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Wyszukujesz frazę ""Al-thamili, Dhaifallah M."" wg kryterium: Autor


Wyświetlanie 1-6 z 6
Tytuł :
Multicomponent Domino Synthesis, Anticancer Activity and Molecular Modeling Simulation of Complex Dispirooxindolopyrrolidines.
Autorzy :
Arumugam N; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Almansour AI; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Suresh Kumar R; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Govindasami P; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Al-Thamili DM; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Krishnamoorthy R; Nanobiotecnology and Molecular Biology Research Laboratory, Department of Food Science and Nutrition, College of Food and Agricultural Sciences, King Saud University, Riyadh 11451, Saudi Arabia. .
Periasamy VS; Department of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, IN 47907-2084, USA. .
Alshatwi AA; Nanobiotecnology and Molecular Biology Research Laboratory, Department of Food Science and Nutrition, College of Food and Agricultural Sciences, King Saud University, Riyadh 11451, Saudi Arabia. .
Mahalingam SM; Department of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, IN 47907-2084, USA. .
Thangamani S; Department of Pathology and Population Medicine, College of Veterinary Medicine, Midwestern University, Glendale, AZ 85308, USA. .
Menéndez JC; Unidad de Química Orgánica y Farmacéutica, Departamento de Química en Ciencias Farmacéuticas, Facultad de Farmacia, Universidad Complutense, 28040 Madrid, Spain. .
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2018 May 05; Vol. 23 (5). Date of Electronic Publication: 2018 May 05.
Typ publikacji :
Journal Article
MeSH Terms :
Antineoplastic Agents/*chemical synthesis
Indoles/*chemical synthesis
Piperidones/*chemical synthesis
Proto-Oncogene Proteins c-met/*antagonists & inhibitors
Pyrrolidines/*chemical synthesis
Spiro Compounds/*chemical synthesis
Antineoplastic Agents/pharmacology ; Apoptosis/drug effects ; Binding Sites ; Bleomycin/pharmacology ; Cell Line, Tumor ; Cell Survival/drug effects ; Cycloaddition Reaction ; Drug Design ; Humans ; Imidazoles/chemistry ; Indoles/pharmacology ; Inhibitory Concentration 50 ; Lymphocytes/drug effects ; Lymphocytes/pathology ; Molecular Docking Simulation ; Piperidones/pharmacology ; Protein Binding ; Protein Interaction Domains and Motifs ; Protein Structure, Secondary ; Proto-Oncogene Proteins c-met/chemistry ; Proto-Oncogene Proteins c-met/metabolism ; Pyrrolidines/pharmacology ; Spiro Compounds/pharmacology ; Structure-Activity Relationship
Czasopismo naukowe
Tytuł :
Regio and stereoselective synthesis of anticancer spirooxindolopyrrolidine embedded piperidone heterocyclic hybrids derived from one-pot cascade protocol.
Autorzy :
Arumugam N; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh, 11451, Saudi Arabia. .
Almansour AI; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh, 11451, Saudi Arabia.
Kumar RS; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh, 11451, Saudi Arabia.
Al-Thamili DM; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh, 11451, Saudi Arabia.
Periyasami G; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh, 11451, Saudi Arabia.
Periasamy VS; Nanobiotecnology and Molecular Biology Research Laboratory, Department of Food Science and Nutrition, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.
Athinarayanan J; Nanobiotecnology and Molecular Biology Research Laboratory, Department of Food Science and Nutrition, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.
Alshatwi AA; Nanobiotecnology and Molecular Biology Research Laboratory, Department of Food Science and Nutrition, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.
Mahalingam SM; Department of Atomic and Molecular Physics, MIT Campus, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
Menéndez JC; Unidad de Química Orgánica y Farmacéutica, Departamento de Química en Ciencias Farmacéuticas, Facultad de Farmacia, Universidad Complutense, 28040, Madrid, Spain.
