يعرض 1 - 10 نتائج من 28 نتيجة بحث عن '"Of - 5 – 4"', وقت الاستعلام: 0.89s تنقيح النتائج
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    دورية أكاديمية

    المؤلفون: Sahin, Onur

    المساهمون: Bursa Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji/Genel Biyoloji Bölümü., orcid:0000-0003-4944-0181, orcid:0000-0002-0483-9642, orcid:0000-0002-7687-3284, orcid:0000-0002-3595-6286, Inci, Duygu, Aydin, Rahmiye, Vatan, Ozgür, Cinkılıc, Nilüfer, G-2201-2019, O-7508-2015, AAH-5296-2021, AAH-8936-2021, 55082306300, 56261495600, 16235098100, 26533892300

    العلاقة: 2211-C; Makale - Uluslararası Hakemli Dergi; (OUAP (F)-2015/14); New Journal of Chemistry; Yurt içi; Sanayi; Inci, D. vd. (2019). ''Water-soluble binary and ternary palladium(II) complexes containing amino acids and intercalating ligands: Synthesis, characterization, biomolecular interactions and cytotoxicities''. New Journal of Chemistry, 43(12), 4681-4697.; https://doi.org/10.1039/c8nj05934aTest; https://hdl.handle.net/11452/39613Test; 000462541900003; 2-s2.0-85063220833; 4681; 4697; 43; 12

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    المساهمون: UCL - SSS/LDRI - Louvain Drug Research Institute, Groupe de Recherche Interdiscipinaire Innovation et Optimisation Thérapeutique - EA 4481 (GRIIOT), Université de Lille, Droit et Santé, Institut pour la Recherche sur le Cancer de Lille (U837 INSERM - IRCL), Institut pour la recherche sur le cancer de Lille [Lille] (IRCL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre de Recherche Jean-Pierre AUBERT - Neurosciences et Cancer -JPArc [Lille], Institut de Chimie Pharmaceutique Albert Lespagnol (ICPAL), Laboratorio di Chimica Bioinorganica (LCBI), Università degli Studi di Firenze = University of Florence [Firenze] (UNIFI), Laboratorio di Chimica Bioinorganica, Université de Namur [Namur] (UNamur), EA 4481 Groupe de Recherche Interdiscipinaire (GRIIOT), Faculté des Sciences Pharmaceutiques et Biologiques, Università degli Studi di Firenze = University of Florence [Firenze], Université de Namur [Namur], Plasticité Cellulaire et Cancer (CPAC) - U908 (CPAC), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille, Centre de Recherche en Cancérologie de Marseille (CRCM), Aix Marseille Université (AMU)-Institut Paoli-Calmettes, Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Université Catholique de Louvain (UCL), Génétique moléculaire et approches thérapeutiques des hémopathies malignes, IRCL-Institut National de la Santé et de la Recherche Médicale (INSERM)

    المصدر: Bioorganic & Medicinal Chemistry
    Bioorganic & Medicinal Chemistry : the tetrahedron journal for research at the interface of chemistry and biology, Vol. 21, no. 6, p. 1451-1464 (2013)
    Bioorganic & Medicinal Chemistry; Vol 21
    Bioorganic and Medicinal Chemistry
    Bioorganic and Medicinal Chemistry, Elsevier, 2013, 21 (6), pp.1451-1464. ⟨10.1016/j.bmc.2012.10.029⟩

    مصطلحات موضوعية: 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (4 bromophenyl) 1h pyrazole, Carbonate dehydratase ix inhibitor, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (2 phenantryl) 1h pyrazole, Unclassified drug, Clinical Biochemistry, Cell, Pharmaceutical Science, Drug structure, Antiproliferative activity, 1 (3 aminosulfonylphenyl) 3 hydroxymethyl 5 phenyl 1h pyrazole, 01 natural sciences, Biochemistry, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (4 methoxyphenyl) 1h pyrazole, 1 (4 aminosulfonylphenyl) 4 hydroxymethyl 5 (2 naphthyl) 1h pyrazole, Breast cancer, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (5 bromo 6 methoxynaphtalen 2 yl) 1h pyrazole, Catalytic Domain, Drug Discovery, Cytotoxicity, Hypoxia, Carbonic Anhydrase Inhibitors, ComputingMilieux_MISCELLANEOUS, Enzyme active site, Carbonic Anhydrases, chemistry.chemical_classification, 0303 health sciences, Sulfonamides, Carbonic anhydrase, biology, Chemistry, Aryl sulfonamide inhibitors, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (2 methoxyphenyl) 1h pyrazole, Carbonate dehydratase IX, 3. Good health, 1 (3 aminosulfonylphenyl) 3 hydroxymethyl 5 (6 methoxy 2 naphthalenyl) 1h pyrazole, Molecular Docking Simulation, Enzyme inhibition, medicine.anatomical_structure, Drug screening, Drug selectivity, Molecular Medicine, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (6 methoxynaphtalen 2 yl) 1h pyrazole, Simulation, medicine.drug, 1 (4 aminosulfonylphenyl) 5 hydroxymethyl 3 phenyl 1h pyrazole, Protein Binding, 1 (3 aminosulfonylphenyl) 3 hydroxymethyl 5 naphthyl 1h pyrazole, Drug cytotoxicity, 1 (4 aminosulfonylphenyl) 5 hydroxymethyl 3 (2 naphthyl) 1h pyrazole, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 pyridinyl 1h pyrazole, Drug binding, Sulfonamide, Article, Molecular model, 03 medical and health sciences, Drug synthesis, Structure-Activity Relationship, Drug potency, [CHIM.ANAL]Chemical Sciences/Analytical chemistry, Antigens, Neoplasm, Cell Line, Tumor, medicine, Humans, Doxorubicin, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (1 naphthyl) 1h pyrazole, 1 (4 aminosulfonylphenyl) 4 hydroxymethyl 5 phenyl 1h pyrazole, Carbonic Anhydrase IX, Molecular Biology, 1 (4 aminosulfonylphenyl) 3 hydroxyethyl 5 phenyl 1h pyrazole, 030304 developmental biology, Cell Proliferation, 1 (4 aminosulfonylphenyl) 4 hydroxymethyl 5 (6 methoxy 2 naphtalenyl) 1h pyrazole, Carbonate dehydratase inhibitor, Cell strain MDA MB 231, Binding Sites, 010405 organic chemistry, Organic Chemistry, Active site, In vitro, 0104 chemical sciences, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (2 naphthyl) 1h pyrazole, Kinetics, Enzyme, Binding kinetics, Tumor progression, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (4 tolyl) 1h pyrazole, Pyrazole, biology.protein, Pyrazoles, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 (3 methoxyphenyl) 1h pyrazole, 1 (4 aminosulfonylphenyl) 3 hydroxymethyl 5 phenyl 1h pyrazole, Cell line, 4 (5 aryl 2 hydroxymethyl pyrazol 1 yl)benzenesulfonamide

