ent-Kaurane diterpenes from the stem bark of Annona vepretorum (Annonaceae) and cytotoxic evaluation

This work describes a novel ent-kaurane diterpene, ent-3β-hydroxy-kaur-16-en-19-al along with five known ent-kaurane diterpenes, ent-3β,19-dihydroxy-kaur-16-eno, ent-3β-hydroxy-kaur-16-eno, ent-3β-acetoxy-kaur-16-eno, ent-3β-hydroxy-kaurenoic acid and kaurenoic acid, as well as caryophyllene oxide, humulene epoxide II, β-sitosterol, stigmasterol and campesterol from the stem bark of Annona vepretorum Mart. (Annonaceae). Cytotoxic activities towards tumor B16-F10, HepG2, K562 and HL60 and non-tumor PBMC cell lines were evaluated for ent-kaurane diterpenes. Among them, ent-3β-hydroxy-kaur-16-en-19-al was the most active compound with higher cytotoxic effect over K562 cell line (IC₅₀ of 2.49 μg/mL) and lower over B16-F10 cell line (IC₅₀ of 21.02 μg/mL).     

Isoquinoline alkaloids from the leaves of Annona leptopetala (Annonaceae)

The phytochemical investigation of the leaves of Annona leptopetala (R. E. Fr.) H. Rainer led to the characterization of tetrahydroprotoberberine corypalmine, and four aporphine (laurotetanine, anonaine, norannuradhapurine and nornuciferine) alkaloids. The structures were established after analysis of their NMR spectral data including 2D NMR experiments. This is the first report of laurotetanine and nornuciferine in A. leptopetala as well as norannuradhapurine in the genus Annona. The ¹³C NMR data of the natural alkaloid norannuradhapurine are reported here for the first time, and the NMR data for the compound corypalmine are reviewed.     

Isoquinoline alkaloids from the leaves of Xylopia laevigata (Annonaceae)

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Natural products from the medicinal plant Duguetia staudtii (Annonaceae)

The phytochemical investigation of the ethyl acetate soluble fraction of Duguetia staudtii stem bark led to the isolation of eight compounds consisting into a new bisnorlignan named pachypolignan (1), a known bisnorlignan (2), four flavonoids (3–6), one alkaloid (7), and one triterpenoid (8). The structures of all the compounds were established with help of spectral data including IR, UV, MS, 1D- and 2D-NMR spectroscopic data, as well as by comparison with previously-reported data in literature. The anti-inflammatory and urease inhibitory activities of the isolated compounds were assessed. Furthermore, the chemotaxonomic significance of these compounds was discussed.     

Chemical constituents from the bark of Annona salzmannii (Annonaceae)

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Highlights? Bark of Annona salzmannii yielded sesquiterpenes, steroids, and isoquinoline alkaloids. ? Isoquinoline alkaloids are the chemotaxonomic marker of the genus Annona. ? The NMR data for reticuline (12) were revised. ? Selin-11-en-4α-ol (3) is reported for the first time in the genus Annona.     

Chemical constituents from the leaves and branches of Annona coriacea Mart. (Annonaceae)

The phytochemical investigation of the leaves and branches of Annona coriacea Mart. (Annonaceae) led to the isolation and characterization of eight compounds: five isoquinoline-derived alkaloids, including pukateine (1), liriodenine (4), anonaine (5), obovanine (6), and norisocorydine (7); one terpene lactone known as loliolide (3); one benzoic acid derivative, 2-methoxybenzoic acid (2), and 3,4,5-trimethoxyphenol (8). All compounds, except liriodenine, are being described for the first time in the species A. coriacea, and their chemophenetics relationships were discussed. The structures were elucidated by extensive analyses of 1D and 2D NMR (COSY, HSQC, and HMBC) spectroscopy in combination with MS, and the data were compared with literature values. The NMR dataset of pukateine and obovanine was reviewed. Our results showed that A. coriacea is a typical species of the Annonaceae family and an important source of aporphine alkaloids with chemophenetic relationships with Xylopia, Duguetia, Guatteria, Artabotrys, and Goniothalamus genera.     

