茎花葱臭木化学成分的研究

从茎花葱臭木种子中分离得到5个化合物,经理化与波谱分析鉴定为β-谷甾醇(1)、没食子酸乙酯(2)、胡萝卜苷(3)、1-O-β-D-吡喃葡萄糖基-(2S,3S,4R,8Z)-2-N-(2 ′-羟基二十四烷酰氨基)十八二氧鞘氨-8-烯(4)和2,3,2″,3″-四氢穗花杉双黄酮(5).这5个化合物均首次从该植物中分离得到.其中化合物5进行细胞毒活性测试,没有显示抑制活性.     

Terpenes from leaves of Guarea macrophylla (Meliaceae)

The dichloromethane extract from the leaves of Guarea macrophylla (Meliaceae) was submitted to adsorption chromatography. Guai-6-en-10beta-ol, isopimara-7,15-dien-2alpha-ol and cycloarta-23,25-dien-3-one were isolated and identified by spectroscopic data, mainly by 1H and 13C NMR analyses; eight other known terpenoids were also isolated.     

The pollen of Dysoxylum (Meliaceae): the demise of Pseudocarapa

An account of the pollen morphology found in the genera Dysoxylum and Pseudocarapa (Meliaceae) is presented. Pollen grains are illustrated by means of electron and some light micrographs. The majority of taxa release grains as tetra-colporate monads. Tetrads have previously only been known in Pseudocarapa. They are also recorded here in three species of Dysoxylum. The taxonomic implications of this are discussed and Pseudocarapa is reduced to a synonym of Dysoxylum.     

Chrotacumines E and F,Two New Chromone‐Alkaloid Analogs from Dysoxylum acutangulum (Meliaceae) Leaves

A chemical investigation of the alkaloidal fraction of Dysoxylum acutangulum leaves led to the isolation and characterization of two new chromone alkaloid analogs named chrotacumines E and F ( 1 and 2 , resp.). Structure elucidation of 1 and 2 was achieved by spectroscopic analyses, including 2D‐NMR. Both of these alkaloids exhibited modest activities as tyrosinase inhibitors with 29.2 and 25.8% inhibition at 100 μg/ml, respectively.     

Cytotoxic steroids from the leaves of Dysoxylum binectariferum

Four new cholestane-type (1–4) and two new ergostane-type (5, 6) steroids were isolated from the leaves of Dysoxylum binectariferum. Their structures were elucidated on the basis of spectroscopic analysis, including 1D and 2D NMR techniques. The absolute configurations were established by comparison with the literature and Mo₂(OAc)₄-induced electronic circular dichroism (ECD) data. All the isolates were evaluated for cytotoxicity against A549 (lung carcinoma), MCF-7 (breast adenocarcinoma), and HepG2 (hepatocellular carcinoma) human cancer cell lines. Three of the new cholestane-type steroids displayed potent antiproliferative effects on the tumor cells with IC₅₀ values ranging from 1.5 to 9.6 μM, whereas the two new ergostane-type (5, 6) steroids were deemed inactive.     

Effects of Dysoxylum malabaricum Bedd. (Meliaceae) extract on the malarial vector Anopheles stephensi Liston (Diptera: Culicidae)

In recent years, use of environmentally friendly and biodegradable natural insecticides of plant origin have received renewed attention as agents for disease vector control. Methanol extracts of leaves from the Indian white cedar Dysoxylum malabaricum Bedd. (Meliaceae) were tested against mature and immature Anopheles stephensi Liston (Diptera) mosquitoes under laboratory conditions. The extract showed strong larvicidal, pupicidal, adulticidal, and antiovipositional activity. The maximum leaf extract concentration tested in this study was 4%, which produced pronounced effects. In general, first and second instars were more susceptible to leaf extract than older insects. Clear dose-response relationships were established, with the highest dose of 4% plant extract causing 97% mortality of first instars.     

Limonoids from Turraea floribunda (Meliaceae)

Six novel limonoids and limonoid derivatives, turraflorins D-I along with the known turraflorins A and B have been isolated from seed of the South African Turraea floribunda (Meliaceae).     

