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Natural Products from Glycyrrhiza uralensis

Natural Products Isolated from Glycyrrhiza uralensis

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  • Broad structural diversity and coverage of biological activities.
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Natural products isolated from Glycyrrhiza uralensis
Natural products isolated from Glycyrrhiza uralensis

Natural Products from Glycyrrhiza uralensis

40 natural product s associated with Glycyrrhiza uralensis

Natural products and bioactive compounds from Glycyrrhiza uralensis
Catalog No. Product Name CAS Number COA
BCN9061 (±)-Naringenin
(±)-Naringenin chemical structure
67604-48-2 COA
BCN4294 2,3-Dehydrokievitone
2,3-Dehydrokievitone chemical structure
74161-25-4 COA
BCN5549 Astragalin
Astragalin chemical structure
480-10-4 COA
BCN5524 Betulinic acid
Betulinic acid chemical structure
472-15-1 COA
BCN5930 Calycosin
Calycosin chemical structure
20575-57-9 COA
BCN5891 Daidzin
Daidzin chemical structure
552-66-9 COA
BCN6277 Echinatin
Echinatin chemical structure
34221-41-5 COA
BCN1209 Eriodictyol
Eriodictyol chemical structure
552-58-9 COA
BCN5024 Fisetin
Fisetin chemical structure
528-48-3 COA
BCN1061 Formononetin
Formononetin chemical structure
485-72-3 COA
BCN5730 Galangin
Galangin chemical structure
548-83-4 COA
BCN5488 Genkwanin
Genkwanin chemical structure
437-64-9 COA
BCN1221 Glabridin
Glabridin chemical structure
59870-68-7 COA
BCN5895 Glycitin
Glycitin chemical structure
40246-10-4 COA
BCN5942 Glycyrrhetinic acid
Glycyrrhetinic acid chemical structure
471-53-4 COA
BCN2930 Glycyrrhisoflavone
Glycyrrhisoflavone chemical structure
116709-70-7 COA
BCN5941 Glycyrrhizic acid
Glycyrrhizic acid chemical structure
1405-86-3 COA
BCN5943 Glycyrrhizic acid ammonium salt
Glycyrrhizic acid ammonium salt chemical structure
53956-04-0 COA
BCN5415 Isobavachalcone
Isobavachalcone chemical structure
20784-50-3 COA
BCN4512 Isoliquiritigenin
Isoliquiritigenin chemical structure
961-29-5 COA
BCN5945 Isoliquiritin
Isoliquiritin chemical structure
5041-81-6 COA
BCN2914 Isoliquiritin apioside
Isoliquiritin apioside chemical structure
120926-46-7 COA
BCN5569 Isoquercitrin
Isoquercitrin chemical structure
482-35-9 COA
BCN6332 Licochalcone A
Licochalcone A chemical structure
58749-22-7 COA
BCN6333 Licochalcone B
Licochalcone B chemical structure
58749-23-8 COA
BCN2929 Licoisoflavone A
Licoisoflavone A chemical structure
66056-19-7 COA
BCN5946 Liquiritigenin
Liquiritigenin chemical structure
578-86-9 COA
BCN5944 Liquiritin
Liquiritin chemical structure
551-15-5 COA
BCN6312 Naringin
Naringin chemical structure
10236-47-2 COA
BCN2907 Neoglycyrol
Neoglycyrol chemical structure
23013-84-5 COA
BCX1186 Neoisoliquiritigenin
Neoisoliquiritigenin chemical structure
7014-39-3 COA
BCN6663 Neoliquiritin
Neoliquiritin chemical structure
5088-75-5 COA
BCN5616 Oleanolic acid
Oleanolic acid chemical structure
508-02-1 COA
BCN5926 Ononin
Ononin chemical structure
486-62-4 COA
BCN5553 Orobol
Orobol chemical structure
480-23-9 COA
BCN5581 Osthol
Osthol chemical structure
484-12-8 COA
BCN5556 Pinocembrin
Pinocembrin chemical structure
480-39-7 COA
BCN1684 Rutin
Rutin chemical structure
153-18-4 COA
BCN2931 Semilicoisoflavone B
Semilicoisoflavone B chemical structure
129280-33-7 COA
BCN3013 Vicenin -2
Vicenin -2 chemical structure
23666-13-9 COA

References

Prenylated Flavonoids from Roots of Glycyrrhiza uralensis Induce Differentiation of B16-F10 Melanoma Cells.[Pubmed: 30115883]


None


[Complex network analysis of law on Chinese herbal drugs intervention on radiation induced lung injury].[Pubmed: 30111064]


To mainly analyze the prescription rules of Chinese herbal drugs for radiation induced lung injury, optimize the prescriptions, and provide a reference for the clinical treatment of radiation induced lung injury. The major Chinese databases CNKI, CBM and Wanfang data were searched to obtain the literature on Chinese herbal drugs for radiation induced lung injury. BICOMS 2 software was used to extract and collect all Chinese herbal drugs information and generate the co-occurrence matrix; NetDraw and Gcluto software were then used to make network map and visualization matrix for analysis. A total of 552 articles (19 types and 304 Chinese herbal drugs) were included. Ophiopogon japonicus had the highest frequency (229 times), followed by Astragalus membranaceus(181 times), Glycyrrhiza uralensis (166 times), and Scutellaria baicalensis (150 times). After the classification of efficacy, deficiency-supplementing medicinal (69 kinds of Chinese herbs), heat-clearing medicine (51 kinds of Chinese herbs) and phlegm cough medicine (42 kinds of Chinese herbs) accounted for 53.29% of all the Chinese herbs, acting in the main position. After the prescription analysis for the top 25 herbal prescriptions, six main structures of common prescriptions were found for the treatment of radiation induced lung injury. There are many kinds of Chinese herbal drugs for the treatment of radiation induced lung injury in clinical application. In the future, researchers can mainly focus on Ophiopogon japonicus etc. as the main drugs, combine with other high-frequency Chinese herbal drugs found in this study, or directly refer to the main structures of commonly used prescriptions found in this analysis.


