Segetoside L, A New Triterpenoid Saponin from Vaccaria segetalis

A new triterpenoid saponin, named segetoside L, was isolated from the seeds of Vaccaria segetalis. On the basis of spectral data and chemical reaction, its structure was established as 28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl oleanolic acid 3-O-β-D-glucopyranosyl-(1→3)- [β-D-galactopyranosyl-(1→2)]-β-D-galactopyranoside.     

A New Triterpenoid Saponin from the Seeds of Vaccaria segetalis

A new triterpenoid saponin, named segetoside k, has been isolated from the seeds of Vaccaria segetalis.On the basis of chemical reaction and spectral analysis, the structure of segetoside K was established as: olean-12-ene-23a ,28b -dioic acid 3b , 16a -dihydroxy-28-O-[b -D-glucopyranosyl-(1→ 3)]-b -D-glucopyra-nosyl-(1→ 2)-b -D-glucopyranosyl-(1→ 6)-b -D-gluco-pyranoside(1).     

Triterpenoid Saponins from Vaccaria segetalis

Four novel triterpenoid saponins, Vaccariside B‐E (1–4), were isolated from the seeds of Vaccaria segetalis and their structures were elucidated as 3‐O‐β‐D‐galactopyranosyl‐(1–2)‐β‐D‐glucuronopyranosyl quillaic add 28‐O‐β‐D‐xylopyranosyl‐(1–3)‐α‐L rhamno‐pyranosyl‐(1–2)‐[α‐L‐arabinofura‐nosyl‐(1–3)]‐4‐O‐acetyl‐β‐D)‐fucopyranoside (1), 3‐O‐β‐D‐galactopyranosyl ‐ (1–2) ?3‐O‐acetyl‐β‐D ‐ glucuronopyranosyl quillaic acid 28‐O‐β‐D‐xylopyranosyl‐(1–3)‐α‐L‐rhamnopyra‐nosyl‐(1–2)‐[α‐L‐arabinofuranosyl‐(1–3)]‐4‐O‐acetyl‐β‐D‐fucopyranoside (2), 3‐O‐β‐D‐galactopyranosyl‐(1–2)‐β‐D‐glucuronopyranosyl quillaic add 28‐O‐α‐L‐arabinopyranosyl‐(1–3)‐α‐L‐rhamnopyranosyl‐(1–2)‐[α‐L‐arabinofuranosyl‐(1–3)]‐4‐O‐acetyl‐β‐D‐fucopyranoside (3), 3‐O‐β‐D‐galacto‐pyranosyl‐(1–2)‐[β‐D‐xytopyranosyl‐(1–3)]‐β‐D‐glucurono‐pyranosyl quillaic add 28‐O‐β‐D‐xylopyranosyl‐(1–3)‐α‐L‐rhamnopyranosyl‐(1–2)‐[α‐L‐arabinofuranosyl‐(1–3)]‐4‐O‐acetyl‐β‐D‐fucopyranoside (4), respectively.     

A New Triterpenoid Saponin from the Seeds of Deccaria segetalis

The seeds of Vaccaria segetalis (Neck) Garcke, which is distributed all over China,except southern China, are used in Chinese folk medicine for promoting diuresis,activating blood circulation and relieving carbuncles 1. Previous studies on the seeds ofthis plant have led to the isolation of seven cyclic peptides 2-5 and several saponins 6-]o.We have repoyted the isolation and structural elucidation of Segetosides A, C-E from theseeds of Vaccaria segetalis I I-13. FuFther investigation of…     

A New Triterpenoid Saponin from Aralia subcapitata

The plants of Aralia genus are used as folk medicines for rheumathism, hepatitis and bruise in China 1. Aralia subcapitata Hoo is distributed in Anhui Province of China and also used for the treatment of diabetes. Yang et al. 2 reported the isolation of four known triterpenoids from this plant. In this paper, we report the structural elucidation of a new triterpenoid saponin, subcapitatoside A, isolated from the roots of this plant. Figure 1: structure of compound 1 Subcapitatoside A (1), …     

川麦冬中的新呋甾皂苷的分离与鉴定

从川麦冬块根总皂苷中分离并鉴定了4个双糖链甾体皂苷化合物, 其中化合物1为新化合物, 化合物2~4是已知化合物.     

