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Wyszukujesz frazę ""Alkaloids"" wg kryterium: Temat


Tytuł:
Untargeted LC-MS/MS-Based Multi-Informative Molecular Networking for Targeting the Antiproliferative Ingredients in Tetradium ruticarpum Fruit.
Autorzy:
Su CH; Agricultural Biotechnology Research Center, Academia Sinica, Taipei 115201, Taiwan.; Research Center for Chinese Herbal Medicine, Graduate Institute of Health Industry Technology, College of Human Ecology, Chang Gung University of Science and Technology, Taoyuan 333324, Taiwan.; Department of Food Science, College of Human Ecology, Fu Jen Catholic University, New Taipei City 242062, Taiwan.
Cheng YC; Agricultural Biotechnology Research Center, Academia Sinica, Taipei 115201, Taiwan.; Biotechnology Center in Southern Taiwan, Academia Sinica, Tainan 711010, Taiwan.
Chang YC; Research Center for Chinese Herbal Medicine, Graduate Institute of Health Industry Technology, College of Human Ecology, Chang Gung University of Science and Technology, Taoyuan 333324, Taiwan.
Kung TH; Graduate Institute of Natural Products, College of Medicine, Chang Gung University, Taoyuan 333323, Taiwan.; Department of Anesthesiology, Chang Gung Memorial Hospital, Taoyuan 333423, Taiwan.
Chen YL; Research Center for Chinese Herbal Medicine, Graduate Institute of Health Industry Technology, College of Human Ecology, Chang Gung University of Science and Technology, Taoyuan 333324, Taiwan.; Graduate Institute of Natural Products, College of Medicine, Chang Gung University, Taoyuan 333323, Taiwan.
Lai KH; PhD Program in Clinical Drug Development of Herbal Medicine, College of Pharmacy, Taipei Medical University, Taipei 110301, Taiwan.; Graduate Institute of Pharmacognosy, College of Pharmacy, Taipei Medical University, Taipei 110301, Taiwan.
Hsieh HL; Research Center for Chinese Herbal Medicine, Graduate Institute of Health Industry Technology, College of Human Ecology, Chang Gung University of Science and Technology, Taoyuan 333324, Taiwan.; Division of Basic Medical Sciences, Department of Nursing, Chang Gung University of Science and Technology, Taoyuan 333324, Taiwan.; Department of Neurology, Chang Gung Memorial Hospital, Taoyuan 333423, Taiwan.
Chen CY; Graduate Institute of Natural Products, College of Medicine, Chang Gung University, Taoyuan 333323, Taiwan.; Department of Anesthesiology, Chang Gung Memorial Hospital, Taoyuan 333423, Taiwan.; Graduate Institute of Clinical Medical Sciences, College of Medicine, Chang Gung University, Taoyuan 333323, Taiwan.
Hwang TL; Research Center for Chinese Herbal Medicine, Graduate Institute of Health Industry Technology, College of Human Ecology, Chang Gung University of Science and Technology, Taoyuan 333324, Taiwan.; Graduate Institute of Natural Products, College of Medicine, Chang Gung University, Taoyuan 333323, Taiwan.; Department of Anesthesiology, Chang Gung Memorial Hospital, Taoyuan 333423, Taiwan.; Department of Chemical Engineering, Ming Chi University of Technology, New Taipei City 243303, Taiwan.
Yang YL; Agricultural Biotechnology Research Center, Academia Sinica, Taipei 115201, Taiwan.; Biotechnology Center in Southern Taiwan, Academia Sinica, Tainan 711010, Taiwan.
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Źródło:
Molecules (Basel, Switzerland) [Molecules] 2022 Jul 12; Vol. 27 (14). Date of Electronic Publication: 2022 Jul 12.
Typ publikacji:
Journal Article
MeSH Terms:
Alkaloids*/analysis
Alkaloids*/pharmacology
Evodia*/chemistry
Quinolones*/analysis
Chromatography, Liquid ; Fruit/chemistry ; Humans ; Indole Alkaloids/analysis ; Indole Alkaloids/pharmacology ; Plant Extracts/chemistry ; Tandem Mass Spectrometry
Czasopismo naukowe
Tytuł:
Monoterpenoid Quinoline Alkaloids from Stems and Leaves of Melodinus tenuicaudatus.
Autorzy:
Wu F; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan, 430074, China.
Chen Y; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan, 430074, China.
Yin JL; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan, 430074, China.
Zhu CH; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan, 430074, China.
Zhang Y; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan, 430074, China.
Liu JK; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan, 430074, China.
He J; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan, 430074, China.
