Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

English (EN)·Polski (PL)·Ukraiński (UK)
Przejdź do strony domowej biblioteki Uniwersytet Ekonomiczny we Wrocławiu Link otwiera się w nowym oknie Logo biblioteki Prolib Integro - strona głównaUniwersytet Ekonomiczny we Wrocławiu

Wyszukujesz frazę ""Cholinesterases"" wg kryterium: Temat

  Lista filtrów
Wyrównaj
Wyświetlanie 21-40 z 4868
Tytuł:
Design, synthesis, in silico, and in vitro evaluation of novel benzyloxybenzene substituted (S)‐α‐amino amide derivatives as cholinesterases and monoaminoxidases inhibitor.
Autorzy:
Akıncıoğlu, Akın (AUTHOR)
Pokaż więcej
Źródło:
Drug Development Research. Apr2024, Vol. 85 Issue 2, p1-16. 16p.
Czasopismo naukowe
Szczegóły
Tytuł:
Identification, Baculoviral Expression, and Biochemical Characterization of a Novel Cholinesterase of Amblyomma americanum (Acari: Ixodidae).
Autorzy:
Temeyer KB; Knipling-Bushland U.S. Livestock Insects Research Laboratory and Arthropod Genomics Center, USDA-ARS, 2700 Fredericksburg Road, Kerrville, TX 78028, USA.
Schlechte KG; Knipling-Bushland U.S. Livestock Insects Research Laboratory and Arthropod Genomics Center, USDA-ARS, 2700 Fredericksburg Road, Kerrville, TX 78028, USA.
Gross AD; Molecular Physiology and Toxicology Laboratory, Department of Entomology (MC 0390), Virginia Polytechnic Institute and State University, Latham Hall (Rm 307), 220 Ag Quad Lane, Blacksburg, VA 24061, USA.
Lohmeyer KH; Knipling-Bushland U.S. Livestock Insects Research Laboratory and Arthropod Genomics Center, USDA-ARS, 2700 Fredericksburg Road, Kerrville, TX 78028, USA.
Pokaż więcej
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Apr 22; Vol. 24 (9). Date of Electronic Publication: 2023 Apr 22.
Typ publikacji:
Journal Article
MeSH Terms:
Ixodidae*/genetics
Ticks*
Animals ; Rabbits ; Amblyomma/genetics ; Cholinesterases/metabolism ; DNA, Complementary/genetics ; DNA, Complementary/metabolism ; Acetylthiocholine/metabolism ; Butyrylthiocholine/metabolism ; Antibodies/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Anti-Cholinesterase and Anti-α-Amylase Activities and Neuroprotective Effects of Carvacrol and p -Cymene and Their Effects on Hydrogen Peroxide Induced Stress in SH-SY5Y Cells.
Autorzy:
Caputo L; Department of Pharmacy, University of Salerno, Via Giovanni Paolo II, 132, 84084 Fisciano, Italy.
Amato G; Department of Pharmacy, University of Salerno, Via Giovanni Paolo II, 132, 84084 Fisciano, Italy.
De Martino L; Department of Pharmacy, University of Salerno, Via Giovanni Paolo II, 132, 84084 Fisciano, Italy.
De Feo V; Department of Pharmacy, University of Salerno, Via Giovanni Paolo II, 132, 84084 Fisciano, Italy.; Institute of Food Sciences, CNR-ISA, Via Roma, 64, 83100 Avellino, Italy.
Nazzaro F; Institute of Food Sciences, CNR-ISA, Via Roma, 64, 83100 Avellino, Italy.
Pokaż więcej
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Mar 23; Vol. 24 (7). Date of Electronic Publication: 2023 Mar 23.
Typ publikacji:
Journal Article
MeSH Terms:
Neuroblastoma*/drug therapy
Neuroprotective Agents*/pharmacology
Humans ; Acetylcholinesterase/metabolism ; Amylases/metabolism ; Butyrylcholinesterase/metabolism ; Caspase 3/metabolism ; Cell Line, Tumor ; Cholinesterase Inhibitors/pharmacology ; Hydrogen Peroxide/toxicity ; Oxidative Stress ; alpha-Amylases/antagonists & inhibitors ; Cholinesterases
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Conjugates of Methylene Blue with Cycloalkaneindoles as New Multifunctional Agents for Potential Treatment of Neurodegenerative Disease.
