornane-6-hydroxy-2-carboxylic acid, y-lactone and some related compounds have been prepared and examined for phytotoxic activity. The 3-exo-propionyl, and 3-exo-5-exo-dibromo substituted compounds have been found to have the greatest activity.