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1.
Over 100 benzyl esters of pyrethroidal acids were synthesised and tested for insecticidal activity to establish detailed structure–activity relationships in compounds with side-chains similar to those in the natural pyrethrins. Alkenyl, and corresponding alkynyl, side-chains were effective, both at the 3- and 4-positions, as were side-chains with extended substitution in either E or Z forms. A cyano group at the α-position increases activity if the side-chain is at C-3, but lowers it drastically if the substituent is at C-4. Similarly, methyl groups at C-2 and/or C-6 may increase activity whether the unsaturated side-chain is at C-3 or C-4, but only in the absence of an α-cyano group.  相似文献   

2.
The insecticidal activities of esters from a series of alcohols with four different groups (H, -CH3, -C?CH and -C?N) in the α-position, and containing different A-rings or bridging groups, were evaluated. The results show a complex interaction between these two parts of the molecule; the strongest enhancement of activity by some α-substituents was found in 3-phenoxybenzyl esters, while other systems responded weakly or even negatively to the substitution.  相似文献   

3.
The insecticidal activities to Musca domestica L. and Phaedon cochleariae Fab. of a series of 3-phenoxybenzyl pyrethroid esters with a cyano substituent at the 2-, 6-. (R)-α-, or (S)-α-position are compared with those of the unsubstituted analogues. Only an (S)-α-substituent enhances activity; others diminish or almost eliminate it. (RS)-α-mixtures are generally less active than would be predicted from the potencies of their separate constituents.  相似文献   

4.
A complexometric method has been developed for the selective determination of glyphosate and related compounds. The method is based upon the different pH-dependence of tridentate and tetradentate ligand-metal complex stabilities. Glyphosate, the tridentate ligand forms a stable copper complex at pH ≥ 8 only, whereas N-carboxymethyl-N-phosphonomethylglycine and N,N-bis(phosphonomethyl)glycine, the tetradentate ligands, form sufficiently stable bismuth complexes even at low pH. The method, therefore, consists of aliquot titrations in basic and acidic media, using metal ion titrant solutions. The first aliquot containing N-(phosphonomethyl)glycine plus N-carboxymethyl-N-phosphonomethylglycine or N,N,-bis(phosphonomethyl)glycine is titrated with bismuth volumetric solution at pH 1.8–2–5 in the presence of methylthymol blue indicator. Quantities of the tetradentate ligands can be calculated from the bismuth consumption. The second aliquot is titrated with copper volumetric solution at pH 8–10, in the presence of murexide indicator. The content of glyphosate can be calculated from the difference between the copper and bismuth consumptions. Efficacy of the method is verified by analyses of standard mixtures and industrial samples.  相似文献   

5.
Comparing insecticidal activities of a wide range of pyrethroids with polarities measured by reversed phase, thin-layer chromatography suggests that there are optimum polarities for potency in both Musca domestica and Phaedon cochleariae, and that these optima have closely similar values. The significance of these conclusions is discussed.  相似文献   

6.
Synthesis and bioassay of a series of esters based on pyrethroidal acids established that the activity of halosubstituted allylbenzyl esters depends on the position and stereochemistry of substitution in the allyl side-chain, on the substitution pattern on benzyl, on the esterifying acid, and, to a lesser extent, on the nature of the halogen substituent itself. The most powerful combination of the first four parameters for activity against houseflies is in (Z)-3-haloallylbenzyl esters of the (1R)-cis 3-(2,2-dibromovinyl) acid. Other combinations have moderate to low activity. Some aspects of the variation conform to previously recognised patterns, others define more precisely the requirements for the side-chain to confer activity. The pattern of response of activity to cyano-substitution at the α-position, noted earlier, persists in the current compounds, and is here analysed quantitatively.  相似文献   

7.
The effects on root geotropism of three series of compounds related to 2-phenyl-8H-pyrazolo[5,1-a]isoindol-8-one (IV), its 3,3a-dihydro derivative (V) and 5-(2-carboxyphenyl)-3-phenylpyrazole (VI) have been assessed using cress seedlings. Compounds (IV) and (VI), and their derivatives, are highly active, destroying geotropism at concentrations of 10?7-10?9M. Substitution with various functional groups and increased molecular size resulted in only minor variation in the level of activity.  相似文献   