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Źródło:
Chemistry & biodiversity [Chem Biodivers] 2022 Jul; Vol. 19 (7), pp. e202200209. Date of Electronic Publication: 2022 Jun 23.
Typ publikacji:
Journal Article
MeSH Terms:
Alkaloids*/chemistry
Apocynaceae*/chemistry
Quinolines*/pharmacology
Indole Alkaloids/chemistry ; Molecular Structure ; Monoterpenes/analysis ; Plant Leaves/chemistry
Czasopismo naukowe
Tytuł:
Characterization of alkaloids in bark extracts of Geissospermum vellosii by HPLC-UV-diode array-multistage high-resolution mass spectrometry.
Autorzy:
Aigotti R; Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.
Santoro V; Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.
Gastaldi D; Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.
Zorzi M; Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.
Dal Bello F; Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.
Grandi M; La Torre Medical Center, Turin, Italy.
Baiocchi C; Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy. Electronic address: .
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Źródło:
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences [J Chromatogr B Analyt Technol Biomed Life Sci] 2022 Jul 01; Vol. 1203, pp. 123307. Date of Electronic Publication: 2022 May 20.
Typ publikacji:
Journal Article
MeSH Terms:
Alkaloids*/chemistry
Apocynaceae*/chemistry
Chromatography, High Pressure Liquid/methods ; Indole Alkaloids/analysis ; Mass Spectrometry ; Plant Bark/chemistry ; Plant Extracts/chemistry
Czasopismo naukowe
Tytuł:
Phosphodiesterase-5 Inhibitory Activity of Canthin-6-One Alkaloids and the Roots of Eurycoma longifolia and Eurycoma harmandiana.
Autorzy:
Choonong R; Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen, 40002, Thailand.
Chaingam J; Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen, 40002, Thailand.
Chantakul R; Center of Excellence in Cannabis Research, Faculty of Pharmaceutical Sciences and Center of Excellence for Innovation in Chemistry, Naresuan University, Phitsanulok, 65000, Thailand.
Mukda S; Center of Excellence in Cannabis Research, Faculty of Pharmaceutical Sciences and Center of Excellence for Innovation in Chemistry, Naresuan University, Phitsanulok, 65000, Thailand.
Temkitthawon P; Center of Excellence in Cannabis Research, Faculty of Pharmaceutical Sciences and Center of Excellence for Innovation in Chemistry, Naresuan University, Phitsanulok, 65000, Thailand.
Ingkaninan K; Center of Excellence in Cannabis Research, Faculty of Pharmaceutical Sciences and Center of Excellence for Innovation in Chemistry, Naresuan University, Phitsanulok, 65000, Thailand.
Juengwatanatrakul T; Faculty of Pharmaceutical Sciences, Ubon Ratchathani University, Ubon Ratchathani, 34190, Thailand.
Yusakul G; School of Pharmacy, Walailak University, 222 Thaiburi, Thasala, Nakhon Si Thammarat 80160, Thailand.
Kanchanapoom T; Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen, 40002, Thailand.
Putalun W; Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen, 40002, Thailand.
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Źródło:
Chemistry & biodiversity [Chem Biodivers] 2022 Jul; Vol. 19 (7), pp. e202200121. Date of Electronic Publication: 2022 Jun 15.
Typ publikacji:
Journal Article
MeSH Terms:
Alkaloids*/pharmacology
Eurycoma*
Carbolines/pharmacology ; Cyclic Nucleotide Phosphodiesterases, Type 5 ; Indole Alkaloids ; Plant Extracts/pharmacology ; Plant Roots
Czasopismo naukowe
Tytuł:
Pharmacokinetics of Veratramine and Jervine from Alcohol Extracts of Radix Veratri.
Autorzy:
Wang S; Yunnan Institute of Materia Medica, Kunming, 650111 Yunnan, China.; Yunnan Technology and Business University, 651701, China.
Cui J; Yunnan Institute of Materia Medica, Kunming, 650111 Yunnan, China.; Yunnan Province Company Key Laboratory for TCM and Ethnic Drug of New Drug Creation, 650111, China.
Zhao G; Yunnan Institute of Materia Medica, Kunming, 650111 Yunnan, China.; Yunnan Province Company Key Laboratory for TCM and Ethnic Drug of New Drug Creation, 650111, China.
Liu H; Yunnan Institute of Materia Medica, Kunming, 650111 Yunnan, China.; Yunnan Province Company Key Laboratory for TCM and Ethnic Drug of New Drug Creation, 650111, China.
Wang J; Yunnan Institute of Materia Medica, Kunming, 650111 Yunnan, China.; Yunnan Province Company Key Laboratory for TCM and Ethnic Drug of New Drug Creation, 650111, China.