Autorzy:
Bachurin SO; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Shevtsova EF; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Makhaeva GF; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Aksinenko AY; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Grigoriev VV; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Goreva TV; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Epishina TA; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Kovaleva NV; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Boltneva NP; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Lushchekina SV; Emanuel Institute of Biochemical Physics, Russian Academy of Sciences, 119334 Moscow, Russia.
Rudakova EV; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Vinogradova DV; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Shevtsov PN; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Pushkareva EA; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Dubova LG; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Serkova TP; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Veselov IM; Institute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 142432 Chernogolovka, Russia.
Fisenko VP; Department of Pharmacology, Institute of Biodesign and Complex System Modelling, Biomedical Science & Technology Park, Sechenov I.M. First Moscow State Medical University, 119991 Moscow, Russia.
Richardson RJ; Department of Neurology, University of Michigan, Ann Arbor, MI 48109, USA.
Pokaż więcej
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 Nov 11; Vol. 23 (22). Date of Electronic Publication: 2022 Nov 11.
Typ publikacji:
Journal Article
MeSH Terms:
Neurodegenerative Diseases*/drug therapy
Alzheimer Disease*/metabolism
Humans ; Cholinesterase Inhibitors/pharmacology ; Methylene Blue/pharmacology ; Ligands ; Receptors, N-Methyl-D-Aspartate ; Calcium/metabolism ; Cholinesterases/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
N -Hydroxy- N -Propargylamide Derivatives of Ferulic Acid: Inhibitors of Cholinesterases and Monoamine Oxidases.
Autorzy:
Bautista-Aguilera ÓM; Universidad de Alcalá, Departamento de Química Orgánica y Química Inorgánica, Ctra, Madrid-Barcelona Km 33.6, 28871 Alcalá de Henares, Madrid, Spain.
Alonso JM; Universidad de Alcalá, Departamento de Química Orgánica y Química Inorgánica, Ctra, Madrid-Barcelona Km 33.6, 28871 Alcalá de Henares, Madrid, Spain.
Catto M; Department of Pharmacy-Pharmaceutical Sciences, University of Bari Aldo Moro, Via E. Orabona 4, 70125 Bari, Italy.
Iriepa I; Universidad de Alcalá, Departamento de Química Orgánica y Química Inorgánica, Ctra, Madrid-Barcelona Km 33.6, 28871 Alcalá de Henares, Madrid, Spain.; Institute of Chemical Research Andrés M. del Río, Alcalá University, 28805 Alcalá de Henares, Madrid, Spain.
Knez D; University of Ljubljana, Faculty of Pharmacy, Askerceva 7, 1000 Ljubljana, Slovenia.
Gobec S; University of Ljubljana, Faculty of Pharmacy, Askerceva 7, 1000 Ljubljana, Slovenia.
Marco-Contelles J; Laboratory of Medicinal Chemistry (IQOG, CSIC), C/Juan de la Cierva 3, 28006 Madrid, Spain.; Center for Biomedical Network Research on Rare Diseases (CIBERER), CIBER, ISCIII, 28029 Madrid, Spain.
Pokaż więcej
Źródło:
Molecules (Basel, Switzerland) [Molecules] 2022 Nov 01; Vol. 27 (21). Date of Electronic Publication: 2022 Nov 01.
Typ publikacji:
Journal Article
MeSH Terms:
Monoamine Oxidase*/metabolism
Alzheimer Disease*/metabolism
Humans ; Cholinesterases/metabolism ; Amyloid beta-Peptides/metabolism ; Monoamine Oxidase Inhibitors/chemistry ; Cholinesterase Inhibitors/chemistry ; Ligands ; Antioxidants/chemistry ; Acetylcholinesterase/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Cholinesterases Inhibition, Anticancer and Antioxidant Activity of Novel Benzoxazole and Naphthoxazole Analogs.
Autorzy:
Skrzypek, Alicja (AUTHOR)
Karpińska, Monika (AUTHOR)
Juszczak, Małgorzata (AUTHOR)
Grabarska, Aneta (AUTHOR)
Wietrzyk, Joanna (AUTHOR)
Krajewska-Kułak, Elżbieta (AUTHOR)
Studziński, Marek (AUTHOR)
Paszko, Tadeusz (AUTHOR)
Matysiak, Joanna (AUTHOR)
Pokaż więcej
Źródło:
Molecules. Dec2022, Vol. 27 Issue 23, p8511. 16p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Exploring Biological Activity of 4-Oxo-4 H -furo[2,3- h ]chromene Derivatives as Potential Multi-Target-Directed Ligands Inhibiting Cholinesterases, β-Secretase, Cyclooxygenase-2, and Lipoxygenase-5/15.
