Publications by authors named "Hao-fu Dai"

Ethnopharmacological Relevance: Nauclea officinalis Pierre ex Pitard, a traditional medicinal plant cherished by the Li ethnic group, is renowned for its potent anti-allergic properties in the clinic, especially in alleviating respiratory inflammations. This plant is now extensively cultivated to harness its valuable extracts for the production of traditional cough syrup.

Aim Of The Study: To identify the active components responsible for its anti-allergic inflammatory properties and to elucidate the underlying mechanisms of action.

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A new 12-membered resorcylic acid lactone, cochliomycin H (), and one known resorcylic acid lactone, -demethylated-zeaenol (), were isolated from sponge-derived fungus sp. ZYX-Z-4. The structure of was elucidated by 1D and 2D NMR spectroscopic as well as HR-ESI-MS analysis.

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A novel actinomycete, designated strain ZYX-F-249, was isolated from the gill of a leopard coral grouper in Yongxing Island, Hainan Province, China. Based on 16S rRNA gene sequence analysis, strain ZYX-F-249 belonged to the genus , with high similarities to ATCC 12950 (98.7 %), 211020 (98.

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Four new isocoumarin derivatives 12-O-acetyl-isocitreoisocoumarinol (1), (+)-(10R)-O-acetyl-diaportinol (2-a), (-)-(10S)-O-acetyl-diaportinol (2-b), peyroisocoumarin E (3) and new stereoconfigurations of three isocoumarin derivatives desmethyldichlorodiaportinol A (4), threo-monochlorodiaportinol A (5-a), erytheo-monochlorodiaportinol A (5-b), together with nine known ones (6-14), were separated from the rice fermentation of endophytic fungus Diaporthe arengae M2 isolated from Camellia oleifera. The structures of new compounds were determined by extensive spectroscopic analyses including nuclear magnetic resonance (NMR) and high resolution electrospray ionization mass spectroscopy (HR-ESI-MS). Compounds 4, 7, 8, 12, 13 exhibited definite inhibition against five strains of bacteria with the MIC values range from 16 μg/mL to 64 μg/mL.

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Agarwood, derived from the genus, is widely utilized in perfumery, traditional medicine, and cultural practices throughout Asia. Agarwood is rich in terpenes, especially sesquiterpenes, which are considered to be the source of its rare and exquisite fragrance. This Review consolidates recent research on sesquiterpene biosynthesis in agarwood and the influence of fungi on these processes, alongside a discussion of the potential medicinal value of agarwood sesquiterpenes.

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A new steroid named persteroid () and seven known compounds (-) were isolated from the marine-derived fungus sp. ZYX-Z-143. The structure of was determined by HRESIMS, NMR, and ECD calculations.

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Two new indole-diterpenoids, penpaxilloids F and G (1 and 2), along with 11 known analogues (3-13), were isolated from the marine fungus Penicillium sp. ZYX-Z-718. The structures of the new compounds were identified by extensive spectroscopic analyses including HR-ESI-MS, UV, and NMR, as well as theoretical NMR chemical shifts and ECD calculations.

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Rubber tree () is reproduced by bud grafting for commercial planting, but significant intraclonal variations exist in bud-grafted clones. DNA methylation changes related to grafting may be partly responsible for intraclonal variations. In the current study, whole-genome DNA methylation profiles of grafted rubber tree plants (GPs) and their donor plants (DPs) were evaluated by whole-genome bisulfite sequencing.

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A novel actinobacterium, strain ZYX-F-186, was isolated from marine sediment sampled on Yongxing Island, Hainan Province, PR China. Based on the results of 16S rRNA gene sequence analysis, strain ZYX-F-186 belongs to the genus , with high similarity to KK1-3 (98.3 %), K11-0047 (98.

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Twelve undescribed 2-(2-phenethyl)chromone dimers (1-12) were isolated from EtOAc extract of agarwood originating from Aquilaria filaria in the Philippines, guided by a UHPLC-MS analysis. Their structures were elucidated by 1D NMR, 2D NMR, and HR-ESI-MS spectra. The absolute configuration of 2-(2-phenylethyl)chromone dimers was determined by single-crystal X-ray diffraction analysis and comparison of the experimental and calculated ECD spectra.

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Five new cytochalasins, diaporchalasins A-E (1-5), together with 14 known congeners (6-19) were isolated from the endophytic fungus Diaporthe sp. BMX12, which was isolated from the branches of Aquilaria sinensis. The structures of the new compounds were elucidated by extensive spectroscopic analyses including high-resolution electron spray ionization mass spectrometry (HR-ESI-MS) and nuclear magnetic resonance (NMR).

