Inheritance of triterpene methyl ethers in Cortaderia (Gramineae)

The distribution of triterpene methyl ethers in several generations of interspecific hybrids of Cortaderia indicates dominant gene control of their synthesis. The hybrid C. richardii × C. toetoe is an exception because synthesis of α- and β-amyrin methyl ethers is suppressed in F₁ and F₂, but is restored in the backcross F₁ × C. toetoe; this backcross generation was heterozygous for genes for the amyrin methyl ethers, and on selfing segregated in a simple Mendelian ratio.     

Flavonoids in leaves and inflorescences of australian cyperaceae

A survey of 170 Australian species of Cyperaceae belonging to 35 genera has confirmed that this family has a highly characteristic flavonoid pattern in leaf and inflorescence. Aurone pigments, the most distinctive family constituents, were found in the leaves of 25% of the sample and in the inflorescences of 40%. Sulphuretin was found for the first time in the family, in Carex appressa. Flavones, such as tricin and luteolin, are very common; in addition, a variety of methyl ethers were detected. Luteolin 5-methyl ether was found in further genera, while luteolin 7-methyl ether, diosmetin and acacetin were detected for the first time in the Cyperaceae. Flavonols and their methyl ethers occurred in over one-third of the species, particularly in the leaves, being especially well represented in the genera Fuirena, Gahnia, Lepidosperma and Mesomelaena. Myricetin was found only twice, in two Baumea species. The 3-desoxyanthocyanidin carexidin was found in the inflorescences of eight species, i.e. in 5% of the sample. Taxonomically, the results are mainly of interest at the generic and specific level, where the patterns sometimes show useful correlations with morphology. At the tribal level, the Sclerieae are the most distinctive, with higher than average frequency of flavone C-glycosides, flavonols, proanthocyanidins and aurones, and lower than average frequency of flavones.     

A new chromone from the stems of Cneorum tricoccum

From the stems of Cneorum tricoccum L. 3,3-dimethylallylspatheliachromene, spatheliabischromene and alloptaeroxylin methyl ether have been isolated as well as the new natural product ptaerochromenol methyl ether, which was chemically interconverted to isoheteropeucenin methyl ether.     

Les sesquiterpenes de Cupressus dupreziana

Heartwood extractives of C. dupreziana were investigated. Carvacrol methyl ether, cedrol and α-cedrene are present, together with sesquiterpene hydrocarbons. A comparison is made with those found in C. sempervirens and other Cupressus species.     

Capillary gas chromatographic analysis of serum bile acids as the n-butyl ester–trimethylsilyl ether derivatives

Gas chromatographic separations of n-butyl ester-trimethylsilyl ether derivatives of several common bile acids were compared with those of the corresponding methyl ester-trimethylsilyl ether derivatives on a CP-Sil-5 CB capillary column. Both types of derivatives were similarly resolved from each other. However, the n-butyl ester-trimethylsilyl ether derivatives of the bile acids showed longer retention times than the corresponding methyl ester-trimethylsilyl ethers and unlike the methyl ester-trimethylsilyl ether derivatives, were completely resolved from and eluted later than the trimethylsilyl ethers of common plasma sterols including sitosterol. A simplified method of plasma work-up for quantitation of bile acids and application of the above method in quantification of plasma bile acids in humans is described.     

Flavonoids from the stem bark of Millettia hemsleyana

The stem bark of Millettia hemsleyana has yielded six simple flavonoids of which three are novel. Dihydromilletenone methyl ether and dihydroisomilletenone methyl ether represent the two keto—enol tautomers of the known β-hydroxychalcone milletenone, trapped by methylation and reduction, and the third new compound, 3′,4′-methylenedioxy-7-methoxyflavone, is the cyclized form of a demethylated milletenone. All compounds were identified on the basis of detailed spectral analysis.     

