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1.
Bioorg Chem ; 148: 107461, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38788363

ABSTRACT

Stachybatranones A-F (1a/1b and 2-6) and three known analogues, namely methylatranones A and B (7 and 8) and atranone B (9), were isolated and identified from a toxigenic fungus Stachybotrys chartarum. Their structures and absolute configurations were elucidated via the extensive spectroscopic data, comparison of the experimental electronic circular dichroism (ECD) data, and single-crystal X-ray diffraction analyses. Structurally, compounds 2-6 belonged to a rare class of C-alkylated dolabellanes, featuring a unique five-membered hemiketal ring and a γ-butyrolactone moiety both fused to an 11-membered carbocyclic system, while compound 1 (1a/1b) represented the first example of a 5-11-6-fused atranone possessing a 2,3-butanediol moiety. The cardiomyocyte protective activity assay revealed that compounds 1-9 ameliorated cold ischemic injury at 24 h post cold ischemia (CI), with compounds 1 and 4 acting in a dose-dependent manner. Moreover, compound 1 prevented cold ischemia induced dephosphorylation of PI3K and AKT acting in a dose-dependent manner. In this study, a new class of natural products were found to protect cardiomyocytes against cold ischemic injury, providing a potential option for the development of novel cardioprotectants in heart transplant medicine.


Subject(s)
Myocytes, Cardiac , Stachybotrys , Stachybotrys/chemistry , Animals , Myocytes, Cardiac/drug effects , Molecular Structure , Structure-Activity Relationship , Dose-Response Relationship, Drug , Rats , Drug Discovery , Biological Products/pharmacology , Biological Products/chemistry , Biological Products/isolation & purification , Protective Agents/pharmacology , Protective Agents/chemistry , Protective Agents/isolation & purification
2.
Bioorg Chem ; 147: 107329, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38608410

ABSTRACT

By co-culturing two endophytic fungi (Chaetomium virescens and Xylaria grammica) collected from the medicinal and edible plant Smilax glabra Roxb. and analyzing them with MolNetEnhancer module on GNPS platform, seven undescribed chromone-derived polyketides (chaetoxylariones A-G), including three pairs of enantiomer ones (2a/2b, 4a/4b and 6a/6b) and four optical pure ones (1, 3, 5 and 7), as well as five known structural analogues (8-12), were obtained. The structures of these new compounds were characterized by NMR spectroscopy, single-crystal X-ray diffraction, 13C NMR calculation and DP4+ probability analyses, as well as the comparison of the experimental electronic circular dichroism (ECD) data. Structurally, compound 1 featured an unprecedented chromone-derived sulfonamide tailored by two isoleucine-derived δ-hydroxy-3-methylpentenoic acids via the acylamide and NO bonds, respectively; compound 2 represented the first example of enantiomeric chromone derivative bearing a unique spiro-[3.3]alkane ring system; compound 3 featured a decane alkyl side chain that formed an undescribed five-membered lactone ring between C-7' and C-10'; compound 4 contained an unexpected highly oxidized five-membered carbocyclic system featuring rare adjacent keto groups; compound 7 featured a rare methylsulfonyl moiety. In addition, compound 10 showed a significant inhibition towards SW620/AD300 cells with an IC50 value of PTX significantly decreased from 4.09 µM to 120 nM, and a further study uncovered that compound 10 could obviously reverse the MDR of SW620/AD300 cells.


Subject(s)
Antineoplastic Agents , Chaetomium , Chromones , Drug Screening Assays, Antitumor , Polyketides , Xylariales , Chromones/chemistry , Chromones/pharmacology , Chromones/isolation & purification , Polyketides/chemistry , Polyketides/pharmacology , Polyketides/isolation & purification , Molecular Structure , Xylariales/chemistry , Chaetomium/chemistry , Humans , Antineoplastic Agents/pharmacology , Antineoplastic Agents/chemistry , Antineoplastic Agents/isolation & purification , Structure-Activity Relationship , Dose-Response Relationship, Drug , Cell Line, Tumor , Coculture Techniques , Cell Proliferation/drug effects
3.
J Org Chem ; 89(2): 1209-1219, 2024 01 19.
Article in English | MEDLINE | ID: mdl-38192075

ABSTRACT

Guided by the Global Natural Products Social (GNPS) molecular networking strategy, five undescribed eremophilane-type sesquiterpenoid derivatives (1-5) were isolated and identified from fungus Penicillium roqueforti, which was separated from the root soil of plant Hypericum beanii collected in Shennongjia Forestry District, Hubei Province. Dipeniroqueforins A-B (1-2), representing a lactam-type sesquiterpenoid skeleton with a highly symmetrical and homodimeric 5/6/6-6/6/5 hexacyclic system, are reported within the eremophilane-type family for the first time. Peniroqueforin D (5) represents the first example of a 1,2-seco eremophilane-type sesquiterpenoid derivative featuring an undescribed 7/6-fused ring system. The structures of these compounds were elucidated by various spectroscopic analyses, DP4+ probability analyses, ECD calculations, and single-crystal X-ray diffraction experiments. Furthermore, these isolates were evaluated for cytotoxicity, and the result uncovered that compound 1 displayed broad-spectrum activity. Further mechanistic study revealed that compound 1 could significantly upregulate the mRNA expression of genes related to the oxidative induction, leading to the abnormal ROS levels in tumor cells and ultimately causing tumor cell apoptosis.


Subject(s)
Antineoplastic Agents , Penicillium , Sesquiterpenes , Polycyclic Sesquiterpenes , Molecular Structure , Sesquiterpenes/chemistry , Penicillium/chemistry , Antineoplastic Agents/chemistry
4.
Phytochemistry ; 212: 113722, 2023 Aug.
Article in English | MEDLINE | ID: mdl-37230212

ABSTRACT

Nine undescribed eremophilane sesquiterpenes, one undescribed guaiane sesquiterpene, along with ten known analogues were isolated and identified from fungus Penicillium roqueforti, which was separated from the root soil of Hypericum beanii N. Robson collected from the Shennongjia Forestry District, Hubei Province. Their structures were elucidated on the basis of various spectroscopic analyses, mainly including NMR and HRESIMS data, 13C NMR calculations with DP4+ probability analyses, ECD calculations, and single-crystal X-ray diffraction experiments. Furthermore, all twenty compounds were evaluated for the in vitro cytotoxic activities against seven human tumor cell lines, and the result suggested that 14-hydroxymethylene-1(10)-ene-epi-guaidiol A exhibited considerable cytotoxic activity against the Farage (IC50 < 10 µM, 48 h), SU-DHL-2, and HL-60 cells. Further mechanism study demonstrated that 14-hydroxymethylene-1(10)-ene-epi-guaidiol A could significantly promote apoptosis by inhibiting tumor cell respiration and decreasing intracellular ROS levels, thereby inducing S-phase blockade in tumor cells.


Subject(s)
Penicillium , Sesquiterpenes , Humans , Polycyclic Sesquiterpenes , Sesquiterpenes, Guaiane , Molecular Structure , Sesquiterpenes/chemistry , Penicillium/chemistry
5.
Nat Prod Res ; : 1-7, 2022 Nov 28.
Article in English | MEDLINE | ID: mdl-36441184

ABSTRACT

Armochaetoglasins L (1) and M (2), two new cytochalasans, were isolated from the EtOAc extract of an arthropod-derived fungus Chaetomium globosum. Armochaetoglasin L (1) is a rare 19,20-seco-chaetoglobosin. Their structures were elucidated by NMR spectroscopy and comparison of their electronic circular dichroism (ECD) data. Compounds 1 and 2 were evaluated for anti-inflammatory activity against the NO production by using LPS-stimulated murine macrophage RAW264.7 cells and antibacterial activity against three drug-resistant microbial pathogens.

6.
R Soc Open Sci ; 6(7): 181696, 2019 Jul.
Article in English | MEDLINE | ID: mdl-31417692

ABSTRACT

Coal is still a major energy source, mostly used in power plants. However, the coal combustion emits harmful SO2 and fly ash. Wet flue gas desulfurization (WFGD) technology is extensively used to control SO2 emissions in power plants. However, only limited studies have investigated the synergistic dust removal by the WFGD system. Spray scrubbers and sieve-tray spray scrubbers are often used in WFGD systems to improve the SO2 removal efficiency. In this study, the synergistic dust removal of WFGD systems for a spray scrubber and a sieve-tray spray scrubber was investigated using the experimental and modelling approaches, respectively. For the spray scrubber, the influence of parameters, including dust particle diameters and inlet concentrations of dust particles, and the flow rates of flue gas and slurry of limestone/gypsum on the dust removal efficiency, was investigated. For the sieve-tray spray scrubber, the influence of parameters such as the pore diameter and porosity of sieve trays on the dust removal efficiency was examined. The study found that the dust removal efficiency in the sieve-tray spray scrubber was approximately 1.1-10.6% higher than that of the spray scrubber for the same experimental conditions. Based on the parameters investigated and geometric parameters of a scrubber, a novel droplets swarm model for dust removal efficiency was developed from the single droplet model. The enhanced dust removal efficiency of sieve tray was expressed by introducing a strength coefficient to an inertial collision model. The dust removal efficiency model for the sieve-tray spray scrubber was developed by combining the droplets swarm model for the spray scrubber with the modified inertial collision model for the sieve tray. The results simulated using both models are consistent with the experimental data obtained.

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