A partial peroxisome proliferator-activated receptor gamma agonist isolated from the roots of Euphorbia sikkimensis.

Chemical constituents of the Euphorbia sikkimensis roots was investigated and twelve known compounds were isolated, including three ent-atisane diterpenes: ent-(13S)-hydroxyatis-16-ene-3,14-dione (1), ent-(5ß,8α,9ß,10α,11α,12α)-11-hydroxyatis-16-ene-3,14-dione (2), ent-atisane-3-oxo-16α,17-diol (3); two kaurene diterpenes: ent-kaurane-3-oxo-16α,17-diol (4), ent-kaurane-3-oxo-16ß,17-diol (5); one lathyane diterpene of latilagascene B (6); two flavonoids: quercetin (7), luteolin (8); one lignin d-pinoresinol (9); one coumarin scopoletin (10); together with ethyl gallate (11), p-hydroxybenzaldehyde (12). Their structures were identified based on the extensive spectroscopic analysis in comparison with the literature data. Compounds 1, 2, 4, 6 and 9 were isolated from Euphorbia sikkimensis for the first time. The agonistic activity of peroxisome proliferator-activated receptor gamma (PPARγ) for compounds 1, 7, 8, 9 and 11 was evaluated. Compound 1 exhibited moderate agonistic activity for PPARγ receptor with relative fluorescence intensity of 10.19 at 30.0 µM, in comparison with that of the positive control of rosiglitazone (28.50 at 2.0 µM).

Constructed a novel of Znln2S4/S-C3N4 heterogeneous catalyst for efficient photodegradation of tetracycline.

Despite S-doped C3N4 can exhibit more efficient photo-reactivity than pure C3N4, there is still some space to further improve the detaching efficiency of electron-hole and enhance the photocatalytic efficiency of S-C3N4. The construction of heterojunction is an effective method to promote the photocatalytic efficiency. ZnIn2S4, as a novel photocatalyst, its VB (1.37 V) and CB (- 1.09 V) can match with S-C3N4. Therefore, we hope to construct the ZnIn2S4/S-C3N4 heterojunction for boosting the photocatalytic activity of S-C3N4. In this paper, ZnIn2S4/S-C3N4 heterojunction was prepared through hydrothermal method using S-C3N4, ZnCl2, InCl3·4H2O, and thioacetamide as raw materials and heated at 160 °C for 16 h. The optimum 18% ZnIn2S4/S-C3N4 nanocomposites exhibit dramatically enhanced photocatalytic performance for degradation of tetracycline with 86.3% removal rate within 120 min, higher than 50% degradation efficiency of pure S-C3N4. And in the process of photodegradation for tetracycline, the largest contribution rate is the photo-excited cavity (h+), followed by ·O2- and ·OH. Herein, we have provided a good example for removing antibiotic residues by using S-C3N4-based heterojunction towards environmental remediation.

Construction of 3D sheet-packed hierarchical MoS2/BiOBr heterostructures with remarkably enhanced photocatalytic performance for tetracycline and levofloxacin degradation.

In this paper, MoS2 nanosheets were prepared and deposited on BiOBr microflowers through deposition-hydrothermal strategy. MoS2 exhibited a string of nanosheets with wrinkled layer outlook, and MoS2/BiOBr composites displayed a micro-flower morphology with the diameter of 2-3 µm. Visible-light harvesting performance was significantly improved in the region of 400-600 nm for MoS2/BiOBr. The obtained MoS2/BiOBr samples exhibited tremendous enhanced catalytic activity, which could degrade 92.96% of tetracycline and 90.31% of levofloxacin within 70 min. The photo-generated holes and ⋅OH radicals played the dominant roles in the whole photocatalytic decomposition process. Based on the analysis of DRS, BET, PL, and electrochemical results, the remarkably improved photocatalytic performance may be ascribed to the synergistic effect of strong visible-light harvesting ability, enhanced BET surface area, and faster separation or transfer efficiency of photo-generated charges.

