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Wyszukujesz frazę ""Chemical synthesis"" wg kryterium: Temat


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Tytuł :
Exploring the Synthetic Potential of γ-Lactam Derivatives Obtained from a Multicomponent Reaction-Applications as Antiproliferative Agents.
Autorzy :
López-Francés A; Departamento de Química Orgánica I, Centro de Investigación y Estudios Avanzados 'Lucio Lascaray', Facultad de Farmacia, University of the Basque Country, UPV/EHU Paseo de la Universidad 7, 01006 Vitoria-Gasteiz, Spain.
Del Corte X; Departamento de Química Orgánica I, Centro de Investigación y Estudios Avanzados 'Lucio Lascaray', Facultad de Farmacia, University of the Basque Country, UPV/EHU Paseo de la Universidad 7, 01006 Vitoria-Gasteiz, Spain.
Serna-Burgos Z; Departamento de Química Orgánica I, Centro de Investigación y Estudios Avanzados 'Lucio Lascaray', Facultad de Farmacia, University of the Basque Country, UPV/EHU Paseo de la Universidad 7, 01006 Vitoria-Gasteiz, Spain.
Martínez de Marigorta E; Departamento de Química Orgánica I, Centro de Investigación y Estudios Avanzados 'Lucio Lascaray', Facultad de Farmacia, University of the Basque Country, UPV/EHU Paseo de la Universidad 7, 01006 Vitoria-Gasteiz, Spain.
Palacios F; Departamento de Química Orgánica I, Centro de Investigación y Estudios Avanzados 'Lucio Lascaray', Facultad de Farmacia, University of the Basque Country, UPV/EHU Paseo de la Universidad 7, 01006 Vitoria-Gasteiz, Spain.
Vicario J; Departamento de Química Orgánica I, Centro de Investigación y Estudios Avanzados 'Lucio Lascaray', Facultad de Farmacia, University of the Basque Country, UPV/EHU Paseo de la Universidad 7, 01006 Vitoria-Gasteiz, Spain.
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2022 Jun 05; Vol. 27 (11). Date of Electronic Publication: 2022 Jun 05.
Typ publikacji :
Journal Article
MeSH Terms :
Antineoplastic Agents*/chemical synthesis
Antineoplastic Agents*/pharmacology
Lactams*/chemical synthesis
Lactams*/chemistry
beta-Lactams/*chemical synthesis
Cycloaddition Reaction ; Imines ; Stereoisomerism ; beta-Lactams/chemistry
Czasopismo naukowe
Tytuł :
Isatin thiazoles as antidiabetic: Synthesis, in vitro enzyme inhibitory activities, kinetics, and in silico studies.
Autorzy :
Solangi M; International Center for Chemical and Biological Sciences, H. E. J. Research Institute of Chemistry, University of Karachi, Karachi, Pakistan.
Kanwal; International Center for Chemical and Biological Sciences, H. E. J. Research Institute of Chemistry, University of Karachi, Karachi, Pakistan.; Institute of Marine Biotechnology, Universiti Malaysia Terengannu, Kuala Terengganu, Terengganu, Malaysia.
Khan KM; International Center for Chemical and Biological Sciences, H. E. J. Research Institute of Chemistry, University of Karachi, Karachi, Pakistan.; Department of Clinical Pharmacy, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
Chigurupati S; Department of Medicinal Chemistry and Pharmacognosy, Qassim University, Buraydah, Saudi Arabia.
Saleem F; International Center for Chemical and Biological Sciences, H. E. J. Research Institute of Chemistry, University of Karachi, Karachi, Pakistan.
Qureshi U; Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.
Ul-Haq Z; Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.
Jabeen A; Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.
Felemban SG; Department of Medical Laboratory Science, Fakeeh College for Medical Sciences, Jeddah, Kingdom of Saudi Arabia.
Zafar F; Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.
Perveen S; PCSIR Laboratories Complex, Shahrah-e-Dr. Salimuzzaman Siddiqui, Karachi, Pakistan.
Taha M; Department of Clinical Pharmacy, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
Bhatia S; Natural and Medical Sciences Research Center, University of Nizwa, Nizwa, Oman.
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Źródło :
Archiv der Pharmazie [Arch Pharm (Weinheim)] 2022 Jun; Vol. 355 (6), pp. e2100481. Date of Electronic Publication: 2022 Mar 30.
Typ publikacji :
Journal Article
MeSH Terms :
Hypoglycemic Agents*/chemical synthesis
Hypoglycemic Agents*/pharmacology
Isatin*/chemical synthesis
Isatin*/pharmacology
Thiazoles*/chemical synthesis
Thiazoles*/pharmacology
Diabetes Mellitus ; Glycoside Hydrolase Inhibitors/chemical synthesis ; Glycoside Hydrolase Inhibitors/pharmacology ; Humans ; Kinetics ; Molecular Docking Simulation ; Molecular Structure ; Structure-Activity Relationship ; alpha-Amylases/antagonists & inhibitors ; alpha-Glucosidases/metabolism
Czasopismo naukowe
Tytuł :
Synthesis of silver nanoparticle-decorated hydroxyapatite nanocomposite with combined bioactivity and antibacterial properties.
Autorzy :
Bee SL; School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, 14300, Nibong Tebal, Penang, Malaysia. .
Bustami Y; School of Biological Sciences, Universiti Sains Malaysia, 11800, Pulau Pinang, Malaysia.
Ul-Hamid A; Center for Engineering Research, Research Institute, King Fahd University of Petroleum & Minerals, Dhahran, 31261, Saudi Arabia.