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Źródło :
Chemistry Central journal [Chem Cent J] 2018 Sep 01; Vol. 12 (1), pp. 95. Date of Electronic Publication: 2018 Sep 01.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Highly functionalized 2-amino-4H-pyrans as potent cholinesterase inhibitors.
Autorzy :
Kumar RS; Department of Chemistry, College of Sciences, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. Electronic address: .
Almansour AI; Department of Chemistry, College of Sciences, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Arumugam N; Department of Chemistry, College of Sciences, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Al-Thamili DM; Department of Chemistry, College of Sciences, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Basiri A; Department of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, NE 68198, United States.
Kotresha D; Department of Microbiology, East West Group of Institution, no. 63, Anjananagar, Vishwaneedam post, Bangaluru 560091, Karnataka, India.
Manohar TS; Department of Biosciences, Sri Sathya Sai Institute of Higher Learning, Prasanthi Nilayam, A.P. 515 134, India.
Venketesh S; Department of Biosciences, Sri Sathya Sai Institute of Higher Learning, Prasanthi Nilayam, A.P. 515 134, India.
Asad M; Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah 21589, Saudi Arabia; Center of Excellence for Advanced Materials Research (CEAMR), King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Asiri AM; Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah 21589, Saudi Arabia; Center of Excellence for Advanced Materials Research (CEAMR), King Abdulaziz University, Jeddah 21589, Saudi Arabia.
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Źródło :
Bioorganic chemistry [Bioorg Chem] 2018 Dec; Vol. 81, pp. 134-143. Date of Electronic Publication: 2018 Aug 12.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Acetylcholinesterase/*metabolism
Butyrylcholinesterase/*metabolism
Cholinesterase Inhibitors/*pharmacology
Pyrans/*pharmacology
Cholinesterase Inhibitors/chemical synthesis ; Cholinesterase Inhibitors/chemistry ; Dose-Response Relationship, Drug ; Humans ; Molecular Docking Simulation ; Molecular Structure ; Pyrans/chemical synthesis ; Pyrans/chemistry ; Structure-Activity Relationship
Czasopismo naukowe
Tytuł :
Domino Multicomponent Approach for the Synthesis of Functionalized Spiro-Indeno[1,2- b ]quinoxaline Heterocyclic Hybrids and Their Antimicrobial Activity, Synergistic Effect and Molecular Docking Simulation.
Autorzy :
Almansour AI; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Arumugam N; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Suresh Kumar R; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Al-Thamili DM; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Periyasami G; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Ponmurugan K; Department of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia. .
Al-Dhabi NA; Department of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia. .
Perumal K; Department of Chemistry and Biochemistry, The Ohio State University, 151 W. Woodruff Ave, Columbus, OH 43210, USA. .
Premnath D; Department of Bioscience and Technology, Karunya Institute of Technology and Science, Branch of Bioinformatics, School of Agriculture and Biosciences, Karunya Nagar, Coimbatore-641114, India. .
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2019 May 22; Vol. 24 (10). Date of Electronic Publication: 2019 May 22.
Typ publikacji :
Journal Article
MeSH Terms :
Anti-Bacterial Agents/*chemical synthesis
Anti-Bacterial Agents/*pharmacology
Quinoxalines/*chemical synthesis
Quinoxalines/*pharmacology
Anti-Bacterial Agents/chemistry ; Cycloaddition Reaction ; Drug Synergism ; Escherichia coli/drug effects ; Imidazoles/chemistry ; Microbial Sensitivity Tests ; Molecular Docking Simulation ; Molecular Structure ; Quinoxalines/chemistry ; Streptomycin/pharmacology ; Structure-Activity Relationship ; Vancomycin/pharmacology
Czasopismo naukowe
Tytuł :
A New Class of β-Pyrrolidino-1,2,3-Triazole Derivatives as β-Adrenergic Receptor Inhibitors: Synthesis, Pharmacological, and Docking Studies.
