Biochemical Systematics and Ecology最新文献

{"title":"Sesquiterpenes from Tinospora sinensis and their chemotaxonomic significance","authors":"Rui Ao,&nbsp;Ming-Hui Li,&nbsp;Zi-Nan Xiao,&nbsp;Xue-Lian Tang,&nbsp;Jun-Sheng Zhang,&nbsp;Hua Zhang","doi":"10.1016/j.bse.2024.104877","DOIUrl":"10.1016/j.bse.2024.104877","url":null,"abstract":"<div><p>Chemical investigation of the <em>Tinospora sinensis</em> led to the isolation of a new cadinane sesquiterpene (<strong>1</strong>) and twelve known sesquiterpenes (<strong>2</strong>−<strong>13</strong>). The structures of these compounds were deduced using a suite of comprehensive spectroscopic techniques including NMR, MS <em>etc.</em>, and the absolute configuration of <strong>1</strong> was established through a combination of TDDFT calculations and chemical methods. Compound <strong>1</strong> demonstrated mild cytotoxicity against MDA-MB-231 cell line, with an inhibition rate of 46.8% and 54.2% at 50 μmol/L and 100 μmol/L, respectively. Compounds <strong>1</strong>, <strong>5</strong>−<strong>13</strong> were reported to exist in the Menispermaceae family for the first time. Furthermore, the chemotaxonomic significance of the isolates is also discussed.</p></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"116 ","pages":"Article 104877"},"PeriodicalIF":1.4,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141946554","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Chemical constituents from Alnus mandshurica and their chemotaxonomic significance","authors":"Chengyu Cui ,&nbsp;Nan Wu ,&nbsp;Xiongjie Yin,&nbsp;Mingjing Zhao,&nbsp;Chonghao Sun,&nbsp;Sihong Wang,&nbsp;Jingyan Zhang,&nbsp;Lili Jin,&nbsp;Changhao Zhang","doi":"10.1016/j.bse.2024.104879","DOIUrl":"10.1016/j.bse.2024.104879","url":null,"abstract":"<div><p>A phytochemical study of <em>Alnus mandshurica</em> (Callier) Hand.-Mazz. (dried stem bark) led to the isolation of 28 compounds, including twelve simple phenols and simple phenol glycosides (<strong>1</strong>–<strong>12</strong>), eleven flavonoids (<strong>13</strong>–<strong>23</strong>), among them, compounds 13, 15, 17, 18, and 23 are flavan-3-ols compounds, two coumarins (<strong>24</strong> and <strong>25</strong>), one diarylheptanoid (<strong>26</strong>), one lupine triterpenoid (<strong>27</strong>), one sterol (<strong>28</strong>). The structures of these isolated compounds were identified using NMR spectroscopy (¹H and ¹³C) by comparison with previously reported data. Compounds <strong>2</strong>, <strong>5</strong>–<strong>14</strong>, <strong>18</strong>, <strong>20</strong>, <strong>22</strong>, <strong>25</strong>–<strong>27</strong> were isolated from <em>A. mandshurica</em> for the first time. The chemotaxonomic significance of the isolates was also discussed.</p></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"116 ","pages":"Article 104879"},"PeriodicalIF":1.4,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141946553","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Chemical composition and bioactivity of essential oils from Cistus ladanifer L., Pistacia lentiscus L., and Matricaria chamomilla L","authors":"Taoufiq Benali ,&nbsp;Mustapha Laghmari ,&nbsp;Jihane Touhtouh ,&nbsp;Tarik Aanniz ,&nbsp;Ahmed Lemhadri ,&nbsp;Mostapha Drissi Daoudi ,&nbsp;Abdelhakim Bouyahya ,&nbsp;Learn-Han Lee ,&nbsp;Riaz Ullah ,&nbsp;Amal Alotaibi ,&nbsp;Mohamed Akhazzane ,&nbsp;Gokhan Zengin ,&nbsp;Khalil Hammani","doi":"10.1016/j.bse.2024.104880","DOIUrl":"10.1016/j.bse.2024.104880","url":null,"abstract":"<div><p>The objective of this study was to characterize the volatile compounds from the aerial part of <em>Cistus ladanifer</em> L., <em>Pistacia lentiscus</em> L., and <em>Matricaria chamomilla</em> L., members of <em>Cistaceae</em>, Anacardiaceae, and