A sensitive and selective LC‐MS/MS method for the quantitative determination of segetalin A from the plasma of rats

A sensitive and selective LC‐MS/MS method was developed and validated for the determination and pharmacokinetic investigation of segetalin A in rat plasma. Sample preparation was accomplished through a simple SPE procedure for the removal and preconcentration of the analyte and IS. Plasma samples were separated by HPLC on a Symmetry C₁₈ column using a mobile phase consisting of methanol and 0.1% formic acid in water (70:30, v/v) with isocratic elution. The quantification was performed using multiple reaction monitoring with the transitions m/z 610.3 → 511.2 for segetalin A and m/z 779.4 → 751.4 for IS, respectively. The calibration curve was linear over the range of 8.0–4000 ng/mL with a limit of quantitation (LOQ) of 8.0 ng/mL. This method was applied in a pharmacokinetic study of segetalin A in rats. For intravenous (i.v.) administration, the plasma concentrations of segetalin A decreased quickly (t_1/2z, 1.31 ± 0.341 h). For oral administration, the plasma concentrations of segetalin A increased to a peak value at 1.50 ± 0.577 h, followed by a gradual decrease to the LOQ in 12 h. The mean AUC values after i.v. and oral administration were 553 ± 105 and 1482 ± 110 ng h/mL, respectively. Copyright © 2015 John Wiley & Sons, Ltd.     

A New Furospirostanol Saponin, Ophiofurospiside B from Ophiopogon japonicus（ Thunb. ） Ker-Gawl

Introduction The tuber ofOphiopogon japonicus(L.f)KerGawl,which is a Chinese traditional medicine named "maidong"have been recorded to have various medical functions for curing cardiovascular diseases and bacterial infections,especially heart diseases.Phytochemical studies on this plant were reported previously[1].     

A Triterpenoid Saponin from Polycarpon prostratum

FromPo{1'cal'Ponproslraluln(Forssk.)Aschers.etSchwein.ExAscherswhichissaidtobetoxicandhasanti-inflammatoryandanodynicactivities',anewtriterpenoidsaponin.namedprostratosideA.wasisolated.ProstratosideA1.mpf250-252"C,[a]5'= 4.3(c0.88,MeOH).0.0018%yield.ItsHRFAB-MSgavea[M-1]'ionatm/zI117.>505,inagreementwiththemolecularformulaC..H,.O:.(cafed."l/zI117.5431).TheiRspectrumshowedabsorptionbandsat3371.1717.1646and1046cm-'.AcomparisonofIwith22a-hydroxy-saikogeninG=showedIwasverysimilarto22a-…     

Septemloside III： A Nonasaccharide Saponin from the Bark of Kalopanax septemlobus （Thunb.） Koidz.

A nonasaccharide saponin, new hederagenin saponin, had been isolated from the bark ofKalopanax septemlobus (Thunb.) Koidz., and its structure was elucidated by HRESI-MS, NMR experi-ments and chemical analyses as 3-O-β-D-xylopyranosyl-(1→4)-13-D-xylopyranosyl-(1→3)-α-L-rhamno-pyranosyl-(1→2)-α-L-arabinopyranosyl hederagenin 28-O-β-D-xylopyranosyl-(1→3)-β-D-xylopyra-nosyl-(1→2)-[α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)]-β-D-glucopyranoside.     

A New Triterpenoid Saponin: Se-saponin A

In continuation of our studies on the constituents of Clerodendrum serratum var.amplexghlium Moldenke'-"', a new triterpenoid saponin, sc-saponin A (l), was isolated.To the best of our knowledge, it is the second instance oftriterpenoid saponin from theClerodendrum genus. This paper deals with the structural elucidation of the newcompound.Se-saponin A (l) an amorphous powder, gave positive Liebermann-Burchardreaction. It was deduced to have a molecular formula of C58H,,O,, by high resoluti…     