Glycopeptide-Conjugated Aggregation-Induced Emission Luminogen: A pH-Responsive Fluorescence Probe with Tunable Self-Assembly Morphologies for Cell Imaging.

pH values play an important role in various cell biological processes. Abnormal pH values in living systems are frequently associated with the development of diseases such as cancers, infection, and other diseases. Real-time monitoring of the changes of pH values in vivo will give us the significant indication for these diseases' progression. Within those pH-sensitive imaging probes, aggregation-induced emission (AIE) molecules exhibit great potential in aqueous imaging environment due to their high fluorescence quantum yield and stability. However, the modulation of the AIE probe with pH sensitivity and light-up property face challenges. Here, we introduced a new glycopeptide-modified AIE probe (TGO) based on the optimized solid-phase peptide synthesis approach. The response to pH of the peptide: DDDD progression changed hydrophobicity and hydrophilicity, resulting in the change of the amphipathicity balance. When modulating the pH from 5.5 to 8.0, the adverse protonation of the peptide induced assembled nanostructure transformation from nanolamellae to nanomicelles. Meanwhile, the pH-induced charge change in peptides can greatly influence the microenvironment of the AIEgen, resulting in the increase of fluorescence intensity.

Preparation and analysis of photochromic behavior of carboxymethyl chitin derivatives containing spiropyran moieties.

1'-(2-Acryloxyethyl)-3,3'-dimethyl-6-nitrospiro[2 H-1-benzopyran-2,2'-indoline] (SPA) was synthesized and grafted onto a water-soluble carboxymethyl chitin (CMCH) macromolecule to prepare a photochromic copolymer (CMCH-g-SPA). The structure of CMCH-g-SPA was characterized by Fourier-transform infrared (FT-IR) spectroscopy, thermogravimetric (TG) analysis, X-ray diffraction (XRD) analysis, water-solubility evaluation, and UV-vis spectroscopy. XRD patterns of CMCH-g-SPA revealed that grafting copolymerization disrupts the CMCH semicrystalline structure, thus improving water solubility. UV-vis spectroscopy results supported the negative photochromic behavior of the merocyanine (MC) form of CMCH-g-SPA (CMCH-g-MCA) present in a water solution of the target copolymer. In addition to high solvent polarity, the intermolecular and intramolecular electrostatic attraction between the indolenine cation and the COO- anion were found to be influencing factors, which stabilize these MC form of spiropyran groups grafted onto CMCH. In a water solution, visible light bleaching was completed over a short period (8 minutes) under artificial visible light irradiation and the thermal coloration reaction, whose rate constant at 25 °C was 4.64 × 10-4 s-1, which fit the first-order reaction equation. After ten photochromic cycles in water solution, the relative absorption intensity of CMCH-g-MCA decreased by 7.92%.

Construction of a new cascade photogenerated charge transfer system for the efficient removal of bio-toxic levofloxacin and rhodamine B from aqueous solution: Mechanism, degradation pathways and intermediates study.

In this work, a novel cascade system (i.e., SnTCPP/g-C3N4/Bi2WO6) is successfully constructed using stannum (II) meso-tetra (4-carboxyphenyl) porphyrin (SnTCPP) as the key photovoltaic agent for the first time. Visible light driven photocatalytic experiments indicated that wt. 12% SnTCPP and 30% Bi2WO6 codecorated g-C3N4 demonstrates the highest photodecomposition capabilities for levofloxacin and rhodamine B, achieving 85.64% and 93.64% degradation rates, respectively. The dramatically enhanced photocatalytic performance mainly raised from the synergetic co-effects among SnTCPP, g-C3N4 and Bi2WO6, including: i) the incorporation of SnTCPP extends the visible light response of the binary Bi2WO6/g-C3N4 heterojunctions, resulting in the highly efficient visible light harvesting; ii) we find that the g-C3N4 not only serves as a promising supporter to trap electrons from Bi2WO6, but also as an interfacial electron-hole pairs transfer moderator, like "volleyball setter" to facilitate the charges transfer between Bi2WO6 and SnTCPP. The presence of the "setter" endows a cascade system for boosting the photodegradation efficiency of levofloxacin and rhodamine B. This study provides a promising design strategy to construct efficient g-C3N4 based heterojunctions suitable for removing pharmaceutical antibiotics and hazardous dyes from various real wastewaters.

The antioxidant compounds isolated from the fruits of chinese wild raspberry Rubus Chingii Hu.

