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  1. Article ; Online: A Review on Anomalin: A Natural Bioactive Pyranocoumarin from the Past to the Future.

    Onder, Alev / Trendafilova, Antoaneta

    Chemistry & biodiversity

    2022  Volume 19, Issue 9, Page(s) e202200167

    Abstract: Anomalin is a seselin-type pyranocoumarin isolated for the first time from Angelica anomala Avé-Lal, but is also found in several other plant species, especially in Apiaceae. This lipophilic molecule possesses pharmacologically beneficial activities for ... ...

    Abstract Anomalin is a seselin-type pyranocoumarin isolated for the first time from Angelica anomala Avé-Lal, but is also found in several other plant species, especially in Apiaceae. This lipophilic molecule possesses pharmacologically beneficial activities for human health. The major scientific databases Scopus, Web of Science, Google Scholar, and PubMed up to the end of 2021 and the combining terms anomalin, praeruptorin, isolation, structure elucidation, and biological activity were used in the research of this review. This review focuses on the sources, structural properties, and biological functions of anomalin and provides future trends in the investigation of anomalin, particularly in therapies for many common diseases such as anti-inflammatory and neurodegenerative illnesses. As a potential bioactive molecule, prospective studies on anomalin should be done through supported clinical trials. At the end, this review confirms the significant pharmacological potential of anomalin.
    MeSH term(s) Anti-Inflammatory Agents ; Apiaceae/chemistry ; Coumarins ; Ethnopharmacology ; Humans ; Phytochemicals ; Plant Extracts/pharmacology ; Prospective Studies ; Pyranocoumarins/pharmacology
    Chemical Substances Anti-Inflammatory Agents ; Coumarins ; Phytochemicals ; Plant Extracts ; Pyranocoumarins ; anomalin (81740-07-0)
    Language English
    Publishing date 2022-08-31
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2139001-0
    ISSN 1612-1880 ; 1612-1872
    ISSN (online) 1612-1880
    ISSN 1612-1872
    DOI 10.1002/cbdv.202200167
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: The comparison of the phytochemical composition, antioxidant and enzyme inhibition activity of two moss species: Plagiomnium ellipticum (Brid.) T. Kop. and Antitrichia californica Sull., from southwest ecological region in Turkey

    Onder, Alev / Yıldız, Aybala / Cinar, Ahsen Sevde / Zengin, Gokhan / Ak, Gunes / Ozenoğlu, Hatice

    Natural product research. 2022 May 23, v. 36, no. 10

    2022  

    Abstract: A limited number of mosses have been studied regarding antioxidant activity and enzyme inhibition effects. In the present study, the phytochemical content, antioxidant, and enzyme inhibition properties of the ether extracts from T.J.Kop.. were ... ...

    Abstract A limited number of mosses have been studied regarding antioxidant activity and enzyme inhibition effects. In the present study, the phytochemical content, antioxidant, and enzyme inhibition properties of the ether extracts from T.J.Kop.. were investigated as promising bryophyte sources. The ether extracts of P. ellipticum had the highest flavonoid content (52.41 ± 0.52, Rutin equivalent), and A. californica had the highest total phenolic content (25.84 ± 0.23, Gallic acid equivalent). While the P. ellipticum had the highest ABTS (mg TE/g extract) 6.60 ± 0.4); A. californica showed the highest metal chelating capacity (mg EDTA/g extract) with the values of 51.46 ± 0.26. In the enzyme activity tests, almost all values of the species were closed the each other, but P. ellipticum was exhibited higher tyrosinase activity (mg/KAE/g extract) with 48.64 ± 1.02. The results have indicated for the first time the potential importance of the selected mosses.
    Keywords Antitrichia californica ; Plagiomnium ; antioxidant activity ; antioxidants ; chemical constituents of plants ; ecoregions ; enzyme activity ; enzyme inhibition ; gallic acid ; mosses and liverworts ; research ; rutin
    Language English
    Dates of publication 2022-0523
    Size p. 2660-2665.
    Publishing place Taylor & Francis
    Document type Article
    ZDB-ID 2185747-7
    ISSN 1478-6427 ; 1478-6419
    ISSN (online) 1478-6427
    ISSN 1478-6419
    DOI 10.1080/14786419.2021.1916745
    Database NAL-Catalogue (AGRICOLA)