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    المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Deney Hayvanları Yetiştirme ve Araştırma Merkezi., Bağdaş, Deniz

    مصطلحات موضوعية: Target, Male, Nociception, Mouse, Inflammatory pain, medicine.medical_treatment, Pharmacology, Signal transduction, Antagonists and inhibitors, Cannabinoid receptor antagonists, Antinociception, Mice, 0302 clinical medicine, Models, Peroxisome proliferator activated receptor antagonist, Nicotinic Antagonist, Oxazoles, Azabicyclo derivative, Pain measurement, GW 6471, Analogs and derivatives, Neurology, Ethanolamines, Mechanism, Cholinergic receptor stimulating agent, Agonist, medicine.medical_specialty, Tonic pain, Alpha7 nicotinic acetylcholine receptor, Article, 03 medical and health sciences, Palmitic acid derivative, Cannabinoid receptor antagonist, Bridged bicyclo compounds, PPAR alpha, Palmidrol, Animal model, Positive allosteric modulator, Animal experiment, Palmitoylethanolamide, Nociceptive pain, 5 (4 chloro 3 methylphenyl) 1 (4 methylbenzyl) n (1,3,3 trimethylbicyclo[2.2.1]heptan 2 yl) 3 pyrazolecarboxamide, Animal, Inflammation, Methyllycaconitine, 3-(2,4-Dimethoxybenzylidene)Anabaseine, Amides, Institute for cancer research mouse, Pnu-120596, 030104 developmental biology, Endocrinology, chemistry, Peroxisome proliferator activated receptor alpha, 030217 neurology & neurosurgery, 0301 basic medicine, Cannabinoid 2 receptor, Nicotinic acetylcholine receptors, Unclassified drug, Neuropathic pain, Gat107, Azabicyclo compounds, Nicotinic antagonists, Oleoylethanolamide, chemistry.chemical_compound, Bungarotoxin receptor, 1 (5 chloro 2,4 dimethoxyphenyl) 3 (5 methyl 3 isoxazolyl)urea, Priority journal, Benzamide derivative, Palmitic acids, Pamgat 107, Ethanolamine derivative, Nicotinic acetylcholine receptor, Nicotinic agonist, Mice, inbred ICR, Benzamides, G-proteins, Rimonabant, 1,4-diazabicyclo(3.2.2)nonan-4-yl(5-(3-(trifluoromethyl)phenyl)furan-2-yl)methanone, Furan derivative, medicine.drug_class, Nuclear peroxisome proliferator-activated receptor type-α, Neurosciences & neurology, PNU-282987, Nicotinic receptor blocking agent, Developmental Neuroscience, Internal medicine, medicine, Animals, Furans, Drug effects, Neurosciences, Alpha7, Oxazole derivative, Cannabinoid 1 receptor, Nonhuman, Receptor cross-talk, Protein protein interaction, Tyrosine, NS 6740, Cannabinoid, Cell nucleus, Controlled study, 4 chloro n (3 quinuclidinyl)benzamide

    وصف الملف: application/pdf

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    المؤلفون: Ceyda Icsel, Veysel T. Yilmaz

    المساهمون: Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü., İçsel, Ceyda, Yılmaz, Veysel Turan, AAI-3342-2021, L-7238-2018

    المصدر: Journal of Photochemistry and Photobiology B: Biology. 130:115-121

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    المصدر: Medicinal Chemistry. 4:110-115