Lim K; School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, 14300, Nibong Tebal, Penang, Malaysia.
Abdul Hamid ZA; School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, 14300, Nibong Tebal, Penang, Malaysia. .
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Źródło :
Journal of materials science. Materials in medicine [J Mater Sci Mater Med] 2021 Aug 23; Vol. 32 (9), pp. 106. Date of Electronic Publication: 2021 Aug 23.
Typ publikacji :
Journal Article
MeSH Terms :
Anti-Bacterial Agents*/chemical synthesis
Anti-Bacterial Agents*/chemistry
Anti-Bacterial Agents*/pharmacology
Coated Materials, Biocompatible/*chemical synthesis
Metal Nanoparticles/*chemistry
Silver/*chemistry
Animals ; Bone Substitutes/chemical synthesis ; Bone Substitutes/chemistry ; Bone Substitutes/pharmacology ; Chickens ; Coated Materials, Biocompatible/chemistry ; Coated Materials, Biocompatible/pharmacology ; Durapatite/chemistry ; Durapatite/pharmacology ; Materials Testing ; Microbial Sensitivity Tests ; Microscopy, Electron, Transmission ; Nanocomposites/chemistry ; Prostheses and Implants ; Silver/pharmacology ; Staphylococcus aureus/drug effects ; Staphylococcus aureus/growth & development
Czasopismo naukowe
Tytuł :
Novel amino acid Schiff base Zn(II) complexes as new therapeutic approaches in diabetes and Alzheimer's disease: Synthesis, characterization, biological evaluation, and molecular docking studies.
Autorzy :
Şenocak A; Chemistry Department, Art and Science Faculty, Tokat Gaziosmanpasa University, Tokat, Turkey.
Taş NA; Chemistry Department, Art and Science Faculty, Tokat Gaziosmanpasa University, Tokat, Turkey.; Department of Biotechnology, Faculty of Science, Bartin University, Bartin, Turkey.
Taslimi P; Department of Biotechnology, Faculty of Science, Bartin University, Bartin, Turkey.
Tüzün B; Chemistry Department, Science Faculty, Sivas Cumhuriyet University, Sivas, Turkey.
Aydin A; Department of Basic Medical Science, Yozgat Bozok University, Yozgat, Turkey.
Karadağ A; Department of Chemistry, Faculty of Arts and Sciences, Yozgat Bozok University, Yozgat, Turkey.
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Źródło :
Journal of biochemical and molecular toxicology [J Biochem Mol Toxicol] 2022 Mar; Vol. 36 (3), pp. e22969. Date of Electronic Publication: 2021 Nov 23.
Typ publikacji :
Journal Article
MeSH Terms :
Acetylcholinesterase*/chemistry
Cholinesterase Inhibitors*/chemical synthesis
Cholinesterase Inhibitors*/chemistry
Cholinesterase Inhibitors*/therapeutic use
Coordination Complexes*/chemical synthesis
Coordination Complexes*/chemistry
Coordination Complexes*/therapeutic use
Molecular Docking Simulation*
Zinc*/chemistry
Zinc*/therapeutic use
Alzheimer Disease/*drug therapy
Butyrylcholinesterase/*chemistry
GPI-Linked Proteins/antagonists & inhibitors ; GPI-Linked Proteins/chemistry ; Humans ; Schiff Bases/chemical synthesis ; Schiff Bases/chemistry ; Schiff Bases/therapeutic use
Czasopismo naukowe
Tytuł :
Cellulose Acetate-g-Polycaprolactone Copolymerization Using Diisocyanate Intermediates and the Effect of Polymer Chain Length on Surface, Thermal, and Antibacterial Properties.
Autorzy :
Benahmed A; Laboratory of Applied Chemistry and Environment (LCAE), Faculty of Sciences, University Mohammed Premier, PB 4808, Oujda 60046, Morocco.
Azzaoui K; Laboratory of Applied Chemistry and Environment (LCAE), Faculty of Sciences, University Mohammed Premier, PB 4808, Oujda 60046, Morocco.
El Idrissi A; Laboratory of Applied Chemistry and Environment (LCAE), Faculty of Sciences, University Mohammed Premier, PB 4808, Oujda 60046, Morocco.
Belkheir H; Laboratory of Applied Chemistry and Environment (LCAE), Faculty of Sciences, University Mohammed Premier, PB 4808, Oujda 60046, Morocco.; Centre de Recherche, Ecole des Hautes Etudes d'Ingénierie EHEIO, Oujda 60046, Morocco.
Said Hassane SO; Département de Physique Chimie Faculté des Sciences et Techniques, Université des Comores, BP 2585, Moroni 99999, Comoros.
Touzani R; Laboratory of Applied Chemistry and Environment (LCAE), Faculty of Sciences, University Mohammed Premier, PB 4808, Oujda 60046, Morocco.
Rhazi L; Institut Polytechnique UniLaSalle Transformations & Agro-ResourcesResearch Unit (ULR7519) 19 rue Pierre Waguet, BP 30313, 60026 Beauvais, France.
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2022 Feb 19; Vol. 27 (4). Date of Electronic Publication: 2022 Feb 19.
Typ publikacji :
Journal Article
MeSH Terms :
Anti-Bacterial Agents*/chemical synthesis
Anti-Bacterial Agents*/chemistry
Anti-Bacterial Agents*/pharmacology
Food Packaging*
Polyesters*/chemical synthesis
Polyesters*/chemistry
Polyesters*/pharmacology
Polymerization*
Bacteria/*growth & development
Cellulose/*analogs & derivatives
Cellulose/chemical synthesis ; Cellulose/chemistry ; Cellulose/pharmacology
Czasopismo naukowe
Tytuł :
Novel Selective Galectin-3 Antagonists Are Cytotoxic to Acute Lymphoblastic Leukemia.