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Źródło:
Computational and mathematical methods in medicine [Comput Math Methods Med] 2022 Jun 23; Vol. 2022, pp. 8289548. Date of Electronic Publication: 2022 Jun 23 (Print Publication: 2022).
Typ publikacji:
Journal Article
MeSH Terms:
Alkaloids*
Veratrum*/chemistry
Animals ; Chromatography, Liquid ; Female ; Humans ; Male ; Mice ; Plant Extracts ; Rats ; Rats, Sprague-Dawley ; Tandem Mass Spectrometry ; Veratrum Alkaloids/chemistry ; Veratrum Alkaloids/pharmacokinetics
Czasopismo naukowe
Tytuł:
Development of a Fully Continuous-Flow Approach Towards Asymmetric Total Synthesis of Tetrahydroprotoberberine Natural Alkaloids.
Autorzy:
Li W; Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu, 610041, China.
Jiang M; Engineering Center of Catalysis and Synthesis for Chiral Molecules, Department of Chemistry, Fudan University, Shanghai, 200433, China.; Shanghai Engineering Center of Industrial Asymmetric Catalysis for Chiral Drugs, Shanghai, 200433, China.
Liu M; Engineering Center of Catalysis and Synthesis for Chiral Molecules, Department of Chemistry, Fudan University, Shanghai, 200433, China.; Shanghai Engineering Center of Industrial Asymmetric Catalysis for Chiral Drugs, Shanghai, 200433, China.
Ling X; Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu, 610041, China.
Xia Y; Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu, 610041, China.
Wan L; Engineering Center of Catalysis and Synthesis for Chiral Molecules, Department of Chemistry, Fudan University, Shanghai, 200433, China.; Shanghai Engineering Center of Industrial Asymmetric Catalysis for Chiral Drugs, Shanghai, 200433, China.
Chen F; Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu, 610041, China.; Engineering Center of Catalysis and Synthesis for Chiral Molecules, Department of Chemistry, Fudan University, Shanghai, 200433, China.; Shanghai Engineering Center of Industrial Asymmetric Catalysis for Chiral Drugs, Shanghai, 200433, China.
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Źródło:
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2022 Jun 10; Vol. 28 (33), pp. e202200700. Date of Electronic Publication: 2022 May 04.
Typ publikacji:
Journal Article
MeSH Terms:
Alkaloids*/chemistry
Biological Products*/chemistry
Berberine Alkaloids ; Cyclization ; Stereoisomerism
Czasopismo naukowe
Tytuł:
Exploration by molecular networking of Strychnos alkaloids reveals the unexpected occurrence of strychnine in seven Strychnos species.
Autorzy:
Bonnet O; Laboratory of Pharmacognosy, Center of Interdisciplinary Research on Medicines (CIRM), University of Liège, B36, 4000, Liège, Belgium. Electronic address: .
Beniddir MA; Équipe 'Chimie des Substances Naturelles' BioCIS, CNRS, Université Paris-Saclay, 5 Rue J.-B. Clément, 92290, Châtenay-Malabry, France.
Champy P; Équipe 'Chimie des Substances Naturelles' BioCIS, CNRS, Université Paris-Saclay, 5 Rue J.-B. Clément, 92290, Châtenay-Malabry, France.
Kagisha V; Laboratory of Pharmacognosy, Center of Interdisciplinary Research on Medicines (CIRM), University of Liège, B36, 4000, Liège, Belgium; School of Medicine and Pharmacy, College of Medicine and Health Sciences, University of Rwanda, Kigali, P.O. Box 3286, Rwanda.
Nyirimigabo A; Laboratory of Pharmacognosy, Center of Interdisciplinary Research on Medicines (CIRM), University of Liège, B36, 4000, Liège, Belgium; School of Medicine and Pharmacy, College of Medicine and Health Sciences, University of Rwanda, Kigali, P.O. Box 3286, Rwanda.
Hamann C; Laboratory of Pharmacognosy, Center of Interdisciplinary Research on Medicines (CIRM), University of Liège, B36, 4000, Liège, Belgium.
Jgerenaia G; Laboratory of Pharmacognosy, Center of Interdisciplinary Research on Medicines (CIRM), University of Liège, B36, 4000, Liège, Belgium; Department of Pharmaceutical Technology, Faculty of Pharmacy, Tbilisi State Medical University, 33, Vazha Pshavela Ave., Tbilisi, 0177, Georgia.
Ledoux A; Laboratory of Pharmacognosy, Center of Interdisciplinary Research on Medicines (CIRM), University of Liège, B36, 4000, Liège, Belgium.
Tchinda AT; Laboratory of Pharmacognosy, Center of Interdisciplinary Research on Medicines (CIRM), University of Liège, B36, 4000, Liège, Belgium; Institute of Medical Research and Medicinal Plants Studies (IMPM), PO Box 13033, Yaoundé, Cameroon.
