Germacrane Sesquiterpene Dilactones from and Their Antibacterial and Cytotoxic Activity.

Four new germacrane sesquiterpene dilactones, 2-hydroxyl-11,13-dihydrodeoxymikanolide (), 3-hydroxyl-11,13-dihydrodeoxymikanolide (), 1,3-dihydroxy-4,9-germacradiene-12,8:15,6-diolide (), and (11,13-dihydrodeoxymikanolide-13-yl)-adenine (), together with five known ones (-) were isolated from the aerial parts of . Their structures were elucidated on the basis of extensive spectroscopic analysis. Compound is featured with an adenine moiety in the molecule, which is the first nitrogen-containing sesquiterpenoid so far isolated from this plant species.

Thymol derivatives with antibacterial and cytotoxic activity from the aerial parts of .

Three new thymol derivatives, 7-formyl-9-isobutyryloxy-8-hydroxythymol (1), 7,9-di-isobutyryloxy-8,10-dehydrothymol (2) and 2α-methoxyl-3β-methyl-6-methylol-2,3-dihydrobenzofuran (3), along with five known ones (4-8), were isolated from the aerial parts of the invasive plant . Their structures were elucidated by extensive spectroscopic analysis and they were all isolated from the aerial part of for the first time. These compounds, except 8, selectively showed antimicrobial activity against three Gram-(+) and two Gram-(-) bacterial strains.

Biodiversity and antifouling activity of fungi associated with two soft corals from the South China Sea.

Bacteria in corals have been studied in detail in the past decades. However, the biodiversity and bioactivity of fungi in corals are still poorly understood. This study investigated the biodiversity and antifouling activity of fungi in soft corals Cladiella krempfi and Sarcophyton tortuosum from the South China Sea.

Triterpenoids with α-glucosidase inhibitory activity and cytotoxic activity from the leaves of .

Ten pentacyclic triterpenoids including a new multiflorane triterpene acid, 2α,3β,23-trihydroxymultiflor-7-en-28-oic acid (1), and a new lupane triterpene monoglucoside named akebiaoside C (2), were obtained from the leaves of . Their structures were elucidated by extensive spectroscopic analysis, and they were all isolated from the leaves of for the first time. These compounds, except 4 and 5, showed α-glucosidase inhibitory activity much stronger than acarbose.

Anti-MRSA Sesquiterpenes from the Semi-Mangrove Plant A. Gray.

The striking rise of methicillin-resistant (MRSA) infections has become a serious threat to public health worldwide. In an effort to search for new anti-MRSA agents from natural products, a bioassay-guided phytochemical study was conducted on the semi-mangrove plant A. Gray, which led to the isolation of two new sesquiterpene alkaloids ( and ) and six known furanosesquiterpenes (⁻).

Characterization and immunological activity of polysaccharides from Ixeris polycephala.

A water-soluble polysaccharide, named KMCP, was isolated and purified from edible plant Ixeris polycephala by using DEAE-52 cellulose chromatography. Its structure was determined by chemical analysis, methylation analysis, and NMR analysis, coupled with characterization by scanning electron spectroscopy (SEM). The resulting data indicated that KMCP was an arabinogalactan, with an average molecular weight of 1.

Phenolics from Mikania micrantha and Their Antioxidant Activity.

A phytochemical study on the aerial parts of led to the isolation of two new phenolic compounds, benzyl 5--β-d-glucopyranosyl-2,5-dihydroxybenzoate () and (7,8)--dihydroxydehydrodiconiferyl alcohol 9-acetate (), together with twelve known compounds, benzyl 2--β-d-glucopyranosyl-2,6-dihydroxybenzoate (), 4-allyl-2,6-dimethoxyphenol glucoside (), (+)-isolariciresinol (), icariol A₂ (), 9,10-dihydroxythymol (), 8,9,10-trihydroxythymol (), caffeic acid (), -coumaric acid (), ethyl protocatechuate (), procatechuic aldehyde (), 4-hydroxybenzoic acid (), and hydroquinone (). Their structures were elucidated on the basis of extensive spectroscopic analysis. Except and , all the other compounds were isolated from this plant species for the first time.

Two New Thymol Derivatives from the Roots of Ageratina adenophora.

Two new thymol derivatives, 7,9-diisobutyryloxy-8-ethoxythymol () and 7-acetoxy-8-methoxy-9-isobutyryloxythymol (), were isolated from fresh roots of , together with four known compounds, 7,9-di-isobutyryloxy-8-methoxythymol (), 9-oxoageraphorone (), (-)-isochaminic acid () and (1α,6α)-10-hydroxycar-3-ene-2-one (). Their structures were established on the basis of detailed spectroscopic analysis, and they were all isolated from the roots of for the first time. All the compounds were tested for their in vitro antibacterial activity toward three Gram-positive and two Gram-negative bacterial strains.

Two New Pentacyclic Triterpene Saponins from the Leaves of Akebia trifoliata.

Two new pentacyclic triterpene saponins, named akebiaoside K (1) and akebiaoside N (2), were isolated from the leaves of Akebia trifoliata, together with five known triterpenoids 3-7. They were all isolated from the leaves of A. trifoliata for the first time.

[Chemical Constituents from Sphagneticola trilobata].

Objective: To study the chemical constituents of the whole plant of Sphagneticola trilobata.

Methods: The compounds were isolated and purified by column chromatography and their structures were determined by spectroscopic techniques.

Results: Three lignans, two indolics and two phenolic glycosides were isolated from the whole plant of Sphagneticola trilobata and identified as syringaresinol-4-O-β-D-glucopyranoside(1), pinoresinol-4-sulfate(2), pinoresinol-4-O-β-D-glucopyranoside(3), 1H-indole-3-carboxylic acid (4), 1H-indole-3-carbaldehyde(5), 2,6-dimethoxy-4-hydroxyphenol-1-O-β-D-glucopyranoside (6), and 3,5-dimethoxy-4-hydroxyphenol-1-O-β-D-glucopyranoside (7).

[Minimally invasive treatment for fresh acromioclavicular dislocation and the distal clavicle fracture].

Objective: To explore the minimally invasive treatment for fresh acromioclavicular dislocation and the distal clavicle fracture.

Methods: Thirty skeletons of human shoulder were measured and compared, and the normal data on healthy people were measured with the help of ultrasound-guided. So the invasion point was located at the cross between subclavian axis and the line from coracoid tip to apophysis behind cone ligament node.