Autorzy :
Bum-Erdene K; Institute for Glycomics, Griffith University, Gold Coast Campus, Queensland 4222, Australia.
Collins PM; Institute for Glycomics, Griffith University, Gold Coast Campus, Queensland 4222, Australia.
Hugo MW; Institute for Glycomics, Griffith University, Gold Coast Campus, Queensland 4222, Australia.
Tarighat SS; Section of Molecular Carcinogenesis, Division of Hematology/Oncology and Bone Marrow Transplant, The Saban Research Institute of Children's Hospital Los Angeles, Los Angeles, California 90027, United States.
Fei F; Section of Molecular Carcinogenesis, Division of Hematology/Oncology and Bone Marrow Transplant, The Saban Research Institute of Children's Hospital Los Angeles, Los Angeles, California 90027, United States.
Kishor C; Institute for Glycomics, Griffith University, Gold Coast Campus, Queensland 4222, Australia.
Leffler H; Department of Laboratory Medicine, Section MIG, Lund University, BMC-C1228b, Klinikgatan 28, 221 84 Lund, Sweden.
Nilsson UJ; Centre for Analysis and Synthesis, Department of Chemistry, Lund University, P.O. Box 124, 221 00 Lund, Sweden.
Groffen J; Section of Molecular Carcinogenesis, Division of Hematology/Oncology and Bone Marrow Transplant, The Saban Research Institute of Children's Hospital Los Angeles, Los Angeles, California 90027, United States.
Grice ID; Institute for Glycomics, Griffith University, Gold Coast Campus, Queensland 4222, Australia.; School of Pharmacy and Medical Sciences, Griffith University, Gold Coast Campus, Queensland 4222, Australia.
Heisterkamp N; Section of Molecular Carcinogenesis, Division of Hematology/Oncology and Bone Marrow Transplant, The Saban Research Institute of Children's Hospital Los Angeles, Los Angeles, California 90027, United States.
Blanchard H; Institute for Glycomics, Griffith University, Gold Coast Campus, Queensland 4222, Australia.
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Źródło :
Journal of medicinal chemistry [J Med Chem] 2022 Apr 28; Vol. 65 (8), pp. 5975-5989. Date of Electronic Publication: 2022 Apr 15.
Typ publikacji :
Journal Article
MeSH Terms :
Antineoplastic Agents*/chemical synthesis
Antineoplastic Agents*/chemistry
Antineoplastic Agents*/pharmacology
Precursor Cell Lymphoblastic Leukemia-Lymphoma*/drug therapy
Precursor Cell Lymphoblastic Leukemia-Lymphoma*/metabolism
Binding Sites ; Drug Design ; Galectin 3/antagonists & inhibitors ; Galectin 3/metabolism ; Humans ; Polysaccharides/chemical synthesis ; Polysaccharides/chemistry ; Polysaccharides/pharmacology
Czasopismo naukowe
Tytuł :
Structural and Biochemical Basis for Development of Diketo Acid Inhibitors Targeting the Cap-Snatching Endonuclease of the Ebinur Lake Virus (Order: Bunyavirales ).
Autorzy :
Kuang W; Department of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.; State Key Laboratory of Virology, Wuhan Institute of Virology Chinese Academy of Sciences, Wuhan, Hubei, China.
Zhang H; State Key Laboratory of Virology, Wuhan Institute of Virology Chinese Academy of Sciences, Wuhan, Hubei, China.
Cai Y; State Key Laboratory of Medicinal Chemical Biology, College of Life Sciences, Nankai University, Tianjin, China.; Tianjin International Joint Academy of Biotechnology and Medicine, Tianjin, China.
Zhang G; Center for Disease Control and Prevention of Xinjiang Military Command, Urumqi, Xinjiang, China.
Deng F; State Key Laboratory of Virology, Wuhan Institute of Virology Chinese Academy of Sciences, Wuhan, Hubei, China.
Li H; Center for Disease Control and Prevention of Xinjiang Military Command, Urumqi, Xinjiang, China.
Zhou Y; Department of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Wang M; State Key Laboratory of Virology, Wuhan Institute of Virology Chinese Academy of Sciences, Wuhan, Hubei, China.
Gong P; Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, China.; Drug Discovery Center for Infectious Diseases, Nankai University, Tianjin, China.
Guo Y; State Key Laboratory of Medicinal Chemical Biology, College of Life Sciences, Nankai University, Tianjin, China.
Hu Z; State Key Laboratory of Virology, Wuhan Institute of Virology Chinese Academy of Sciences, Wuhan, Hubei, China.
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Źródło :
Journal of virology [J Virol] 2022 Apr 13; Vol. 96 (7), pp. e0217321. Date of Electronic Publication: 2022 Mar 10.
Typ publikacji :
Journal Article
MeSH Terms :
Antiviral Agents*/chemical synthesis
Antiviral Agents*/pharmacology
Antiviral Agents*/therapeutic use
Bunyaviridae*/enzymology
Endonucleases*/metabolism
Viral Proteins*/metabolism
Bunyaviridae Infections/drug therapy ; Bunyaviridae Infections/virology ; Enzyme Activation/drug effects ; Enzyme Inhibitors/chemical synthesis ; Enzyme Inhibitors/pharmacology ; Enzyme Inhibitors/therapeutic use ; Humans ; Hydroxybutyrates/chemistry ; Hydroxybutyrates/pharmacology ; Hydroxybutyrates/therapeutic use ; Piperidines/chemistry ; Piperidines/pharmacology ; Piperidines/therapeutic use ; Structure-Activity Relationship
Czasopismo naukowe
Tytuł :
Structural variation in the linkage region of pharmaceutical heparin arising from oxidative treatments during manufacture.
