Plagiochilines C,D, E and F,four novel secoaromadendrane-type sesquiterpene hemiacetals from Plagiochila asplenioides and Plagiochila semidecurrens

Four novel secoaromadendrane-type sesquiterpene hemiacetals, plagiochilines C, D, E and F, together with the previously known (?)-bicyclogermacrene, have been isolated from the liverwort, Plagiochila asplenioides and their structures have been spectroscopically elucidated. From Plagiochila semidecurrens plagiochilines A and C have been obtained along with (?)-bicyclogermacrene and its related sesquiterpene hydrocarbons.     

Insect antifeedant secoaromadendrane-type sesquiterpenes from Plagiochila species

The characteristic pungency of the liverworts Plagiochila species P. fruticosa, P. hattoriana, P. ovalifolia and P. yokogurensis is due to a new ent-secoaromadendrane-type sesquiterpene hemiacetal, plagiochiline A, which exhibits very strong antifeedant activity against the African army worm, Spodoptera exempta at 1–10ng/cm². Two new secoaromadendranes, plagiochilide and furanoplagiochilal A, together with the previously known plagiochiline C were isolated from P. yokogurensis. Plagiochilal A, which may be a precursor of plagiochilide and its related hemiacetals, and a bitter principle, plagiochiline B were also isolated from P. hattoriana. P. ovalifolia contained plagiochilines A, B and C. From P. fruticosa, plagiochilide and plagiochilines A, B and C were isolated. The structures of the new secoaromadendrane-type sesquiterpenes were elucidated by extensive ¹H NMR and ¹³CNMR studies.     

Sesquiterpene lactones from Artemisia herba alba

A new chemotype of Artemisia herba alba has been analysed and been shown to contain two known sesquiterpene lactones, herbolides E and F, and three new ones, herbolides G, H and I.     

Three new dolabrane diterpenes from the Chinese mangrove plant of Ceriops tagal

Three new dolabranes, tagalenes G − I (1 − 3), together with five known analogues (4 − 8), were isolated from the twigs of the Chinese mangrove, Ceriops tagal. Their structures were determined on the basis of extensive spectroscopic analysis and the comparison with the previous data. Tagalene G (1) is a 16-nordolabrane with a 15-hydroxymethyl scaffold, tagalene H (2) possesses an 18-hydroxymethyl moiety, whereas tagalene I (3) is a further addition to the small group of dolabranes with a rare 4, 18-epoxy ring. Compounds 6 − 7 were isolated from C. tagal for the first time.     

Physalins E and H,new physalins from Physalis angulata and P. lancifolia

From the stems and leaves of Physalis angulata and P. lancifolia, the isolation of five new physalins E, F, G, H and I is reported. The structures of physalins E and H are established respectively as 5,6-dihydro-5α,7α-dihydroxy and 7β-hydroxy derivatives of physalin B.     

Immunomodulatory sesquiterpene glycosides from Dendrobium nobile

Four sesquiterpene glycosides with alloaromadendrane, emmotin, and picrotoxane type aglycones were isolated from the stems of Dendrobium nobile Lindl (Orchidaceae). Their structures were determined by spectroscopic methods and chemical reactions. Immunomodulatory activity of the isolates was evaluated in vitro.     

Two guaiane-type sesquiterpene lactones and their related sesquiterpene lactones from Porella japonica

Two new guaiane-type sesquiterpene dilactones, porelladiolide and 3α,4α-epoxyporelladiolide and a new germacranolide, 3β-hydroxycostunolide, together with the previously known germacranolides, guaianolides, pinguisane-type sesquiterpenes, and a sacculatane-type diterpene dialdehyde have been isolated from the liverwort, Porella japonica and their structures have been established by the spectral evidence and some chemical transformations. Porelladiolide, 3α,4α-epoxyporelladiolide and the sesquiterpene with α-methylene γ-lactone group showed inhibitory activity toward the germination and growth of roots of rice in the husk.     

Three ent-eudesmenones from the liverwort Plagiochila bifaria

The essential oil of the liverwort Plagiochila bifaria was analysed by GC and GC-MS. Three eudesmane type sesquiterpenes, ent-eudesm-4-en-6-one, ent-eudesm-4(15)-en-6-one, ent-7-hydroxyeudesm-4-en-6-one were isolated and identified as new natural products. Structure elucidation and the determination of absolute configurations are described.     