Isoquinoline-derived alkaloids from the bark of Guatteria olivacea (Annonaceae)

Phytochemical investigation of the bark of Guatteria olivacea R. E. Fries (Annonaceae) led to the isolation and identification of ten isoquinoline-derived alkaloids, including three phenanthrenes, atherosperminine, argentinine, and atherosperminine N-oxide; three aporphines, asimilobine, puterine, and discoguattine; two oxoaporphines, liriodenine and oxoputerine; and two tetrahydroprotoberberines, corypalmine and discretine. All these alkaloids are described for the first time in G. olivacea and their chemotaxonomic significance was discussed. The structure elucidation of these isolated alkaloids was established by extensive analyses of 1D and 2D NMR spectroscopy in combination with MS. The NMR data for atherosperminine, argentinine, and atherosperminine N-oxide were reviewed.     

Aporphine alkaloids from the stem bark of Guatteria pogonopus (Annonaceae)

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紫玉盘中的新内酰胺

从紫玉盘(UvariamicrocarpaChamp.exBenth.)的茎枝分离到7个生物碱,经光谱数据分析鉴定为紫玉盘内酰胺(uvarilactam,1)、马兜铃内酰胺AⅡ(2)、马兜铃内酰胺BⅠ(3)、马兜铃内酰胺BⅡ(4)、马兜铃内酰胺AⅠa(aristololactamAⅠa,5)、4,5_dioxodehydroasimilobine(6)和oxoanolobin(7)。1～5属于菲甲酸内酰胺类化合物,6～7是阿扑菲生物碱类,化合物3与4以混合物出现。其中1是新化合物,其余化合物均首次从该植物中分离得到     

A new species of Annona (Annonaceae) from the northeastern Guayana Shield

Annona prevostiae, a new species from the northeastern margin of the Guayana Shield, is described and illustrated.     

Alkaloids of Toddalia asiatica (Rutaceae)

Phytochemical investigation of the alkaloidal extract of the roots of Toddalia asiatica led to the isolation of a new seco-benzophenanthridine alkaloid (1) and twelve known alkaloids (2–13). The new structure was elucidated by means of spectroscopic analysis, and the known alkaloids were identified by comparison with the literature. Among these alkaloids, 1 and 5–7 were reported from the genus Toddalia for the first time. The distribution of the isolated alkaloids at genus/family level was presented via network analysis and their chemotaxonomic significance was also discussed.     

Phylogenetics of Annona cherimola (Annonaceae) and some of its closest relatives

Annona cherimola is a woody perennial species in the Annonaceae family that produces edible fruits and has economic importance in several regions of the world with subtropical climates. Together with other 10‐12 species, A. cherimola belongs to the section Atta of the Annona genus with a center of origin in Central America and the Caribbean. Species of the section Atta produce soft skin ripe fruits with raised areoles bounded by recessed furrows. Annona cherimola is the only species of the section naturally found in the Andean region of South America. Currently, no information is available at the molecular level on the phylogenetic relationships of most of the species of Atta and closely related sections in Annona. In order to fill this gap, in this work a phylogenetic approach was performed using five coding and non‐coding plastid DNA regions, to determine the phylogenetic relationships between A. cherimola and other related species included in Atta and other sections of the genus. The results obtained support recent studies that demonstrated the likely Mesoamerican origin of A. cherimola based on biogeographical analysis with SSR markers, rather than the previously considered South American origin hypothesis. In addition, the species belonging to the Atta section did not show monophyly. Finally, A. cherimola and A. pruinosa seem to be phylogenetically close species and additional studies are needed to discern the relations between them.     

Isoquinoline-derived alkaloids and one terpene lactone from the leaves of Duguetia pycnastera (Annonaceae)

The phytochemical investigation from the leaves of Duguetia pycnastera Sandwith (Annonaceae) led to the isolation and identification of ten compounds: nine isoquinoline-derived alkaloids, including five aporphines, anonaine, isopiline, O-methylisopiline, nornuciferine, and norstephalagine; three oxoaporphines, O-methylmoschatoline, liriodenine, and lysicamine; and one tetrahydroprotoberberine, isocorypalmine; in addition, one C₁₁-terpene lactone known as loliolide. The isolated compounds (except for O-methylmochatoline and lysicamine) are described for the first time in the species and their chemophenetics relationships were discussed. The occurrence of loliolide is reported for the first time in the Duguetia. The structure elucidation of these compounds was established by extensive analyzes of 1D and 2D NMR spectroscopy in combination with MS. The NMR spectroscopic data for norstephalagine and isocorypalmine were reviewed.     