Asteraceae families, respectively; and assess their potential antioxidant, antimicrobial, and enzyme inhibitory properties. The essential oils were analyzed using gas chromatography-mass spectrometry (GC-MS-MS) analysis. The outcomes revealed distinct chemical profiles indicative of specific chemotypes within each species. Indeed, <em>M. chamomilla</em> essential oil (MCEO) contained sabinene (16.03 %), camphor (11.22 %), 3,6-dihydrochamazulene (14.22 %), and chamazulene (12.84 %) as its primary constituents. <em>C. ladanifer</em> essential oil (CLEO) prominently featured camphene (31.5 %), α-pinene (15.76%), and bornyl acetate (15.73 %), while <em>P. lentiscus</em> essential oil (PLEO) was rich in D-limonene (21 %), β-myrcene (14.89 %), α-pinene (13.93 %), and terpinen-4-ol (9.75 %). Remarkably, PLEO exhibited significant antioxidant activity across multiple assays, demonstrating inhibitory values of 72.07 ± 4.06 mg TE/g of extract (Cuprac), 45.74 ± 1.23 mg TE/g of extract (FRAP), 30.89 ± 1.69 mg EDTAE/g of extract (Chelating), 26.71 ± 1.84 mmol TE/g of extract (Phosphomolybdenum), 15.55 ± 0.84 mg TE/g of extract (ABTS), and 2.30 ± 0.22 mg TE/g of extract (DPPH). The results showed that the microorganisms under examination varied in their sensitivity to essential oils and the inhibitory zone ranged between 25 and 57 mm. The inhibitory effects of the essential oils were investigated against enzymes associated with human pathologies. As findings, CLEO demonstrated substantial inhibition of tyrosinase (10.22 ± 0.13 mg KAE/g of extract) and acetylcholinesterase (4.71 ± 0.97 mg GALAE/g of extract), outperforming other essential oils that displayed moderate activities. These important biological effects of the oils tested qualify these plants as an interesting source of phytochemicals with medicinal actions.</p></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"116 ","pages":"Article 104880"},"PeriodicalIF":1.4,"publicationDate":"2024-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141946555","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"GC-MS-MS analysis and biological properties determination of Mentha piperita L., essential oils","authors":"Nasreddine El Omari ,&nbsp;Imane Chamkhi ,&nbsp;Abdelaali Balahbib ,&nbsp;Taoufiq Benali ,&nbsp;Mohamed Akhazzane ,&nbsp;Riaz Ullah ,&nbsp;Amal Alotaibi ,&nbsp;Youssef Elouafy ,&nbsp;Hamza Elhrech ,&nbsp;Abdelhakim Bouyahya","doi":"10.1016/j.bse.2024.104875","DOIUrl":"10.1016/j.bse.2024.104875","url":null,"abstract":"<div><p>This research explores the therapeutic properties and medicinal potential of <em>Mentha piperita</em> L. (<em>M. piperita</em>) essential oil (EO) (MPEO) harvested in the province of Ouezzane, northwestern Morocco. We conducted a comprehensive chemical composition analysis of MPEO using gas chromatography-mass spectrometry (GC-MS) to identify its major components. The predominant constituents were pulegone (17.56%), mintlactone (10.62%), _D-carvone (9.24%), eucalyptol (7.53%), and thymol (6.06%). The antidiabetic effects were assessed by measuring the inhibition of two digestive enzymes (α-glucosidase and α-amylase). The dermatoprotective effect was evaluated based on the inhibition of elastase and tyrosinase, and neuroprotective activity was studied by examining the inhibition of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). Additionally, molecular docking analysis was used to determine the interactions between the main MPEO compounds and the enzymes targeted. Antioxidant activity was estimated using <em>in vitro</em> FRAP, DPPH, and ABTS assays. Furthermore, the antibacterial potential was evaluated against pathogenic strains using the micro-broth dilution method. Our results indicate significant antioxidant and neuroprotective activities of MPEO, along with promising