Publications by authors named "Dongxiao Guo"

Article Synopsis
  • - Seahorses are valuable for their health benefits and have many species with varying market prices, often leading to confusion in their identification.
  • - A new method utilizing peptide biomarkers through advanced techniques like Nano-LC-MS/MS and chemometrics has been developed to accurately identify different seahorse species.
  • - This method shows promise for ensuring proper identification of seahorses and their products, which is important for trade and conservation efforts.
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  • Deer horn gelatin (DHG) is a popular dietary supplement, but its quality varies significantly, making it important to identify its source.
  • The manufacturing process complicates the distinction between DHG and gelatin from other sources, as similar properties and the loss of genetic material hinder quality assessment.
  • Researchers identified 18 unique peptide markers from five deer species using advanced methods, leading to the development of strategies for evaluating DHG quality effectively.
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A synergetic strategy was proposed to address the critical issue in the brand characterization of (Ejiao, CCA), a precious traditional Chinese medicine (TCM). In all brands of CCA, Dong'e Ejiao (DEEJ) is an intangible cultural heritage resource. Seventy-eight CCA samples (including forty DEEJ samples and thirty-eight samples from other different manufacturers) were detected by laser-induced breakdown spectroscopy (LIBS) and near-infrared spectroscopy (NIR).

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Searching for new adjuvants of conventional chemotherapeutic approaches against colorectal cancer cells is extremely urgent. In current research, a non-targeted analytical approach was established by combining proton nuclear magnetic resonance spectroscopy with a chemometrics data mining tool to identify chemosensitizing agents from . This approach enabled the identification of potential active constituents in the initial fractionation process and provided their structural information.

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Background: Naolingsu capsule (NLSC) is a well-known traditional Chinese medicine (TCM) prescription in China. It is widely used to treat neurasthenia, insomnia, cardiovascular and cerebrovascular disease, and other diseases. However, its inalienable chemical groups have not been carried out.

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North Patrininae herba, a perennial herbaceous plant, has long been used in traditional Chinese medicine to treat appendicitis, enteritis, and dysentery. Sonchus arvensis L., Sonchus oleraceus L.

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Deer antler is a globally widely used precious natural medicine and the material of deer horn gelatin. However, identification of deer antler species based on traditional approaches are problematic because of their similarity in appearance and physical-chemical properties. In this study, we performed a comprehensive antler peptidome analysis using a label-free approach: nano LC-Orbitrap MS was applied to discover peptide biomarkers in deer adult beta-globin (HBB), and HPLC-Triple Quadrupole MS was used to verify their specificity.

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Members of the R2R3-MYB transcription factor superfamily have been implicated in plant development, improved disease resistance, and defense responses to several types of stresses. To study the function of TaMYB29 transcription factor-a member of the R2R3-MYB superfamily-in response to an avirulent race of stripe rust pathogen, f. sp.

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Background: Imported malaria has been an important challenge for China. Fatality rates from malaria increased in China, particularly in Henan Province, primarily due to malpractice and misdiagnoses in healthcare institutions, and the level of imported malaria. This study aims to investigate the relationship between the state of diagnosis and subsequent complications among imported malaria cases at healthcare institutions, based on malaria surveillance data in Henan Province from 2012 to 2017.

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Article Synopsis
  • - Artemisinin-based combination therapy effectively treats uncomplicated Plasmodium falciparum malaria, with piperaquine (PQ) being a key partner drug; however, its interactions with human serum albumin (HSA) and its metabolites had not been previously studied.
  • - The study used fluorescence, circular dichroism (CD) spectroscopy, and molecular docking to demonstrate that PQ and its metabolites bind to HSA, with binding mainly involving hydrogen bonds, van der Waals forces, and hydrophobic interactions, indicating varied affinities.
  • - Additionally, binding of PQs to HSA caused structural changes in HSA, and further investigation into PQs' mechanism against malaria parasites suggested interactions with heme using H NMR spectroscopy
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Interaction of riociguat with human serum albumin (HSA) is extremely important in understanding the drug's disposition and efficiency. In the current study, the binding of riociguat to HSA was explored using spectroscopic methods and molecular docking. The quenching constant, the binding constant, the number of binding sites, thermodynamic parameters, and the secondary structure of protein were determined.