Angenot L; Laboratory of Pharmacognosy, Center of Interdisciplinary Research on Medicines (CIRM), University of Liège, B36, 4000, Liège, Belgium.
Frédérich M; Laboratory of Pharmacognosy, Center of Interdisciplinary Research on Medicines (CIRM), University of Liège, B36, 4000, Liège, Belgium.
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Źródło:
Toxicon : official journal of the International Society on Toxinology [Toxicon] 2022 Aug; Vol. 215, pp. 57-68. Date of Electronic Publication: 2022 Jun 09.
Typ publikacji:
Journal Article
MeSH Terms:
Alkaloids*/chemistry
Strychnos*/chemistry
Indole Alkaloids ; Plant Leaves ; Strychnine/chemistry ; Strychnine/pharmacology
Czasopismo naukowe
Tytuł:
The Pharmacologically Active Alkaloid Cryptolepine Activates a Type 1 Interferon Response That Is Independent of MAVS and STING Pathways.
Autorzy:
Domfeh SA; West African Centre for Cell Biology of Infectious Pathogens, University of Ghana, Legon, Ghana.; Department of Biochemistry, Cell and Molecular Biology, School of Biological Sciences University of Ghana, Legon, Ghana.; Department of Biochemistry and Biotechnology, College of Science, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
Narkwa PW; Department of Clinical Microbiology, School of Medicine and Dentistry, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
Quaye O; West African Centre for Cell Biology of Infectious Pathogens, University of Ghana, Legon, Ghana.; Department of Biochemistry, Cell and Molecular Biology, School of Biological Sciences University of Ghana, Legon, Ghana.
Kusi KA; West African Centre for Cell Biology of Infectious Pathogens, University of Ghana, Legon, Ghana.; Department of Biochemistry, Cell and Molecular Biology, School of Biological Sciences University of Ghana, Legon, Ghana.; Department of Immunology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana.
Addy BS; Department of Biochemistry and Biotechnology, College of Science, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
Lant S; Department of Microbial Sciences, University of Surrey, Guildford, UK.
Sumner RP; Department of Microbial Sciences, University of Surrey, Guildford, UK.
Maluquer de Motes C; Department of Microbial Sciences, University of Surrey, Guildford, UK.
Awandare GA; West African Centre for Cell Biology of Infectious Pathogens, University of Ghana, Legon, Ghana.; Department of Biochemistry, Cell and Molecular Biology, School of Biological Sciences University of Ghana, Legon, Ghana.
Ansah C; Department of Pharmacology, Faculty of Pharmacy and Pharmaceutical Sciences, College of Health Sciences, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
Mutocheluh M; Department of Clinical Microbiology, School of Medicine and Dentistry, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
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Źródło:
Journal of immunology research [J Immunol Res] 2022 Jul 26; Vol. 2022, pp. 8873536. Date of Electronic Publication: 2022 Jul 26 (Print Publication: 2022).
Typ publikacji:
Journal Article
MeSH Terms:
Alkaloids*/pharmacology
Antineoplastic Agents*
Interferon Type I*
Quinolines*/pharmacology
Humans ; Indole Alkaloids/pharmacology
Czasopismo naukowe
Tytuł:
Insights into the Cardiotoxic Effects of Veratrum Lobelianum Alkaloids: Pilot Study.
Autorzy:
Taldaev A; Laboratory of Nanobiotechnology, Institute of Biomedical Chemistry, 119121 Moscow, Russia.; A.P. Nelyubin Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University (Sechenov University), 119991 Moscow, Russia.
Terekhov RP; A.P. Nelyubin Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University (Sechenov University), 119991 Moscow, Russia.
Melnik EV; A.P. Nelyubin Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University (Sechenov University), 119991 Moscow, Russia.
Belova MV; A.P. Nelyubin Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University (Sechenov University), 119991 Moscow, Russia.; N.V. Sklifosovsky Research Institute for Emergency Medicine, 129090 Moscow, Russia.
Kozin SV; A.P. Nelyubin Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University (Sechenov University), 119991 Moscow, Russia.
Nedorubov AA; A.P. Nelyubin Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University (Sechenov University), 119991 Moscow, Russia.
Pomerantseva TY; A.P. Nelyubin Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University (Sechenov University), 119991 Moscow, Russia.
Ramenskaya GV; A.P. Nelyubin Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University (Sechenov University), 119991 Moscow, Russia.
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Źródło:
Toxins [Toxins (Basel)] 2022 Jul 15; Vol. 14 (7). Date of Electronic Publication: 2022 Jul 15.
