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Tytuł :
A Chiral Molecular Cage Comprising Diethynylallenes and N-Heterotriangulenes for Enantioselective Recognition.
Autorzy :
Míguez-Lago S; Departamento de Química Orgánica, Universidade de Vigo, Campus Lagoas-Marcosende, 36310, Vigo, Spain.; Department of Chemistry and Pharmacy, Chair of Organic Chemistry I, Friedrich-Alexander-Universität Erlangen-Nürnberg, Nikolaus-Fiebiger-Str. 10, 91058, Erlangen, Germany.
Gliemann BD; Department of Chemistry and Pharmacy, Chair of Organic Chemistry I, Friedrich-Alexander-Universität Erlangen-Nürnberg, Nikolaus-Fiebiger-Str. 10, 91058, Erlangen, Germany.
Kivala M; Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120, Heidelberg, Germany.; Centre for Advanced Materials, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 225, 69120, Heidelberg, Germany.
Cid MM; Departamento de Química Orgánica, Universidade de Vigo, Campus Lagoas-Marcosende, 36310, Vigo, Spain.
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Źródło :
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2021 Sep 20; Vol. 27 (53), pp. 13352-13357. Date of Electronic Publication: 2021 Aug 12.
Typ publikacji :
Journal Article
MeSH Terms :
Stereoisomerism*
Molecular Structure
Czasopismo naukowe
Tytuł :
Green Multi-Platform Solution for the Quantification of Levodopa Enantiomeric Excess in Solid-State Mixtures for Pharmacological Formulations.
Autorzy :
Biancolillo A; Department of Physical and Chemical Sciences, University of L'Aquila, Via Vetoio, 67100 L'Aquila, Italy.
Battistoni S; Department of Chemistry, University of Rome 'La Sapienza', Piazzale Aldo Moro 5, 00185 Rome, Italy.
Presutto R; Department of Chemistry, University of Rome 'La Sapienza', Piazzale Aldo Moro 5, 00185 Rome, Italy.
Marini F; Department of Chemistry, University of Rome 'La Sapienza', Piazzale Aldo Moro 5, 00185 Rome, Italy.
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2021 Aug 15; Vol. 26 (16). Date of Electronic Publication: 2021 Aug 15.
Typ publikacji :
Journal Article
MeSH Terms :
Drug Compounding*
Stereoisomerism*
Levodopa/*chemistry
Solutions/*chemistry
Green Chemistry Technology ; Spectroscopy, Near-Infrared
Czasopismo naukowe
Tytuł :
Analysis of Stereochemical Stability of Dynamic Chiral Molecules Using an Automated Microflow Measurement System.
Autorzy :
Igawa K
Asano S
Yoshida Y
Kawasaki Y
Tomooka K
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Źródło :
The Journal of organic chemistry [J Org Chem] 2021 Jul 16; Vol. 86 (14), pp. 9651-9657. Date of Electronic Publication: 2021 Jul 07.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Stereoisomerism*
Chromatography, High Pressure Liquid ; Kinetics
Czasopismo naukowe
Tytuł :
Activated Self-Resolution and Error-Correction in Catalytic Reaction Networks*.
Autorzy :
Schaufelberger F; Department of Chemistry, KTH - Royal Institute of Technology Teknikringen 36, 10044 Stockholm (Sweden).
Ramström O; Department of Chemistry, KTH - Royal Institute of Technology Teknikringen 36, 10044 Stockholm (Sweden).; Department of Chemistry, University of Massachusetts Lowell, One University Ave., Lowell, MA, 01854, USA.; Department of Chemistry and Biomedical Sciences, Linnaeus University, 39182, Kalmar, Sweden.
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Źródło :
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2021 Jul 16; Vol. 27 (40), pp. 10335-10340. Date of Electronic Publication: 2021 Apr 30.
Typ publikacji :
Journal Article
MeSH Terms :
Stereoisomerism*
Catalysis
Czasopismo naukowe
Tytuł :
Enantioconvergent Substitution Reactions of Racemic Electrophiles by Organocatalysis.
Autorzy :
Kikuchi J; Department of Chemistry, Graduate School of Science, Tohoku University, Aramaki, Aoba-ku, Sendai, 980-8578, Japan.
Terada M; Department of Chemistry, Graduate School of Science, Tohoku University, Aramaki, Aoba-ku, Sendai, 980-8578, Japan.