Autorzy:
Mphahlele MJ; Department of Chemistry, College of Science, Engineering and Technology, University of South Africa, Private Bag X06, Florida 1710, South Africa.
Agbo EN; Department of Chemistry, College of Science, Engineering and Technology, University of South Africa, Private Bag X06, Florida 1710, South Africa.
Gildenhuys S; Department of Life & Consumer Sciences, College of Agriculture and Environmental Sciences, University of South Africa, Private Bag X06, Florida 1710, South Africa.
Setshedi IB; Department of Life & Consumer Sciences, College of Agriculture and Environmental Sciences, University of South Africa, Private Bag X06, Florida 1710, South Africa.
Pokaż więcej
Źródło:
Biomolecules [Biomolecules] 2019 Nov 13; Vol. 9 (11). Date of Electronic Publication: 2019 Nov 13.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Amyloid Precursor Protein Secretases*/antagonists & inhibitors
Amyloid Precursor Protein Secretases*/chemistry
Amyloid Precursor Protein Secretases*/metabolism
Arachidonate 5-Lipoxygenase*/chemistry
Arachidonate 5-Lipoxygenase*/metabolism
Cholinesterase Inhibitors*/chemistry
Cholinesterase Inhibitors*/pharmacology
Cholinesterases*/chemistry
Cholinesterases*/metabolism
Cyclooxygenase 2*/chemistry
Cyclooxygenase 2*/metabolism
Cyclooxygenase 2 Inhibitors*/chemistry
Lipoxygenase Inhibitors*/chemistry
Lipoxygenase Inhibitors*/pharmacology
HEK293 Cells ; Humans ; Ligands ; MCF-7 Cells ; Molecular Docking Simulation
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Genome-wide association studies reveal genetic loci associated with plasma cholinesterase activity in ducks.
Autorzy:
Xu Y; Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.; College of Animal Science and Technology, Northwest A&F University, Yangling, Shanxi, 712100, China.
Liu H; Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Jiang Y; Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Fan W; Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Hu J; Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Zhang Y; Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Guo Z; Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Xie M; Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Huang W; Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Liu X; College of Animal Science and Technology, Northwest A&F University, Yangling, Shanxi, 712100, China.
Zhou Z; Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Hou S; Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Pokaż więcej
Źródło:
Animal genetics [Anim Genet] 2019 Jun; Vol. 50 (3), pp. 287-292. Date of Electronic Publication: 2019 Apr 17.
Typ publikacji:
Journal Article
MeSH Terms:
Cholinesterases/*genetics
Ducks/*genetics
Animals ; Avian Proteins/blood ; Avian Proteins/genetics ; Avian Proteins/metabolism ; Butyrylcholinesterase/genetics ; Cholinesterases/blood ; Cholinesterases/metabolism ; Crosses, Genetic ; Ducks/blood ; Ducks/metabolism ; Female ; Genetic Association Studies ; Male ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Benzophenone Derivatives with Histamine H 3 Receptor Affinity and Cholinesterase Inhibitory Potency as Multitarget-Directed Ligands for Possible Therapy of Alzheimer's Disease.
Autorzy:
Godyń J; Department of Physicochemical Drug Analysis, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Zaręba P; Department of Physicochemical Drug Analysis, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Stary D; Department of Physicochemical Drug Analysis, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.; Doctoral School of Medical and Health Sciences, Jagiellonian University Medical College, św. Łazarza 16 St., 31-530 Krakow, Poland.
Kaleta M; Department of Technology and Biotechnology of Drugs, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Kuder KJ; Department of Technology and Biotechnology of Drugs, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Latacz G; Department of Technology and Biotechnology of Drugs, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Mogilski S; Department of Pharmacodynamics, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Reiner-Link D; Institute of Pharmaceutical and Medicinal Chemistry, Heinrich Heine University Duesseldorf, Universitaetsstr. 1, 40225 Duesseldorf, Germany.
Frank A; Institute of Pharmaceutical and Medicinal Chemistry, Heinrich Heine University Duesseldorf, Universitaetsstr. 1, 40225 Duesseldorf, Germany.