Typ publikacji:
Journal Article
MeSH Terms:
Alkaloids*/toxicity
Veratrum*
Cardiotoxicity ; Humans ; Molecular Docking Simulation ; Pilot Projects ; Tandem Mass Spectrometry ; Veratrum Alkaloids/pharmacology
Czasopismo naukowe
Tytuł:
Semi-syntheses and interrogation of indole-substituted Aspidosperma terpenoid alkaloids.
Autorzy:
Kang J; Department of Chemistry, Temple University, 1901 N. 13th Street, Philadelphia, PA, 19122, USA. .
Lewis TR; Department of Chemistry, Temple University, 1901 N. 13th Street, Philadelphia, PA, 19122, USA. .
Gardner A; Department of Chemistry, Temple University, 1901 N. 13th Street, Philadelphia, PA, 19122, USA. .
Andrade RB; Department of Chemistry, Temple University, 1901 N. 13th Street, Philadelphia, PA, 19122, USA. .
Wang RE; Department of Chemistry, Temple University, 1901 N. 13th Street, Philadelphia, PA, 19122, USA. .
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Źródło:
Organic & biomolecular chemistry [Org Biomol Chem] 2022 May 18; Vol. 20 (19), pp. 3988-3997. Date of Electronic Publication: 2022 May 18.
Typ publikacji:
Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Alkaloids*/chemistry
Alkaloids*/pharmacology
Aspidosperma*/chemistry
Indole Alkaloids/chemistry ; Indole Alkaloids/pharmacology ; Plant Extracts ; Terpenes
Czasopismo naukowe
Tytuł:
Molecular and biochemical characterization of Catharanthus roseus perivine-N β -methyltransferase.
Autorzy:
Levac D; Department of Biological Sciences, Brock University, 500 Glenridge Avenue, St. Catharines, ON, L2S 3A1, Canada. Electronic address: .
Flores PC; Department of Biological Sciences, Brock University, 500 Glenridge Avenue, St. Catharines, ON, L2S 3A1, Canada. Electronic address: .
De Luca V; Department of Biological Sciences, Brock University, 500 Glenridge Avenue, St. Catharines, ON, L2S 3A1, Canada. Electronic address: .
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Źródło:
Phytochemistry [Phytochemistry] 2022 Sep; Vol. 201, pp. 113266. Date of Electronic Publication: 2022 Jun 06.
Typ publikacji:
Journal Article
MeSH Terms:
Apocynaceae*
Catharanthus*/metabolism
Secologanin Tryptamine Alkaloids*/metabolism
Gene Expression Regulation, Plant ; Indole Alkaloids/chemistry ; Methyltransferases/genetics ; Methyltransferases/metabolism ; Phytochemicals/metabolism ; Plant Proteins/metabolism
Czasopismo naukowe
Tytuł:
Indole Alkaloids and Chromones from the Stem Bark of Cassia alata and Their Antiviral Activities.
Autorzy:
Yang PS; Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan Minzu University, Kunming 650031, China.; Yunnan Key Laboratory of Tobacco Chemistry, China Tobacco Yunnan Industrial Co., Ltd., Kunming 650231, China.
Dai JM; Yunnan Key Laboratory of Tobacco Chemistry, China Tobacco Yunnan Industrial Co., Ltd., Kunming 650231, China.
Gu XJ; Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan Minzu University, Kunming 650031, China.
Xiong W; Yunnan Key Laboratory of Tobacco Chemistry, China Tobacco Yunnan Industrial Co., Ltd., Kunming 650231, China.
Huang DQ; Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan Minzu University, Kunming 650031, China.
Qiu SY; Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan Minzu University, Kunming 650031, China.
Zheng JN; Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan Minzu University, Kunming 650031, China.
Li Y; Yunnan Key Laboratory of Tobacco Chemistry, China Tobacco Yunnan Industrial Co., Ltd., Kunming 650231, China.
Yang FX; Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan Minzu University, Kunming 650031, China.; Yunnan Key Laboratory of Tobacco Chemistry, China Tobacco Yunnan Industrial Co., Ltd., Kunming 650231, China.
Zhou M; Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, Yunnan Minzu University, Kunming 650031, China.; Yunnan Key Laboratory of Tobacco Chemistry, China Tobacco Yunnan Industrial Co., Ltd., Kunming 650231, China.
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Źródło:
Molecules (Basel, Switzerland) [Molecules] 2022 May 13; Vol. 27 (10). Date of Electronic Publication: 2022 May 13.
Typ publikacji:
Journal Article
MeSH Terms:
Alkaloids*/pharmacology
Cassia*/chemistry
Senna Plant*
Tobacco Mosaic Virus*
Antiviral Agents/chemistry ; Chromones/chemistry ; Indole Alkaloids ; Plant Bark
Czasopismo naukowe
Tytuł:
Construction of ajmalicine and sanguinarine de novo biosynthetic pathways using stable integration sites in yeast.