Autorzy :
Urso E; Istituto di Ricerche Chimiche e Biochimiche G. Ronzoni, via G. Colombo 81, 20133, Milan, Italy. Electronic address: .
Mantione G; Istituto di Ricerche Chimiche e Biochimiche G. Ronzoni, via G. Colombo 81, 20133, Milan, Italy.
Sala F; Istituto di Ricerche Chimiche e Biochimiche G. Ronzoni, via G. Colombo 81, 20133, Milan, Italy.
Yates EA; Department of Biochemistry and Systems Biology, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.
Guerrini M; Istituto di Ricerche Chimiche e Biochimiche G. Ronzoni, via G. Colombo 81, 20133, Milan, Italy.
Naggi A; Istituto di Ricerche Chimiche e Biochimiche G. Ronzoni, via G. Colombo 81, 20133, Milan, Italy.
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Źródło :
Carbohydrate research [Carbohydr Res] 2022 Apr; Vol. 514, pp. 108540. Date of Electronic Publication: 2022 Mar 05.
Typ publikacji :
Journal Article
MeSH Terms :
Heparin*/chemical synthesis
Heparin*/chemistry
Oligosaccharides*/chemistry
Animals ; Carbohydrate Sequence ; Heparin Lyase ; Oxidative Stress ; Pharmaceutical Preparations/chemical synthesis ; Swine
Czasopismo naukowe
Tytuł :
Synthesis and some enzyme inhibition effects of isoxazoline and pyrazoline derivatives including benzonorbornene unit.
Autorzy :
Yavari MA; Department of Chemistry, Faculty of Science, Atatürk University, Erzurum, Turkey.
Adiloglu Y; Department of Chemistry, Faculty of Science, Sakarya University, Sakarya, Turkey.
Saglamtas R; Central Research and Application Laboratory, Agri Ibrahim Cecen University, Agri, Turkey.
Tutar A; Department of Chemistry, Faculty of Science, Sakarya University, Sakarya, Turkey.
Gulcin I; Department of Chemistry, Faculty of Science, Atatürk University, Erzurum, Turkey.
Menzek A; Department of Chemistry, Faculty of Science, Atatürk University, Erzurum, Turkey.
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Źródło :
Journal of biochemical and molecular toxicology [J Biochem Mol Toxicol] 2022 Feb; Vol. 36 (2), pp. e22952. Date of Electronic Publication: 2021 Nov 16.
Typ publikacji :
Journal Article
MeSH Terms :
Acetylcholinesterase*/chemistry
Carbonic Anhydrase I*/antagonists & inhibitors
Carbonic Anhydrase I*/chemistry
Carbonic Anhydrase II*/antagonists & inhibitors
Carbonic Anhydrase II*/chemistry
Carbonic Anhydrase Inhibitors*/chemical synthesis
Carbonic Anhydrase Inhibitors*/chemistry
Butyrylcholinesterase/*chemistry
Animals ; Cholinesterase Inhibitors/chemical synthesis ; Cholinesterase Inhibitors/chemistry ; Electrophorus ; GPI-Linked Proteins/antagonists & inhibitors ; GPI-Linked Proteins/chemistry ; Structure-Activity Relationship
Czasopismo naukowe
Tytuł :
Tunable and high tissue adhesive properties of injectable chitosan based hydrogels through polymer architecture modulation.
Autorzy :
Jung HY; Department of Molecular Science and Technology, Ajou University, 5 Woncheon, Yeongtong, Suwon, 443-749, Republic of Korea. Electronic address: .
Le Thi P; Department of Molecular Science and Technology, Ajou University, 5 Woncheon, Yeongtong, Suwon, 443-749, Republic of Korea. Electronic address: .
HwangBo KH; Department of Material Development, GENOSS, 906-5 Iuidong, Yeongtong, Suwon, Republic of Korea. Electronic address: .
Bae JW; Department of Material Development, GENOSS, 906-5 Iuidong, Yeongtong, Suwon, Republic of Korea. Electronic address: .
Park KD; Department of Molecular Science and Technology, Ajou University, 5 Woncheon, Yeongtong, Suwon, 443-749, Republic of Korea. Electronic address: .
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Źródło :
Carbohydrate polymers [Carbohydr Polym] 2021 Jun 01; Vol. 261, pp. 117810. Date of Electronic Publication: 2021 Feb 14.
Typ publikacji :
Journal Article
MeSH Terms :
Tissue Adhesives*/administration & dosage
Tissue Adhesives*/chemical synthesis
Tissue Adhesives*/chemistry
Tissue Adhesives*/pharmacology
Chitosan/*chemistry
Hydrogels/*chemical synthesis
Adhesiveness ; Animals ; Cells, Cultured ; Dermis/cytology ; Dermis/drug effects ; Female ; Fibroblasts/drug effects ; Fibroblasts/physiology ; Hemostasis/drug effects ; Humans ; Hydrogels/chemistry ; Hydrogels/pharmacology ; Injections ; Male ; Materials Testing ; Mice ; Mice, Inbred C57BL ; Molecular Structure ; Polymerization ; Polymers/administration & dosage ; Polymers/chemical synthesis ; Polymers/chemistry ; Polymers/pharmacology ; Rats ; Rats, Sprague-Dawley ; Stress, Mechanical ; Tissue Engineering/methods
Czasopismo naukowe
Tytuł :
Antimicrobial, Cytotoxic and Mutagenic Activity of Gemini QAS Derivatives of 1,4:3,6-Dianhydro-l-iditol.