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One undescribed 6,7-secofusicoccane-type diterpene, albifolione (1), and one new aromadendrane-type sesquiterpenoid ketone, methyl 2-oxoaromadendra-1(10),3-dien-12-oate (2), along with four known compounds, δ-cuparenol (3), fusicoauritone (4), chiloscyphenols A and B (5 and 6, resp.), were isolated from the liverwort Bazzania albifolia Horik. The structures and relative configurations of 1 and 2 were established unequivocally on the basis of spectroscopic data analysis.

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Chemical investigation of the fungus Phellinus baumii has resulted in characterization of five previously undescribed hispidin derivatives, phellibaumins A-E (1-5), as well as two pairs of new non-equivalent epimeric benzyl dihydroflavones, methylphelligrin A (9), epi-methylphelligrin A (10), methylphelligrin B (11), and epi-methylphelligrin B (12), together with five known compounds, interfungin B (6), phelligridin H (7), phelligridimer A (8), phelligrin A (13), and epi-phelligrin A (14). Phellibaumin A (1) was a novel hispidin derivative with a unique 3,4-dihydroxybenzofuran unit. These compounds exhibited NF-κB inhibitory activity with IC(50) values of 52.

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Two undescribed dimeric ArC2 derivatives, cis- and trans-1,2-bis(3,4-dimethoxyphenyl)cyclobutane (1 and 2), one new monoterpenes esters, 2alpha,5beta-dihydroxybornane-2-cis-cinnamate (3), along with eight known compounds, 2alpha,5beta-dihydroxybornane-2-trans-cinnamate (4), perrottetin E (5), isoriccardin C (6), marchantin A (7), marchantin E (8), marchantin C (9), and isomarchantin C (10) were isolated from the liverwort Conocephalum japonicum. All the structures were established by extensive spectroscopic analysis. The isolated compounds 3-10 were evaluated for their cytotoxicity against the human KB cell line with IC50 values ranging from 16.

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Article Synopsis
  • A new compound called scaparvin A was discovered from the Chinese liverwort Scapania parva, featuring a unique C-6/C-11 bond and a ketal ring structure.
  • In addition to scaparvin A, four new derivatives named scaparvins B-E were also isolated.
  • The structures of these compounds were determined using techniques like NMR, CD analysis, and electronic circular dichroism calculations, with a proposed enzymatic mechanism explaining the formation of scaparvin A.
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Four undescribed labdane diterpenoids, 1,2-dehydro-3,7-dioxo-manoyl oxide (1), 1,2-dehydro-7 beta-hydroxy-3-oxo-manoyl oxide (2), 3,7-dioxo-manoyl oxide (3), and 3beta-hydroxy-7-oxo-manoyl oxide (4) together with three known diterpenoids (5-7) and four highly methoxylated bibenzyls (8-11) were isolated from the liverwort Frullania inouei. The absolute structures of 1-4 were established by combined analysis of NMR data, CD data coupled with TDDFT CD calculations, and single-crystal X-ray diffraction measurement. Cytotoxicity tests to human tumor KB, KB/VCR, K562 or K562/A02 cells showed bibenzyls 8-11 inhibited cell proliferation with ID(50) values ranging from 11.

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A new trinortriterpenoid, diospyrolide acetate (1) and a new diphenylmethane derivative, pulcherrimumin (12), together with ten known pentacyclic triterpenoids (2-11) and four aromatic compounds (13-16), were isolated from the liverwort Ptilidium pulcherrimum. Their structures were established on the basis of extensive analysis of NMR data and by chemical methods. The cytotoxicity of compounds 1-16 was evaluated against the PC3, MDA-MB-231, and Hela cells lines.

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