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Źródło :
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2021 Jul 16; Vol. 27 (40), pp. 10215-10225. Date of Electronic Publication: 2021 Jun 04.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Stereoisomerism*
Catalysis
Czasopismo naukowe
Tytuł :
Stereoselective Synthesis of 1-Aminocyclopropanecarboxylic Acid Carnosadines via Inter-intramolecular Double Alkylation with Optically Active 2-Methylaziridine Derivatives.
Autorzy :
Ohsawa K; Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aza-aoba, Aramaki, Aoba-ku, Sendai, 980-8578, Japan.
Kubota J; Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aza-aoba, Aramaki, Aoba-ku, Sendai, 980-8578, Japan.
Ochiai S; Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aza-aoba, Aramaki, Aoba-ku, Sendai, 980-8578, Japan.
Doi T; Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aza-aoba, Aramaki, Aoba-ku, Sendai, 980-8578, Japan.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2021 May 21; Vol. 86 (10), pp. 7304-7313. Date of Electronic Publication: 2021 May 11.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Stereoisomerism*
Alkylation ; Aziridines
Czasopismo naukowe
Tytuł :
Left-handed DNA-PAINT for improved super-resolution imaging in the nucleus.
Autorzy :
Geertsema HJ; Institute of Chemistry and Biochemistry, Department for Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany.
Aimola G; Institute of Virology, Department of Veterinary Science, Freie Universität Berlin, Berlin, Germany.
Fabricius V; Institute of Chemistry and Biochemistry, Department for Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany.
Fuerste JP; Institute of Chemistry and Biochemistry, Department for Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany.
Kaufer BB; Institute of Virology, Department of Veterinary Science, Freie Universität Berlin, Berlin, Germany.
Ewers H; Institute of Chemistry and Biochemistry, Department for Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany. .
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Źródło :
Nature biotechnology [Nat Biotechnol] 2021 May; Vol. 39 (5), pp. 551-554. Date of Electronic Publication: 2021 Jan 04.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Stereoisomerism*
Cell Nucleus/*ultrastructure
DNA/*genetics
Molecular Imaging/*methods
Cell Nucleus/genetics ; DNA/ultrastructure ; DNA, Z-Form ; Microscopy, Fluorescence ; Nucleic Acid Conformation
Czasopismo naukowe
Tytuł :
Synthesis of Chiral Helic[1]triptycene[3]arenes and Their Enantioselective Recognition Towards Chiral Guests Containing Aminoindan Groups.
Autorzy :
Li J; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.; University of Chinese Academy of Sciences, Beijing 100049, China.
Han Y; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Chen CF; Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.; University of Chinese Academy of Sciences, Beijing 100049, China.
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2021 Jan 20; Vol. 26 (3). Date of Electronic Publication: 2021 Jan 20.
Typ publikacji :
Journal Article
MeSH Terms :
Stereoisomerism*
Anthracenes/*chemistry
Indans/*chemistry
Ammonium Compounds/chemistry ; Anthracenes/chemical synthesis ; Circular Dichroism ; Indans/chemical synthesis
Czasopismo naukowe
Tytuł :
Enantiomer-specific activities of an LRH-1 and SF-1 dual agonist.
Autorzy :
Mays SG; Department of Biochemistry, Emory University, Atlanta, GA, 30322, USA.; Centre for Genomic Regulation, Carrer Dr. Aiguader, 88, 08003, Barcelona, Spain.
Stec J; School of Chemistry, University of Southampton, Southampton, Hants, SO17, United Kingdom.; Department of Pharmaceutical Sciences, College of Pharmacy, Marshall B. Ketchum University, 2575 Yorba Linda Blvd, Fullerton, CA, 82831, USA.
Liu X; Department of Biochemistry, Emory University, Atlanta, GA, 30322, USA.
D'Agostino EH; Department of Biochemistry, Emory University, Atlanta, GA, 30322, USA.
Whitby RJ; School of Chemistry, University of Southampton, Southampton, Hants, SO17, United Kingdom.
Ortlund EA; Department of Biochemistry, Emory University, Atlanta, GA, 30322, USA. .