Autorzy :
Sikora K; Department of Inorganic Chemistry, Faculty of Pharmacy, Medical University of Gdańsk, Al. Gen. J. Hallera 107, 80-416 Gdańsk, Poland.; Faculty of Chemistry, University of Gdańsk, Wita Stwosza 63, 80-308 Gdańsk, Poland.
Nowacki A; Faculty of Chemistry, University of Gdańsk, Wita Stwosza 63, 80-308 Gdańsk, Poland.
Szweda P; Department of Pharmaceutical Technology and Biochemistry, Faculty of Chemistry, Gdańsk University of Technology, ul. G. Narutowicza 11/12, 80-233 Gdańsk, Poland.
Woziwodzka A; Laboratory of Biophysics, Intercollegiate Faculty of Biotechnology, University of Gdańsk and Medical University of Gdańsk, Abrahama 58, 80-307 Gdańsk, Poland.
Bartoszewska S; Department of Inorganic Chemistry, Faculty of Pharmacy, Medical University of Gdańsk, Al. Gen. J. Hallera 107, 80-416 Gdańsk, Poland.
Piosik J; Laboratory of Biophysics, Intercollegiate Faculty of Biotechnology, University of Gdańsk and Medical University of Gdańsk, Abrahama 58, 80-307 Gdańsk, Poland.
Dmochowska B; Faculty of Chemistry, University of Gdańsk, Wita Stwosza 63, 80-308 Gdańsk, Poland.
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2022 Jan 24; Vol. 27 (3). Date of Electronic Publication: 2022 Jan 24.
Typ publikacji :
Journal Article
MeSH Terms :
Quaternary Ammonium Compounds*/chemical synthesis
Quaternary Ammonium Compounds*/chemistry
Quaternary Ammonium Compounds*/pharmacology
Sugar Alcohols/*chemistry
Sugar Alcohols/*pharmacology
Anti-Infective Agents/chemical synthesis ; Anti-Infective Agents/chemistry ; Anti-Infective Agents/pharmacology ; Candida albicans ; Cytotoxins/chemical synthesis ; Cytotoxins/chemistry ; Cytotoxins/pharmacology ; Escherichia coli ; HaCaT Cells ; Humans ; Microbial Sensitivity Tests ; Mutagenicity Tests ; Mutagens/chemical synthesis ; Mutagens/chemistry ; Mutagens/pharmacology ; Staphylococcus aureus ; Sugar Alcohols/chemical synthesis
Czasopismo naukowe
Tytuł :
Preparation of Naringenin Nanosuspension and Its Antitussive and Expectorant Effects.
Autorzy :
Dong Z; Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 151, Malianwa North Road, Haidian District, Beijing 100193, China.
Wang R; College of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin 150040, China.
Wang M; Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 151, Malianwa North Road, Haidian District, Beijing 100193, China.; College of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin 150040, China.
Meng Z; Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 151, Malianwa North Road, Haidian District, Beijing 100193, China.; College of Pharmacy, Harbin University of Commerce, No. 138, Tongda Street, Daoli District, Harbin 150076, China.
Wang X; Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 151, Malianwa North Road, Haidian District, Beijing 100193, China.; College of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin 150040, China.
Han M; Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 151, Malianwa North Road, Haidian District, Beijing 100193, China.
Guo Y; Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 151, Malianwa North Road, Haidian District, Beijing 100193, China.
Wang X; Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 151, Malianwa North Road, Haidian District, Beijing 100193, China.
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2022 Jan 24; Vol. 27 (3). Date of Electronic Publication: 2022 Jan 24.
Typ publikacji :
Journal Article
MeSH Terms :
Antitussive Agents*/chemical synthesis
Antitussive Agents*/chemistry
Antitussive Agents*/pharmacology
Antitussive Agents*/therapeutic use
Expectorants*/chemical synthesis
Expectorants*/chemistry
Expectorants*/pharmacology
Expectorants*/therapeutic use
Flavanones/*pharmacology
Animals ; Biological Availability ; Cough/drug therapy ; Cough/pathology ; Disease Models, Animal ; Drug Delivery Systems ; Drug Evaluation, Preclinical ; Drug Liberation ; Flavanones/chemical synthesis ; Flavanones/chemistry ; Flavanones/therapeutic use ; Mice ; Nanoparticles ; Particle Size ; Solubility ; Suspensions
Czasopismo naukowe
Tytuł :
Antifungal, Antibacterial, and Cytotoxic Activities of Silver Nanoparticles Synthesized from Aqueous Extracts of Mace-Arils of Myristica fragrans .
Autorzy :
Rizwana H; Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 22452, Riyadh 11495, Saudi Arabia.
Bokahri NA; Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 22452, Riyadh 11495, Saudi Arabia.
S Alkhattaf F; Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 22452, Riyadh 11495, Saudi Arabia.
Albasher G; Department of Zoology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
A Aldehaish H; Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 22452, Riyadh 11495, Saudi Arabia.
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2021 Dec 20; Vol. 26 (24). Date of Electronic Publication: 2021 Dec 20.
