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1دورية أكاديمية
المؤلفون: Carolin Thomas, Reto Erni, Jia Yee Wu, Fabian Fischer, Greta Lamers, Giovanna Grigolon, Sarah J. Mitchell, Kim Zarse, Erick M. Carreira, Michael Ristow
المصدر: Nature Communications, Vol 14, Iss 1, Pp 1-18 (2023)
مصطلحات موضوعية: Science
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2041-1723
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2دورية أكاديمية
المؤلفون: Giovanna Grigolon, Elisa Araldi, Reto Erni, Jia Yee Wu, Carolin Thomas, Marco La Fortezza, Beate Laube, Doris Pöhlmann, Markus Stoffel, Kim Zarse, Erick M. Carreira, Michael Ristow, Fabian Fischer
المصدر: Nature Communications, Vol 13, Iss 1, Pp 1-17 (2022)
مصطلحات موضوعية: Science
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2041-1723
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المؤلفون: Giovanni Appendino, Michael A. Schafroth, Erick M. Carreira, Andrea Chicca, Jürg Gertsch, Diego Caprioglio, Giulio Grassi, Gianna Allegrone, Federica Pollastro, Francesco Gasparrini, Bruno Botta, Giulia Mazzoccanti, Ines Reynoso-Moreno, Reto Erni
المصدر: Journal of Natural Products, 84 (9)
Schafroth, Michael A; Mazzoccanti, Giulia; Reynoso-Moreno, Ines; Erni, Reto; Pollastro, Federica; Caprioglio, Diego; Botta, Bruno; Allegrone, Gianna; Grassi, Giulio; Chicca, Andrea; Gasparrini, Francesco; Gertsch, Jürg; Carreira, Erick M; Appendino, Giovanni (2021). Δ9-cis-Tetrahydrocannabinol: Natural Occurrence, Chirality, and Pharmacology. Journal of natural products, 84(9), pp. 2502-2510. American Chemical Society 10.1021/acs.jnatprod.1c00513 <http://dx.doi.org/10.1021/acs.jnatprod.1c00513>مصطلحات موضوعية: Pharmacology, biology, Chemistry, Narcotic, Stereochemistry, medicine.medical_treatment, Organic Chemistry, Enantioselective synthesis, Absolute configuration, Pharmaceutical Science, 610 Medicine & health, biology.organism_classification, Analytical Chemistry, Complementary and alternative medicine, Drug Discovery, medicine, Molecular Medicine, 570 Life sciences, Δ9-cis-Tetrahydrocannabinol, Chirality, Natural occurrence, Pharmacology, Cannabinoid, Cannabis, Enantiomer, Tetrahydrocannabinol, Chirality (chemistry), medicine.drug
وصف الملف: application/application/pdf; application/pdf
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المؤلفون: Michael A, Schafroth, Giulia, Mazzoccanti, Ines, Reynoso-Moreno, Reto, Erni, Federica, Pollastro, Diego, Caprioglio, Bruno, Botta, Gianna, Allegrone, Giulio, Grassi, Andrea, Chicca, Francesco, Gasparrini, Jürg, Gertsch, Erick M, Carreira, Giovanni, Appendino
المصدر: Journal of natural products. 84(9)
مصطلحات موضوعية: Male, Mice, Mice, Inbred BALB C, Molecular Structure, Cannabinoids, Animals, Stereoisomerism, Dronabinol, Cannabis
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5Total Synthesis Establishes the Biosynthetic Pathway to the Naphterpin and Marinone Natural Products
المؤلفون: Lauren A. M. Murray, Shaun M. K. McKinnie, Henry P. Pepper, Reto Erni, Zachary D. Miles, Michelle C. Cruickshank, Borja López‐Pérez, Bradley S. Moore, Jonathan H. George
المصدر: Angewandte Chemie (International ed. in English), vol 57, iss 34
مصطلحات موضوعية: Biological Products, Halogenation, Terpenes, 010405 organic chemistry, meroterpenoids, Organic Chemistry, Reproducibility of Results, Naphthols, General Medicine, 010402 general chemistry, 01 natural sciences, dearomatization, 0104 chemical sciences, Biomimetics, Cyclization, Chemical Sciences, biomimetic synthesis, biosynthesis, Chloride Peroxidase, total synthesis, Oxidation-Reduction, Naphthoquinones
وصف الملف: application/pdf
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المؤلفون: Thomas A. Lutz, Michael Ristow, Reto Erni, Jia Yee Wu, Fabian Fischer, Christina N. Boyle, Carolin Thomas, Erick M. Carreira
المصدر: Free Radical Biology and Medicine. 165:22
مصطلحات موضوعية: Promotion (rank), Chemistry, Physiology (medical), media_common.quotation_subject, Biochemistry, Transcription factor, Small molecule, Redox sensitive, Cell biology, media_common
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7
المؤلفون: Erick M. Carreira, Vanessa Petrucci, Reto Erni, Michael A. Schafroth, Ines Reynoso-Moreno, Andrea Chicca, Jürg Gertsch
المصدر: Science Advances, 4 (10)
Chicca, Andrea; Schafroth, M A; Reynoso, Ines del Carmen; Erni, R; Petrucci, Vanessa; Carreira, E M; Gertsch, Jürg (2018). Uncovering the psychoactivity of a cannabinoid from liverworts associated with a legal high. Science Advances, 4(10), eaat2166. American Association for the Advancement of Science 10.1126/sciadv.aat2166 <http://dx.doi.org/10.1126/sciadv.aat2166>
Science Advancesمصطلحات موضوعية: 0301 basic medicine, Hepatophyta, Male, Cannabinoid receptor, medicine.medical_treatment, Prostaglandin, Neurophysiology, Biological Availability, 610 Medicine & health, CHO Cells, Hypothermia, Catalepsy, Pharmacology, 03 medical and health sciences, chemistry.chemical_compound, Cricetulus, medicine, Animals, Dronabinol, Receptor, Receptors, Cannabinoid, Research Articles, Analgesics, Mice, Inbred BALB C, Multidisciplinary, Natural product, Drug discovery, Chemistry, Cannabinoids, Plant Sciences, SciAdv r-articles, Brain, Stereoisomerism, medicine.disease, Endocannabinoid system, 3. Good health, Enzymes, 030104 developmental biology, 570 Life sciences, biology, lipids (amino acids, peptides, and proteins), Cannabinoid, Research Article, Endocannabinoids
وصف الملف: application/application/pdf; application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61f48304633569e7ebf5d277e0be180f
https://hdl.handle.net/20.500.11850/302458 -
8Total Synthesis Establishes the Biosynthetic Pathway to the Naphterpin and Marinone Natural Products
المؤلفون: Reto Erni, Bradley S. Moore, Henry P. Pepper, Jonathan H. George, Borja López-Pérez, Michelle C. Cruickshank, Zachary D. Miles, Lauren A. M. Murray, Shaun M. K. McKinnie
المصدر: Angewandte Chemie (International ed. in English). 57(34)
مصطلحات موضوعية: Halogenation, Stereochemistry, Chloride peroxidase, Naphthols, 010402 general chemistry, 01 natural sciences, Catalysis, Article, Terpene, chemistry.chemical_compound, Biosynthesis, Biomimetics, Biomimetic synthesis, chemistry.chemical_classification, Biological Products, 010405 organic chemistry, Chemistry, Terpenes, Total synthesis, Reproducibility of Results, General Chemistry, Naphthoquinone, 0104 chemical sciences, Enzyme, Cyclization, Chloride Peroxidase, Oxidation-Reduction, Naphthoquinones