Autorzy:
Liu T; Key Laboratory of Biomass Chemical Engineering of Ministry of Education, Zhejiang University, Hangzhou, China.
Gou Y; Key Laboratory of Biomass Chemical Engineering of Ministry of Education, Zhejiang University, Hangzhou, China.; Hangzhou Global Scientific and Technological Innovation Center, Zhejiang University, Hangzhou, China.
Zhang B; Key Laboratory of Biomass Chemical Engineering of Ministry of Education, Zhejiang University, Hangzhou, China.
Gao R; Key Laboratory of Biomass Chemical Engineering of Ministry of Education, Zhejiang University, Hangzhou, China.; Hangzhou Global Scientific and Technological Innovation Center, Zhejiang University, Hangzhou, China.
Dong C; Key Laboratory of Biomass Chemical Engineering of Ministry of Education, Zhejiang University, Hangzhou, China.; Hangzhou Global Scientific and Technological Innovation Center, Zhejiang University, Hangzhou, China.
Qi M; Key Laboratory of Biomass Chemical Engineering of Ministry of Education, Zhejiang University, Hangzhou, China.
Jiang L; Key Laboratory of Biomass Chemical Engineering of Ministry of Education, Zhejiang University, Hangzhou, China.
Ding X; Key Laboratory of Medical Molecule Science and Pharmaceutics Engineering, Ministry of Industry and Information Technology, Institute of Biochemical Engineering, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, China.
Li C; Key Laboratory of Medical Molecule Science and Pharmaceutics Engineering, Ministry of Industry and Information Technology, Institute of Biochemical Engineering, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, China.
Lian J; Key Laboratory of Biomass Chemical Engineering of Ministry of Education, Zhejiang University, Hangzhou, China.; Hangzhou Global Scientific and Technological Innovation Center, Zhejiang University, Hangzhou, China.
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Źródło:
Biotechnology and bioengineering [Biotechnol Bioeng] 2022 May; Vol. 119 (5), pp. 1314-1326. Date of Electronic Publication: 2022 Jan 31.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Biosynthetic Pathways*/genetics
Secologanin Tryptamine Alkaloids*/metabolism
Benzophenanthridines ; Indole Alkaloids/metabolism ; Isoquinolines ; Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/metabolism
Czasopismo naukowe
Tytuł:
Engineered Production of Strictosidine and Analogues in Yeast.
Autorzy:
Misa J; Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, California 90095, United States.
Billingsley JM; Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, California 90095, United States.
Niwa K; Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, California 90095, United States.
Yu RK; Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, California 90095, United States.
Tang Y; Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, California 90095, United States.; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States.
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Źródło:
ACS synthetic biology [ACS Synth Biol] 2022 Apr 15; Vol. 11 (4), pp. 1639-1649. Date of Electronic Publication: 2022 Mar 16.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Biological Products*
Vinca Alkaloids*
Indole Alkaloids ; Plants ; Saccharomyces cerevisiae/genetics
Czasopismo naukowe
Tytuł:
Analysis of alkaloids in Gelsemium elegans Benth using an online heart-cutting + comprehensive RPLC×RPLC system tandem mass spectrometry.
Autorzy:
Liu D; Key Lab of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, China; University of Chinese Academy of Sciences, Beijing, China.
Liu Y; Key Lab of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, China; Ganjiang Chinese Medicine Innovation Center, Nanchang, 330000, China. Electronic address: .
Shen A; Key Lab of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, China; Ganjiang Chinese Medicine Innovation Center, Nanchang, 330000, China.
Li X; Ganjiang Chinese Medicine Innovation Center, Nanchang, 330000, China.
Yu L; Key Lab of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, China.
Wang C; Key Lab of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, China.
Liang X; Key Lab of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, China; Ganjiang Chinese Medicine Innovation Center, Nanchang, 330000, China. Electronic address: .
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Źródło:
Talanta [Talanta] 2022 Mar 01; Vol. 239, pp. 123069. Date of Electronic Publication: 2021 Nov 20.
Typ publikacji:
Journal Article
MeSH Terms:
Alkaloids*
Gelsemium*
Chromatography, High Pressure Liquid ; Indole Alkaloids ; Tandem Mass Spectrometry
Czasopismo naukowe
Tytuł:
Activity of alkaloids from Aspidosperma nitidum against Leishmania (Leishmania) amazonensis.
Autorzy:
do Socorro Silva da Veiga A; Postgraduate Program in Pharmaceutical Innovation, Institute of Health Sciences, Federal University of Pará, Belém, PA, Brazil.