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  3. Article: Coumarins from Seseli petraeum M. Bieb. (Apiaceae) and their α-glucosidase inhibitory activity

    Onder, Alev / Cinar, Ahsen Sevde / Baran, Merve Yuzbasioglu / Kuruüzüm-Uz, Ayşe / Trendafilova, Antoaneta

    SAAB South African journal of botany. 2022 Jan., v. 144

    2022  

    Abstract: Seseli L. species from the Apiaceae family are well-known medicinal plants with rich bioactive components. In the present study, the phytochemical investigation of the n-hexane extract of the aerial parts from Seseli petraeum M. Bieb., a fairly narrow ... ...

    Abstract Seseli L. species from the Apiaceae family are well-known medicinal plants with rich bioactive components. In the present study, the phytochemical investigation of the n-hexane extract of the aerial parts from Seseli petraeum M. Bieb., a fairly narrow growing plant on the northern side of Turkey, led to the isolation of one new pyranocoumarin called 3′-isovaleryl-4′-oxo-lomatin (petracoumarin, (1) along with 12 known coumarins octanoyllomatin (2), selinidin (3), anomalin (4), 3′-isobutryl-lomatin (5), 3′-angeloyl-4′-isovaleryl-cis-khellactone (6), 3′-isovaleryl-4′-angeloyl-cis-khellactone (7), calipteryxin (8), samidin (9), 4′-senecioyl-cis-khellactone (10), 3′-senecioyl-cis-khellactone (11), cis-khellactone (12) and angelicin (13), and six plant sterols (campesterol, stigmasterol, β-sitosterol, stigmastanol, stigma-7-en-3-ol and γ-ergosterol, 14–19). The structures of the coumarins were elucidated by spectroscopic methods, including extensive 1D/2D NMR, and MS techniques. In addition, several coumarins have been tested for their inhibitory activity against α-amylase and α-glucosidase enzymes. The coumarins exhibited notable inhibitory activity against the α-glucosidase enzyme and low inhibitory potential against α-amylase. Among the tested compounds, octanoyllomatin (2) was found to be the best inhibitor of α-glucosidase with IC₅₀ = 69.00 ± 0.43 µg/mL. The promising results will guide our future studies and suggest that more detailed studies can be done on in vivo models.
    Keywords Seseli ; alpha-amylase ; campesterol ; coumarins ; hexane ; stigmasterol
    Language English
    Dates of publication 2022-01
    Size p. 458-463.
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 2126918-X
    ISSN 0254-6299
    ISSN 0254-6299
    DOI 10.1016/j.sajb.2021.09.022
    Database NAL-Catalogue (AGRICOLA)

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  4. Article: The characterization of phenolic compounds via LC-ESI-MS/MS, antioxidant, enzyme inhibitory activities of Salvia absconditiflora, Salvia sclarea, and Salvia palaestina: A comparative analysis

    Onder, Alev / Izgi, Mehmet Necat / Cinar, Ahsen Sevde / Zengin, Gokhan / Yilmaz, Mustafa Abdullah

    SAAB South African journal of botany. 2022 Nov., v. 150

    2022  

    Abstract: Salvia L. genus, one of the medicinal and aromatic plants belonging to the Lamiaceae family, is represented by many endemic species in temperate regions worldwide. The Salvia species have plenty of usages in traditional medicine, important ... ...