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Źródło :
Scientific reports [Sci Rep] 2020 Dec 17; Vol. 10 (1), pp. 22279. Date of Electronic Publication: 2020 Dec 17.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Stereoisomerism*
Homeodomain Proteins/*ultrastructure
Receptors, Cytoplasmic and Nuclear/*ultrastructure
Steroidogenic Factor 1/*genetics
Homeodomain Proteins/chemistry ; Homeodomain Proteins/genetics ; Humans ; Metabolic Diseases/drug therapy ; Molecular Dynamics Simulation ; Neoplasms/drug therapy ; Receptors, Cytoplasmic and Nuclear/antagonists & inhibitors ; Receptors, Cytoplasmic and Nuclear/chemistry ; Receptors, Cytoplasmic and Nuclear/genetics ; Steroidogenic Factor 1/antagonists & inhibitors
Czasopismo naukowe
Tytuł :
Application of Infrared Multiple Photon Dissociation (IRMPD) Spectroscopy in Chiral Analysis.
Autorzy :
Shi Y; State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.
Du M; State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.
Ren J; State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.
Zhang K; State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.; School of Precision Instrument and Opto-Electronics Engineering, Tianjin University, Tianjin 300072, China.
Xu Y; State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.
Kong X; State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.; Collaborative Innovation Center of Chemical Science and Engineering, Nankai University, Tianjin 300071, China.
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2020 Nov 05; Vol. 25 (21). Date of Electronic Publication: 2020 Nov 05.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Stereoisomerism*
Mass Spectrometry/*methods
Photochemistry/*methods
Spectrophotometry, Infrared/*methods
Spectrophotometry, Infrared/*trends
Calixarenes/chemistry ; Dimerization ; Gases/chemistry ; Ions ; Ligands ; Peptides/chemistry ; Photons ; Physical Phenomena ; Reproducibility of Results ; Serine/chemistry ; beta-Cyclodextrins/chemistry
Czasopismo naukowe
Tytuł :
Synergistic, additive, and antagonistic antioxidant effects in the mixtures of curcumin with (-)-epicatechin and with a green tea fraction containing (-)-epicatechin.
Autorzy :
Slavova-Kazakova A; Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria. Electronic address: .
Janiak MA; Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Tuwima 10, 10-748 Olsztyn, Poland. Electronic address: .
Sulewska K; Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Tuwima 10, 10-748 Olsztyn, Poland. Electronic address: .
Kancheva VD; Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria. Electronic address: .
Karamać M; Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Tuwima 10, 10-748 Olsztyn, Poland. Electronic address: .
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Źródło :
Food chemistry [Food Chem] 2021 Oct 30; Vol. 360, pp. 129994. Date of Electronic Publication: 2021 May 02.
Typ publikacji :
Journal Article
MeSH Terms :
Antioxidants/*chemistry
Catechin/*chemistry
Curcumin/*chemistry
Tea/*chemistry
Chromatography, High Pressure Liquid ; Chromatography, Thin Layer ; Drug Synergism ; Kinetics ; Plant Extracts/chemistry ; Stereoisomerism ; Tea/metabolism
Czasopismo naukowe
Tytuł :
Enantioselective determination of plasma protein binding of common amphetamine-type stimulants.
Autorzy :
Losacker M; Department of Forensic Toxicology, Institute of Legal Medicine, Johannes Gutenberg University Mainz, Am Pulverturm 3, D-55131, Mainz, Germany. Electronic address: .
Roehrich J; Department of Forensic Toxicology, Institute of Legal Medicine, Johannes Gutenberg University Mainz, Am Pulverturm 3, D-55131, Mainz, Germany.
Hess C; Department of Forensic Toxicology, Institute of Legal Medicine, Johannes Gutenberg University Mainz, Am Pulverturm 3, D-55131, Mainz, Germany; Reference Institute for Bioanalytics, Friesdorfer Str. 153, D-53175, Bonn, Germany.
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Źródło :
Journal of pharmaceutical and biomedical analysis [J Pharm Biomed Anal] 2021 Oct 25; Vol. 205, pp. 114317. Date of Electronic Publication: 2021 Aug 13.
Typ publikacji :
Journal Article
MeSH Terms :
Central Nervous System Stimulants*
Illicit Drugs*
Amphetamine ; Chromatography, Liquid ; Humans ; Protein Binding ; Stereoisomerism ; Tandem Mass Spectrometry
Czasopismo naukowe
Tytuł :
Efficient enantioresolution of aromatic α-hydroxy acids with Cinchona alkaloid-based zwitterionic stationary phases and volatile polar-ionic eluents.
Autorzy :
Varfaj I; Department of Pharmaceutical Sciences, University of Perugia, Via Fabretti 48, 06123, Perugia, Italy.