Oleanane trietrpenoids from Cedrela montana (Meliaceae)

Two new oleanane-type triterpenes, characterized as 3-oxo-11alpha,12alpha-epoxy-oleanan-28,13beta-olide and 3-oxo-olean-11-en-28,13beta-olide , were isolated from the fruits and seeds of Cedrela montana (Meliaceae). In addition, the known compounds oleanonic acid, a mixture of beta-sitosterol and stigmasterol, and the limonoid photogedunin were also isolated. The structures of the new compounds were established by spectroscopic methods, including 2D NMR.     

Tetranortriterpenoid derivatives from Turraea parvifolia (Meliaceae)

The methanol extract of the seeds of Turraea parvifolia has yielded seven novel triterpenoid derivatives: 12alpha-acetoxyazadironolide, turraparvin A (12alpha-acetoxy-7alpha,23-dihydroxy-24,25,26,27-tetranor-3-oxoapotirucalla-1,14,20(22)-trien-21,23-olide), turraparvin B (12alpha-acetoxy-7alpha,21-dihydroxy-24,25,26,27-tetranor-3-oxoapotirucalla-1,14,20(22)-trien-23,21-olide), turraparvin C (7alpha,12alpha-diacetoxy-21-hydroxy-24,25,26,27-tetranor-3-oxoapotirucalla-1,14,20(22)-trien-23,21-olide), 11-epi-21-hydroxytoonacilide, 11-epi-23-hydroxytoonacilide and turraparvin D (12alpha-acetoxy-7alpha-hydroxy-24,25,26,27-tetranor-3-oxoapotirucalla-1,14,20(22)-trien-21,23-lactam).     

Indeterminate leaves of Chisocheton (Meliaceae): survey of structure and development

Pinnately compound leaves in the Malesian genus Chisocheton (Meliaceae) have leaf-tip buds that continue to produce new pinnae (leaflets) periodically for many years. Juvenile leaves form a terminal pinna in place of the leaf-tip bud found in adult leaves. The histology of an old leaf-tip bud is similar to the entire leaf primordium in other species of Meliaceae with large pinnate leaves (e.g. Chukrasia and Dysoxylum ) which serve as examples of more typical leaves. Pinna initiation from this meristem continues after the first stage of leaf expansion as seen in the relatively constant number of pinna primordia in a large sampling of leaf-tip buds of varying ages. Structure and development are compared in leaves of nine species of Chisocheton , out of a total of approxiamtely 50 species in the genus. Species having small leaves (e.g. C. pentandrus ) show more branch-like, indeterminate leaf growth as compared with species with large leaves (e.g. C. macranthus ). The structure and development of leaves of Chisocheton are like the similar indeterminate leaves of the American and African genus Guarea . Some authors have used the indeterminate leaves of Chisocheton and Guarea as examples of intermediate organs showing 'fuzzy morphology' or 'partial homology.' Nevertheless, these unusual organs are considered here as being homologous with leaves of other Meliaceae based on their position, histology and ontogeny. © 2002 The Linnean Society of London, Botanical Journal of the Linnean Society , 2002, 139 , 207–221.     

Insecticidal rocaglamide derivatives from Aglaia spectabilis (Meliaceae)

Bark of Aglaia spectabilis collected on the island of Phu Quoc (Vietnam) yielded insecticidal cyclopentatetrahydrobenzofurans of the rocaglamide type including four new natural products. Structure elucidation of the new compounds is described. All rocaglamide derivatives isolated exhibited strong insecticidal activity towards neonate larvae of the polyphagous pest insect Spodoptera littoralis when incorporated into an artificial diet. LC50 values varied from 0.8 to 80 ppm. The most active compounds isolated, methylrocaglate and C-3' hydroxylmethylrocaglate, were similar with regard to their insecticidal activity to the well-known natural insecticide azadirachtin.     