Anti-melanogenesis effect of dehydroglyasperin C through the downregulation of MITF via the reduction of intracellular cAMP and acceleration of ERK activation in B16F1 melanoma cells.[Pubmed: 30099299]


In mammals, UV radiation induces melanin synthesis in melanocyte for protecting their skin through the stimulation of α-melanocyte stimulating hormone (α-MSH) from keratinocytes. In this study, the inhibitory effects of dehydroglyasperin C (DGC), an useful component of Glycyrrhiza uralensis (G. uralensis), was investigated on melanogenesis induced by α-melanocyte stimulating hormone (α-MSH) and its mechanisms.


Isoliquiritigenin suppresses human melanoma growth by targeting miR-301b/LRIG1 signaling.[Pubmed: 30081934]


Isoliquiritigenin (ISL), a natural flavonoid isolated from the root of licorice (Glycyrrhiza uralensis), has shown various pharmacological properties including anti-oxidant, anti-inflammatory and anti-cancer activities. MicroRNAs (miRNAs), a class of small non-coding RNAs, have been reported as post-transcriptional regulators with altered expression levels in melanoma. This study aims to investigate the anti-melanoma effect of ISL and its potential mechanism.


Biological Effects Of Licochalcones.[Pubmed: 30049263]


Licorice root (Radix Glycyrrhizae) is a common perennial plants native to Mediterranean countries, central to southern Russia, Asia, Turkey, Iraq and Iran used in traditional Chinese medicine for centuries and licorice has been described as 'the grandfather of herbs' .The genus name Glycyrrhiza (family Leguminoseae) is derived from the ancient Greek words glycos (meaning sweet) and rhiza (meaning root). It consists of about 30 species, but most common ones are Glycyrrhiza glabra L., Glycyrrhiza uralensis Fisch and Glycyrrhiza Inflata. It is known that licorice root contains various chalcones which are an important class of natural products, precursors of flavonoids. Chemically, chalcones consist of open-chain flavonoids, wherein two aromatic rings are joined by a three-carbon α, β-unsaturated ketone, which represent the fundamental nucleus of the structure. They are classified according to chemical structures in Licochalcone A, B, C, D, E, F and G. This review aims to highlight all the in vitro and in vivo studies that have been conducted on the licochalcones, extracted from Glycyrrhiza species. The most important effects are: anti-inflammatory, antioxidant, anticancer, antimicrobial, antiviral, antiallergic, antidiabetic, hepatotoxic and osteogenic. Natural bioactive compounds are mostly value to implement the introduction of biologically active molecules from the bench (research) to the bedside (clinical practice). However, in a future perspective it is necessary to perform additional studies to confirm these biological effects.


Isoliquiritigenin attenuates glutamate-induced mitochondrial fission via calcineurin-mediated Drp1 dephosphorylation in HT22 hippocampal neuron cells.[Pubmed: 30048666]


Numerous studies suggest that glutamate toxicity is a major contributor to neuronal dysfunction and death in several neurodegenerative diseases. In our previous study, isoliquiritigenin (ISL) isolated from Glycyrrhiza uralensis showed neuroprotective effects against neuronal cell death mediated by intracellular reactive oxygen species (ROS) generation and loss of mitochondrial membrane potential. However, the mechanisms by which ISL protects against glutamate-induced oxidative stress are unknown. In the present study, we focused on the cellular and molecular mechanisms underlying the inhibition of ROS production and induction of mitochondrial dysfunction by ISL in glutamate-stimulated HT22 mouse hippocampal neuron cells. The results revealed that ISL inhibited glutamate-induced mitochondrial ROS production and decline of glutathione levels and ATP generation in HT22 cells. Interestingly, we discovered that ISL prevents glutamate-induced mitochondrial fission by inhibiting the dephosphorylation of Drp1 at the serine 637 residue, which is a regulatory factor of mitochondrial dynamics, and both a S637D mutation of Drp1, which resulted in a phosphorylation-mimetic form of Drp1 at Ser637, and mitochondria-targeted antioxidant Mito-TEMPO inhibited glutamate-induced mitochondrial fission. Furthermore, ISL also prevented the increase of intracellular calcium accompanied by activation of calcineurin, which is a key regulator of dephosphorylation of Drp1 (Ser637), in glutamate-treated HT22 cells. Taken together, our results demonstrated that ISL protects against glutamate-induced mitochondrial fission by inhibiting the increase of mitochondrial ROS and intracellular calcium, which are accompanied by dephosphorylation of Drp1 (Ser637), and consequently attenuates glutamate-induced neuronal cell death. Therefore, these findings suggest that ISL exhibits the potential for protection against glutamate toxicity. These results may contribute to the development of new drugs and novel strategies for the treatment of neurodegenerative disorders related to glutamate toxicity.


UGT73F17, a new glycosyltransferase from Glycyrrhiza uralensis, catalyzes the regiospecific glycosylation of pentacyclic triterpenoids.[Pubmed: 30010690]


The regiospecific glycosylation of pentacyclic triterpenoids by UGT73F17, a new glycosyltransferase from Glycyrrhiza uralensis, is highlighted. UGT73F17 exhibited strict substrate specificity toward the carboxyl group at C-30/C-29 of pentacyclic triterpenoids, and showed high promiscuity to sugar donors. UGT73F17 represents the first identified triterpenoid 30/29-O-glycosyltransferase, and could be used as an effective biocatalyst to synthesize glycosyl ester saponins.