Protti M; Department of Pharmacy and Biotechnology (FaBiT), Alma Mater Studiorum, University of Bologna, Via Belmeloro 6, 40126, Bologna, Italy.
Di Michele A; Department of Physics and Geology, University of Perugia, Via Pascoli 1, 06123, Perugia, Italy.
Macchioni A; Department of Chemistry, Biology and Biotechnology, University of Perugia, Via Elce di Sotto 8, 06123, Perugia, Italy.
Lindner W; Department of Analytical Chemistry, University of Vienna, Währinger Strasse 38, 1090, Vienna, Austria.
Carotti A; Department of Pharmaceutical Sciences, University of Perugia, Via Fabretti 48, 06123, Perugia, Italy. Electronic address: .
Sardella R; Department of Pharmaceutical Sciences, University of Perugia, Via Fabretti 48, 06123, Perugia, Italy; Center for Perinatal and Reproductive Medicine, University of Perugia, Santa Maria Della Misericordia University Hospital, 06132, Perugia, Italy. Electronic address: .
Mercolini L; Department of Pharmacy and Biotechnology (FaBiT), Alma Mater Studiorum, University of Bologna, Via Belmeloro 6, 40126, Bologna, Italy.
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Źródło :
Analytica chimica acta [Anal Chim Acta] 2021 Oct 02; Vol. 1180, pp. 338928. Date of Electronic Publication: 2021 Aug 09.
Typ publikacji :
Journal Article
MeSH Terms :
Cinchona Alkaloids*
Pharmaceutical Preparations*
Chromatography, High Pressure Liquid ; Hydroxy Acids ; Ions ; Stereoisomerism
Czasopismo naukowe
Tytuł :
Enantioselective multiple heart cutting online two-dimensional liquid chromatography-mass spectrometry of all proteinogenic amino acids with second dimension chiral separations in one-minute time scales on a chiral tandem column.
Autorzy :
Karongo R; Institute of Pharmaceutical Sciences, Pharmaceutical (Bio-)Analysis, University of Tübingen, Auf der Morgenstelle 8, 72076, Tübingen, Germany.
Ge M; Institute of Pharmaceutical Sciences, Pharmaceutical (Bio-)Analysis, University of Tübingen, Auf der Morgenstelle 8, 72076, Tübingen, Germany.
Geibel C; Institute of Pharmaceutical Sciences, Pharmaceutical (Bio-)Analysis, University of Tübingen, Auf der Morgenstelle 8, 72076, Tübingen, Germany.
Horak J; Institute of Pharmaceutical Sciences, Pharmaceutical (Bio-)Analysis, University of Tübingen, Auf der Morgenstelle 8, 72076, Tübingen, Germany; Division of Metabolic and Nutritional Medicine, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University Munich Medical Center, Lindwurmstraße 4, 80337, Munich, Germany. Electronic address: .
Lämmerhofer M; Institute of Pharmaceutical Sciences, Pharmaceutical (Bio-)Analysis, University of Tübingen, Auf der Morgenstelle 8, 72076, Tübingen, Germany. Electronic address: .
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Źródło :
Analytica chimica acta [Anal Chim Acta] 2021 Oct 02; Vol. 1180, pp. 338858. Date of Electronic Publication: 2021 Jul 19.
Typ publikacji :
Journal Article
MeSH Terms :
Amino Acids*
Tandem Mass Spectrometry*
Chromatography, High Pressure Liquid ; Chromatography, Liquid ; Stereoisomerism
Czasopismo naukowe
Tytuł :
A lipase-based chiral stationary phase for direct chiral separation in capillary electrochromatography.
Autorzy :
Li Z; Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, Hubei Province Engineering and Technology Research Center for Fluorinated Pharmaceuticals, Wuhan University School of Pharmaceutical Sciences, Wuhan, 430071, China; State Key Laboratory of Transducer Technology, Chinese Academy of Sciences, Beijing, 100080, China.
Li Q; Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, Hubei Province Engineering and Technology Research Center for Fluorinated Pharmaceuticals, Wuhan University School of Pharmaceutical Sciences, Wuhan, 430071, China.
Fu Y; Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, Hubei Province Engineering and Technology Research Center for Fluorinated Pharmaceuticals, Wuhan University School of Pharmaceutical Sciences, Wuhan, 430071, China.