8.
The insecticidal activities against houseflies (Musca domestica L.) and mustard beetles (Phaedon cochleariae Fab.) of the chrysanthemate bioresmethrin, and of 31 related 5-benzyl-3-furylmethyl 2,2-dimethylcyclopropanecarboxylates with alkenyl, alkadienyl or alkoxycarbonylalkenyl substituents at position 3 of the cyclopropane ring are compared to determine the relative influence of the isobutenyl sidechain (as in chrysanthemates) and of the other side chains. Several substituents, in particular (E)- or (Z)-butadienyl or -pentadienyl, give considerably greater activity than isobutenyl but alkoxycarbonyl compounds are less potent.  相似文献   

9.
Eleven sesquiterpene lactone derivatives of parthenin ( 1 ), obtained from wild feverfew, Parthenium hysterophorus, were prepared by chemical and photochemical transformations. The compounds tested were a pyrazoline adduct ( 2 ) of parthenin, its cyclopropyl ( 3 ) and propenyl ( 4 ) derivatives, anhydroparthenin ( 5 ), a dihydro‐deoxygenated product ( 6 ), a formate ( 7 ) and its corresponding alcohol ( 8 ) and acetate ( 9 ), a rearranged product ( 10 ), lactone ( 11 ) and hemiacetal ( 12 ). All these derivatives, along with parthenin, were tried for their antifeedant action against sixth‐instar larvae of Spodoptera litura, for insecticidal activity against the adults of store grain pest Callosobruchus maculatus, for phytotoxic activity against Cassia tora, and for nematicidal activity against the juvenile stage‐II (J2) of the root knot nematode Meloidogyne incognita. Antifeedent bioassay revealed that parthenin is moderately antifeedant. Among the derivatives, the saturated lactone ( 11 ) was found to be about 2.25 times more active than parthenin. The pyrazoline adduct ( 2 ) was found to be the most effective as an insecticide, with LC50 values after 24, 48 and 72 h of 96, 43 and 32 mg litre−1, respectively, which are comparable with neem extract. Compound 4 was found to be the most effective inhibitor of germination and seedling growth of C tora, with ID50 values for germination, plumule length and radicle length of 136, 326 and 172 compared with 364, 738 and 427 mg litre−1, respectively, for parthenin. Compound 10 was found to be the most effective in terms of nematicidal activity. The LC50 values for this compound were 273 and 104 mg litre−1, respectively, after 48 and 72 h compared with 862 and 512 mg litre−1 observed for parthenin after 48 and 72 h. © 2001 Society of Chemical Industry  相似文献   

10.
Esters of 3-phenoxybenzyl alcohol and its α-cyano derivative with 2,2-dimethylcyclopropanecarboxylic acids bearing (E)- or (Z)-3-monohalovinyl side chains (haloiodo, bromo, chloro or fluoro) were synthesised and had moderate to high insecticidal activities, but these were generally lower than those of established pyrethroids with the corresponding 3-(dihalovinyl) side chains. Compounds with 3-(2-chloroprop-1-enyl) side chains were intermediate in potency between the related chrysanthemates and 3-(dichlorovinyl) esters.  相似文献   

11.
Pretreatment of tobacco callus (Nicotiana tabacum L.) with glyphosate and related compounds promoted to a different degree the metabolism of radiolabeled indole-3-acetic acid ([2-14C]IAA) by increasing both conjugation and oxidation, and consequently lowered the level of free [2-14C]IAA. At identical concentrations, glufosinate ammonium was more active than glyphosate whereas glyphosine and aminomethylphosphonic acid were less active. These compounds also selectively reduced ethylene production and inhibited fresh-weight growth of tobacco callus. The activities of the tested compounds on IAA metabolism were correlated with those on inhibition of growth, suggesting that, under the experimental condition, the effect on IAA metabolism was a major contribution to their toxic action. This information may be useful for the design and testing of new herbicides and plant growth regulators of this type.  相似文献   