Three acetylated polyacetylenes from the roots of Panax ginseng

Three new acetylated polyacetylenes named ginsenoynes F, G and H were isolated from the hexane extract of the roots of Panax ginseng. The structures were determinated by spectral and chemical methods.     

Neurotrophic secoaromadendrane-type sesquiterpenes from the liverwort Plagiochila fruticosa

A new sesquiterpene dialdehyde, plagiochilal B, isolated from the liverwort Plagiochila fruticosa exhibits not only acceleration of neurite sprouting but also enhancement of choline acetyltransferase activity on a neuronal cell culture of fetal rat cerebral hemisphere at 10⁻⁵ M. Additionally, two new secoaromadendranes, plagiochilines J and K were isolated. The structures of the new secoaromadendrane-type sesquiterpenes were established by extensive 2D NMR data and chemical correlation with plagiochiline A.     

Bullatantriol,a sesquiterpene from annona bullata

Bullatantriol has been isolated from Annona bullata. Its constitution and relative configuration have been established by X-ray analysis. Its absolute configuration has been assigned by chiroptical investigation of the corresponding 7-ketone.     

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).     

New physalins from Physalis angulata and Physalis lancifolia. Structure and reactions of physalins D,I, G and K

The structures of physalins I, G and K are established respectively as 5,6-dihydro-5α-methoxy-6β-hydroxy, 4,5-dehydro-5,6-dihydro-4β-hydroxy and 5,6-dihydro-4α,5α-epoxy-6α-hydroxy derivatives of physalin B. The chemistry of physalin D, and the synthesis of physalins D and I from physalin F and physalin K from physalin G are described.     

通光藤甙F,G,H和I结构

从通光藤(Marsdeniatenacissima)的茎中分离得到4个新的C21甾体甙———通光藤甙F(3),G(4),H(5)和I(6),以及2个已知化合物通光藤甙A(1)和B(2)。根据光谱数据和化学方法推定了其结构。同时,通过COLOC谱和二维核磁共振谱指定了这些化合物中甙元上11和12位的酯基确切连接位置。     

Lyonin A, a new 9,10-Secograyanotoxin from Lyonia ovalifolia

Phytochemical studies on the branches and leaves of Lyonia ovalifolia yielded a new grayanane diterpenoid, lyonin A ( 1 ), together with two known compounds, secorhodomollolides A and D ( 2 and 3 , resp.). The structure of 1 was elucidated by combination of 1D‐ and 2D‐NMR, and MS analyses. Compound 1 turned out to be a new, highly O‐acylated grayanane diterpenoid, of which ring B has undergone an oxidative cleavage between C(9) and C(10), yielding a system differing from the previously reported grayanane type with a 5/7/6/5 ring system. Results of the cAMP regulation activity assay showed that compounds 2 and 3 at 50 μM induced a significantly decreased cAMP level in N1E‐115 neuroblastoma cells (p<0.001), indicating neuropharmacological potential.     

Elemanolide sesquiterpenes and eudesmane sesquiterpene glycosides from Centaurea hierapolitana

Two elemanolide sesquiterpenes and two eudesmane-type sesquiterpene glycosides named hierapolitanins A-D, were isolated, together with five known compounds, two flavones; hispidulin and jaceosidin, a flavon-C-glycoside, shaftoside, a flavonol glycoside, kaempferol-3-O-rutinoside and a neolignan, dehydrodiconiferyl alcohol from the aerial parts of Centaurea hierapolitana Boiss. (Asteraceae). Structure elucidations were based on spectroscopic evidence.     

Argophyllone-B,a sesquiterpene lactone from Helianthus argophyllus

The sesquiterpene lactone, 2-methyl-2-butenoic acid dodecahydro-4-(hydroxymethyl)-10a-methyl-8-methylene-3,7-dioxooxineno[5,6]cyclodeca[1,2-b]furan-9-yl ester [1aR^*-[1aS^*,4R^*,5aS^*,8aR^*,9R^*(E)]], argophyllone-B, was isolated from acetone extracts from the leaves of Helianthus argophyllus. Its structure has been determined by single crystal X-ray analysis. Complete ¹H NMR and ¹³C NMR assignments have been made.