Autorzy :
Easwaramoorthi K; Department of Chemistry, Loyola College, Chennai-600034, TN, India. .; R&D Centre, Malladi Drugs & Pharmaceuticals Ltd., Chennai-600124, TN, India. .
Rajendran JA; Department of Chemistry, Loyola College, Chennai-600034, TN, India. .
Rao KC; R&D Centre, Malladi Drugs & Pharmaceuticals Ltd., Chennai-600124, TN, India. .; Organic & Bioorganic Chemistry Laboratory, CSIR-Central Leather Research Institute, Adyar, Chennai-600020, TN, India. .
Balachandran C; Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2641 Yamazaki, Noda 278-8510, Japan. .
Arun Y; Organic & Bioorganic Chemistry Laboratory, CSIR-Central Leather Research Institute, Adyar, Chennai-600020, TN, India. .
Mahalingam SM; Department of Chemistry, SRM institute of Science and Technology, Kattankulathur, Kancheepuram 603203, India. .
Arumugam N; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Almansour AI; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Kumar RS; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Al-Thamili DM; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. .
Aoki S; Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2641 Yamazaki, Noda 278-8510, Japan. .; Research Institute of Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda 278-8510, Japan. .
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2019 Sep 26; Vol. 24 (19). Date of Electronic Publication: 2019 Sep 26.
Typ publikacji :
Journal Article
MeSH Terms :
Adrenergic beta-Antagonists/*chemical synthesis
Adrenergic beta-Antagonists/*pharmacology
Triazoles/*chemical synthesis
Triazoles/*pharmacology
Adrenergic beta-Antagonists/chemistry ; Anti-Infective Agents/chemistry ; Anti-Infective Agents/pharmacology ; Antineoplastic Agents/chemistry ; Antineoplastic Agents/pharmacology ; Chemistry Techniques, Synthetic ; Dose-Response Relationship, Drug ; Humans ; Microbial Sensitivity Tests ; Molecular Conformation ; Molecular Docking Simulation ; Molecular Dynamics Simulation ; Molecular Structure ; Protein Binding ; Receptors, Adrenergic, beta-2/chemistry ; Structure-Activity Relationship ; Triazoles/chemistry
Czasopismo naukowe
Tytuł :
Discovery of novel cage-like heterocyclic hybrids as anti-inflammatory agents through the inhibition of nitrite, PGE2 and TNF-α.
Autorzy :
Kumar RS; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia. Electronic address: .
Antonisamy P; Department of Korean Physiology, Wonkwang University School of Korean Medicine, 460 Iksan-daero, Iksan City, Jeonbuk 570-749, Republic of Korea.
Almansour AI; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Arumugam N; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Al-Thamili DM; Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Kumar RR; Department of Organic Chemistry, School of Chemistry, Madurai Kamaraj University, Madurai 625 021, Tamil Nadu, India.
Kim HR; Department of Korean Physiology, Wonkwang University School of Korean Medicine, 460 Iksan-daero, Iksan City, Jeonbuk 570-749, Republic of Korea.
Kwon KB; Department of Korean Physiology, Wonkwang University School of Korean Medicine, 460 Iksan-daero, Iksan City, Jeonbuk 570-749, Republic of Korea.
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Źródło :
Bioorganic chemistry [Bioorg Chem] 2019 Oct; Vol. 91, pp. 103180. Date of Electronic Publication: 2019 Aug 03.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Drug Discovery*
Anti-Inflammatory Agents/*pharmacology
Dinoprostone/*antagonists & inhibitors
Edema/*drug therapy
Granuloma/*drug therapy
Heterocyclic Compounds/*chemistry
Nitrites/*antagonists & inhibitors
Tumor Necrosis Factor-alpha/*antagonists & inhibitors
Animals ; Anti-Inflammatory Agents/chemistry ; Carrageenan/toxicity ; Edema/chemically induced ; Edema/pathology ; Granuloma/chemically induced ; Granuloma/pathology ; Mice ; Rats ; Rats, Wistar
Czasopismo naukowe
    Wyświetlanie 1-6 z 6

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