antidiabetic and dermatoprotective potential, surpassing references. Additionally, all bacterial strains tested were susceptible to MPEO, with MIC values lower than those of MBC for all bacteria except <em>L. monocytogenes</em>. These <em>in vitro</em> findings were supported by <em>in silico</em> analysis, showing that menthelactone and pulegone presented strong binding affinities with key enzymes involved in glucose regulation and pigmentation. MPEO, rich in bioactive compounds, has shown promising potential. The main components of this oil offer innovative prospects for the development of drugs and natural therapeutic applications.</p></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"116 ","pages":"Article 104875"},"PeriodicalIF":1.4,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141946556","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Secondary metabolites from the barks of Garcinia griffithii T. Anderson (Clusiaceae) and their chemophenetic significance","authors":"Noor Aimi Othman ,&nbsp;Sook Yee Liew ,&nbsp;Kooi Yeong Khaw ,&nbsp;Abdulwali Ablat ,&nbsp;Saiful Anuar Karsani ,&nbsp;Kok Hoong Leong ,&nbsp;Patricia Blanchard ,&nbsp;Severine Derbré ,&nbsp;Khalijah Awang","doi":"10.1016/j.bse.2024.104869","DOIUrl":"10.1016/j.bse.2024.104869","url":null,"abstract":"<div><p>A total of thirteen compounds consisting of nine xanthones; cowagarcinone C (<strong>1</strong>), doitunggarcinone C (<strong>2</strong>), nigrolineaxanthone E (<strong>3</strong>), nigrolineaxanthone Q (<strong>4</strong>), β-mangostin (<strong>5</strong>), 7-<em>O</em>-methylgarcinone E (<strong>6</strong>), dulcisxanthone F (<strong>7</strong>), ananixanthone (<strong>8</strong>) and nigrolineaxanthone N (<strong>9</strong>), two polycyclic polyprenylated acylphloroglucinols (PPAPs); garcinielliptone J (<strong>13</strong>) and garcinialone (<strong>14</strong>) as well as two terpenoids; 30-hydroxycycloartenol (<strong>15</strong>) and garcinane (<strong>16</strong>), were putatively identified with a good confidence level from dichloromethane extract of <em>Garcinia griffithii</em> T. Anderson using the ¹³C NMR-based dereplication and MixONat software. In addition, three xanthones; euxanthone (1,7-dihydroxyxanthone) (<strong>10</strong>), forbexanthone (<strong>11</strong>) and 1,5-hydroxy-3,6-dimethoxy-2,7-diprenylxanthone (<strong>12</strong>) were successfully isolated. The structure of the isolated compounds was confirmed through the analysis of spectroscopic data and comparison with reported data. The ¹³C NMR data of forbexanthone (<strong>11</strong>) was reported for the first time. Interestingly, the dichloromethane extract and 1,5-dihydroxy-3,6-dimethoxy-2,7-diprenylxanthone (<strong>12</strong>) which were evaluated for their exhibited α-glucosidase inhibitory activity exhibited potent inhibition toward the enzyme with IC₅₀ values of 0.66 μg/mL and 3.02 μM, respectively as compared to the standard, acarbose (IC₅₀ = 392 μg/mL or 608 μM). Notably, ananixanthone (<strong>8</strong>) has not been reported from the genus <em>Garcinia</em> while compounds <strong>1</strong>–<strong>7</strong>, <strong>9</strong>, <strong>11</strong> and <strong>13</strong>–<strong>16</strong> being reported from <em>Garcinia griffithii</em> for the first time. In addition, the chemophenetic significance of all the compounds has also been discussed.