Publications by authors named "Nilufar Mamadalieva"

Ajuga turkestanica preparations are used as anti-aging cosmeceuticals and for medicinal purposes. Herein we describe the characterization and quantification of its metabolites in different organs using UHPLC-MS and NMR spectroscopy. A total of 51 compounds belonging to various phytochemical classes (11 flavonoids, 10 ecdysteroids, 9 diterpenes, 6 fatty acids, 5 iridoids, 3 phenylpropanoids, 3 sugars, 2 phenolics, 1 coumarin, 1 triterpene) were annotated and tentatively identified by UHPLC-ESI-QqTOF-MS/MS of methanolic extracts obtained separately from the organs.

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  • A detailed metabolite profiling of a medicinal plant using UHPLC-ESI-MS/MS was performed for the first time, identifying 71 compounds, mostly flavonoids, triterpene glycosides, and ecdysteroids.
  • The compounds schaftoside, 26-hydroxyecdysone, and silviridoside were highlighted as important markers for evaluating preparation quality.
  • The methanol extract demonstrated cytotoxic and Wnt pathway-inhibiting effects against triple-negative breast cancer, identifying 2-Deoxy-20-hydroxyecdysone as potent, while the presence of a hydroxyl group at C-2 in ecdysteroids was linked to reduced cytotoxicity against cancer cells.
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Introduction: Boswellic acids (BAs) are a group of pentacyclic triterpenoids of the ursane and oleanane type. They have shown very interesting biological properties that have led to the development of a number of synthesis protocols. Both natural BAs and their synthetic derivatives may be useful in the treatment of a variety of cancers, viral infections and inflammatory diseases.

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Infectious diseases are a significant challenge to global healthcare, especially in the face of increasing antibiotic resistance. This urgent issue requires the continuous exploration and development of new antimicrobial drugs. In this regard, the secondary metabolites derived from endophytic microorganisms stand out as promising sources for finding antimicrobials.

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  • Isoquinoline alkaloids are important for medicinal purposes, and methods to improve their safety and efficacy are crucial.
  • A one-step synthesis of various tetrahydroisoquinolines was achieved with high yields using the Pictet-Spengler reaction, confirming the structures with advanced spectroscopic techniques.
  • Toxicity studies on these compounds in mice revealed varying levels of toxicity, with some exhibiting promising local anesthetic activity while showing potential safety differences among the derivatives.
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A new triterpene glycoside, silviridoside, was isolated from the aerial parts of (Caryophyllaceae) using different chromatographic techniques. The structure of silviridoside was comprehensively elucidated as 3-β-D-galacturonopyranosyl-quillaic acid 28--β-D-glucopyranosyl-(1→2)-[α-L-rhamnopyranosyl-(1→3)]-β-D-fucopyranosyl ester by one- and two-dimensional nuclear magnetic resonance (NMR) spectroscopy and high-resolution mass spectrometry (HR-MS). Silviridoside showed promising antioxidant activity in different antioxidant assays such as 2,2-diphenyl-1-picrylhydrazyl (DPPH) (2.

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is a potentially valuable aromatic herb that has been used since ancient times. The present work studied the chemical profile of three species essential oils (EO): , and , as well as assessing their antioxidant and enzyme inhibitory activities. A total of 144 compounds were detected by GC-MS analysis, representing 91.

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Ecdysteroids represent arthropods' steroidal hormones, and they exist in about 5-6% of plant species. In this study, the enzyme inhibitory activity of 20 ecdysteroids was assessed for the first time via determining their inhibition versus acetylcholinesterase, butyrylcholinesterase, tyrosinase, as well as α-amylase enzymes. Furthermore, 20-Hydroxyecdysone-2,3,22-tri--acetate () showed the highest inhibition of acetylcholinesterase and butyrylcholinesterase with values of 5.

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Fruits along with vegetables are crucial for a balanced diet. These not only have delicious flavors but are also reported to decrease the risk of contracting various chronic diseases. Fruit by-products are produced in huge quantity during industrial processing and constitute a serious issue because they may pose a harmful risk to the environment.

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The chemical composition of the essential oils (EOs) of , and growing in Uzbekistan were determined, and their antioxidant and enzyme inhibitory activity were assessed. A gas chromatography-mass spectrometry (GC-MS) analysis revealed the presence of 143 metabolites accounting for 70.34, 76.

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  • The study explored the antioxidant and enzyme inhibitory effects of fifteen cycloartane-type triterpenes through various assays.
  • Cycloalpioside D showed the highest antioxidant activity in the phosphomolybdenum method, while cycloorbicosides A and B exhibited strong results in DPPH* and ABTS assays, respectively.
  • Compounds demonstrated powerful inhibition of enzymes like AChE and BChE, with significant activity for tyrosinase and α-amylase, suggesting their potential for pharmacological applications.
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The chemical composition of the essential oils obtained from the aerial parts of four Apiaceae species, namely (EA), (EP), (FC), and (HI), were determined using gas chromatography. Altogether, 100 volatile metabolites representing 78.97, 81.