Typ publikacji :
Journal Article
MeSH Terms :
Anti-Bacterial Agents*/chemical synthesis
Anti-Bacterial Agents*/chemistry
Anti-Bacterial Agents*/isolation & purification
Anti-Bacterial Agents*/pharmacology
Antifungal Agents*/chemical synthesis
Antifungal Agents*/chemistry
Antifungal Agents*/isolation & purification
Antifungal Agents*/pharmacology
Metal Nanoparticles*/chemistry
Metal Nanoparticles*/therapeutic use
Silver*/chemistry
Silver*/pharmacology
Myristica/*chemistry
Plant Extracts/*chemistry
Bacteria/growth & development ; Cytotoxins/chemical synthesis ; Cytotoxins/chemistry ; Cytotoxins/isolation & purification ; Cytotoxins/pharmacology ; Fungi/growth & development ; HeLa Cells ; Humans
Czasopismo naukowe
Tytuł :
ROS-Responsive Selenium-Containing Carriers for Coencapsulation of Photosensitizer and Hypoxia-Activated Prodrug and Their Cellular Behaviors.
Autorzy :
Song F; Shanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials and Science and Engineering, East China University of Science and Technology, Shanghai, 200237, China.
Li S; Shanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials and Science and Engineering, East China University of Science and Technology, Shanghai, 200237, China.
Sun C; Shanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials and Science and Engineering, East China University of Science and Technology, Shanghai, 200237, China.
Ji Y; Institute of Textiles and Clothing, Hong Kong Polytechnic University, Hunghom, Kowloon, Hong Kong SAR, 999077, China.
Zhang Y; Shanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials and Science and Engineering, East China University of Science and Technology, Shanghai, 200237, China.; Key Laboratory of Smart Drug Delivery, Ministry of Education (Fudan University), Shanghai, 201203, China.
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Źródło :
Macromolecular bioscience [Macromol Biosci] 2021 Dec; Vol. 21 (12), pp. e2100229. Date of Electronic Publication: 2021 Aug 12.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Drug Carriers*/chemical synthesis
Drug Carriers*/chemistry
Drug Carriers*/pharmacokinetics
Drug Carriers*/pharmacology
Nanoparticles*/chemistry
Nanoparticles*/therapeutic use
Photochemotherapy*
Photosensitizing Agents*/chemical synthesis
Photosensitizing Agents*/chemistry
Photosensitizing Agents*/pharmacokinetics
Photosensitizing Agents*/pharmacology
Prodrugs*/chemical synthesis
Prodrugs*/chemistry
Prodrugs*/pharmacokinetics
Prodrugs*/pharmacology
Selenium*/chemistry
Selenium*/pharmacokinetics
Selenium*/pharmacology
Reactive Oxygen Species/*metabolism
Cell Line, Tumor ; Delayed-Action Preparations/chemical synthesis ; Delayed-Action Preparations/chemistry ; Delayed-Action Preparations/pharmacokinetics ; Delayed-Action Preparations/pharmacology ; Humans
Czasopismo naukowe
Tytuł :
Structural Design, Synthesis and Antioxidant, Antileishmania, Anti-Inflammatory and Anticancer Activities of a Novel Quercetin Acetylated Derivative.
Autorzy :
da Silva SVS; Department of Life Sciences, State University of Bahia (UNEB), Salvador 41150-000, BA, Brazil.
Barboza OM; Department of Life Sciences, State University of Bahia (UNEB), Salvador 41150-000, BA, Brazil.
Souza JT; Laboratory of Neurochemistry and Cell Biology, Department of Biochemistry and Biophysics, Federal University of Bahia, Salvador 40231-300, BA, Brazil.
Soares ÉN; Laboratory of Neurochemistry and Cell Biology, Department of Biochemistry and Biophysics, Federal University of Bahia, Salvador 40231-300, BA, Brazil.
Dos Santos CC; Laboratory of Neurochemistry and Cell Biology, Department of Biochemistry and Biophysics, Federal University of Bahia, Salvador 40231-300, BA, Brazil.
Pacheco LV; Department of Life Sciences, State University of Bahia (UNEB), Salvador 41150-000, BA, Brazil.; Gonçalo Moniz Institute, FIOCRUZ, Salvador 40296-710, BA, Brazil.
Santos IP; Gonçalo Moniz Institute, FIOCRUZ, Salvador 40296-710, BA, Brazil.
Magalhães TBDS; Department of Life Sciences, State University of Bahia (UNEB), Salvador 41150-000, BA, Brazil.
Soares MBP; Gonçalo Moniz Institute, FIOCRUZ, Salvador 40296-710, BA, Brazil.; SENAI Institute of Innovation in Health Advanced Systems (CIMATEC ISI SAS), University Center SENAI/CIMATEC, Salvador 41650-010, BA, Brazil.
Guimarães ET; Department of Life Sciences, State University of Bahia (UNEB), Salvador 41150-000, BA, Brazil.; Gonçalo Moniz Institute, FIOCRUZ, Salvador 40296-710, BA, Brazil.
Meira CS; Department of Life Sciences, State University of Bahia (UNEB), Salvador 41150-000, BA, Brazil.; Gonçalo Moniz Institute, FIOCRUZ, Salvador 40296-710, BA, Brazil.; SENAI Institute of Innovation in Health Advanced Systems (CIMATEC ISI SAS), University Center SENAI/CIMATEC, Salvador 41650-010, BA, Brazil.
Costa SL; Laboratory of Neurochemistry and Cell Biology, Department of Biochemistry and Biophysics, Federal University of Bahia, Salvador 40231-300, BA, Brazil.
da Silva VDA; Laboratory of Neurochemistry and Cell Biology, Department of Biochemistry and Biophysics, Federal University of Bahia, Salvador 40231-300, BA, Brazil.
de Santana LLB; Department of Life Sciences, State University of Bahia (UNEB), Salvador 41150-000, BA, Brazil.
de Freitas Santos Júnior A; Department of Life Sciences, State University of Bahia (UNEB), Salvador 41150-000, BA, Brazil.