Doroz-Płonka A; Department of Technology and Biotechnology of Drugs, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Olejarz-Maciej A; Department of Technology and Biotechnology of Drugs, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Sudoł-Tałaj S; Doctoral School of Medical and Health Sciences, Jagiellonian University Medical College, św. Łazarza 16 St., 31-530 Krakow, Poland.; Department of Technology and Biotechnology of Drugs, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Nolte T; Department of Technology and Biotechnology of Drugs, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Handzlik J; Department of Technology and Biotechnology of Drugs, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Stark H; Institute of Pharmaceutical and Medicinal Chemistry, Heinrich Heine University Duesseldorf, Universitaetsstr. 1, 40225 Duesseldorf, Germany.
Więckowska A; Department of Physicochemical Drug Analysis, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Malawska B; Department of Physicochemical Drug Analysis, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Kieć-Kononowicz K; Department of Technology and Biotechnology of Drugs, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Łażewska D; Department of Technology and Biotechnology of Drugs, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Bajda M; Department of Physicochemical Drug Analysis, Jagiellonian University Medical College, Medyczna 9 St., 30-688 Krakow, Poland.
Pokaż więcej
Źródło:
Molecules (Basel, Switzerland) [Molecules] 2022 Dec 28; Vol. 28 (1). Date of Electronic Publication: 2022 Dec 28.
Typ publikacji:
Journal Article
MeSH Terms:
Alzheimer Disease*/drug therapy
Alzheimer Disease*/metabolism
Receptors, Histamine H3*/metabolism
Mice ; Animals ; Cholinesterases/metabolism ; Histamine ; Cholinesterase Inhibitors/pharmacology ; Receptors, Histamine ; Ligands ; Structure-Activity Relationship
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Metabolomic Profiling, Antioxidant and Enzyme Inhibition Properties and Molecular Docking Analysis of Antarctic Lichens.
Autorzy:
Torres-Benítez A; Instituto de Farmacia, Facultad de Ciencias, Campus Isla Teja, Universidad Austral de Chile, Valdivia 5090000, Chile.
Ortega-Valencia JE; Tecnológico Nacional de México/Instituto Tecnológico de Tlalnepantla, Av. Instituto Tecnológico, S/N. Col. La Comunidad, Tlalnepantla de Baz 54070, Mexico.
Sanchez M; Departamento de Farmacología, Farmacognosia y Botánica, Facultad de Farmacia, Universidad Complutense de Madrid, Plaza Ramón y Cajal s/n, Ciudad Universitaria, 28040 Madrid, Spain.
Divakar PK; Departamento de Farmacología, Farmacognosia y Botánica, Facultad de Farmacia, Universidad Complutense de Madrid, Plaza Ramón y Cajal s/n, Ciudad Universitaria, 28040 Madrid, Spain.
Simirgiotis MJ; Instituto de Farmacia, Facultad de Ciencias, Campus Isla Teja, Universidad Austral de Chile, Valdivia 5090000, Chile.
Gómez-Serranillos MP; Departamento de Farmacología, Farmacognosia y Botánica, Facultad de Farmacia, Universidad Complutense de Madrid, Plaza Ramón y Cajal s/n, Ciudad Universitaria, 28040 Madrid, Spain.
Pokaż więcej
Źródło:
Molecules (Basel, Switzerland) [Molecules] 2022 Nov 21; Vol. 27 (22). Date of Electronic Publication: 2022 Nov 21.
Typ publikacji:
Journal Article
MeSH Terms:
Lichens*
Eczema*
Keratosis*
Molecular Docking Simulation ; Antioxidants/pharmacology ; Cholinesterases
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Composite biscuits from sandpaper and acha flour restore the altered activity of arginase, cholinergic, and purinergic enzymes in hypertensive-diabetic rats.
Autorzy:
Oboh G; Department of Biochemistry, Federal University of Technology, Akure, Nigeria.
Bello TG; Department of Biochemistry, Federal University of Technology, Akure, Nigeria.
Agunloye OM; Department of Biochemistry, Federal University of Technology, Akure, Nigeria.
Pokaż więcej
Źródło:
Journal of food biochemistry [J Food Biochem] 2022 Nov; Vol. 46 (11), pp. e14336. Date of Electronic Publication: 2022 Jul 18.