Hu C; Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, Hubei Province Engineering and Technology Research Center for Fluorinated Pharmaceuticals, Wuhan University School of Pharmaceutical Sciences, Wuhan, 430071, China.
Liu Y; Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, Hubei Province Engineering and Technology Research Center for Fluorinated Pharmaceuticals, Wuhan University School of Pharmaceutical Sciences, Wuhan, 430071, China.
Li W; Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, Hubei Province Engineering and Technology Research Center for Fluorinated Pharmaceuticals, Wuhan University School of Pharmaceutical Sciences, Wuhan, 430071, China.
Chen Z; Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, Hubei Province Engineering and Technology Research Center for Fluorinated Pharmaceuticals, Wuhan University School of Pharmaceutical Sciences, Wuhan, 430071, China; State Key Laboratory of Transducer Technology, Chinese Academy of Sciences, Beijing, 100080, China. Electronic address: .
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Źródło :
Talanta [Talanta] 2021 Oct 01; Vol. 233, pp. 122488. Date of Electronic Publication: 2021 May 11.
Typ publikacji :
Journal Article
MeSH Terms :
Capillary Electrochromatography*
Basidiomycota ; Lipase ; Spectroscopy, Fourier Transform Infrared ; Stereoisomerism
SCR Organism :
Moesziomyces antarcticus
Czasopismo naukowe
Tytuł :
First Synthesis of the Inherently Chiral Trans-4' Bisadduct of C 59 N Azafullerene by Using Cyclo-[2]-dodecylmalonate as a Tether.
Autorzy :
Asad K; Department of Chemistry, University of Cyprus, University str. 1, Building No. 13, 2109, Aglantzia, Nicosia, Cyprus.
Stergiou A; Theoretical and Physical Chemistry Institute, National Hellenic Research Foundation, 48 Vassileos Constantinou Avenue, 11635, Athens, Greece.
Kourtellaris A; Department of Chemistry, University of Cyprus, University str. 1, Building No. 13, 2109, Aglantzia, Nicosia, Cyprus.
Tagmatarchis N; Theoretical and Physical Chemistry Institute, National Hellenic Research Foundation, 48 Vassileos Constantinou Avenue, 11635, Athens, Greece.
Chronakis N; Department of Chemistry, University of Cyprus, University str. 1, Building No. 13, 2109, Aglantzia, Nicosia, Cyprus.
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Źródło :
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2021 Oct 01; Vol. 27 (55), pp. 13879-13886. Date of Electronic Publication: 2021 Aug 31.
Typ publikacji :
Journal Article
MeSH Terms :
Fullerenes*
Crystallography, X-Ray ; Magnetic Resonance Spectroscopy ; Stereoisomerism
Czasopismo naukowe
Tytuł :
Monitoring the behavior of imazalil and its metabolite in grapes, apples, and the processing of fruit wine at enantiomeric level.
Autorzy :
Li R; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, P. R. China.
Pan X; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, P. R. China.
An X; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, P. R. China.
Wang K; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, P. R. China.
Dong F; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, P. R. China.
Xu J; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, P. R. China.
Liu X; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, P. R. China.
Wu X; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, P. R. China.
Zheng Y; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, P. R. China.
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Źródło :
Journal of the science of food and agriculture [J Sci Food Agric] 2021 Oct; Vol. 101 (13), pp. 5478-5486. Date of Electronic Publication: 2021 Mar 21.
Typ publikacji :
Journal Article
MeSH Terms :
Fungicides, Industrial/*chemistry
Imidazoles/*chemistry
Malus/*chemistry
Vitis/*chemistry
Wine/*analysis
Drug Residues/chemistry ; Drug Residues/metabolism ; Food Contamination/analysis ; Food Handling ; Fruit/chemistry ; Fruit/metabolism ; Fungicides, Industrial/metabolism ; Imidazoles/metabolism ; Malus/metabolism ; Stereoisomerism ; Vitis/metabolism
Czasopismo naukowe
Tytuł :
Fragment-based in silico design of SARS-CoV-2 main protease inhibitors.
Autorzy :
Ahmad S; Drug Design Development Research Group, Department of Chemistry, Faculty of Science, Universiti Malaya, Kuala Lumpur, Malaysia.
Usman Mirza M; Department of Chemistry and Biochemistry, University of Windsor, Windsor, ON, Canada.
Yean Kee L; Drug Design Development Research Group, Department of Chemistry, Faculty of Science, Universiti Malaya, Kuala Lumpur, Malaysia.