    Abstract Salvia L. genus, one of the medicinal and aromatic plants belonging to the Lamiaceae family, is represented by many endemic species in temperate regions worldwide. The Salvia species have plenty of usages in traditional medicine, important pharmacological effects and economic value. In this context, this study was conducted to evaluate the chemical profile and potential bioactivity of ethyl acetate extracts from 3 different Salvia species; Salvia absconditiflora (Salvia cryptantha- an endemic species), S. sclarea and S. palaestina collected from different localities in Anatolia. Total phenolic-flavonoid contents, antioxidant properties and enzyme inhibition experiments were investigated in tested Salvia species. The phenolic profiles were also determined by liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). The analysis revealed the presence of phenolic compounds in ethyl acetate extracts such as cynaroside, rosmarinic acid, cosmosiin, luteolin, apigenin and acacetin. The highest level of phenolic components was detected in S. absconditiflora with 74.16 mg GAE/g. The best radical scavenging and reducing abilities were found in S. absconditiflora (DPPH: 251.39 mg TE/g; ABTS: 340.16 mg TE/g; CUPRAC: 496.20 mg TE/g; FRAP: 322.94 mg TE/g). Moreover, the inhibition of AChE, BChE, and α-amylase has also been studied. The most potent AChE inhibitory ability was recorded in S. sclarea (4.00 mg GALAE/g), followed by S. palaestina (3.38 mg GALAE/g) and S. absconditiflora (3.01 mg GALAE/g). The extracts exhibited similar amylase inhibitory effects. These results reveal that Salvia species [S. absconditiflora (S. cryptantha), S. sclarea and S. palaestina] confirming their potential can be rich sources of promising bioactive compounds as a starting point for further analysis. In addition, it is thought that this study may be the new report for the construction of helpful databases in terms of shedding light on future research and researchers with the valuable information obtained about these economically important Salvia species.
    Keywords Salvia absconditiflora ; Salvia sclarea ; Turkey (country) ; alpha-amylase ; antioxidants ; apigenin ; economic valuation ; enzyme inhibition ; ethyl acetate ; indigenous species ; luteolin ; rosmarinic acid ; tandem mass spectrometry ; traditional medicine
    Language English
    Dates of publication 2022-11
    Size p. 313-322.
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 2126918-X
    ISSN 0254-6299
    ISSN 0254-6299
    DOI 10.1016/j.sajb.2022.07.030
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  5. Article ; Online: Seseli petraeum M. Bieb. (Apiaceae) Significantly Inhibited Cellular Growth of A549 Lung Cancer Cells through G0/G1 Cell Cycle Arrest.

    Cinar, Ahsen S / Bakar-Ates, Filiz / Onder, Alev

    Anais da Academia Brasileira de Ciencias

    2020  Volume 92, Issue 4, Page(s) e20191533

    Abstract: Seseli L. is an important genus of the Apiaceae family, with a large number of aromatic species. It is used in traditional medicine extensively, but there is quite limited information on their phytochemicals and biological activities. Seseli petraeum M. ... ...

    Abstract Seseli L. is an important genus of the Apiaceae family, with a large number of aromatic species. It is used in traditional medicine extensively, but there is quite limited information on their phytochemicals and biological activities. Seseli petraeum M. Bieb. grows in Northern Anatolia, and there are no phytochemical studies on this species. In the present study, we aimed to investigate the effect of the extracts of S. petraeum on A549 lung cancer cell proliferation. For this purpose, the antiproliferative effect was determined via MTT assay, and the extracts obtained from the root of S. petraeum showed a significant inhibitory effect on cell proliferation. The hexane extract of the root exhibited potent inhibition on A549 cancer cell growth at the 24th hour with 3.432 mg/mL IC50 value. The results also showed that the hexane extract had displayed cytotoxic effect through an arrest at the G0/G1 phase of the cell cycle and induced apoptosis as well as DNA damage of A549 cells. Consequently, this study demonstrated the antiproliferative potential of the extracts from S. petraeum, especially hexane extract from the roots. Further studies are required to identify the mechanisms underlying these effects.
    MeSH term(s) A549 Cells ; Apiaceae ; Apoptosis ; Cell Cycle ; Cell Line, Tumor ; Cell Proliferation ; G1 Phase Cell Cycle Checkpoints ; Humans ; Lung Neoplasms/drug therapy ; Plant Extracts/pharmacology
    Chemical Substances Plant Extracts
    Language English
    Publishing date 2020-11-20
    Publishing country Brazil
    Document type Journal Article
    ZDB-ID 2046885-4
    ISSN 1678-2690 ; 0001-3765
    ISSN (online) 1678-2690
    ISSN 0001-3765
    DOI 10.1590/0001-3765202020191533
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Identifying phenolics by UPLC-MS/MS in some Prangos Lindl. species and α-glucosidase inhibitory activities.

    Onder, Alev / Gülmez, Nazif / Baran, Merve Yuzbasioglu / Kuruuzum-Uz, Ayse / Trendafilova, Antoaneta / Cinar Koc, Ahsen Sevde / Cakir, Oguz / Yilmaz, Mustafa Abdullah

    Journal of pharmaceutical and biomedical analysis

    2023  Volume 236, Page(s) 115733

    Abstract: Diabetes mellitus is a chronic metabolic disorder associated with biochemical, physiological, and pathological changes in the liver and characterized by some deficiencies in insulin secretion or insulin action. Prangos Lindl. species are important plants ...

    Abstract Diabetes mellitus is a chronic metabolic disorder associated with biochemical, physiological, and pathological changes in the liver and characterized by some deficiencies in insulin secretion or insulin action. Prangos Lindl. species are important plants used as spice and medicine in Asian countries, including Türkiye. This study first aimed to evaluate the antidiabetic potential of the aerial parts of the 5 different Prangos species (Apiaceae) collected from various locations to discover and identify bioactive phenolic components. The results revealed that the methanolic extract of P. heyniae exhibited the highest activity against α-glucosidase inhibition compared to the other Prangos species (IC
    MeSH term(s) alpha-Glucosidases ; Plant Extracts/chemistry ; Antioxidants/pharmacology ; Chromatography, Liquid ; alpha-Amylases ; Tandem Mass Spectrometry ; Hypoglycemic Agents/chemistry
    Chemical Substances alpha-Glucosidases (EC 3.2.1.20) ; Plant Extracts ; Antioxidants ; alpha-Amylases (EC 3.2.1.1) ; Hypoglycemic Agents
    Language English
    Publishing date 2023-09-21
    Publishing country England
    Document type Journal Article
    ZDB-ID 604917-5
    ISSN 1873-264X ; 0731-7085
    ISSN (online) 1873-264X
    ISSN 0731-7085
    DOI 10.1016/j.jpba.2023.115733
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  7. Article: Anti-allergic activities of Umbelliferone against histamine- and Picryl chloride-induced ear edema by targeting Nrf2/iNOS signaling in mice

    Younas / Khan, Ashrafullah / Shehzad, Omer / Seo, Eun Kyoung / Onder, Alev / Khan, Salman

    BMC complementary medicine and therapies. 2021 Dec., v. 21, no. 1

    2021  

    Abstract: BACKGROUND: The current study was aimed to investigate the anti-allergic activities of the Umbelliferone (UMB) against the acute Histamine and chronic Picryl chloride (PiCl)-induced allergy in mice. UMB is a coumarin derivative (isolated from Angelica ... ...

    Abstract BACKGROUND: The current study was aimed to investigate the anti-allergic activities of the Umbelliferone (UMB) against the acute Histamine and chronic Picryl chloride (PiCl)-induced allergy in mice. UMB is a coumarin derivative (isolated from Angelica decursiva) found in various parts of the plants such as flowers, roots and, stems isolated from the plants of Umbelliferae family. METHODS: The UMB (1, 10, 50 mg/kg) was administered intraperitoneally (i.p) half an h before or 2 h after the induction of allergic ear edema. The acute ear edema was induced by histamine (intradermally, i.d), while the chronic ear edema was induced by painting the PiCl (sensitized with the toluene) on the ear. The antioxidants and oxidative stress markers were assessed. The histological changes were assessed using Hematoxylin and eosin (H and E) and giemsa staining. The immunohistochemistry studies were performed to assess the expression of the nuclear factor erythroid 2-related factor 2 (Nrf2) and inducible nitric oxide synthase (iNOS). The data was analyzed using one-way ANOVA tests followed by Tukey’s test with p < 0.05 was chosen as criteria for statistical significance. RESULTS: UMB treatment markedly reduced the allergic ear edema and ear weight compared to the negative control. Furthermore, the UMB attenuated the oxidative stress markers, while induced the antioxidants enzymes. Similarly, the UMB treatment significantly attenuated the serum immunoglobulin E (IgE) level. The UMB treatment markedly improved the histological parameters using H and E staining and Giemsa staining. The UMB administration induced the Nrf2 expression, while attenuated the iNOS expression. Furthermore, the computational analysis was performed to assess the interaction of the UMB with the various protein targets and to determine the mechanism of interaction with the target proteins. CONCLUSION: In conclusion, the UMB treatment significantly alleviated the allergic symptoms, attenuating the oxidative stress, improved the histological features using in vivo and computational approaches.
    Keywords Angelica ; alternative medicine ; anti-allergic agents ; blood serum ; chlorides ; coumarin ; ears ; edema ; eosin ; histamine ; hypersensitivity ; immunoglobulin E ; immunohistochemistry ; inducible nitric oxide synthase ; oxidative stress ; toluene ; umbelliferones
    Language English
    Dates of publication 2021-12
    Size p. 215.
    Publishing place BioMed Central
    Document type Article
    ISSN 2662-7671
    DOI 10.1186/s12906-021-03384-1
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  8. Article ; Online: A review on the recent advances in HPLC, UHPLC and UPLC analyses of naturally occurring cannabinoids (2010-2019).

    Nahar, Lutfun / Onder, Alev / Sarker, Satyajit D

    Phytochemical analysis : PCA

    2019  Volume 31, Issue 4, Page(s) 413–457

    Abstract: Introduction: Organic molecules that bind to cannabinoid receptors are called cannabinoids, and they have similar pharmacological properties like the plant, Cannabis sativa L. Hyphenated liquid chromatography (LC), incorporating high-performance liquid ... ...

    Abstract Introduction: Organic molecules that bind to cannabinoid receptors are called cannabinoids, and they have similar pharmacological properties like the plant, Cannabis sativa L. Hyphenated liquid chromatography (LC), incorporating high-performance liquid chromatography (HPLC) and ultra-performance liquid chromatography (UPLC, also known as ultrahigh-performance liquid chromatography, UHPLC), usually coupled to an ultraviolet (UV), UV-photodiode array (PDA) or mass spectrometry (MS) detector, has become a popular analytical tool for the analysis of naturally occurring cannabinoids in various matrices.
    Objective: To review literature on the use of various LC-based analytical methods for the analysis of naturally occurring cannabinoids published since 2010.
    Methodology: A comprehensive literature search was performed utilising several databases, like Web of Knowledge, PubMed and Google Scholar, and other relevant published materials including published books. The keywords used, in various combinations, with cannabinoids being present in all combinations, in the search were Cannabis, hemp, cannabinoids, Cannabis sativa, marijuana, analysis, HPLC, UHPLC, UPLC, quantitative, qualitative and quality control.
    Results: Since 2010, several LC methods for the analysis of naturally occurring cannabinoids have been reported. While simple HPLC-UV or HPLC-UV-PDA-based methods were common in cannabinoids analysis, HPLC-MS, HPLC-MS/MS, UPLC (or UHPLC)-UV-PDA, UPLC (or UHPLC)-MS and UPLC (or UHPLC)-MS/MS, were also used frequently. Applications of mathematical and computational models for optimisation of different protocols were observed, and pre-analyses included various environmentally friendly extraction protocols.
    Conclusions: LC-based analysis of naturally occurring cannabinoids has dominated the cannabinoids analysis during the last 10 years, and UPLC and UHPLC methods have been shown to be superior to conventional HPLC methods.
    MeSH term(s) Cannabinoids ; Cannabis ; Chromatography, High Pressure Liquid ; Tandem Mass Spectrometry
    Chemical Substances Cannabinoids
    Language English
    Publishing date 2019-12-17
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 1073576-8
    ISSN 1099-1565 ; 0958-0344
    ISSN (online) 1099-1565
    ISSN 0958-0344
    DOI 10.1002/pca.2906
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  9. Article ; Online: Anti-allergic activities of Umbelliferone against histamine- and Picryl chloride-induced ear edema by targeting Nrf2/iNOS signaling in mice.

    Younas / Khan, Ashrafullah / Shehzad, Omer / Seo, Eun Kyoung / Onder, Alev / Khan, Salman

    BMC complementary medicine and therapies

    2021  Volume 21, Issue 1, Page(s) 215

    Abstract: Background: The current study was aimed to investigate the anti-allergic activities of the Umbelliferone (UMB) against the acute Histamine and chronic Picryl chloride (PiCl)-induced allergy in mice. UMB is a coumarin derivative (isolated from Angelica ... ...

    Abstract Background: The current study was aimed to investigate the anti-allergic activities of the Umbelliferone (UMB) against the acute Histamine and chronic Picryl chloride (PiCl)-induced allergy in mice. UMB is a coumarin derivative (isolated from Angelica decursiva) found in various parts of the plants such as flowers, roots and, stems isolated from the plants of Umbelliferae family.
    Methods: The UMB (1, 10, 50 mg/kg) was administered intraperitoneally (i.p) half an h before or 2 h after the induction of allergic ear edema. The acute ear edema was induced by histamine (intradermally, i.d), while the chronic ear edema was induced by painting the PiCl (sensitized with the toluene) on the ear. The antioxidants and oxidative stress markers were assessed. The histological changes were assessed using Hematoxylin and eosin (H and E) and giemsa staining. The immunohistochemistry studies were performed to assess the expression of the nuclear factor erythroid 2-related factor 2 (Nrf2) and inducible nitric oxide synthase (iNOS). The data was analyzed using one-way ANOVA tests followed by Tukey's test with p < 0.05 was chosen as criteria for statistical significance.
    Results: UMB treatment markedly reduced the allergic ear edema and ear weight compared to the negative control. Furthermore, the UMB attenuated the oxidative stress markers, while induced the antioxidants enzymes. Similarly, the UMB treatment significantly attenuated the serum immunoglobulin E (IgE) level. The UMB treatment markedly improved the histological parameters using H and E staining and Giemsa staining. The UMB administration induced the Nrf2 expression, while attenuated the iNOS expression. Furthermore, the computational analysis was performed to assess the interaction of the UMB with the various protein targets and to determine the mechanism of interaction with the target proteins.
    Conclusion: In conclusion, the UMB treatment significantly alleviated the allergic symptoms, attenuating the oxidative stress, improved the histological features using in vivo and computational approaches.
    MeSH term(s) Animals ; Anti-Allergic Agents/pharmacology ; Antioxidants/pharmacology ; Dose-Response Relationship, Drug ; Ear Auricle/drug effects ; Edema/chemically induced ; Edema/drug therapy ; Mice ; Oxidative Stress/drug effects ; Plant Extracts/pharmacology ; Umbelliferones/pharmacology
    Chemical Substances Anti-Allergic Agents ; Antioxidants ; Plant Extracts ; Umbelliferones
    Language English
    Publishing date 2021-08-27
    Publishing country England
    Document type Journal Article
    ISSN 2662-7671
    ISSN (online) 2662-7671
    DOI 10.1186/s12906-021-03384-1
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  10. Article ; Online: The comparison of the phytochemical composition, antioxidant and enzyme inhibition activity of two moss species:

    Onder, Alev / Yıldız, Aybala / Cinar, Ahsen Sevde / Zengin, Gokhan / Ak, Gunes / Ozenoğlu, Hatice

    Natural product research

    2021  Volume 36, Issue 10, Page(s) 2660–2665

    Abstract: A limited number of mosses have been studied regarding antioxidant activity and enzyme inhibition effects. In the present study, the phytochemical content, antioxidant, and enzyme inhibition properties of the ether extracts from T.J.Kop.. were ... ...

    Abstract A limited number of mosses have been studied regarding antioxidant activity and enzyme inhibition effects. In the present study, the phytochemical content, antioxidant, and enzyme inhibition properties of the ether extracts from T.J.Kop.. were investigated as promising bryophyte sources. The ether extracts of
    MeSH term(s) Antioxidants/chemistry ; Antioxidants/pharmacology ; Bryophyta ; Ethers ; Phytochemicals/chemistry ; Phytochemicals/pharmacology ; Plant Extracts/chemistry ; Plant Extracts/pharmacology ; Turkey
    Chemical Substances Antioxidants ; Ethers ; Phytochemicals ; Plant Extracts
    Language English
    Publishing date 2021-05-05
    Publishing country England
    Document type Journal Article
    ZDB-ID 2185747-7
    ISSN 1478-6427 ; 1478-6419
    ISSN (online) 1478-6427
    ISSN 1478-6419
    DOI 10.1080/14786419.2021.1916745
    Database MEDical Literature Analysis and Retrieval System OnLINE

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