Typ publikacji:
Journal Article
MeSH Terms:
Diabetes Mellitus, Experimental*/drug therapy
Hypertension*/drug therapy
Animals ; Rats ; Arginase ; Flour ; NG-Nitroarginine Methyl Ester/adverse effects ; Cholinergic Agents/adverse effects ; Nitric Oxide ; Cholinesterases
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Synthesis, characterization, and α‐glucosidase, cholinesterases, and tyrosinase inhibitory effects of axial substituted silicon and peripheral tetra‐substituted copper (II), manganese (III) phthalocyanines.
Autorzy:
Öztürmen, Berivan Arin (AUTHOR)
Barut, Burak (AUTHOR)
Biyiklioglu, Zekeriya (AUTHOR)
Pokaż więcej
Źródło:
Applied Organometallic Chemistry. Aug2022, Vol. 36 Issue 8, p1-10. 10p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Validation and kinetic of enzymatic method for the detection of organophosphate insecticides based on cholinesterase inhibition.
Autorzy:
Badawy SM; National Center for Clinical and Environmental Toxicology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Pokaż więcej
Źródło:
Toxicology mechanisms and methods [Toxicol Mech Methods] 2020 Feb; Vol. 30 (2), pp. 134-138. Date of Electronic Publication: 2019 Sep 25.
Typ publikacji:
Journal Article
MeSH Terms:
Models, Biological*
Cholinesterase Inhibitors/*analysis
Cholinesterases/*blood
Fenitrothion/*analysis
Insecticides/*analysis
Organophosphorus Compounds/*analysis
Cholinesterases/metabolism ; Dose-Response Relationship, Drug ; Enzyme Assays ; Humans ; Kinetics ; Limit of Detection ; Time Factors
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Ameliorative effect of oregano (Origanum vulgare) versus silymarin in experimentally induced hepatic encephalopathy.
Autorzy:
Abdelghffar EAR; Department of Zoology, Faculty of Science, Ain Shams University, Cairo, Egypt. eman_.
El-Nashar HAS; Department of Pharmacognosy, Faculty of Pharmacy, Ain-Shams University, Cairo, Egypt.; Centre of Drug Discovery Research and Development, Ain Shams University, Cairo, Egypt.
Fayez S; Department of Pharmacognosy, Faculty of Pharmacy, Ain-Shams University, Cairo, Egypt.; Centre of Drug Discovery Research and Development, Ain Shams University, Cairo, Egypt.
Obaid WA; Department of Biology, College of Science, Taibah University, Al-Madīnah Al-Munawarah, Saudi Arabia.
Eldahshan OA; Department of Pharmacognosy, Faculty of Pharmacy, Ain-Shams University, Cairo, Egypt. .; Centre of Drug Discovery Research and Development, Ain Shams University, Cairo, Egypt. .
Pokaż więcej
Źródło:
Scientific reports [Sci Rep] 2022 Oct 25; Vol. 12 (1), pp. 17854. Date of Electronic Publication: 2022 Oct 25.
Typ publikacji:
Journal Article
MeSH Terms:
Hepatic Encephalopathy*/metabolism
Origanum*/chemistry
Silymarin*/pharmacology
Animals ; Rats ; alpha-Tocopherol/metabolism ; Ammonia/metabolism ; Antioxidants/metabolism ; Biomarkers/metabolism ; Cholinesterases/metabolism ; Cytokines/metabolism ; Dopamine/metabolism ; gamma-Tocopherol/pharmacology ; Hexanes ; Liver/metabolism ; Neurotransmitter Agents/metabolism ; Norepinephrine/metabolism ; Oxidative Stress ; Rats, Wistar ; Serotonin/metabolism ; Thioacetamide ; Water/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Conformational Stability and Denaturation Processes of Proteins Investigated by Electrophoresis under Extreme Conditions.
Autorzy:
Masson P; Biochemical Neuropharmacology Laboratory, Kazan Federal University, Kremlievskaya Str. 18, 420111 Kazan, Russia.
Lushchekina S; Emanuel Institute of Biochemical Physics, Russian Academy of Sciences, Kosygin Str. 4, 119334 Moscow, Russia.
Pokaż więcej
Źródło:
Molecules (Basel, Switzerland) [Molecules] 2022 Oct 13; Vol. 27 (20). Date of Electronic Publication: 2022 Oct 13.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Aryldialkylphosphatase*
Biological Products*
Protein Denaturation ; Protein Conformation ; Deuterium Oxide ; Electrophoresis, Polyacrylamide Gel ; Cholinesterases ; Thermodynamics ; Protein Folding
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Resveratrol-Maltol and Resveratrol-Thiophene Hybrids as Cholinesterase Inhibitors and Antioxidants: Synthesis, Biometal Chelating Capability and Crystal Structure.