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2021 Nov 17; Vol. 26 (22). Date of Electronic Publication: 2021 Nov 17.
Typ publikacji :
Journal Article
MeSH Terms :
Anti-Inflammatory Agents*/chemical synthesis
Anti-Inflammatory Agents*/chemistry
Anti-Inflammatory Agents*/pharmacology
Antineoplastic Agents*/chemical synthesis
Antineoplastic Agents*/chemistry
Antineoplastic Agents*/pharmacology
Antioxidants*/chemical synthesis
Antioxidants*/chemistry
Antioxidants*/pharmacology
Antiprotozoal Agents*/chemical synthesis
Antiprotozoal Agents*/chemistry
Antiprotozoal Agents*/pharmacology
Quercetin/*analogs & derivatives
Acetylation ; Animals ; HL-60 Cells ; Hep G2 Cells ; Humans ; Mice ; Mice, Inbred BALB C ; Quercetin/chemical synthesis ; Quercetin/chemistry ; Quercetin/pharmacology
Czasopismo naukowe
Tytuł :
Amidine- and Amidoxime-Substituted Heterocycles: Synthesis, Antiproliferative Evaluations and DNA Binding.
Autorzy :
Maračić S; Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Marulićev trg 19, HR-10000 Zagreb, Croatia.
Grbčić P; Department of Biotechnology, University of Rijeka, Ulica Radmile Matejčić 2, HR-51000 Rijeka, Croatia.
Shammugam S; Division of Organic Chemistry and Biochemistry, Laboratory for Biomolecular Interactions and Spectroscopy, Ruđer Bošković Institute, Bijenička 54, HR-10000 Zagreb, Croatia.
Radić Stojković M; Division of Organic Chemistry and Biochemistry, Laboratory for Biomolecular Interactions and Spectroscopy, Ruđer Bošković Institute, Bijenička 54, HR-10000 Zagreb, Croatia.
Pavelić K; Faculty of Medicine, Juraj Dobrila University of Pula, HR-52100 Pula, Croatia.
Sedić M; Centre for Applied Bioanthropology, Institute for Anthropological Research, Ljudevita Gaja 32, HR-10000 Zagreb, Croatia.
Kraljević Pavelić S; Faculty of Health Studies, University of Rijeka, Ulica Viktora Cara Emina 5, HR-51000 Rijeka, Croatia.
Raić-Malić S; Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Marulićev trg 19, HR-10000 Zagreb, Croatia.
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2021 Nov 22; Vol. 26 (22). Date of Electronic Publication: 2021 Nov 22.
Typ publikacji :
Journal Article
MeSH Terms :
Cell Proliferation*
DNA, Neoplasm*/chemistry
DNA, Neoplasm*/metabolism
Intercalating Agents*/chemical synthesis
Intercalating Agents*/chemistry
Intercalating Agents*/pharmacology
Neoplasms*/drug therapy
Neoplasms*/metabolism
Oximes/*chemistry
A549 Cells ; Antineoplastic Agents/chemical synthesis ; Antineoplastic Agents/chemistry ; Antineoplastic Agents/pharmacology ; HeLa Cells ; Hep G2 Cells ; Humans
Czasopismo naukowe
Tytuł :
Synthesis, Antifungal Activity, 3D-QSAR, and Molecular Docking Study of Novel Menthol-Derived 1,2,4-Triazole-thioether Compounds.
Autorzy :
Huang M; School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China.; Guangxi Research Institute of Chemical Industry Co., Ltd., Nanning 530001, China.
Duan WG; School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China.
Lin GS; School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China.
Li BY; School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China.
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2021 Nov 17; Vol. 26 (22). Date of Electronic Publication: 2021 Nov 17.
Typ publikacji :
Journal Article
MeSH Terms :
Fungicides, Industrial*/chemical synthesis
Fungicides, Industrial*/chemistry
Fungicides, Industrial*/pharmacology
Molecular Docking Simulation*
Fusarium/*growth & development
Menthol/chemistry ; Microbial Sensitivity Tests ; Structure-Activity Relationship ; Sulfides/chemical synthesis ; Sulfides/chemistry ; Sulfides/pharmacology ; Triazoles/chemistry
SCR Organism :
Fusarium oxysporum; Fusarium zeae
Czasopismo naukowe
Tytuł :
Calcium hydroxyapatite nanoparticles as a reinforcement filler in dental resin nanocomposite.
Autorzy :
Akhtar K; National Centre of Excellence in Physical Chemistry, University of Peshawar, Peshawar, 25120, Khyber Pakhtunkhwa, Pakistan. .
Pervez C; National Centre of Excellence in Physical Chemistry, University of Peshawar, Peshawar, 25120, Khyber Pakhtunkhwa, Pakistan.
Zubair N; National Centre of Excellence in Physical Chemistry, University of Peshawar, Peshawar, 25120, Khyber Pakhtunkhwa, Pakistan.
Khalid H; National Centre of Excellence in Physical Chemistry, University of Peshawar, Peshawar, 25120, Khyber Pakhtunkhwa, Pakistan.
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Źródło :
Journal of materials science. Materials in medicine [J Mater Sci Mater Med] 2021 Oct 03; Vol. 32 (10), pp. 129. Date of Electronic Publication: 2021 Oct 03.