12.
Close isosteres of fenvalerate [(RS)-α-cyano-3-phenoxybenzyl (RS)-2-(4-chlorophenyl)-3-methylbutyrate], in which cyclopropyl groups replace isopropyl have insecticidal activity close to or greater than the parent compounds, and diminished intravenous toxicity to rats. A direct toxicological relationship of these compounds to fenvalerate itself and to chrysanthemate esters is indicated by the consistently greater activity of esters from one of an enantiomeric pair of acids. Other esters with larger alkyl or cycloalkyl groups, or spiropentane analogues of chrysanthemates are less active insecticides. 13C-Nuclear magnetic resonance spectra suggest that in the α-cyanobenzyl esters there is an intramolecular through-space interaction in solution. The relationships between the chemical structures of the compounds synthesised and their relative activities to different insect species and toxicity to rats are discussed.  相似文献   

13.
Pimaricin-resistant mutants of Aspergillus nidulans were selected on a medium containing the polyene-antibiotic. Some resistant mutants contained markedly reduced amounts of ergosterol, but others contained almost normal levels of this sterol. Most resistant mutants which lacked ergosterol had a biochemical lesion in sterol C-22 desaturation. Analysis of sterols in one of these isolates showed the presence of 5,7-ergostadienol, 5,7,24(28)-ergostatrienol, and 5,8-ergostadienol. The sterol C-14 demethylation inhibitor, fenarimol, was more toxic to this mutant than to the wild type. On the other hand, mutants inactive in sterol C-22 desaturation were resistant to oligomycin but showed wild type sensitivity to carboxin. Attempts to select sterol C-14-demethylation-deficient mutants of Aspergillus nidulans, Monilinia fructicola, and Pyricularia oryzae on polyene-containing media were unsuccessful. Apparently C-14-methyl sterols do not support growth of these filamentous fungi.  相似文献   

14.
The fungistatic activity against Penicillium digitatum and Diplodia natalensis decreased slightly in ascending a homologous series of alkyl esters of benzimidazol-2-ylcarbamic acid from the methyl ester (carbendazim) to the pentyl ester; the hexyl and octyl esters were inactive. 2-(Acylamino)benzimidazoles were slightly less active than the analogous alkyl benzimidazol-2-ylcarbamates. Introduction of a methylene bridge between the benzimidazole ring and the 2-methoxycarbonylamino group abolished antifungal activity. Methylation of either the carbamate nitrogen or an imidazole nitrogen of carbendazim produced inactive compounds. Replacement of the benzimidazole ring of carbendazim with various other ring systems was accompanied by marked reduction in antifungal activity.  相似文献   

15.
1-(4′-Ethylphenoxy)-3,7-dimethyl-6,7-epoxy-trans-2-octene (the ethyl-epoxide), a potent insect morphogenetic agent, is converted to 6,7-diol and other derivatives in living cockroaches and mealworms. Enzyme preparations of these organisms, and of houseflies and several other insect species, also carry out these hydration and/or oxidation reactions. In addition, housefly microsomes epoxidize the ethyl-epoxide to a diepoxide. The diepoxide and diol are then converted by microsomes to at least six cyclic diols, probably via an epoxy-diol intermediate, the major ones being the cis- and trans-tetrahydrofurandiol derivatives. The metabolites formed by these reactions have little or no morphogenetic activity in Tenebrio assays. Attempts to find potent inhibitors for housefly epoxide hydratases were unsuccessful. The corresponding ethylphenyl geranyl ether is epoxidized by housefly microsomes, forming the more morphogenetically active ethyl-epoxide, but the major reaction is oxidation on the geranyl moiety to an unidentified olefinic carboxylic acid. The chemical modifications needed for improved stability and morphogenetic activity in this juvenoid series depend on the insect species and strain and the relative activities of their enzymes involved in various inactivation pathways.  相似文献   