Raspberry, the fruit of Rubus Chingji Hu, is a widely distributed economic staple food in China. It has long been used as a traditional medicine in mainland China to treat kidney enuresis, nocturnal emission and premature ejaculation in clinic. In this paper, six known compounds (1 - 6) were purified from the fruits of Rubus chingji. Their structures were elucidated as (16α)-16,17-dihydroxy-ent-kauran-2-one17-O-ß-D-glucopyranoside (1), (16R) -16,17-dihydroxy-ent-kaurane-2-one (2), 3,3'-di-O-methylellagic acid 4-(5''-acetyl)-α-L-arabinofuranoside (3), quercilicoside A (4), esculetine (5) and ethyl-ß-D-glucoside (6). All the compounds were isolated from Rubus Chingji Hu for the first time. Compounds 3 and 5 shown distinctive free radical scavenging activities in DPPH and FRAP assays. In addition, no cytotoxicity was observed for compounds 3 and 5 against different cancer cells, suggesting that they might be useful as potential antioxidant agents against various reactive oxygen species.[Formula: see text].

An effective strategy for boosting photoinduced charge separation of Ag3PO4 by BiVO4 with enhanced visible light photodegradation efficiency for levofloxacin and methylene blue.

In this paper, a Z-scheme Ag3PO4/BiVO4 photocatalyst was successfully prepared by precipitation-deposition method. The Ag3PO4/BiVO4 composite exhibited enhanced photocatalytic activity and recyclability for levofloxacin and methylene blue degradation under visible light irradiation. In the Ag3PO4/BiVO4-0.4 system, up to 92.44% of the levofloxacin molecules can be decomposed within 180 min and the photocatalytic degradation efficiency can maintain at 92.02% for methylene blue after recycled for 5 times. The enhanced photocatalytic activity of Ag3PO4/BiVO4 heterojunctions could be mainly attributed to the fabrication of hetero-structure between BiVO4 and Ag3PO4. The photogenerated electron-hole pair separation was effectively enhanced based on the photocurrent, electro-chemical impedance spectra and photoluminescence data. Furthermore, the electrons transfer from photoinduced BiVO4 to Ag3PO4 and the visible light harvesting efficiencies were significantly increased due to the BiVO4 hybridization. The ·OH was the main oxidative species in the Ag3PO4/BiVO4 system for the methylene blue decomposition. Finally, a purposed photocatalytic mechanism for methylene blue degradation was discussed in detail on the basis of experimental results.

Delphatisine D and Chrysotrichumine A, two new diterpenoid alkaloids from Delphinium chrysotrichum.

Chemical investigations of the aerial parts of Tibetan folk medicine Delphinium chrysotrichum resulted in the isolation of two new diterpenoid alkaloids, delphatisine D (1) and chrysotrichumine A (2), together with ten known diterpenoid alkaloids (3-12) and 3ß,6α-dihydroxysclareolida (13). Delphatisine D (1) is a rare atisine-type alkaloid from genus Delphinium and is the C-15 epimer of spiramine C which bears an internal carbinolamine ether linkage (N-C-O-C) between C-7 and C-20. Chrysotrichumine A (2) is a rare natural C19-diterpenoid alkaloid possessing a nitrone group between C-17 and C-19. Their structures were elucidated on the basis of extensive spectroscopic analysis. Compound 13 is a sesquiterpene first isolated from this genus. Compounds 1, 3-7 and 13 were investigated for cytotoxicity against human breast cancer cell lines of MCF-7 and MDA-MB-23, none of them presented significant activity except compound 7 which exhibited slight activity at 100 µM against MDA-MB-231, but did not reach the EC50.

Hydrothermal synthesis of p-C3N4/f-BiOBr composites with highly efficient degradation of methylene blue and tetracycline.