Triterpene methyl ethers in leaf waxes of Saccharum and related genera

The triterpene methyl ethers in the leaf waxes of over 80 clones of Saccharum officinarum, S. edule, S. robustum, S. spontaneum and a limited number of related species were compared as possible chemotaxonomic markers by GLC. The principal components were arundoin, crusgallin and cylindrin. The overall interspecific variation was small, but arundoin was particularly characteristic of S. officinarum. However, each species showed marked interclonal variation, which was related to chromosome numbers and geographical origin. Most S. spontaneum clones from India were atypical containing no triterpene methyl ethers.     

假酸浆中新的醉茄内酯类化合物

从假酸浆（Nicandra physaloides）全草中分离得到12个化合物,其中两个为新的醉茄内酯类化合物,经波谱学方法将其结构鉴定为nicandrenone methyl ether （1） 和26S-nicandrenone methyl ether （2）;已知化合物为三个醉茄内酯,nicandrenone （3）,Nic-7 （4）,nicaphysalin E （5）,以及pinosylvin monomethyl ether （6）,2S-pinocembrin （7）,（1S, 2R）-1, 2-bis （4-hydroxy-3-methoxyphenyl）-1, 3-propanediol （8）,vanillin （9）,indole-3-carboxylic acid （10）,vanillic acid （11） 和drummondol （12）。     

6-Hydroxy- and 6-methoxyflavonoids from Neurolaena lobata and N. macrocephala

Twelve flavonoids including one new sulfate were isolated from Neurolaena lobata, and six known flavonoids were obtained from N. macrocephala. The new compound isolated from N. lobata is 6-hydroxykaempferol 3-methyl ether 7-sulfate, and the known flavonoids are 6-hydroxykaempferol 3,7-di-dimethyl ether, 6-hydroxykaempferol, 3-methyl ether 7-glucoside, 6-hydroxykaempferol 7-glucoside, quercetagetin and its 7-glucoside, quercetagetin 3,6- and 3,7-dimethyl ethers, quercetagetin 3-methyl ether 7-glucoside and 7-sulfate, 6-hydroxyluteolin 3′-methyl ether and 6-hydroxyluteolin 7-glucoside. The known flavonoids identified from N. macrocephala are quercetagetin 3,6- and 3, 7-dimethyl ethers, quercetagetin 6-methyl ether 7-glucoside, quercetagetin 3,6-dimethyl ether 7-glucoside, quercetagetin 7-glucoside and quercetagetin 3-methyl ether 7-sulfate.     

Radiolabeled cholesteryl ethers: A need to analyze for biological stability before use

Radiolabeled cholesteryl ethers are widely used as non-metabolizable tracers for lipoproteins and lipid emulsions in a variety of in vitro and in vivo experiments. Since cholesteryl ethers do not leave cells after uptake and are not hydrolyzed by mammalian cellular enzymes, these compounds can act as markers for cumulative cell uptakes of labeled particles. We have employed [³H]cholesteryl oleoyl ether to study the uptake and distribution of triglyceride-rich emulsion particles on animal models. However, questionable unexpected results compelled us to analyze the stability of these ethers. We tested the stability of two commercially available radiolabeled cholesteryl ethers - [³H]cholesteryl oleoyl ether and [³H]cholesteryl hexadecyl ether from different suppliers, employing in vitro, in vivo and chemical model systems. Our results show that, among the two cholesteryl ethers tested, one ether was hydrolyzed to free cholesterol in vitro, in vivo and chemically under alkaline hydrolyzing agent. Free cholesterol, unlike cholesteryl ether, can then re-enter the circulation leading to confounding results. The other ether was not hydrolyzed to free cholesterol and remained as a stable ether. Hence, radiolabeled cholesteryl ethers should be analyzed for biological stability before utilizing them for in vitro or in vivo experiments.     