16.
TwoPenicillium species, vizP. brevicompactum andP. corymbiferum, were isolated from senescent petioles of cyclamen and from bulbs of lilies, respectively, both samples treated previously with benomyl. The isolates turned out to be very resistant to this fungicide when grown on malt agar, supplied with the fungicide; at a concentration of 2000 g/ml they were less inhibited than randomly chosen isolates of the same species on agar with 1 g/ml.The strains retained their resistance at the same level for at least 3 months after repeated subculturing on fungicide-free agar.Resistance to benomyl coincided with resistance to methyl-thiophanate and, to a lesser extent, also to thiabendazole and furidazol.Samenvatting Uit afstervende bladstelen van cyclamen en uit schubben van leliebollen, welke eerder met benomyl waren behandeld, konden respectievelijkPenicillium brevicompactum enPenicillium corymbiferum worden geïsoleerd. De isolaten blekenin vitro zeer resistent tegen het fungicide. De myceliumgroei van deze isolaten werd op moutagar met 2000 g/ml benomyl minder geremd dan die van willekeurige isolaten van dezelfde soorten op agar met 1 g/ml (Fig. 1).De isolaten bleven gedurende tenminste 3 maanden resistent na regelmatig overenten op voedingsbodems zonder het fungicide.De resistente stammen van de beidePenicillium-soorten bleken eveneens resistent tegen methyl-thiophanaat en in mindere mate ook tegen thiabendazol en furidazol (Tabel 1). De volgorde van de groeiremmende werking van deze fungiciden was voor de willekeurig gekozen (gevoelige) isolaten: benomyl>thiabendazol>methyl-thiophanaat >furidazol. Voor de resistente stammen was deze: thiabendazol en furidazol >benomyl>methyl-thiophanaat. In het feit dat een dergelijke verandering in volgorde van remmend effect ook voorBotrytis cinerea geldt, ligt een aanwijzing, dat de wijze waarop de resistentie werkt, voor deze schimmels gelijk is.  相似文献   

17.
Preparation of 3-phenoxybenzyl chrysanthemates and their dihalovinyl analogues substituted with a cyano group at the 2-, 6-, (R)-α-, or (S)-α- positions is described. The (R)- and (S)- isomers of α-cyano-3-phenoxybenzyl esters of 2,2-difluoro-, -dichloro-, and -dibromo-vinyl analogues of cis- and trans- chrysanthemic acid are separated chromatographically, as are the separate pairs of enantiomers of fenvalerate, (RS)-α- cyano-3-phenoxybenzyl (RS)-2-(4-chlorophenyl)-3-methylbutyrate. An optically active ester of α-cyano-3-phenoxybenzyl alcohol (obtained using D -oxynitrilase) with 2,2,3,3-tetramethylcyclopropanecarboxylic acid is synthesised.  相似文献   

18.
A series of compounds containing fluorine atoms in place of hydrogen in olefinic non-ester pyrethroids has been synthesised using a route based on novel intermediates, ie 2-fluoroallyl acetates, which are coupled with aryl Grignard reagents, and tested against several insect species. In most cases, after introduction of fluorine at the olefinic position, the activity remains high in both the 1-aryl-1-(3-arylprop-2-enyl)cyclopropane and the (1-aryl-4-arylbut-2-enyl)cyclopropane series. In particular, the former series have potential as soil insecticides, because in tests against Diabrotica balteata, activities were high, and dose-transferability factors were increased by the introduction of fluorine. © 1999 Society of Chemical Industry  相似文献   

19.
The insecticidal activities against houseflies (Musca domestica L.) and mustard beetles (Phaedon cochleariae Fab.) of 29 new 5-benzyl-3-furylmethyl 2,2-dimethyl-cyclopropane-carboxylates are compared with those of the corresponding chrysanthe-mate (bioresmethrin) to assess the influence of non-ethylenic and isobutenyl substituents at position 3 of the cyclopropane ring. Of the new groups investigated, only 3-methoxyiminomethyl gives equal or enhanced activity; 3-(2-furyl) esters are moderately effective, but 3-phenyl and 3-alkoxycarbonyl compounds show weak activity. A 3-(2,2,2-trihaloethyl) compound was more active than compounds with other saturated groups, such as isobutyl.  相似文献   

20.
A series of substituted 4-methylcoumarins was synthesised and the members tested for their toxicity towards mycelial growth of seven phytopathogenic fungi in culture. Rhizoctonia solani, Alternaria alternata and Fusarium solani exhibited maximum sensitivity to these compounds whereas Pythium aphanidermatum, Colletotrichum falcatum, Drechslera oryzae and Macrophomina phaseolina were relatively less sensitive. 6-Ethyl-3-n- propyl-7-hydroxy4-methylcoumarin ( I ) was relatively toxic towards all fungi except C. falcatum, P. aphanidermatum and M. phaseolina. The 6-n-butyl ( III ) and 6-(1, 1, 3, 3-tetramethylbutyl) ( VI ) derivatives were highly toxic to R. solani with EC50, values of lμg ml?1.  相似文献   

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