Construction of heterojunctions with band-suitable different semiconductors has been demonstrated to be an efficient approach to enhance the separation of photoinduced electrons and holes. In this paper, highly efficient heterojuction photocatalysts consisted of porous-C3N4 (p-C3N4) and flowerlike-BiOBr (f-BiOBr) were successfully synthesized via a deposition-hydrothermal method. The SEM and HRTEM images indicated that BiOBr were successfully deposited on the surface of p-C3N4 and the layered p-C3N4/f-BiOBr heterojunctions were formed between p-C3N4 and f-BiOBr. The optimum photocatalytic activity of the p-C3N4/f-BiOBr nanocomposites with weight ratio of 3%p-C3N4 exhibited dramatically improved visible-light photocatalytic activities with 98.42% and 94.25% degradation rates for methylene blue (MB) and tetracycline, respectively. The enhanced activity was mainly attributed to the unique heteojunction architecture, which creates large interfacial surface between the constituent materials for facilitating charge transfer and effectively inhibits the fast recombination of photogenerated electrons and holes. The active species trapping experiment indicated that the O2- was the dominating reactive oxidizing species of p-C3N4/f-BiOBr for MB degradation under visible light irradiation. Moreover, the as-prepared photocatalysts displayed excellent stability in the recycling experiments with no obvious decrease of the degradation efficiencies for MB and tetracycline. Furthermore, the possible photocatalytic degradation mechanism of MB over p-C3N4/f-BiOBr was proposed to better understand the reaction process. The work provides a facile route for rational design of heterojunction photocatalysts with promising prospect for the treatment of antibiotic residues in various wastewaters.

Synthesis, characterization and evaluation cytotoxic activity of silver nanoparticles synthesized by Chinese herbal Cornus officinalis via environment friendly approach.

Cornus officinalis has been widely used as a precious herb and as the tonic food to improve kidney function in China. Its fruits have been used in many traditional Chinese medicine prescriptions to treat kidney diseases, diabetes, cancer and shock. In this study, a new eco-friendly approach for green synthesis of silver nanoparticles (AgNPs) by using the fruits of Cornus officinalis aqueous extract as a reducing and stabilizing agent. The so-synthesized AgNPs showed quasi-spherical in shape with uniform dispersal and an average mean size of 11.7nm. Water soluble biomolecules such as flavonoids and/or anthocyanins from the extract played important roles in the nanoparticles formation. The AgNPs displayed distinctive cytotoxicity activities against human prostate cancer (PC-3) and human liver cancer (HepG2) cell lines. The results provided a low cost, nontoxic and eco-friendly approach for synthesizing metal nanoparticles to explore alternative anticancer agents on the way fighting against cancer in future.

Cyclized 9,11-secosterol enol-ethers from the gorgonian Pseudopterogorgia americana.

Chemical investigation of the MeOH extract from the gorgonian Pseudopterogorgia americana afforded two rare sterols, ameristerenol A (1) and B (2), both 9,11-secosterols possesses a seven-membered cyclic enol-ether in ring C, and ameristerol A (3) is the first example of a naturally occurring 9,11-secosterol containing a gorgosterol side chain with a C-24(28) double bond. Ameristerenol A (1) was converted to the sterol derivatives 4-6 to provide additional chemical diversity and comparison for biological screening. The structures of compounds 1-6, along with three related known analogues 7-9, were determined on the basis of extensive spectroscopic analysis and by comparison with literature data. Compound 6 exhibited slight cytotoxicity activity against human breast cancer cell line MDA-MB-231.

An iridoid glucoside and the related aglycones from Cornus florida.

A new iridoid glucoside, cornusoside A (1), and four new natural product iridoid aglycones, cornolactones A-D (2-5), together with 10 known compounds were isolated from the leaves of Cornus florida. The structures of compounds 1-5 were established by interpretation of their spectroscopic data. Cornolactone B (3) is the first natural cis-fused tricyclic dilactone iridoid containing both a five- and a six-membered lactone ring. A biosynthesis pathway is proposed for cornolactones C (4) and D (5), the C-6 epimers of compounds 1-3.

Liver X receptor and peroxisome proliferator-activated receptor agonist from Cornus alternifolia.