Autorzy:
Mlakić M; Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Marulićev trg 19, HR-10000 Zagreb, Croatia.
Fodor L; Department of General and Inorganic Chemistry, Institute of Chemistry, Faculty of Engineering, University of Pannonia, P.O. Box 158, H-8201 Veszprém, Hungary.
Odak I; Department of Chemistry, Faculty of Science and Education, University of Mostar, Matice hrvatske bb, 88000 Mostar, Bosnia and Herzegovina.
Horváth O; Department of General and Inorganic Chemistry, Institute of Chemistry, Faculty of Engineering, University of Pannonia, P.O. Box 158, H-8201 Veszprém, Hungary.
Lovrić MJ; Group for Computational Life Sciences, Division of Physical Chemistry, Ruđer Bošković Institute, Bijenička cesta 54, HR-10000 Zagreb, Croatia.
Barić D; Group for Computational Life Sciences, Division of Physical Chemistry, Ruđer Bošković Institute, Bijenička cesta 54, HR-10000 Zagreb, Croatia.
Milašinović V; Division of Physical Chemistry, Rudjer Bošković Institute, Bijenička cesta 54, HR-10000 Zagreb, Croatia.
Molčanov K; Division of Physical Chemistry, Rudjer Bošković Institute, Bijenička cesta 54, HR-10000 Zagreb, Croatia.
Marinić Ž; NMR Center, Rudjer Bošković Institute, Bijenička cesta 54, HR-10000 Zagreb, Croatia.
Lasić Z; Teva api Analytical R&D, Pliva, Prilaz Baruna Filipovića 25, HR-10000 Zagreb, Croatia.
Škorić I; Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Marulićev trg 19, HR-10000 Zagreb, Croatia.
Pokaż więcej
Źródło:
Molecules (Basel, Switzerland) [Molecules] 2022 Sep 27; Vol. 27 (19). Date of Electronic Publication: 2022 Sep 27.
Typ publikacji:
Journal Article
MeSH Terms:
Alzheimer Disease*/metabolism
Trace Elements*
Antioxidants/chemistry ; Antioxidants/pharmacology ; Chelating Agents/chemistry ; Cholinesterase Inhibitors/chemistry ; Cholinesterase Inhibitors/pharmacology ; Cholinesterases/metabolism ; Galantamine ; Humans ; Ligands ; Molecular Docking Simulation ; Pyrones ; Resveratrol ; Structure-Activity Relationship ; Thiophenes
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Phytochemical Characterization, Anti-Oxidant, Anti-Enzymatic and Cytotoxic Effects of Artemisia verlotiorum Lamotte Extracts: A New Source of Bioactive Agents.
Autorzy:
Suroowan S; Department of Health Sciences, Faculty of Medicine and Health Sciences, University of Mauritius, Réduit, Moka 80837, Mauritius.
Llorent-Martínez EJ; Department of Physical and Analytical Chemistry, University of Jaén, Campus Las Lagunillas S/N, E-23071 Jaén, Spain.
Zengin G; Department of Biology, Science Faculty, Selcuk University, Konya 42130, Turkey.
Dall'Acqua S; Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Via Marzolo 5, 35131 Padova, Italy.
Sut S; Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Via Marzolo 5, 35131 Padova, Italy.
Buskaran K; Laboratory of Natural Medicine and Product Research, Institute of Bioscience, Universiti Putra Malaysia (UPM), Serdang 43400, Selangor Darul Ehsan, Malaysia.
Fakurazi S; Laboratory of Natural Medicine and Product Research, Institute of Bioscience, Universiti Putra Malaysia (UPM), Serdang 43400, Selangor Darul Ehsan, Malaysia.; Department of Human Anatomy, Faculty of Medicine & Health Sciences, Universiti Putra Malaysia (UPM), Serdang 43400, Selangor Darul Ehsan, Malaysia.
Mahomoodally MF; Department of Health Sciences, Faculty of Medicine and Health Sciences, University of Mauritius, Réduit, Moka 80837, Mauritius.; Center for Transdisciplinary Research, Department of Pharmacology, Saveetha Dental College, Saveetha Institute of Medical and Technical Science, Chennai 600077, India.; Centre of Excellence for Pharmaceutical Sciences (Pharmacen), North West University, Potchefstroom 2520, South Africa.