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  • Researchers isolated a new compound called lehmanniaside from the Bunge plant, which is part of the Leguminosae family.
  • The chemical structure of lehmanniaside was determined using advanced techniques like high-resolution mass spectrometry (HR-MS) and nuclear magnetic resonance (NMR) spectroscopy.
  • Preliminary tests revealed that lehmanniaside has some weak biological activities, including anthelmintic (anti-worm), antifungal, and cytotoxic properties.
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Meroterpenoids are secondary metabolites formed due to mixed biosynthetic pathways which are produced in part from a terpenoid co-substrate. These mixed biosynthetically hybrid compounds are widely produced by bacteria, algae, plants, and animals. Notably amazing chemical diversity is generated among meroterpenoids via a combination of terpenoid scaffolds with polyketides, alkaloids, phenols, and amino acids.

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Phytochemical investigation of the methanolic extract obtained from the aerial parts of (Lamiaceae) afforded the new compound 1-methoxy-3---glucopyranosyl-α-l-oliose () together with five known glycosides, namely sitosterol-3---glucoside (), stigmasterol-3---glucoside (), pinitol (), 6-hydroxyl-7--loganin (), and chlorotuberoside (). The structures of these compounds were elucidated by extensive spectroscopic analyses, especially HR-MS, 1D and 2D NMR spectroscopy. The in vitro cytotoxic activity of the methanolic extract and the isolated compounds was assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) and crystal violet (CV) staining assays.

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The genus (Lamiaceae) is native to Central, South-Central, and Eastern Asia. It comprises 44 species, which have been commonly used as herbal medicines for the treatments of various ailments for thousands of years, especially in Asian countries. This review aims to summarize the chemical constituents and pharmacological activities of species from the genus to unveil opportunities for future research.

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The compositions of volatile components in the aerial parts of six species, namely (), (), (), (), () and (), were investigated using gas chromatograph-mass spectrometry (GC-MS) analysis. Ninety-seven metabolites were identified, accounting for 73.28, 87.

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Phytochemical investigation on the aerial parts of a Lamiaceous medicinal plant Perovskia scrophulariifolia collected in Uzbekistan resulted in the isolation of two new 20-norabietane diterpenes, along with thirteen known diterpenes including one 20-norabietane, eight abietanes, one 6,7-secoabietane, and three icetexanes. The structures of new 20-norabietane diterpenes, perovsfolins C (1) and D (2), were elucidated by spectroscopic analyses aided with calculations of ECD spectra. Perovsfolin C (1) is the first 20-norabietane diterpene possessing a 1,11-epoxy moiety, while perovsfolin D (2) is a 20-norabitetane diterpene with a 2-hydroxy-1,4-quinone moiety as C-ring.

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  • The study focuses on L., a spiny fruit buttercup known for its medicinal properties, and isolates four new compounds alongside three previously reported ones.
  • The structures of the new compounds were analyzed using advanced NMR spectroscopy and mass spectrometry techniques.
  • Among the isolated compounds, chalcone showed significant inhibition of acetylcholinesterase, while anthraquinone displayed some alpha-glucosidase inhibition, and another compound exhibited moderate cytotoxic activity against several cancer cell lines.
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  • Two novel C terpenoids, perovsfolins A and B, were discovered from an Uzbek medicinal plant belonging to the Lamiaceae family.
  • Their unique chemical structures feature a rare pentacyclic carbon skeleton with a C-C ester group, determined through advanced spectroscopic methods and computational analysis.
  • Perovsfolin B showed potential anti-neuroinflammatory effects, suggesting possible medicinal applications.
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The differences in the composition of essential oils obtained from the aerial parts of six species viz., (), (), (), (), () and () were detected both qualitatively and semi-quantitatively using GC-MS and GC-FID analyses. One hundred and six metabolites were identified that account for 92.

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species are mainly distributed in Central Asia and widely used in folk medicine as a sedative and haemostatic. The present investigation reports on the extraction by hydrodistillation and the chemical composition of three species ( and ) essential oils from Uzbekistan. The chemical composition of these essential oils was determined by GC-MS.

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The search for new biologically active compounds is a topic of current research because of their ubiquitous availability and low toxicity. Plants of the Silene genus contain secondary metabolites known as phytoecdysteroids that reportedly have various biological activities. α-Ecdysone is a phytoecdysteroid with biological activity that has not been thoroughly investigated to date.

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Essential oils obtained from the aerial parts of and were determined using GC-FID and GC-MS methods. A total of 76 components were identified in the three species representing 97.12, 88.

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