BACKGROUND: Peroxisome proliferator-activated receptors (PPARs) belong to the nuclear receptors superfamily and are transcription factors activated by specific ligands. Liver X receptors (LXR) belong to the nuclear hormone receptors and have been shown to play an important role in cholesterol homeostasis. From the previous screening of several medicinal plants for potential partial PPARγ agonists, the extracts of Cornus alternifolia were found to exhibit promising bioactivity. In this paper, we report the isolation and structural elucidation of four new compounds and their potential as ligands for PPAR. METHODS: The new compounds were extracted from the leaves of C. alternifolia and fractionated by high-performance liquid chromatography. Their structures were elucidated on the basis of spectroscopic evidence and analysis of their hydrolysis products. RESULTS: Three new iridoid glycosides including an iridolactone, alternosides A-C (1-3), a new megastigmane glycoside, cornalternoside (4) and 10 known compounds, were obtained from the leaves of C. alternifolia. Kaempferol-3-O-ß-glucopyranoside (5) exhibited potent agonistic activities for PPARα, PPARγ and LXR with EC50 values of 0.62, 3.0 and 1.8 µM, respectively. CONCLUSIONS: We isolated four new and ten known compounds from C. alternifolia, and one known compound showed agonistic activities for PPARα, PPARγ and LXR. GENERAL SIGNIFICANCE: Compound 1 is the first example of a naturally occurring iridoid glycoside containing a ß-glucopyranoside moiety at C-6.

Diterpenoid alkaloids from a Tibetan medicinal plant Aconitum richardsonianum var. pseudosessiliflorum and their cytotoxic activity.

The chemical constituents from Aconitum richardsonianum var. pseudosessiliflorum were investigated. The roots of this plant were extracted three times with 90% EtOH at the room temperature. The ethanol extracts were combined and concentrated under reduced pressure to yield residue, which was suspended in water and successively partitioned with chloroform. The chloroform extraction was isolated and purified by silica gel and Sephadex LH-20 column chromatography. Six compounds were isolated and elucidated as delelatine (1), isodelpheline (2), 3-acetylaconitine (3), isoatisine (4), nordhagenine A (5) and yunaconitine (6). Compounds 1-5 were obtained from Aconitum Brunneum for the first time. Compound (1) showed significant cytotoxic activities (IC50= 4.36 µM) against the human tumor cell line P388.

Chemical constituents from Delphinium chrysotrichum and their biological activity.

A new diterpene alkaloid named delphatisine C (1) has been isolated from aerial parts of Delphinium chrysotrichum along with three known norditerpenoid alkaloids delpheline (2), delbrunine (3), and delectinine (4). Their structures were characterized on the basis of their spectral data. All of them were determined by SRB assay for their cytotoxicity, and compound (1) showed significant cytotoxic activities (IC(50)=2.36 µmol/L) against the A549 cell line.

A new norditerpenoid alkaloid from Aconitum taipaicum.

To investigate the chemical constituents of the roots of Aconitum taipaicum, silica gel column chromatography was used for the isolation and purification of compounds. A new norditerpenoid alkaloid, isodelelatine (1), along with five known alkaloids, atisine (2), delfissinol (3), liangshanine (4), hypaconitine (5) and delelatine (6) were isolated and identified. The structure of the new compound was elucidated on the basis of spectral data.

[Study on chemical constituents from Delphinium honanense var. piliteram].

OBJECTIVE: To study the chemical constituents from Delphinium honanense var. piliteram. METHOD: The constituents were isolated and purified with chromatographic methods, identified by NMR, MS and IR. RESULT: Six compounds were isolated and elucidated as siwanine E (1), isoatisine (2), 12-epi-napelline (3), acontine (4), ajadelphinine (5) and beta-sitosterol (6). CONCLUSION: Compounds 1-6 are all isolated from the plant for the first time.

[Studies on chemical constituents of Clerodendrum bungei].

OBJECTIVE: To study the constituents from Clerodendrum bungei. METHOD: The constituents were isolated and purified with chromatographic methods, and identified by NMR, MS and IR. RESULT: Five compounds were isolated, beta-sitosterol (1), taraxerol (2), glochidone (3), glochidonol (4), glochidiol (5). CONCLUSION: Compounds (3), (4) and (5) were isolated for the first time from C. bungei.

[Studies on chemical constituents in leafs of Clerodendron fragrans].

OBJECTIVE: To separate and identify the constituents from Clerodendron fragrans. METHOD: The constituents were isolated and purified with chromatographic methods, identified by NMR, MS, IR. RESULT: Beta-sitosterol (1), clerosterol (2), daucosterol (3), caffeic acid (4), kaempferol (5), 5,4'-dihydroxy-kaempferol-7-O-beta-rutinoside (6), acteoside (7) and leucoseceptoside A (8), were isolated and identified. CONCLUSION: Compound 7 and 8 were identified for the first time from Clerodendron fragrans.