Pokaż więcej
Źródło:
Molecules (Basel, Switzerland) [Molecules] 2022 Sep 10; Vol. 27 (18). Date of Electronic Publication: 2022 Sep 10.
Typ publikacji:
Journal Article
MeSH Terms:
Antineoplastic Agents*
Artemisia*
Acetates ; Amylases ; Animals ; Antioxidants/chemistry ; Antioxidants/pharmacology ; Cholinesterases ; Flavonoids/analysis ; Flavonoids/pharmacology ; Flavonols ; Humans ; Methanol/chemistry ; Mice ; Monophenol Monooxygenase ; Phytochemicals/analysis ; Phytochemicals/pharmacology ; Plant Extracts/chemistry ; Plant Extracts/pharmacology ; alpha-Amylases/chemistry ; alpha-Glucosidases/chemistry
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Citrinin and α-pyrone derivatives with pancreatic lipase inhibitory activities from Penicillium sp. SCSIO 41302.
Autorzy:
Han WR; Key Laboratory of Tropical Marine Bio-resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica/Innovation Academy of South China Sea Ecology and Environmental Engineering, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China.; College of Chemical Engineering, Department of Pharmaceutical Engineering, Northwest University, Xi'an 710069, China.
Song MM; Key Laboratory of Tropical Marine Bio-resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica/Innovation Academy of South China Sea Ecology and Environmental Engineering, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China.; College of Chemical Engineering, Department of Pharmaceutical Engineering, Northwest University, Xi'an 710069, China.
Hu YW; Key Laboratory of Tropical Marine Bio-resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica/Innovation Academy of South China Sea Ecology and Environmental Engineering, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China.
Pang XY; Key Laboratory of Tropical Marine Bio-resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica/Innovation Academy of South China Sea Ecology and Environmental Engineering, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China.
Liao SR; Key Laboratory of Tropical Marine Bio-resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica/Innovation Academy of South China Sea Ecology and Environmental Engineering, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China.; Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Guangzhou 511458, China.; Sanya Institute of Oceanology, SCSIO, Sanya 572000, China.
Yang B; Key Laboratory of Tropical Marine Bio-resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica/Innovation Academy of South China Sea Ecology and Environmental Engineering, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China.; Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Guangzhou 511458, China.; Sanya Institute of Oceanology, SCSIO, Sanya 572000, China.
Zhou XF; Key Laboratory of Tropical Marine Bio-resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica/Innovation Academy of South China Sea Ecology and Environmental Engineering, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China.; Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Guangzhou 511458, China.; Sanya Institute of Oceanology, SCSIO, Sanya 572000, China.
Liu YH; Key Laboratory of Tropical Marine Bio-resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica/Innovation Academy of South China Sea Ecology and Environmental Engineering, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China.; Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Guangzhou 511458, China.; Sanya Institute of Oceanology, SCSIO, Sanya 572000, China.
Liu QC; College of Chemical Engineering, Department of Pharmaceutical Engineering, Northwest University, Xi'an 710069, China.
Wang JF; Key Laboratory of Tropical Marine Bio-resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica/Innovation Academy of South China Sea Ecology and Environmental Engineering, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China.; Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Guangzhou 511458, China.; Sanya Institute of Oceanology, SCSIO, Sanya 572000, China.
Pokaż więcej
Źródło:
Journal of Asian natural products research [J Asian Nat Prod Res] 2022 Sep; Vol. 24 (9), pp. 810-819. Date of Electronic Publication: 2021 Nov 11.
Typ publikacji:
Journal Article
MeSH Terms:
Biological Products*/chemistry
Citrinin*
Penicillium*/chemistry
Cholinesterases ; Lipase ; Molecular Structure ; Pyrones/pharmacology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Assessing the Role of a Malonamide Linker in the Design of Potent Dual Inhibitors of Factor Xa and Cholinesterases.
Autorzy:
Purgatorio, Rosa (AUTHOR)
Gambacorta, Nicola (AUTHOR)
Samarelli, Francesco (AUTHOR)
Lopopolo, Gianfranco (AUTHOR)
de Candia, Modesto (AUTHOR)
Catto, Marco (AUTHOR)
Nicolotti, Orazio (AUTHOR)
Altomare, Cosimo D. (AUTHOR)
Pokaż więcej
Źródło:
Molecules. Jul2022, Vol. 27 Issue 13, p4269-N.PAG. 18p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Wyświetlanie 21-40 z 4868

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies