A new flavonol derivative, meliglabrin (1) along with three known flavonols, ternatin (2), meliternatin (3), and 5,4′-dihydroxy-3,7,3′-trimethoxyflavon (4) were isolated from the leaves of Melicope glabra (Blume) T.G. Hartley. Their structures were determined using extensive spectroscopic methods, including UV, IR, HRESIMS, 1D and 2D NMR. Compounds 1 – 4 were evaluated for their cytotoxicity against murine leukemia P-388 cells, compound 4 showed moderate activity.
Flavonols ; Leukemia ; Rutaceae

A new isoprenylated acetophenone, acronyculatin P (1) as well as two known compounds, 3′,5′-diisoprenyl-2′,4′-dihydroxy-6′-methoxyphenylethanone (2) and 3′-isoprenyl-2′,4′,6′-trihydroxyphenylethanone (3) were isolated from the stem bark of Acronychia pedunculata (L.) Miq. The structures were determined by HRESIMS, 1D and 2D NMR. The inhibitory activity of the isoprenylated acetophenone derivatives against murine leukemia P-388 cells showed compound 1 moderate activity with IC₅₀ 15.42 µM.
Leukemia ; Rutaceae ; Thoracica

By isolating and using UV, IR, 1H-MNR and 13C-NMR analysis, the authors determined the structure of heptazolin (8-hydroxy-heptaphillin) - an alcaloid carbazol isolated from Clausena heptaphilla (Roxb.) W & ARN. Results of in vitro study showed the physiochemical characteristics and spectrum of alcaloid carbazol heptazolin
Rutaceae ; plants ; pharmacy ; Medicine, Traditional ; Alkaloids

OBJECTIVEThe spectral imaging method was used to quickly identify the Cortex Dictamni pieces and its counterfeit alangium Chinese, which is a potential method would be applied to control the quality of the Cortex Dictamni pieces.

METHODStandard sample, 5 cortex dictamni samples and its counterfeit alangium Chinese of different sources were tested by the liquid crystal imaging instrument. The spectrum resolution was 5 nm, the spectral range was from 405 nm to 680 nm, and the spatial resolution was 50 lp x mm(-1). The characteristic spectrum curves were picked up from spectral cube and principal analysis method was used to analyze the results.

RESULTThe identification results by the spectral imaging method accorded well with the results by the traditional biology and chemistry analysis method.

CONCLUSIONThe spectral imaging analysis method can be used to identify the cortex dictamni pieces and its counterfeit alangium Chinense. The testing course is convenient, quick and noninvasive.

Alangiaceae ; chemistry ; Quality Control ; Rutaceae ; chemistry ; Spectrum Analysis ; methods

Anticoccidial effects of the root bark of Dictamnus dasycarpus Turcz (Rutaceae) extract (DDE) were evaluated in chickens following oral infection with Eimeria (E.) tenella. Three-day-old chickens (n=30) were assigned to three groups (control, untreated, and DDE 0.1% treated). Chickens were fed a standard diet supplemented with or without DDE for 1 week prior to infection with E. tenella (10,000 sporulated oocysts per chicken). The effects of DDE on E. tenella infection were assessed by two parameters; fecal oocysts shedding and body weights gain. The DDE-fed chickens produced significantly reduced fecal oocysts (P<0.05) when compared to the E. tenella-infected group fed standard diet. Also, DDE-based diet, improved body weight loss caused by E. tenella infection. Our data demonstrated that DDE had remarkable anticoccidial activities against E. tenella. This finding might have implications for the development of anticoccidial drug. This study is the first to demonstrate anticoccidial effect of DDE on Eimeria parasites.
Body Weight ; Chickens ; Dichlorodiphenyl Dichloroethylene ; Dictamnus* ; Diet ; Eimeria ; Eimeria tenella* ; Oocysts ; Parasites ; Rutaceae

Activity-guided separation of the methylene chloride-soluble fraction of the leaves of Zanthoxylum schinifolium, resulted in the isolation of four coumarinoids (1 - 4), two triterpenoids (5, 6) and three fatty acid derivatives (7 - 9) as active principles. Their chemical structures were identified as collinin (1), 8-methoxyanisocoumarin (2), 7-(6'R-hydroxy-3',7'-dimethylocta-2',7'-dienyloxy)-coumarin (3), (E)-4-methly-6-(coumarin-7'-yloxy) hex-4-enal (4), lupeol (5), epi-lupeol (6), phytol (7), hexadec-3-enoic acid (8) and palmitic acid (9), on the basis of spectroscopic (1D, 2D and MS) data analyses and comparing with the data published in the literatures. Compounds 1 and 7 showed potent cytotoxicity against Jurkat T cells with IC50 values of 45.58 and 47.51 microM, respectively. The others showed moderate activity with IC50 values ranging around 80.58 to 85.83 microM, while the positive control, auraptene, possessed an IC50 value of 55.36 microM.
Inhibitory Concentration 50 ; Palmitic Acid ; Phytol ; Rutaceae ; Statistics as Topic ; T-Lymphocytes ; Zanthoxylum*

OBJECTIVETo determine the content of isopimpinellin in root of Toddalia asiatica.

METHODSA HPLC method was set up. Using Hypersil C18 column and methanol-water (70:30) as mobile phase, with the detection wavelength at 306 nm.

RESULTThe linear range of isopimpinellin was 0.004 20 approximately 0.420 microg. The average recovery was 99.7% and the RSD 2.8%.

CONCLUSIONThe method is simple and accurate, with good reproducibility, and can be used as a quantitative analysis method for isopimpinellin.

Chromatography, High Pressure Liquid ; Furocoumarins ; analysis ; Plant Roots ; chemistry ; Plants, Medicinal ; chemistry ; Rutaceae ; chemistry

A new benzene derivative microintegerrin C (1) and a new norsesquiterpenoid microintegerrin D (2), along with six known compounds (3-8), were isolated and identified from stems and leaves of Micromelum integerrimum by various chromatographies such as silica gel, Sephadex LH-20, RP-18 column chromatography and HPLC. Their structures were mainly identified based on the spectral data analysis such as 1D-, 2D-NMR and HR-EI-MS. All known compounds were isolated from this plant for the first time.
Chromatography, High Pressure Liquid ; Plant Leaves ; chemistry ; Plant Stems ; chemistry ; Rutaceae ; chemistry ; Sesquiterpenes ; isolation & purification

Three new coumarins, integmarins A-C (1-3), and a new coumarin glycoside, integmaside A (4) were isolated from the leaves and stems of Micromelum integerrimum. Their structures were elucidated on the basis of 1D and 2D NMR and MS data, and their absolute configurations were assigned according to the ECD data of the in situ formed transition metal complexes and comparison of experimental and calculated ECD data. Compounds 1 and 2 are two rare coumarins with butyl and propyl moieties at the C-6 position; compound 3 is a novel coumarin with a highly oxidized prenyl group, and compound 4 is a rare bisdihydrofuranocoumarin glycoside.
Coumarins/isolation & purification* ; Glycosides/isolation & purification* ; Molecular Structure ; Plant Leaves/chemistry* ; Plant Stems/chemistry* ; Rutaceae/chemistry*

BACKGROUND: Our local calamansi's pulps contain tannin which has been found to have antifungal activity.
OBJECTIVE: To determine the safety and efficacy of calamansi pulp extract cream in the treatment of tinea versicolor.
METHODS: This was a prospective, open-label pilot study. Safety of 20 percent, 40 percent and 80 percent tannin from calamansi pulp was done using patch test. The 40 percent tannin cream determined safe was used for the phase 2 clinical trial. Patients with tinea versicolor applied the test cream twice daily and was re-evaluated weekly for 4-weeks.
RESULTS: Of the 100 volunteers who underwent patch testing, six subjects developed significant irritancy with the 80 percent tannin cream (p= 0.016). The 20 percent and 40 percent tannin creams were deemed safe for topical application. Fifteen patients underwent the 2nd phase evaluation for efficacy using 40 percent tannin cream. Weekly mean global assessment score showed significant clinical improvement from baseline and after the 4-weeks study (p= 0.000). At week 4, clinical cure had occurred in 93 percent (95 percent CI, 81-106) of subjects, mycologic cure in 100 percent (95 percent CI, 100) and complete cure in 93 percent (95 percent CI, 81-106).
CONCLUSION: The 20 percent and 40 percent tannin extracts are safe for topical application. The 40 percent calamansi pulp extract cream is effective against tinea versicolor after 4-weeks of use.

Human ; Citrus ; Eukaryota ; Plants ; Antifungal Agents ; Patch Tests ; Pilot Projects ; Prospective Studies ; Tannins ; Tinea Pedis ; Tinea Versicolor ; Volunteers ; Angiosperms ; Rutaceae