中国瓜馥木属植物叶片结构的解剖观察

采用叶片表皮离析法、扫描电镜和石蜡制片法,研究了中国分布的番荔枝科瓜馥木属19种植物叶片的形态结构。结果表明:瓜馥木属叶片形态和结构具有较多的相似性,如叶片表皮均具有2-多个细胞的单列丝状毛,表皮细胞内具有一个晶簇,气孔器均为平列型,只分布在叶片的远轴面,远轴面的表皮细胞平周壁形成一个乳突,叶片主脉的维管组织除具有正常的维管组织外,还具有一个小的副维管束等,这些特征有助于区分番荔枝科植物的属间关系,支持瓜馥木属是一个很自然的类群。但叶片表皮毛的形态及分布,表皮细胞的形状、叶肉中栅栏组织和海绵组织的结构、远轴面的乳突大小以及叶主脉维管组织的细微结构则具有种间差异。尤其有助于区分小萼瓜馥木和黑风藤、广西瓜馥木和独山瓜馥木、上思瓜馥木和东方瓜馥木等形态相似、难以区分的植物种类。该研究结果为该属的系统研究和种间正确区分提供了重要资料。     

Five new alkaloids from Aconitum apetalum (Ranunculaceae)

Twenty-one alkaloids, including five new ones, acoapetaldines A–E (1–5), were isolated from the whole plants of Aconitum apetalum. Among them, 1 is an aconitine-type diterpenoid alkaloid, 2 and 3 are aporphine alkaloids and 4 and 5 are napelline-type diterpenoid alkaloids. The structures of the new alkaloids were elucidated by spectroscopic data analysis and that of acoapetaldine D (4) was confirmed by single crystal X-ray crystallography. Acoapetaldine A (1) and aconorine (12) exhibited moderate anti-tobacco mosaic virus (anti-TMV) activity, while corydine (15) displayed moderate antimicrobial activity against Pseudomonas aeruginosa.     

Alkaloids from the leaves of Isatis indigotica fortune and their chemotaxonomic significance

From the leaves of Isatis indigotica Fortune, one new alkaloid, namely (2E)-N-(2-hydroxyphenyl)-2-(1-hydroxy-3-oxoindolin-2-ylidene) acetamide (1), together with four known ones, such as phaitanthrin D (2), methyl quindoline-11-carboxylate (3), cephalandole B (4) and 2,2-di (3-indolyl)-3-indolone (5) were isolated and identified. The structure of compound 1 was elucidated by means of spectroscopic analysis, including HRESIMS together with 1D and 2D NMR experiments. Compounds 1, 2 and 5 were obtained from this genus for the first time. Chemotaxonomic significance of these compounds is described herein.     

Chemophenetics as a Tool for Distinguishing Morphotypes of Annona emarginata (Schltdl.) H. Rainer

Annona emarginata (Annonaceae) has two morphological variations (A. emarginata ‘mirim’ and A. emarginata ‘terra-fria’). The species has agricultural value and produces specialized metabolites of pharmacological interest. The objective of this work was to analyze whether chemical and morphological differences contribute to differentiate A. emarginata ‘terra-fria’ from A. emarginata ‘mirim’, as chemophenetic variations of A. emarginata. The analysis of chemical compounds was based on the quantification, profile of root alkaloids and on the leaves volatile profile, together with morphometric analyses of the leaf blade. The samples were collected in three phenological stages (flowering, fruiting, and vegetative) at two places in São Paulo, Brazil. Differences in the composition of the alkaloid profile and leaf volatiles (in both places and in the three phenological stages) allowed us to separate the two morphotypes by multivariate statistical analysis. These differences agreed with the leaf blade morphology and flower color. This first chemophenetic report of A. emarginata demonstrates that, in addition to morphological variations, the specialized metabolism of roots and leaves can be phytochemical characters, which suggest the existence of at least morphochemotypes of A. emarginata.