Typ publikacji :
Journal Article
MeSH Terms :
Resins, Synthetic*/chemical synthesis
Resins, Synthetic*/chemistry
Resins, Synthetic*/pharmacology
Dental Restoration, Permanent/*instrumentation
Durapatite/*pharmacology
Coated Materials, Biocompatible/chemical synthesis ; Coated Materials, Biocompatible/chemistry ; Composite Resins/chemical synthesis ; Composite Resins/chemistry ; Durapatite/chemistry ; Hardness ; Humans ; Materials Testing ; Microscopy, Electron, Scanning ; Nanocomposites/chemistry ; Nanoparticles/chemistry ; Surface Properties
Czasopismo naukowe
Tytuł :
Ecofriendly flame-retardant composite aerogel derived from polysaccharide: Preparation, flammability, thermal kinetics, and mechanism.
Autorzy :
He H; Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, College of Chemistry and Chemical Engineering, Wuhan Textile University, Wuhan 430200, China.
Wang Y; Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, College of Chemistry and Chemical Engineering, Wuhan Textile University, Wuhan 430200, China.
Yu Z; Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, College of Chemistry and Chemical Engineering, Wuhan Textile University, Wuhan 430200, China. Electronic address: .
Liu J; Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, College of Chemistry and Chemical Engineering, Wuhan Textile University, Wuhan 430200, China.
Zhao Y; Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, College of Chemistry and Chemical Engineering, Wuhan Textile University, Wuhan 430200, China.
Ke Y; Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, College of Chemistry and Chemical Engineering, Wuhan Textile University, Wuhan 430200, China.
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Źródło :
Carbohydrate polymers [Carbohydr Polym] 2021 Oct 01; Vol. 269, pp. 118291. Date of Electronic Publication: 2021 Jun 02.
Typ publikacji :
Journal Article; Video-Audio Media
MeSH Terms :
Flame Retardants*/chemical synthesis
Flame Retardants*/pharmacology
Alginates/*chemistry
Carboxymethylcellulose Sodium/*chemistry
Chitosan/*chemistry
Cryogels/*chemistry
Alginates/chemical synthesis ; Alginates/pharmacology ; Anti-Bacterial Agents/chemical synthesis ; Anti-Bacterial Agents/chemistry ; Anti-Bacterial Agents/pharmacology ; Carboxymethylcellulose Sodium/chemical synthesis ; Carboxymethylcellulose Sodium/pharmacology ; Chitosan/chemical synthesis ; Chitosan/pharmacology ; Compressive Strength ; Cryogels/chemical synthesis ; Cryogels/pharmacology ; Escherichia coli/drug effects ; Kinetics ; Materials Testing ; Microbial Sensitivity Tests ; Porosity ; Staphylococcus aureus/drug effects ; Thermal Conductivity
Czasopismo naukowe
Tytuł :
Optimization of (-)-cubebin biotransformation to (-)-hinokinin by the marine fungus Absidia coerulea 3A9.
Autorzy :
de Souza JM; Center for Research in Exact and Technological Sciences, University of Franca, Franca, SP, 14404-600, Brazil.
Santos MFC; Center for Research in Exact and Technological Sciences, University of Franca, Franca, SP, 14404-600, Brazil.
Pedroso RCN; Center for Research in Exact and Technological Sciences, University of Franca, Franca, SP, 14404-600, Brazil.
Pimenta LP; Center for Research in Exact and Technological Sciences, University of Franca, Franca, SP, 14404-600, Brazil.
Siqueira KA; Department of Botany and Ecology, Biosciences Institute, Federal University of Mato Grosso, Cuiabá, MT, 78060-900, Brazil.
Soares MA; Department of Botany and Ecology, Biosciences Institute, Federal University of Mato Grosso, Cuiabá, MT, 78060-900, Brazil.
Dias GM; Center for Natural and Human Sciences, Federal University of ABC, São Bernardo do Campo, SP, 09606-070, Brazil.
Pietro RCLR; Department of Drugs and Medicines, School of Pharmaceutical Sciences, University Estadual Paulista, Araraquara, SP, 14800-903, Brazil.
Ramos HP; Center for Research in Exact and Technological Sciences, University of Franca, Franca, SP, 14404-600, Brazil.
Silva MLA; Center for Research in Exact and Technological Sciences, University of Franca, Franca, SP, 14404-600, Brazil.
Pauletti PM; Center for Research in Exact and Technological Sciences, University of Franca, Franca, SP, 14404-600, Brazil.
Veneziani RCS; Center for Research in Exact and Technological Sciences, University of Franca, Franca, SP, 14404-600, Brazil.
Ambrósio SR; Center for Research in Exact and Technological Sciences, University of Franca, Franca, SP, 14404-600, Brazil.
Braun GH; Center for Research in Exact and Technological Sciences, University of Franca, Franca, SP, 14404-600, Brazil. .
Januário AH; Center for Research in Exact and Technological Sciences, University of Franca, Franca, SP, 14404-600, Brazil. .
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Źródło :
Archives of microbiology [Arch Microbiol] 2021 Sep; Vol. 203 (7), pp. 4313-4318. Date of Electronic Publication: 2021 Jun 10.
Typ publikacji :
Journal Article
MeSH Terms :
Absidia*
Benzodioxoles*/chemical synthesis
Lignans*/chemical synthesis
Lignans*/chemistry
Lignans*/metabolism
4-Butyrolactone/*analogs & derivatives
4-Butyrolactone/chemical synthesis ; Aquatic Organisms/metabolism ; Biotransformation ; Seawater/chemistry
SCR Organism :
Absidia caerulea
Czasopismo naukowe

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