Lignans from the heartwood of Streblus asper and their inhibiting activities to hepatitis B virus

Three new lignans, erythro-strebluslignanol (1), threo-7'-methoxyl strebluslignanol (2) and erythro-7'-methoxyl strebluslignanol (3), together with twelve known compounds were isolated from the n-butanol and chloroform fractions of the heartwood of Streblus asper. Their structures were elucidated through extensive spectroscopic methods, including MS and 2D NMR experiments (HMQC and HMBC). The stereochemistry at the chiral center was determined using CD spectra, as well as analysis of coupling constants and optical rotation data, respectively. Primary bioassays showed that 6-hydroxyl-7-methoxyl-coumarin (5) and ursolic acid (10) showed anti-HBV activities, with IC(50) values of 29.60 μM and 89.91 μM for HBsAg at no cytotoxicity, and IC(50) values of 46.41 μM and 97.61 μM for HBeAg at no cytotoxicity, respectively.     

Anti-HBV activities of Streblus asper and constituents of its roots

The extracts from leaves, heartwood, barks and roots of the Streblus asper were investigated for anti-HBV activities, separately. The results suggested that the MeOH extracts of the heartwood, barks, and roots exhibited good anti-HBV activities. Further investigations displayed that ethyl acetate and n-butanol soluble parts of their MeOH extracts showed more significant anti-HBV activities. Moreover, a new lignan, together with 11 known compounds, was isolated from n-butanol-soluble part of MeOH extract of the roots of S. asper. The structures were elucidated by spectroscopic methods, including 1D NMR ((1)H NMR, (13)C NMR), 2D NMR (HMQC, HMBC) and HR-EI-MS experiments. Compounds 1-3 were evaluated for their anti-HBV activities. Honokiol showed significant anti-HBV activity with IC(50) values of 3.14μM and 4.74μM for HBsAg and HBeAg with no cytotoxicity respectively, while lamivudine (3TC, positive control) exhibited weak anti-HBV activity with IC(50) values of 11.81μM and 25.80μM for HBsAg and HBeAg respectively.     

Antifungal activity of the stem bark of Ailanthus excelsa

The methanol extract of stem barks of Alianthus excelsa was partitioned with chloroform. The chloroform extract showed fungistatic and fungicidal activity against Aspergillus niger, A. fumigatus, Penicillium frequentence, P. notatum and Botrytis cinerea.     

Insecticidal activity of some essential oils against larvae of Spodoptera littoralis

Thirty-four essential oils were tested for insecticidal activity (fumigation or topical application) against larvae Spodoptera littoralis. Twenty essential oils applied by fumigation were highly toxic to the third instar of S. littoralis larvae. Two essential oils Nepeta cataria and Thuja occidentalis were highly toxic, with LC50< or =10.0 ml/m3. Five essential oils Salvia sclarea, Thymus mastichina, Origanum majorana, Pogostemon cablin and Mentha pulegium were toxic with LC50 between 10.1 and 20.0 l ml/m3. Twenty-three essential oils were highly toxic to the third instar of S. littoralis larvae after topical application. Eight essential oils Mentha citrata, N. cataria, S. sclarea, O. vulgare, O. compactum, Melissa officinalis, T. mastichina, and Lavandula angustifolia were highly toxic with LD50 < or =0.05 microl/larvae.     

Antimicrobial properties of Uvaria chamae stem bark

The antimicrobial properties of the methanol extract of Uvaria chamae stembark (ME) were investigated. The more active ethylacetate-soluble fraction (EAS) was separated by PTLC into 18 sub-fractions. Following phytochemical and antimicrobial screening, several sub-fractions, testing positive for the presence of glycosides (8, 11–15) and tannins (18), exhibited activity against a number of microorganisms, being in some cases more active than penicillin G and chloramphenicol.     

Insecticidal activity of certain medicinal plants

The methanol extracts of eight species of medicinal plants were tested for insecticidal activity in third instar larvae of Egyptian cottonworm (Spodoptera littoralis). All extracts showed a certain degree of larval toxicity. The extracts of Ocimum basilicum, Origanum majorana and Salvia officinalis appeared to be highly toxic. The extracts significantly affected the growth indexes [relative growth rate (RGR), efficiency of conversion of ingested food (ECI), efficiency of conversion of digested food (ECD)].     

Antinociceptive activity of Maytenus rigida stem bark

Ethanol extract of Maytenus rigida stem bark and its fractions were assessed for antinociceptive activity in tail-flick test in rats. The activity was located in the chloroform, ethyl acetate and aq.methanol fractions. Phytochemical screening revealed that catechin was the only common class of compounds present on the ethanol extract as well as on the active fractions. 4'-Methylepigallocatechin, isolated from the ethyl acetate and aq.methanol fractions, showed antinociceptive effect in the tail-flick test (75 mg/kg; p.o.), which was reversed by the opiate antagonist naloxone (3 mg/kg; i.p.).     

Malaysianol A, a new trimer resveratrol oligomer from the stem bark of Dryobalanops aromatica

A new resveratrol trimer, malaysianol A (1), five known resveratrol oligomers: laevifonol (2), ampelopsin E (3), α-viniferin (4), ε-viniferin (5), diptoindonesin A (6), and bergenin (7) have been isolated from the acetone extract of the stem bark of Dryobalanops aromatica by combination of vacuum and radial chromatography techniques. Their structures were established on the basis of their spectroscopic evidence and comparison with the published data. The cytotoxic activity of the compounds was tested against several cell lines in which compound 4 was found to inhibit strongly the growth of HL-60 cell line.     

Insecticidal activity of Vitex mollis

Organic extracts from the leaves of Vitex mollis were assessed for their toxic effect on fall armyworm neonate larvae (Spodoptera frugiperda), an important insect pest of corn. The extracts showed insecticidal and insect growth regulatory activity, being CHCl(3)-MeOH (1:1) extract the most active, also found to be toxic in the Artemia salina test.     

Antibacterial and cytotoxic compounds from the bark of Cananga odorata

O-Methylmoschatoline, liriodenine and 3,4-dihydroxybenzoic acid isolated from the barks of Cananga odorata showed antibacterial activities against a number of Gram (+) and Gram (-) bacteria. The compounds also showed antifungal and cytotoxic activities.     

Bioactive polar compounds from stem bark of Magnolia officinalis

Two new phenylethanoid glycosides magnoloside D (1) and E (2), together with nine known compounds, were isolated from the polar part of methanol extract of the stem bark of Magnolia officinalis. The structures of the new compounds were established on the basis of spectral analysis. Anti-spasmodic activity of four major constituents (3, 4, 9 and 11) was tested in isolated colon of rat, compounds 3, 4, and 9 showed inhibition against acetylcholine, with the effect similar to that of magnolol and honokiol. At the same time, antioxidant activity of the isolated compounds was investigated using a DPPH and an ORAC assay. All of the compounds, except compound 8 showed potent antioxidant capacity in the ORAC assay, while compounds 1-5 and 11 exhibited potent antioxidant activity in the DPPH assay.     

Antispasmodic effects of Persea cordata bark fractions on guinea pig ileum

The present study describes the antispasmodic activity of some fractions from the bark of Persea cordata, against guinea pig ileum contracted by acetylcholine and histamine. Hexane and dichloromethane fractions demonstrated the most promising biological effects, having similar potency to that of papaverine, a well-known antispasmodic agent.     

A new seco-friedelolactone acid from the bark and twigs of Itoa orientalis

A new seco-friedelolactone, named itoaic acid, together with 5 known compounds was isolated from the bark and twigs of Itoa orientalis. The structure was elucidated by means of MS, 1D and 2D NMR techniques. Anti-inflammatory activity against COX-2 was evaluated for several compounds from I. orientalis and another Flacourtiaceae plant Xylosma controversum.     

Sedative activity of stem bark of the Sri Lankan endemic plant, Vateria copallifera

An aqueous bark extract of Vateria copallifera showed marked sedative activity, which supports the therapeutic effects claimed by Sri Lankan traditional physicians.     

Mitogenic effect of Carthamus lanatus extracts, fractions and constituents

Extracts, fractions and constituents of Carthamus lanatus were tested for their mitogenic effect on bone marrow cells in mice. Most of the studied samples inhibited cell proliferation and only the flavonoid glycoside rutin caused increasing of mitotic activity.     

New cardenolides from the stem bark of Trewia nudiflora

Phytochemical investigation of the stem bark of Trewia nudiflora led to the isolation of two new cardenolides, trewianin (1) and trewioside (2), along with scopoletin (3) and indole-3-carboxylic acid (4). Structures were established by 1D- and 2D NMR spectroscopy, HR-MS analysis, and by comparison with literature data.     

Two new antioxidant bergenin derivatives from the stem of Rivea hypocrateriformis

Two new bergenin derivatives, named rivebergenin A and B (1, and 2), together with two known compounds, bergenin (3) and norbergenin (4) were isolated from the stem of Rivea hypocrateriformis (Desr.) Choisy. The structures of the new compound have been assigned from ¹H and ¹³C NMR spectra, DEPT, and by 2D COSY, HMQC, and HMBC experiments. Compounds 1-4 showed the strong antioxidant activity.     

Antimutagenic, antioxidant and antimicrobial properties of Maytenus krukovii bark

The hydroalcoholic extract of Maytenus krukovii bark was investigated for its in vitro mutageno-protective activities by means of the Ames Salmonella/microsome assay. The extract showed an inhibitory effect in both T98 and T100 strains against the mutagenic activity of promutagen 2-aminoanthracene but was not protective against directly acting mutagens sodium azide and 2-nitrofluorene. When tested as a radical scavenger and antioxidant it produced a dose-dependent inhibition. The extract did not show significant antibacterial properties, and was weakly active against dermatophyte and phytopathogenic fungi, but inhibited the growth of phytopathogen Pithyum ultimum.     

Insecticidal activity and antifeedant effect of a new type biocide GCSC-BtA against Plutella xylostella L. (Lep., Plutellidae)

Insecticidal activity and antifeedant effect of a new type biocide GCSC-BtA and its two reactants Bacillus thuringiensis (B.t.) crystal and Abamectin against third instar larvae of Plutella xylostella L. (Lep., Plutellidae) were investigated using bioassays. GCSC-BtA showed significantly higher toxicity to P. xylostella with LC₅₀ of 0.021 mg/ml than B.t. crystal with 0.060 mg/ml and Abamectin with 0.139 mg/ml in leaf-dip bioassay. Net leaf-dip test gave LC₅₀s of 0.073, 0.071 and 0.670 mg/ml for GCSC-BtA, B.t. crystal and Abamectin, respectively. The significant differences of the biocide toxicities between leaf-dip and net leaf-dip methods showed the potential of net leaf-dip method for separating ingestion and contact poisons. Variation in toxicity of the biocide and two reactants in net leaf-dip method and in mortality in topical application bioassay showed that GCSC-BtA possessed a combination of strong stomach as well as contact poison property higher than B.t. or Abamectin. GCSC-BtA indicated no fumigant and systemic toxicities, which the two reactants lacked. In the antifeedant bioassay, GCSC-BtA acted as a strong antifeedant to the larvae of P. xylostella. Leaf consumption by the larvae after GCSC-BtA treatment was 0.04–0.60 mm² with a concentration range of 0.04–4.00 mg/ml, which was lower than 0.26–1.02 and 0.04–6.47 mm² for B.t. crystal and Abamectin, respectively. DC₅₀ (concentration resulting in a deterrence index of 50%) value for GCSC-BtA was 0.089 mg/ml, which was also significantly lower than 0.275 and 0.736 mg/ml for B.t. crystal and Abamectin, respectively.     

Constituents and cytotoxicity of Zanthoxylum rhesta stem bark

3,5-Dimethoxy-4-geranyloxycinnamyl alcohol (1), 8-methoxy-N-methylflindersine (2), xanthyletin and sesamin have been isolated from petroleum ether extract of the stem bark of Zanthoxylum rhesta. The petroleum ether extract and 8-methoxy-N-methylflindersine showed cytotoxicity on brine shrimp nauplii.