A New Triterpenoid Saponin from Anemone tomentosa

TherootsofAnemonetomentosa(Maxim.)PeiareusedasafolkmedicineforthetreatmentofdysenteriainChinal.Recently,twonewcoumarinsandnineknowncompoundswereisolatedfromtheethylacetateeXtractwhichexhibitedstrongantifeedantactivityagainstLeucaniaSeparataWailiee.Duringthefurtherinvestigationofthetitleplant,anewminorsaponin,tomentoside,togetherwithfourknownoneswasisolated.Tomentoside(5),amorphouspowder,[a]D-41.5(MeOH,c0.26).MolecularformulawasdeterminedasC,,H,,.O,.byHRFABMS,m/zf1497.7166([M-H]-),caf…     

A New Saponin Transformed from Ginsenoside Rh1 by Bacillus subtilis

A novel saponin was isolated from the transformed products of ginsenoside Rh1 by Bacillus subtilis. It‘s structure was determined to be 3-O-β-D-glucopyranosyl-6-O-β-D-glucopyranosyl-20 (S)-protopanaxatriol on the basis of the spectral data.     

Ginsenoside-Rg6, a Novel Triterpenoid Saponin from the Stem-Leaves of Panax ginseng C. A. Mey.

A novel dammarane-type triterpene oligoglycoside, named ginsenoside-Rg6 3, was isolated from the stem-leaves of Panax ginseng C.A.Mey., together with two known ones, 20(S)-ginsenoside-Rg2 1 and 20(R)-ginsenoside-Rg2 2.On the basis of chemical and physicochemical evidence , the structure of ginsenoside-Rg6 have been elucidated as 6-O-α-L-rhamnosyl-(1→2)-β-D-glucopyranosyl-dammarane-(E)-20(22), 24-diene-3β, 6α, 12β-triol.     

A Furostanol Saponin from the Cytotoxic Fraction of Tupistra chinensis Rhizomes

More than 1800 species of medicinal plants grow in Shennongjia Forest District. Most of them were recorded to be used as anti-inflammatory agents in the folk medicine1. Kaikoujian, a Chinese name for rhizomes of Tupistra chinensis Bak., is a reputed folk …     

云南重楼中的新甾体皂苷

从云南重楼Paris polyphylla Sm. var. yunnanensis(France. )Hand.-Mazz.的干燥根茎中分离鉴定了4个甾体皂苷(1~4), 其中化合物1是新化合物, 采用波谱技术鉴定其结构为24-O-β-D-吡喃半乳糖基-(23S,24S)-螺甾-5, 25(27)-二烯-1β,3β,23,24-四醇-1-O-β-D-吡喃木糖基(1→6)-β-D-吡喃葡萄糖基(1→3)[α-L-吡喃鼠李糖基(1→2)]-β-D-吡喃葡萄糖苷.     

A Cytotoxic Saponin with Two Monoterpenoids from Albizia julibrissin

The dried stem barks of Albl'ziajulibrissin have been specified in Chinese Pharmacopeiaas a sedative agent. In the previous research several novel saponins were reported'-'.T.Ikeda. at al' isolated three similar saponins almost at the same time. In our further studieson the 95O/O etllanol extract from the plant, a new saponin I was obtained. This paper'involves the isolation and structural elucidation of the new saponin.Air-dried powdered stem barks (13.5 kg.) were extracted with 95% ethan…     

A New Triterpenoid Saponin and a New Glycoside from Epigynum aurilum

A new triterpenoid saponin with novel sugar moiety (1), a new trisaccharide derivative (2), as well as a known monosaccharide derivative (3), were isolated from the dried stem of Epigyhum aurilum. The structures of compounds 1 and 2 were determined by MS and NMR spectram analyses.     

A Novel Hexanordammarane Glycoside from the Roots of Panax notoginseng

There are extensive chemical studies on the roots of Panax notoginseng (Burk.) F. H. Chen, a famous traditional Chinese medicine called San-Qi or Tian-Qi, thirty-three dammarane saponins were isolated and their structures were identified by our group and other scientists1-8. Further chemical investigation on this plant led to the isolation of a novel hexanordammarane glycoside, named notoginsenoside R10 (1).Notoginsenoside R10 (1), white powder, negative HRFAB-MS showed a quasimolecular…