</p></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"116 ","pages":"Article 104869"},"PeriodicalIF":1.4,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141946559","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A new 7,9′-monoepoxylignan glucoside and other phytochemicals from Centaurea granatensis and their chemotaxonomic significance","authors":"Meriem Belaid ,&nbsp;Soumia Mouffouk ,&nbsp;Sonia Chabani ,&nbsp;Chaima Mouffouk ,&nbsp;Mohammed Benkhaled ,&nbsp;Hamada Haba","doi":"10.1016/j.bse.2024.104874","DOIUrl":"10.1016/j.bse.2024.104874","url":null,"abstract":"<div><p>The chemical study of <em>Centaurea granatensis</em> Boiss. ex DC. allowed the isolation and structural elucidation of eighteen secondary metabolites (<strong>1</strong>–<strong>18)</strong> from ethyl acetate (EtOAc) and <em>n</em>-butanol (<em>n</em>-BuOH) extracts. These compounds are divided into one new epoxylignan glucoside <strong>(1)</strong> and seventeen known phytochemicals including seven flavonoids <strong>(2</strong>–<strong>8)</strong>, four triterpenes <strong>(9</strong>–<strong>12)</strong>, and six phytosterols <strong>(13</strong>–<strong>18)</strong>. Structures of the isolates were identified using various spectroscopic methods, namely 1D NMR (¹H and ¹³C), 2D NMR (HSQC, ¹H–¹H COSY, HMBC, and NOESY), and mass spectrometry (HR-ESIMS), as well as by comparison with literature data. The obtained results showed the abundance of triterpenoids and flavonoids particularly flavones in <em>C. granatensis</em>. Apigenin <strong>(3)</strong> could be used as a chemotaxonomic marker of this genus due to its presence in approximately forty plant species. Furthermore, tiliroside <strong>(2)</strong> and stigmasteryl-3-<em>O</em>-<em>β</em>-D-glucoside-6′-palmitate <strong>(18)</strong> were first detected in <em>Centaurea</em> genus, but had previously been found in species of the Asteraceae family. Additionally, the chemotaxonomic significance of all isolated molecules was fully discussed.</p></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"116 ","pages":"Article 104874"},"PeriodicalIF":1.4,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141946558","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Extraction of phenolic compounds from Acinos rotundifolius pers. And evaluation of bioactivities","authors":"Raziye Ozturk Urek ,&nbsp;Aylin Oner","doi":"10.1016/j.bse.2024.104876","DOIUrl":"10.1016/j.bse.2024.104876","url":null,"abstract":"<div><p>The aim of the present study was to determine the phenolic profile, antioxidant capacities, inhibition of enzymes related to dermatological and neurodegenerative diseases, and cytotoxic properties of <em>Acinos rotundifolius</em> Pers. For this purpose, three different extraction methods were applied: Soxhlet extraction, ultrasonic-assisted extraction (UAE), and infusion (INF). The use of different solvents (ethyl acetate, methanol, water) has also been applied. The RP-HPLC-DAD data highlighted that Soxhlet extraction in MeOH/water is more effective at extracting flavonoids and phenolic acids. The UAE extract, which was richer in chlorogenic acid, exhibited a better scavenging capacity versus HO^•, NO^• and ABTS^•+ were determined by UAE, whereas the one obtained via Soxhlet extraction in water had a better efficacy to eliminate O₂^•. The greatest inhibitory effects on AChE and tyrosinase enzymes were demonstrated by the infusion. The different composition of the extracts obtained with the different methods also influences the cytotoxic properties which were investigated by MTT test on HepG2 and OE-33 cell lines.</p></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"116 ","pages":"Article 104876"},"PeriodicalIF":1.4,"publicationDate":"2024-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141946557","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Caffeoylhexaric acids in Inuleae: A case study of Geigeria alata, Inula helenium, and Telekia speciosa","authors":"Aleksandra Stefanova ,&nbsp;Reneta Gevrenova ,&nbsp;Vessela Balabanova ,&nbsp;Vesela Lozanova ,&nbsp;Ralitsa Alexova ,&nbsp;Dimitrina Zheleva-Dimitrova","doi":"10.1016/j.bse.2024.104873","DOIUrl":"10.1016/j.bse.2024.104873","url":null,"abstract":"<div><p>In