Nazir M; Department of Pharmacy, The University of Lahore, Lahore, Pakistan.
Abdul Rahman N; Drug Design Development Research Group, Department of Chemistry, Faculty of Science, Universiti Malaya, Kuala Lumpur, Malaysia.
Trant JF; Department of Chemistry and Biochemistry, University of Windsor, Windsor, ON, Canada.
Abdullah I; Drug Design Development Research Group, Department of Chemistry, Faculty of Science, Universiti Malaya, Kuala Lumpur, Malaysia.
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Źródło :
Chemical biology & drug design [Chem Biol Drug Des] 2021 Oct; Vol. 98 (4), pp. 604-619. Date of Electronic Publication: 2021 Jul 02.
Typ publikacji :
Journal Article
MeSH Terms :
Antiviral Agents/*chemistry
COVID-19/*drug therapy
SARS-CoV-2/*drug effects
Viral Protease Inhibitors/*chemistry
Viral Proteases/*metabolism
Antiviral Agents/pharmacology ; Crystallization ; Drug Design ; Humans ; Molecular Docking Simulation ; Molecular Dynamics Simulation ; Multivariate Analysis ; Protein Binding ; Protein Conformation ; Stereoisomerism ; Structure-Activity Relationship ; Viral Protease Inhibitors/pharmacology
Czasopismo naukowe
Tytuł :
Enantioselective toxicity and mechanism of chiral fungicide penflufen based on experiments and computational chemistry.
Autorzy :
Di S; State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products/ Key Laboratory of Detection for Pesticide Residues and Control of Zhejiang, Institute of Agro-product Safety and Nutrition, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, PR China; Agricultural Ministry Key Laboratory for Pesticide Residue Detection, Hangzhou 310021, PR China.
Wang Z; State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products/ Key Laboratory of Detection for Pesticide Residues and Control of Zhejiang, Institute of Agro-product Safety and Nutrition, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, PR China; Agricultural Ministry Key Laboratory for Pesticide Residue Detection, Hangzhou 310021, PR China.
Cang T; State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products/ Key Laboratory of Detection for Pesticide Residues and Control of Zhejiang, Institute of Agro-product Safety and Nutrition, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, PR China; Agricultural Ministry Key Laboratory for Pesticide Residue Detection, Hangzhou 310021, PR China.
Xie Y; Institute of Plant Protection and Microbiology, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, PR China.
Zhao H; State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products/ Key Laboratory of Detection for Pesticide Residues and Control of Zhejiang, Institute of Agro-product Safety and Nutrition, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, PR China; Agricultural Ministry Key Laboratory for Pesticide Residue Detection, Hangzhou 310021, PR China.
Qi P; State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products/ Key Laboratory of Detection for Pesticide Residues and Control of Zhejiang, Institute of Agro-product Safety and Nutrition, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, PR China; Agricultural Ministry Key Laboratory for Pesticide Residue Detection, Hangzhou 310021, PR China.
Wang X; State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products/ Key Laboratory of Detection for Pesticide Residues and Control of Zhejiang, Institute of Agro-product Safety and Nutrition, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, PR China; Agricultural Ministry Key Laboratory for Pesticide Residue Detection, Hangzhou 310021, PR China.
Xu H; State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products/ Key Laboratory of Detection for Pesticide Residues and Control of Zhejiang, Institute of Agro-product Safety and Nutrition, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, PR China; Agricultural Ministry Key Laboratory for Pesticide Residue Detection, Hangzhou 310021, PR China.
Wang X; State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products/ Key Laboratory of Detection for Pesticide Residues and Control of Zhejiang, Institute of Agro-product Safety and Nutrition, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, PR China; Agricultural Ministry Key Laboratory for Pesticide Residue Detection, Hangzhou 310021, PR China. Electronic address: .
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Źródło :
Ecotoxicology and environmental safety [Ecotoxicol Environ Saf] 2021 Oct 01; Vol. 222, pp. 112534. Date of Electronic Publication: 2021 Jul 23.
Typ publikacji :
Journal Article
MeSH Terms :
Fungicides, Industrial*/toxicity
Anilides ; Botrytis ; Computational Chemistry ; Rhizoctonia ; Stereoisomerism
SCR Organism :
Botrytis cinerea; Rhizoctonia solani
Czasopismo naukowe

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