Silveira FT; Institute Evandro Chagas, Ananindeua, PA, Brazil.
da Silva EO; Postgraduate Program in Biology of Infectious and Parasitic Agents, Institute of Biological Sciences, Federal University of Pará, Belém, PA, Brazil.; Postgraduate Program in Biodiversity and Biotechnology of the BIONORTE Network, Institute of Biological Sciences, Federal University of Pará, Belém, PA, Brazil.
Júnior JAPD; Institute Evandro Chagas, Ananindeua, PA, Brazil.
Araújo SC; Institute Evandro Chagas, Ananindeua, PA, Brazil.
Campos MB; Institute Evandro Chagas, Ananindeua, PA, Brazil.
do Rosário Marinho AM; Postgraduate Program in Biodiversity and Biotechnology of the BIONORTE Network, Institute of Biological Sciences, Federal University of Pará, Belém, PA, Brazil.
Brandão GC; School of Pharmacy, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.
Vale VV; Postgraduate Program in Pharmaceutical Innovation, Institute of Health Sciences, Federal University of Pará, Belém, PA, Brazil.
Percário S; Postgraduate Program in Biodiversity and Biotechnology of the BIONORTE Network, Institute of Biological Sciences, Federal University of Pará, Belém, PA, Brazil.; Oxidative Stress Research Laboratory, Institute of Biological Sciences, Federal University of Pará, Belém, PA, Brazil.
Dolabela MF; Postgraduate Program in Pharmaceutical Innovation, Institute of Health Sciences, Federal University of Pará, Belém, PA, Brazil. .; Postgraduate Program in Biodiversity and Biotechnology of the BIONORTE Network, Institute of Biological Sciences, Federal University of Pará, Belém, PA, Brazil. .
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Źródło:
Scientific reports [Sci Rep] 2022 May 23; Vol. 12 (1), pp. 8662. Date of Electronic Publication: 2022 May 23.
Typ publikacji:
Journal Article
MeSH Terms:
Alkaloids*/pharmacology
Antiprotozoal Agents*/chemistry
Aspidosperma*/chemistry
Leishmania*
Indole Alkaloids ; Plant Extracts/chemistry
Czasopismo naukowe
Tytuł:
Sclerotiamides C-H, Notoamides from a Marine Gorgonian-Derived Fungus with Cytotoxic Activities.
Autorzy:
Guo X; State Key Laboratory of Natural and Biomimetic Drugs, Institute of Ocean Research, Peking University, Beijing, 100191, People's Republic of China.
Meng Q; State Key Laboratory of Natural and Biomimetic Drugs, Institute of Ocean Research, Peking University, Beijing, 100191, People's Republic of China.
Liu J; State Key Laboratory of Natural and Biomimetic Drugs, Institute of Ocean Research, Peking University, Beijing, 100191, People's Republic of China.
Wu J; State Key Laboratory of Natural and Biomimetic Drugs, Institute of Ocean Research, Peking University, Beijing, 100191, People's Republic of China.
Jia H; State Key Laboratory of Natural and Biomimetic Drugs, Institute of Ocean Research, Peking University, Beijing, 100191, People's Republic of China.
Liu D; State Key Laboratory of Natural and Biomimetic Drugs, Institute of Ocean Research, Peking University, Beijing, 100191, People's Republic of China.
Gu Y; Syngenta, Jealott's Hill International Research Centre Bracknell, Berks RG42 6EY, U.K.
Liu J; State Key Laboratory of Natural and Biomimetic Drugs, Institute of Ocean Research, Peking University, Beijing, 100191, People's Republic of China.
Huang J; State Key Laboratory of Natural and Biomimetic Drugs, Institute of Ocean Research, Peking University, Beijing, 100191, People's Republic of China.
Fan A; State Key Laboratory of Natural and Biomimetic Drugs, Institute of Ocean Research, Peking University, Beijing, 100191, People's Republic of China.
Lin W; State Key Laboratory of Natural and Biomimetic Drugs, Institute of Ocean Research, Peking University, Beijing, 100191, People's Republic of China.
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Źródło:
Journal of natural products [J Nat Prod] 2022 Apr 22; Vol. 85 (4), pp. 1067-1078. Date of Electronic Publication: 2022 Feb 25.
Typ publikacji:
Journal Article; Review; Research Support, Non-U.S. Gov't
MeSH Terms:
Alkaloids*/pharmacology
Antineoplastic Agents*/pharmacology
Fungi/metabolism ; HeLa Cells ; Humans ; Indole Alkaloids/chemistry ; Molecular Structure
Czasopismo naukowe
Tytuł:
Chevalinulins A and B, Proangiogenic Alkaloids with a Spiro[bicyclo[2.2.2]octane-diketopiperazine] Skeleton from Deep-Sea Cold-Seep-Derived Fungus Aspergillus chevalieri CS-122.
