Abstract:A new alkaloid pyrroloquinolone A (1), along with fifteen known compounds 2-16 were isolated from the petroleum ether, EtOAc and n-BuOH extracts of the whole plant Atractylis cancellata L. Their structures were elucidated on the basis of extensive spectroscopic analysis including 1D-and 2D-NMR and HR-ESI-MS techniques. This is the first report of alkaloids in the genus Atractylis. Some of the isolated compounds and extracts were evaluated for their antioxidant potential (scavenging activity of DPPH and ABTS ra… Show more
“…There are more than ten thousand different natural alkaloids, which can be classified according to their carbon skeletal structures (Ziegler and Facchini, 2008). With the continuous development of modern medication, various biopotentials of natural alkaloids have been explored, including antioxidant (Badaoui et al, 2021), antiproliferative (Hu et al, 2018), anti-obesity (Saunders et al, 2018), antidiabetic (Jan et al, 2018), cardiovascular protection (Li et al, 2021a), anti-aging (Asokan et al, 2018), and antiinflammatory (Hu et al, 2020) effects in experimental trials and clinical applications. At present, natural alkaloids are the mainstream anti-osteoporosis drugs because of their strong efficacy and low toxicity (Ajebli et al, 2021), and some of them have been used clinically.…”
Natural alkaloids are polycyclic, nitrogen-containing, and basic compounds obtained from plants. In this review, the advances in bioactive alkaloids with respect to their chemical structures, herbal sources, and effects for the prevention and treatment of osteoporosis are discussed. Anti-osteoporosis alkaloids are classified into six categories based on the chemical structure, namely, isoquinoline alkaloids, quinolizidine alkaloids, piperidine alkaloids, indole alkaloids, pyrrolizidine alkaloids and steroidal alkaloids. They promote mesenchymal stem cells differentiation, improve osteoblast proliferation, stimulate osteoblast autophagy and suppress osteoclast formation. These natural alkaloids can regulate multiple signaling pathways, including interrupting the tumor necrosis factor receptor associated factor 6- receptor activator of nuclear factor kappa B interaction, inhibiting the nuclear factor kappa B pathway in osteoclasts, activating the p38 mitogen-activated protein kinases pathway in osteoblasts, and triggering the wingless and int-1 pathway in mesenchymal stem cells. This review provides evidence and support for novel drug and clinical treatment of osteoporosis using natural alkaloids.
“…There are more than ten thousand different natural alkaloids, which can be classified according to their carbon skeletal structures (Ziegler and Facchini, 2008). With the continuous development of modern medication, various biopotentials of natural alkaloids have been explored, including antioxidant (Badaoui et al, 2021), antiproliferative (Hu et al, 2018), anti-obesity (Saunders et al, 2018), antidiabetic (Jan et al, 2018), cardiovascular protection (Li et al, 2021a), anti-aging (Asokan et al, 2018), and antiinflammatory (Hu et al, 2020) effects in experimental trials and clinical applications. At present, natural alkaloids are the mainstream anti-osteoporosis drugs because of their strong efficacy and low toxicity (Ajebli et al, 2021), and some of them have been used clinically.…”
Natural alkaloids are polycyclic, nitrogen-containing, and basic compounds obtained from plants. In this review, the advances in bioactive alkaloids with respect to their chemical structures, herbal sources, and effects for the prevention and treatment of osteoporosis are discussed. Anti-osteoporosis alkaloids are classified into six categories based on the chemical structure, namely, isoquinoline alkaloids, quinolizidine alkaloids, piperidine alkaloids, indole alkaloids, pyrrolizidine alkaloids and steroidal alkaloids. They promote mesenchymal stem cells differentiation, improve osteoblast proliferation, stimulate osteoblast autophagy and suppress osteoclast formation. These natural alkaloids can regulate multiple signaling pathways, including interrupting the tumor necrosis factor receptor associated factor 6- receptor activator of nuclear factor kappa B interaction, inhibiting the nuclear factor kappa B pathway in osteoclasts, activating the p38 mitogen-activated protein kinases pathway in osteoblasts, and triggering the wingless and int-1 pathway in mesenchymal stem cells. This review provides evidence and support for novel drug and clinical treatment of osteoporosis using natural alkaloids.
“…In addition, 2-quinolones are embedded as core structures in natural products [ 25 , 26 , 27 , 28 , 29 , 30 , 31 , 32 , 33 , 34 , 35 , 36 , 37 , 38 , 39 , 40 , 41 , 42 , 43 ]. While a number of naturally occurring derivatives have been released, early reports revealed hybrid compounds that are derived from an isoprene unit and quinolones, namely hemiterpenoids [ 35 , 38 , 39 , 40 , 41 , 42 , 43 ].…”
Section: Introductionmentioning
confidence: 99%
“…Targets on this scaffold, β-adrenergic receptors [2][3][4][5], muscarinic acetylcholine receptors [6][7][8], vascular endothelial growth factor receptors [9,10], poly [ADP-ribose] polymerase-1 [11][12][13][14][15], tyrosine-protein kinases [16], and serine/threonine-protein kinases [17][18][19], have been extensively studied for decades. In addition In addition, 2-quinolones are embedded as core structures in natural products [25][26][27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42][43]. While a number of naturally occurring derivatives have been released, early reports revealed hybrid compounds that are derived from an isoprene unit and quinolones, namely hemiterpenoids [35,38- In addition, 2-quinolones are embedded as core structures in natural products [25][26][27][28][29][30][31]…”
Section: Introductionmentioning
confidence: 99%
“…In addition In addition, 2-quinolones are embedded as core structures in natural products [25][26][27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42][43]. While a number of naturally occurring derivatives have been released, early reports revealed hybrid compounds that are derived from an isoprene unit and quinolones, namely hemiterpenoids [35,38- In addition, 2-quinolones are embedded as core structures in natural products [25][26][27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42][43]. While a number of naturally occurring derivatives have been released, early reports revealed hybrid compounds that are derived from an isoprene unit and quinolones, namely hemiterpenoids [35,[38][39][40][41][42][43].…”
It is known that 2-quinolones are broadly applicable chemical structures in medicinal and agrochemical research as well as various functional materials. A number of current publications about their synthesis and their applications emphasize the importance of these small molecules. The early synthetic chemistry originated from the same principle of the classical Friedländer and Knorr procedures for the preparation of quinolines. The analogous processes were developed by applying new synthetic tools such as novel catalysts, the microwave irradiation method, etc., whereas recent innovations in new bond forming reactions have allowed for novel strategies to construct the core structures of 2-quinolones beyond the bond disconnections based on two classical reactions. Over the last few decades, some reviews on structure-based, catalyst-based, and bioactivity-based studies have been released. In this focused review, we extensively surveyed recent examples of one-pot reactions, particularly in view of modular approaches. Thus, the contents are categorized as three major sections (two-, three-, and four-component reactions) according to the number of reagents that ultimately compose atoms of the core structures of 2-quinolones. The collected synthetic methods are discussed from the perspectives of strategy, efficiency, selectivity, and reaction mechanism.
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