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1.
Toxicon ; 233: 107232, 2023 Sep.
Article in English | MEDLINE | ID: mdl-37536653

ABSTRACT

Scorpions are a group of arthropods that strike fear in many people due to their severe medical symptoms, even death, caused by their venomous stings. Even so, not all scorpion species contain harmful venoms against humans but still have valuable bioactive molecules, which could be used in developing new pharmaceutical leads for treating important diseases. This work conducted a comprehensive analysis of the venom from the scorpion Thorellius intrepidus. The venom of T. intrepidus was separated by size exclusion chromatography, and four main fractions were obtained. Fraction IV (FIV) contained small molecules representing over 90% of the total absorbance at 280 nm. Analysis of fraction FIV by RP-HPLC indicated the presence of three main molecules (FIV.1, FIV.2, and FIV.3) with similar UV absorbance spectra profiles. The molecular masses of FIV.1, FIV.2, and FIV.3 were determined, resulting in 175.99, 190.07, and 218.16 Da, respectively. Further confirmation through 1H-NMR and 13C-NMR analyses revealed that these molecules were serotonin, N-methylserotonin, and bufotenidine. These intriguing compounds are speculated to play a pivotal role in self-defense and increasing venom toxicity and could also offer promising biotechnological applications as small bioactive molecules.


Subject(s)
Scorpion Stings , Scorpion Venoms , Animals , Humans , Scorpions , Venoms , Scorpion Venoms/chemistry
2.
Molecules ; 25(19)2020 Oct 01.
Article in English | MEDLINE | ID: mdl-33019706

ABSTRACT

Two new indole alkaloids, Bufotenidine B (2) and Bufocarboline A (6), along with seven known indole alkaloids (1, 3-5, and 7-9) and three organic acids (10-12), were isolated from the water extract of toad venom. The structures of the new alkaloids were elucidated by extensive spectroscopic methods. The absolute configurations of 4, 6, and 8 were determined for the first time by electronic circular dichroism (ECD) calculations. The cytotoxic activity of all compounds was tested against human malignant melanoma cells A375 by the MTT method, and no antitumor activity was observed.


Subject(s)
Amphibian Venoms/chemistry , Bufo bufo/metabolism , Indole Alkaloids/isolation & purification , Animals , Carbon-13 Magnetic Resonance Spectroscopy , Circular Dichroism , Indole Alkaloids/chemistry , Proton Magnetic Resonance Spectroscopy , Water/chemistry
3.
Zhongguo Zhong Yao Za Zhi ; 44(5): 968-974, 2019 Mar.
Article in Chinese | MEDLINE | ID: mdl-30989857

ABSTRACT

In order to clarify the characteristic components of Berberidis Cortex,the preparative liquid chromatography and spectral analysis methods were used to separate and identify the unknown components in the water extract of Berberidis Cortex. Two compounds were isolated and identified as bufotenidine and ferulic acid 4-O-ß-D-glucopyranoside. They were both isolated for the first time from Berberidis Cortex and Berberis. In addition,an HPLC method was successfully established for simultaneously determination of six compounds in Berberidis Cortex,and chemometric methods were used to study the chemical differences among three main species of Berberidis Cortex. The results suggested that jatrorrhizine and bufotenidine are the main difference compounds among the three species.Compared with B. kansuensis and B. diaphana,B. vernae contains significantly more jatrorrhizine(P<0. 01),and the content of bufotenidine in B. vernae was significantly higher than that in B. kansuensis(P<0. 05). Considering these results,further research is necessary to reveal the pharmacological activities of bufotenidine and the pharmacodynamic differences between the three species. The results could provide a reference for quality control,the basic research on effective substances,and development of Berberidis Cortex.


Subject(s)
Berberis/chemistry , Phytochemicals/analysis , Plant Extracts/analysis , Berberine/analogs & derivatives , Berberine/analysis , Berberis/classification , Chromatography, High Pressure Liquid
4.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-777530

ABSTRACT

In order to clarify the characteristic components of Berberidis Cortex,the preparative liquid chromatography and spectral analysis methods were used to separate and identify the unknown components in the water extract of Berberidis Cortex. Two compounds were isolated and identified as bufotenidine and ferulic acid 4-O-β-D-glucopyranoside. They were both isolated for the first time from Berberidis Cortex and Berberis. In addition,an HPLC method was successfully established for simultaneously determination of six compounds in Berberidis Cortex,and chemometric methods were used to study the chemical differences among three main species of Berberidis Cortex. The results suggested that jatrorrhizine and bufotenidine are the main difference compounds among the three species.Compared with B. kansuensis and B. diaphana,B. vernae contains significantly more jatrorrhizine(P<0. 01),and the content of bufotenidine in B. vernae was significantly higher than that in B. kansuensis(P<0. 05). Considering these results,further research is necessary to reveal the pharmacological activities of bufotenidine and the pharmacodynamic differences between the three species. The results could provide a reference for quality control,the basic research on effective substances,and development of Berberidis Cortex.


Subject(s)
Berberine , Berberis , Chemistry , Classification , Chromatography, High Pressure Liquid , Phytochemicals , Plant Extracts
5.
J Agric Food Chem ; 63(16): 4220-7, 2015 Apr 29.
Article in English | MEDLINE | ID: mdl-25893818

ABSTRACT

Citrus genus is characterized by a specific presence of indole metabolites deriving from the N-methylation of tryptamine and its hydroxylated form, 5-hydroxytryptamine (serotonin), which are likely involved in plant defense mechanisms. In this study, we identified for the first time the occurrence in Citrus plants of serotonin 5-O-ß-glucoside and all its N-methylated derivatives, that is, N-methylserotonin 5-O-ß-glucoside, N,N-dimethylserotonin (bufotenine) 5-O-ß-glucoside, and N,N,N-trimethylserotonin (bufotenidine) 5-O-ß-glucoside. The identification of the glucosylated compounds was based on mass spectrometric studies, hydrolysis by glucosidase, and in some cases, comparison to authentic compounds. Beside leaves, the distribution of the glucosylated forms and their aglycones in some Citrus species was evaluated in flavedo, albedo, juice, and seeds. The simultaneous presence of serotonin and its N-methylated derivatives, together with the corresponding glucosylated forms, is consistent with the occurrence of a metabolic pathway, specific for Citrus, aimed at potentiating the defensive response to biotic stress through the optimization of the production and use of the most toxic of such metabolites.


Subject(s)
Citrus/chemistry , Glucosides/chemistry , Plant Extracts/chemistry , Serotonin/chemistry , Citrus/metabolism , Glucosides/metabolism , Methylation , Molecular Structure , Plant Extracts/metabolism , Serotonin/metabolism
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