Autorzy:
Yan LH; CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Nanhai Road 7, Qingdao 266071, People's Republic of China.; Laboratory of Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Nanhai Road 7, Qingdao 266071, People's Republic of China.; College of Marine Science, University of Chinese Academy of Sciences, Yuquan Road 19A, Beijing 100049, People's Republic of China.
Li PH; Engineering Research Center of Zebrafish Models for Human Diseases and Drug Screening of Shandong Province, Shandong Provincial Engineering Laboratory for Biological Testing Technology, Key Laboratory for Biosensor of Shandong Province, Biology Institute, Qilu University of Technology (Shandong Academy of Sciences), Jingshi East Road 28789, Jinan 250103, People's Republic of China.
Li XM; CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Nanhai Road 7, Qingdao 266071, People's Republic of China.; Laboratory of Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Nanhai Road 7, Qingdao 266071, People's Republic of China.
Yang SQ; CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Nanhai Road 7, Qingdao 266071, People's Republic of China.; Laboratory of Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Nanhai Road 7, Qingdao 266071, People's Republic of China.
Liu KC; Engineering Research Center of Zebrafish Models for Human Diseases and Drug Screening of Shandong Province, Shandong Provincial Engineering Laboratory for Biological Testing Technology, Key Laboratory for Biosensor of Shandong Province, Biology Institute, Qilu University of Technology (Shandong Academy of Sciences), Jingshi East Road 28789, Jinan 250103, People's Republic of China.
Wang BG; CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Nanhai Road 7, Qingdao 266071, People's Republic of China.; Laboratory of Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Nanhai Road 7, Qingdao 266071, People's Republic of China.; College of Marine Science, University of Chinese Academy of Sciences, Yuquan Road 19A, Beijing 100049, People's Republic of China.; Center for Ocean Mega-Science, Chinese Academy of Sciences, Nanhai Road 7, Qingdao 266071, People's Republic of China.
Li X; CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Nanhai Road 7, Qingdao 266071, People's Republic of China.; Laboratory of Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Nanhai Road 7, Qingdao 266071, People's Republic of China.
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Źródło:
Organic letters [Org Lett] 2022 Apr 15; Vol. 24 (14), pp. 2684-2688. Date of Electronic Publication: 2022 Apr 07.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Alkaloids*/chemistry
Diketopiperazines*/chemistry
Animals ; Aspergillus ; Fungi ; Indole Alkaloids/chemistry ; Molecular Structure ; Octanes ; Skeleton ; Zebrafish
SCR Organism:
Aspergillus chevalieri
Czasopismo naukowe
Tytuł:
A Compilation of Synthetic Strategies to Access the Most Utilized Indoloquinoline Motifs.
Autorzy:
Thongsornkleeb C; Program on Chemical Sciences, Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), OPS, MHESI, 54 Kamphaeng Phet 6, Laksi, Bangkok, 10210, Thailand.; Laboratory of Medicinal Chemistry, Chulabhorn Research Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok, 10210, Thailand.
Tummatorn J; Program on Chemical Sciences, Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), OPS, MHESI, 54 Kamphaeng Phet 6, Laksi, Bangkok, 10210, Thailand.; Laboratory of Medicinal Chemistry, Chulabhorn Research Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok, 10210, Thailand.
Ruchirawat S; Program on Chemical Sciences, Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), OPS, MHESI, 54 Kamphaeng Phet 6, Laksi, Bangkok, 10210, Thailand.; Laboratory of Medicinal Chemistry, Chulabhorn Research Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok, 10210, Thailand.
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Źródło:
Chemistry, an Asian journal [Chem Asian J] 2022 Apr 01; Vol. 17 (7), pp. e202200040. Date of Electronic Publication: 2022 Feb 21.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Alkaloids*
Quinolines*
Indole Alkaloids
Czasopismo naukowe
Tytuł:
Cascade Benzannulation Approach for the Syntheses of Lipocarbazoles, Carbazomycins, and Related Alkaloids.
Autorzy:
Banerjee A; Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721302, West Bengal, India.
Saha S; Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721302, West Bengal, India.
Maji MS; Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721302, West Bengal, India.
Pokaż więcej
Źródło:
The Journal of organic chemistry [J Org Chem] 2022 Mar 18; Vol. 87 (6), pp. 4343-4359. Date of Electronic Publication: 2022 Mar 07.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Alkaloids*
Carbazoles*
Indole Alkaloids
Czasopismo naukowe

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