Sesquiterpenoid aldehyde quinones and derivatives in pigment glands of Gossypium

The resistance of Gossypium species to insects is enhanced by compounds in their lysigenous pigment glands. In cultivated cottons, glands in achlorophyllous plant parts contained predominately the terpenoid aldehyde gossypol in G. hirsutum, and gossypol and its methyl and dimethyl ethers in G. barbadense. Glands in young green tissues, however, contained hemigossypolone as the predominant terpenoid aldehyde in G. hirsutum, and a new quinone, hemigossypolone-7-methyl ether, in G. barbadense. As glands aged in green tissues, the sesquiterpenoid quinones were replaced by several C₂₅-terpenoids formed by the Diels-Alder reaction of the quinones with myrcene or trans-β-ocimene. Two C₂₅-terpenoids isolated from G. barbadense, but not G. hirsutum, were the methyl ethers of heliocides H₁ and H₄ and were designated heliocides B₁ and B₄, respectively. A dark red pigment, gossyrubilone, from glands of young leaves of both species is the isopentylimine of hemigossypolone. Similar red imines, formed from sesquiterpenoid quinones and amino acids, resembled the red coloration of the envelope cells surrounding the gland sac. The terpenoid quinones of Gossypium had physical characteristics different from quinones in Bombax which apparently were incorrectly identified as being the same. A survey of the terpenoid quinones and their heliocide derivates in wild Gossypium species and related genera in the Gossypieae showed considerable diversity which may be used for establishing biochemical and phylogenetic relationships.     

New Withanolides from Nicandra physaloides (Solanaceae)

Two new withanolides, named nicandrenone methyl ether (1), 26S nicandrenone methyl ether (2), together with ten known compounds were isolated from the whole plants of Nicandra physaloides (Solanaceae). Their chemical structures were deduced on the basis of spectroscopic analysis. Ten known compounds were identified as nicandrenone (3), Nic-7 (4), nicaphysalin E (5), pinosylvin monomethyl ether (6), 2S-pinocembrin (7), (1S, 2R)-1, 2-bis (4-hydroxy-3-methoxyphenyl)-1, 3-propanediol (8), vanillin (9), indole-3-carboxylic acid (10), vanillic acid (11) and drummondol (12).     

8-C-Prenylflavonoids from the seed of Tephrosia bracteolata

Four flavonoids in the seeds of Tephrosia bracteolata were identified as the flavanone obovatin methyl ether and the flavones isopongaflavone, trans-tephrostachin and trans-anhydrotephrostachin.     

The effect of farnesyl methyl ether, a mimic of insect juvenile hormone, on Hymenolepis Diminuta in vitro

The effect of farnesyl methyl ether, a mimic of insect juvenile hormone, on Hymenolepis diminuta in vitro. International journal for Parasitology4: 211–218. The inhibition of weight gain of Hymenolepis diminuta in vitro by farnesyl methyl ether (FME) was not dose-dependent, so that there were no differences produced by FME in concentrations from 10^?5 to 10^?13m. At all concentrations of FME used the weight gain over a 6-day culture period was half of that of controls. The FME-treated and control worms were identical to each other in proglottid number and the degree of maturity. Neither the dry to wet weight ratios of worms nor the carbohydrate, protein or lipid ratios were altered by FME. The release of neurosecretory material from the neurosecretory cells in the rostellum (as measured by the degree of their fuchsinophilia) was more advanced in time in the FME-treated worms than in the controls, and it is suggested that this premature release of neurosecretion, triggered either directly or indirectly by traces of FME in the medium, upset a control mechanism in the germinative tissue of the neck region, which determines the mass, but not the number, of the proglottids in the strobila.     

Flavonoids in leaves and inflorescences of australian Cyperus species

A survey of the flavonoids of some 92 species of Australian Cyperus, mainly of subtropical or tropical origin, has confirmed a correlation previously reported in this family between flavonoid pattern and plant geography. The pattern found was similar to that of African and South American Cyperaceae, particularly in the occurrence of the rare marker substance, luteolin 5-methyl ether. Tricin and luteolin are relatively common, in glycosidic form, in the leaves while the flavonol quercetin is infrequent. When present, quercetin occurs either in glycosidic form or free as a methyl ether. The 3-monomethyl and 3, 7-dimethyl ethers of kaempferol and quercetin and the 3, 7, ?-trimethyl ether of quercetin are reported for the first time from the Cyperaceae. The flavonoid pattern of inflorescences is distinct from that of the leaves in that tricin is not detectable and that luteolin 5-methyl ether appears to be replaced by 7, 3′, 4′-trihydroxyflavone. In addition, the aurone aureusidin is more commonly present than in the leaves and is occasionally accompanied by two further aurones. The glycoxanthones mangiferin and isomangiferin occur rarely in all three species examined in the section Haspani, i.e. in C. haspan, C. prolifer and C. tenuispica. In general, however, the flavonoid data do not offer any markers which separate off different sections within the genus; there are, however, some significant correlations between the frequency of the flavonoid classes and subgeneric groupings.     

