Rotenones

Rotenone is present in the roots of Derris spp., from Malaya and the East Indies, and Lon-chocarpus spp. Rotenone is a selective insecticide with some acaricidal properties for control of garden insects, and lice and ticks on animals. Rotenone is very toxic to fish, so it can be used to control undesirable fish species (to eradicate them from lakes, streams, and reservoirs). Its oral LD50 in rats is 132 mg/kg. 

Rotenone is an important insecticide extracted from various leguminous plants. It inhibits the transfer of electrons from nicotineamide-adenine (NADH) to ubiquinone. 

It is also highly toxic to fish and is often used to eradicate unwanted fish populations, for instance, minnows in lakes before introducing trout, or 

The fungicides are very versatile in the contol of fungi that have become resistant to the demethylase inhibitor (DMI) fungicides described later. They have surprisingly low mammalian toxicity, but as with many other respiratory poisons, they show some toxicity to fish and other aquatic organisms. They may also be toxic to earthworms. In fungi they inhibit spore germination. The structures show the natural products strobilurin B and azoxystrobin, which has been marketed since 1996. 

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Rotenoids. The use of rotenone-bearing roots as insecticides in the United States was developed as a result of federal laws against residues of lead, arsenic, and fluorine upon edible produce. Rotenone [83-79-4] (5) is harmless to plants, highly toxic to many insects, and relatively innocuous to... 

Insects poisoned with rotenone exhibit a steady decline ia oxygen consumption and the iasecticide has been shown to have a specific action ia interfering with the electron transport iavolved ia the oxidation of reduced nicotinamide adenine dinucleotide (NADH) to nicotinamide adenine dinucleotide (NAD) by cytochrome b. Poisoning, therefore, inhibits the mitochondrial oxidation of Krebs-cycle iatermediates which is catalysed by NAD. 

Rotenone-containing iasecticides have been used as dusts of ground roots, dispersible powders, and emulsive extracts. Their principal uses have been for appHcation to edible produce just prior to harvest and for the control of animal ectoparasites and cattle gmbs. 

Rya.nia., The root and stem of the plant yania speciosa family Flacourtiaceae, native to South America, contain from 0.16—0.2% of iasecticidal components, the most important of which is the alkaloid ryanodine [15662-33-9] C25H250 N (8) (mp 219—220°C). This compound is effective as both a contact and a stomach poison. Ryanodine is soluble ia water, methyl alcohol, and most organic solvents but not ia petroleum oils. It is more stable to the action of air and light than pyrethmm or rotenone and has considerable residual action. Ryania has an oral LD q to the rat of 750 mg/kg. The material has shown considerable promise ia the control of the European com borer and codling moth and is used as a wettable powder of ground stems or as a methanohc extract. Ryanodine uncouples the ATP—ADP actomyosia cycle of striated muscle. 

Piscicides. The two piscicides, antimycin and rotenone, are both used in ponds to control nuisance fish. Antimycin is used selectively to remove scaled fishes from catfish ponds, and rotenone is used as a general fish toxicant (9,10). Recent observations by catfish farmers indicate that antimycin at low concentrations also acts as a therapeutant against external parasites. 

Rosin core solder, pyrolysis products Rotenone (commercial)... 

Rotenone is a common insecticide that strongly inhibits the NADH-UQ reductase. Rotenone is obtained from the roots of several species of plants. Tribes in certain parts of the world have made a practice of beating the roots of trees along riverbanks to release rotenone into the water, where it paralyzes fish and makes them easy prey. Ptericidin, Amytal, and other barbiturates, mercurial... 

Although only two protons are pumped out of the matrix, two others from the matrix are consumed in the formation of H2O. There is therefore a net translocation of four positive charges out of the matrix which is equivalent to the extrusion of four protons. If four protons are required by the chemiosmotic mechanism to convert cytosolic ADP + Pj to ATP, then 0.5 mol ATP is made for the oxidation of one mol of ubiquinol and one mol ATP for the oxidation of 2 mols of reduced cytochrome c. These stoichiometries were obtained experimentally when ubiquinol was oxidized when complexes I, II, and IV were inhibited by rotenone, malonate, and cyanide, respectively, and when reduced cytochrome c was oxidized with complex III inhibited by antimycin (Hinkle et al., 1991). (In these experiments, of course, no protons were liberated in the matrix by substrate oxidation.) However, in the scheme illustrated in Figure 6, with the flow of two electrons through the complete electron transport chain from substrate to oxygen, it also appears valid to say that four protons are extmded by complex I, four by complex III, and two by complex 1. 

Pesticides, e.g. aminocarb, captan, difolatan, landrin, rotenone... 

Under the chosen conditions aromatic compounds are nitrated to nitroaromatics [1]. The detection of rotenone [1] (see below) depends on the reduction of silver ions, incorporated into the layer, to metallic silver in the presence of ammonia [4]. The mechanism of the reaction of many substances leading to fluorescent derivatives has not yet been elucidated [2],... 

Rotenone is a complex flavonoid found in the plant Derris ellyptica. It acts by inhibiting electron transport in the mitochondrion. Derris powder is an insecticidal preparation made from the plant, which is highly toxic to hsh. 

Rotenone A complex flavonoid produced by the plant Denis ellyptica. It has insecticidal activity due to its ability to inhibit electron transport in the mitochondrion. 

Pesticides, e.g. aminocarb, captan, difolatan, landrin, rotenone 200 °C, 45 min Induction of fluorescence in weakly [ fluorescent or nonfluorescent pesticides and amplification of natural fluoies-cence. There are some differences between basic and acidic aluminium oxide layers. 

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