the present study, the caffeoylhexaric acids in Inuleae species of Asteraceae family as G<em>eigeria alata</em> Benth. &amp; Hook.f. ex Oliv., <em>Inula helenium</em> L. and <em>Telekia speciosa</em> (Schreb.) Baumg. were profiled by ultra-high performance – liquid chromatography coupled with high resolution mass spectrometry. In the root methanol-aqueous extracts, 32 caffeoylhexaric acids were annotated. A variety of mono-, di-, tri- and terta-caffeoylhexaric acids, as well as their propionyl, isobutyryl, hydroxypropionyl, methylbutyryl/isovaleryl, hydroxybutyryl- and others derivatives were tentatively identified<em>.</em> The study is the first attempt to propose a fragmentation key of caffeoylhexaric acids derivatives by LC-HRMS. The chemophenetic significance of these compounds was discussed based on the results and literature data. The identification of leontopodic acid A and B in the studied Inuleae species highlighted <em>T. speciosa</em> as a new source of caffeoyl-D-glucaric acid derivatives, natural compounds with health-benefit promotion and cosmetic application.</p></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"116 ","pages":"Article 104873"},"PeriodicalIF":1.4,"publicationDate":"2024-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141950142","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Two new anthranilamides with chemotaxonomic value from Delphinium tatsienense","authors":"Xichen Tu ,&nbsp;Jinhuan Chen ,&nbsp;Xiaolin Liu ,&nbsp;Jianmin He","doi":"10.1016/j.bse.2024.104868","DOIUrl":"10.1016/j.bse.2024.104868","url":null,"abstract":"<div><h3>Delphinium</h3><p>L. (Ranunculaceae) is a taxonomically complex genus composed of approximately 365 species of perennial herbs. Chemical taxonomy is highly important for assisting and supplementing the taxonomy of this genus. In the present study, <em>Delphinium tatsienense</em> Franch., a Chinese endemic <em>Delphinium</em> species, was phytochemically investigated, which led to the discovery of two previously undescribed anthranilamide derivatives, tatsieamides A and B (<strong>1</strong>–<strong>2</strong>). The isolated anthranilamides possess chemotaxonomic value and could be utilized as good chemical markers to provide valuable information for the chemotaxonomy of <em>D</em>. <em>tatsienense</em> and related species.</p></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"116 ","pages":"Article 104868"},"PeriodicalIF":1.4,"publicationDate":"2024-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141960072","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Chemical constituents from Elephantopus scaber L. and their chemotaxonomic significant","authors":"Ze-Ming Wu ,&nbsp;Mei-Ya Lian ,&nbsp;Xiao-Yu Han,&nbsp;Ming Bai,&nbsp;Shao-Jiang Song","doi":"10.1016/j.bse.2024.104871","DOIUrl":"10.1016/j.bse.2024.104871","url":null,"abstract":"<div><p>The isolation of eight compounds from <em>Elephantopus scaber</em> L. through phytochemical studies yielded six lignans (<strong>1</strong>–<strong>6</strong>), two flavonoids (<strong>7</strong>–<strong>8</strong>), and two triterpenoids (<strong>9</strong>–<strong>10</strong>). The structures of these compounds were identified using thorough spectroscopic methods and compared with existing literature data. Notably, compounds <strong>1</strong>–<strong>4</strong>, <strong>6</strong>, and <strong>8</strong> were newly discovered in the Asteraceae family as per the analysis. Furthermore, the chemical classification of these isolated compounds was deliberated.</p></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"116 ","pages":"Article 104871"},"PeriodicalIF":1.4,"publicationDate":"2024-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141960073","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}