Cytotoxic sesquiterpenoids from Dysoxylum parasiticum (Osbeck) Kosterm. stem bark

Two undescribed sesquiterpenoid derivatives, 10β,11-dihydroxy-1β-hydroperoxide-4αH,5αH,7βH-guaiane (1) and 10β-hydroxy-4α,4β-dimethyl-5αH,7αH-eudesm-3-one (2) along with three known of guaiane, aromadendrane, and cadinane sesquiterpenoids (3-5) were isolated from the stem bark of Dysoxylum parasiticum (Osbeck) Kosterm. The chemical structure of the compounds were determined by detailed analysis of spectroscopic data, including MS, IR, 1D, and 2D NMR as well as through comparison with data of known analogues. The isolated compounds were also tested for cytotoxic properties against MCF-7 breast cancer line. Compound 4, was found to exhibit the strongest cytotoxic activity with an IC₅₀ value of 12.17 μM, while the other compounds showed moderate or no activity.     

Limonoids from the West African Trichilia welwitschii (Meliaceae)

The seeds of Trichilia welwitschii C.DC. (Meliaceae) yielded three limonoids, dregeanin DM4 (1), reported here from a natural source for the first time, the known rohituka 3 (2) and trichilia lactone D5 (3). The bark yielded 28,29-dinorcycloart-24-ene-3,4,6-triol (4), sitosterol-3-O-β-d-glucoside, 4-hydroxy-N-methyl-l-proline, stigmasterol and sitosterol.     

浆果楝中的新木脂素(英文)

从浆果楝(Cipadessa baccifera)中分离得到两个木脂素,其化学结构通过波谱方法鉴定为:(-)-9′-O-(E)-coumarate-5,5′-dimethoxylariciresinol(1)和(+)-9′-O-(E)-feruloyl-5,5′-dimethoxylariciresinol(2)。其中化合物1为新化合物。     

浆果楝中的新木脂素

从浆果楝（Cipadessa baccifera）中分离得到两个木脂素,其化学结构通过波谱方法鉴定为：（-）-9′-O-（E）-coumarate-5,5′-dimethoxylariciresinol（1）和（＋）-9′-O-（E）-feruloyl-5,5′-dimethoxylariciresinol（2）。其中化合物1为新化合物。     

A New Pregnane from Munronia delavayi Franc （Meliaceae）

To search for pharmacologically active constituents of folk medicine, a new pregnane, 2α,3α,15β-trihydroxy-20（S）-tigloyl-pregnane （compound 1）, and nine known compounds, geranylgeraniol （compound 2）, β-daucosterol （compound 3）, 6-hydroxystigmast-4oen-3-one （compound 4）, sitoindoside Ⅰ （compound 5）, sitoindoside Ⅱ （compound 6）, β-sitosterol （compound 7）, kaempferol （compound 8）, quercetin （compound 9）, and rutin （compound 10）, were isolated from the ethanol extract of whole plants of Munronia delavayi Franch using chromatographic methods. The structures of compounds 1-10 were elucidated on the basis of spectral data.     

Antifeeding activity of limonoids from Khaya senegalensis (Meliaceae)

Abstract: Fifteen B,D-secolimonoids of mexicanolide, rearranged phragmalin, methyl angolensate and glycoside types have been isolated from ether and acetone extracts of the stem bark of Khaya senegalensis (Desr.). The antifeedant activity of the isolated compounds was assessed by conventional choice leaf disc method on the third-instar larvae of Spodoptera littoralis (Boisd.). Khayalactol, 1- O -acetylkhayanolide A, 2-hydroxyseneganolide, khayanolide A, khayanolide D and methyl angolensate displayed strong antifeedant activity at 1000  μ g/ml with antifeedant percentages of 83.8, 61.9, 60.1, 59.5, 57.1 and 55.7, respectively. 2-Hydroxyseneganolide and khayanolide D showed high activity at 500, 300 and 200  μ g/ml while 1- O -acetylkhayanolide A was the only compound that revealed antifeedant activity at a concentration as low as 100  μ g/ml. Antifeedant activity was dose-dependent in some of the isolated compounds. Correlation between antifeedant activity of the isolated compounds and chemical structure was discussed.