Linear furocoumarins and other constituents from thamnosma texana

Eight linear furocoumarins and three coumarins were isolated and identified from Thamnosma texana. They were xanthotoxin, imperatorin, bergapten, alloimperatorin methyl ether epoxide, heraclenin, isopimpinellin, psoralen, oxypeucedanin, and the coumarins herniarin, osthol and thamnosmin. The linear furocoumarins appear to be agents that account for the known photosensitizing properties of Thamnosma texana, and consequently its colloquial name, ‘blisterweed.’ This is the first report on the occurrence of imperatorin, heraclenin, oxypeucedanin, herniarin or osthol in any Thamnosma species.     

Synthesis and fungicidal activities of novel benzothiophene-substituted oxime ether strobilurins

Twenty-one novel benzothiophene-substituted oxime ether strobilurins, which employed a benzothiophene group to stabilise the E-styryl group in Enoxastrobin (an unsaturated oxime strobilurin fungicide developed by Shenyang Research Institute of Chemical Industry, China) were designed and synthesised. The biological assay indicated that most compounds exhibited good or excellent fungicidal activities, especially against Colletotrichum lagenarium and Puccinia sorghi Schw. In addition, methyl 3-methoxypropenoate oxime ethers and N-methoxy-carbamic acid methyl esters exhibited good in vivo fungicidal activities against Erysiphe graminis, Colletotrichum lagenarium and Puccinia sorghi Schw. under the tested concentrations. Notably, (E,E)-methyl 3-methoxy-2-(2-((((6-chloro-1-(1H-benzo[b]thien-2-yl)ethylidene)amino)oxy)methyl)phenyl)propenoate (5E) exhibited more potent in vivo fungicidal activities against nearly all of the tested fungi at a concentration of 0.39 mg/L compared to Enoxastrobin.     

Constitution of the santalin pigments A and B

The heartwood of Pterocarpus santalinus contains two major red pigments, santalin-A and santalin-B which are partial methyl ethers of the same polyphenol (santalin). For locating the position of the methoxyl groups, alkali fission and permanganate oxidation of the mixed ethyl methyl ethers are the most convenient. By this method santalin-A has been shown to be 9,1O,12- tri-O-methylsantalin and santalin-B, 9,10,12,4′-tetra-O-methylsantalin.     

Brickellin,a novel flavone from brickellia veronicaefolia and b. chlorolepis

A new highly oxygenated flavone methyl ether has been isolated from Brickellia veronicaefolia and B. chlorolepis. It has been identified as 5,6′-dihydroxy-6,7,2′,3′,4′-pentamethoxyflavone and given the name brickellin.     

Enzymes involved in the anoxic utilization of phenyl methyl ethers by <Emphasis Type="Italic">Desulfitobacterium hafniense</Emphasis> DCB2 and <Emphasis Type="Italic">Desulfitobacterium hafniense</Emphasis> PCE-S

Phenyl methyl ethers are utilized by Desulfitobacterium hafniense DCB2 and Desulfitobacterium hafniense PCE-S; the methyl group derived from the O-demethylation of these substrates can be used as electron donor for anaerobic fumarate respiration or dehalorespiration. The activity of all enzymes involved in the oxidation of the methyl group to carbon dioxide via the acetyl-CoA pathway was detected in cell extracts of both strains. In addition, a carbon monoxide dehydrogenase activity could be detected. Activity staining of this enzyme indicated that the enzyme is a bifunctional CO dehydrogenase/acetyl-CoA synthase.