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Article Synopsis
  • Scientists found six new special plant compounds called dimeric 2-(2-phenylethyl)chromones from agarwood, a type of wood from the tree Aquilaria filaria in the Philippines.
  • These compounds are linked together in a unique way and were studied using special tools to figure out their structures.
  • The researchers discovered that one of the compounds (compound 2) can help stop a certain enzyme, and another (compound 4) can reduce inflammation in cells, making them interesting for health studies.
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Seven new indole-diterpenoids, penpaxilloids A-E (1-5), 7-methoxypaxilline-13-ene (6), and 10-hydroxy-paspaline (7), along with 20 known ones (8-27), were isolated from the marine-derived fungus Penicillium sp. ZYX-Z-143. Among them, compound 1 was a spiro indole-diterpenoid bearing a 2,3,3a,5-tetrahydro-1H-benzo[d]pyrrolo[2,1-b][1,3]oxazin-1-one motif.

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Article Synopsis
  • * The structures of the new compounds were determined using various spectroscopic techniques, including NMR and ECD calculations.
  • * Some of the compounds showed significant antibacterial activity, particularly against Listeria monocytogenes and methicillin-resistant Staphylococcus aureus (MRSA), with varying effectiveness measured by minimum inhibitory concentrations (MIC).
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Article Synopsis
  • Ganoderma mushrooms are special because they contain unique chemicals called lanostane-type triterpenoids.
  • Researchers studied the Ganoderma amboinense mushrooms and discovered twelve new lanostane triterpenoids that were not known before.
  • Some of these new compounds can help prevent certain health issues, like high blood sugar and inflammation, with different strengths in their abilities.
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Three new sesquiterpenoids, dendrohercoglin A - C (1-3), and one new bibenzyl derivative, dendronbiline D (4), together with nine known sesquiterpenoids (5-13) were isolated from Dendrobium hercoglossum. The structures of the new compounds were elucidated by extensive spectroscopic analysis as well as NMR and ECD calculations. All the compounds were evaluated for their neuroprotective and anti-inflammatory activities.

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is a homology of medicine and food. This study aims to investigate the dominant chemical composition and explore the antioxidant properties of the ethanol extract of the leaves and stems of (AOE) on juvenile shrimp, . An in vitro test showed that AOE and its dominant chemical composition procyanidin B-2 () and epicatechin () presented DPPH and ABTS radical scavenging activities.

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Eight previously undescribed indole-diterpenoids named penerpenes O-V (1-8), together with seven known analogues (9-14), were isolated from the marine soft coral-derived fungus Aspergillus sp. ZF-104. Their structures including the absolute configurations of these compounds were assigned on the basis of spectroscopic data and ECD analysis along with quantum ECD and NMR calculations.

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Twelve previously undescribed and four known lanostane triterpenoids were isolated from the fruiting bodies of Ganoderma calidophilum. The structures of undescribed compounds, ganodecalones H-S (1-12), were elucidated by extensive spectroscopic analysis as well as ECD and NMR calculations. Compound 4 showed significant inhibitory activity against human leukaemia cell line K562, gastric cancer cell line SGC-7901, and cervical cancer cell line HeLa with IC values of 13.

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Two new compounds named 3()-hydroxy-1-(2,4,5-trihydroxy-3,6- dimethylphenyl)-hex-4-en-1-one () and acremonilactone (), together with nine known compounds (-), were isolated from the fermentation broth of . associated with marine sediments collected from South China Sea. NMR and HRESIMS spectroscopic analysis elucidated the structure of two new compounds.

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is a fungus widely distributed on Earth and has a high capacity to adapt to complex environments in soil, plants, or sea. It is an endophyte that can be used as a potential biocontrol agent to protect plants from pathogenic fungi, nematodes, and insects. However, the spectrum of secondary metabolites produced by has only scarcely been studied.

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Two new rare trachylobane euphoratones A-B (-), together with five known diterpenoids (compounds ), were isolated from the aerial parts of . Their structures were unambiguously elucidated through HRESIMS, 1D and 2D NMR spectral analysis. Compounds , , and showed weak anti-inflammatory activities (IC 77.

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Four new compounds ((±)-1-3), including one pair of enantiomers ((±)-1), along with 11 known bibenzyls (4-14) were isolated from Dendrobium nobile. The structures of the new compounds were elucidated by spectroscopic methods including 1D and 2D NMR as well as HRESIMS. The configurations of (±)-1 were established via the electronic circular dichroism (ECD) calculations.

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Article Synopsis
  • - The study focused on analyzing chemical components and bioactivities in unpolar fractions (petroleum ether and chloroform) from the fruits and leaves of a specific plant (Miq.), identifying 95.80% of these compounds using GC-MS.
  • - Nootkatone was the primary compound found in all fractions, while valencene was the second main compound in the petroleum ether fractions and both exhibited various bioactivities, including inhibiting tyrosinase and nitric oxide production in specific cells.
  • - The research also identified critical genes related to nootkatone biosynthesis, providing insights into utilizing plant leaves (previously considered waste) for potential benefits and opening avenues for further exploration of nootkatone production. *
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A novel actinobacterium strain (M4I6) was isolated from marine sediment collected in Megas Gialos, Syros, Greece. On the basis of 16S rRNA gene sequence analysis, strain M4I6 was indicated as belonging to the genus , with high similarity to '' LAM7112 (97.9 %), IFO 15555 (97.

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