Works matching DE "HYDRAZINE derivatives"
Results: 342
A Derivative of L-Allo Threonine Alleviates 2,4-Dinitrofluorobenzene-Induced Atopic Dermatitis Indications.
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- Bioscience, Biotechnology & Biochemistry, 2012, v. 76, n. 11, p. 2021, doi. 10.1271/bbb.120258
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Transient Stabilization Effect of CO<sub>2</sub> in the Electrochemical Hydrogenation of Azo Compounds and the Reductive Coupling of α‐Ketoesters.
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- Angewandte Chemie, 2022, v. 134, n. 48, p. 1, doi. 10.1002/ange.202213636
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Conversion of Ammonia to Hydrazine Induced by High‐Frequency Ultrasound.
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- Angewandte Chemie, 2021, v. 133, n. 48, p. 25434, doi. 10.1002/ange.202109516
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N‐Trifluoromethyl Hydrazines, Indoles and Their Derivatives.
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- Angewandte Chemie, 2020, v. 132, n. 29, p. 12006, doi. 10.1002/ange.202004321
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Synthesis of fused dihydrobenzo [4,5]imidazo[1,2- a]pyrmido[5,4-e]pyrmidin-3(4H)-amine derivatives.
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- Al-Qadisiyah Journal of Pure Science, 2021, v. 26, n. 4, p. 34, doi. 10.29350/qjps.2021.26.4.1371
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Preparation and Identification of Some New HeterocyclicDerivatives fromSuberoyl Chloride and Their Study as Anti-bacterial.
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- Al-Qadisiyah Journal of Pure Science, 2019, v. 24, n. 4, p. 1
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SYNTHESIS, CHARACTERIZATION AND STUDY BIOLOGICAL ACTIVITY SOME NEW DERIVATIVES AMIDE AND PYRAZOLE -PYRAZOLINE OF STEROID ANALOGS.
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- Al-Qadisiyah Journal of Pure Science, 2019, v. 24, n. 3, p. 37
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Synthesis and antimicrobial investigation of some 5H-pyridazino[4,5-b]indoles.
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- Turkish Journal of Chemistry, 2013, v. 37, n. 2, p. 271, doi. 10.3906/kim-1210-22
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Synthesis and Spectroscopic Characterization Study of Some Schiff Bases 1,3[N,N-Bis(5-Methyl-1,3,4-Triazole-2-Thione)] Benzene and 1,4[N,N-Bis(5-Methyl-1,3,4-Triazole-2-Thione)] Benzene.
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- Nanosistemi, Nanomateriali, Nanotehnologii, 2024, v. 22, n. 2, p. 457, doi. 10.15407/nnn.22.02.457
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Synthesis of Novel Pyrazolyl and Isoxazolyl 3-(Furan-2-yl)-5-Methyl-1-(4-Nitrophenyl)-1H-Pyrazol-4-yl Derivatives via Regioselectivity of the 1,3-Dipolar Cycloaddition.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 4, p. 2212, doi. 10.1080/10406638.2023.2214284
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Design, synthesis and biological evaluation of novel 4-anlinoquinazoline derivatives as EGFR inhibitors with the potential to inhibit the gefitinib-resistant nonsmall cell lung cancers.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 203, doi. 10.1080/14756366.2018.1518957
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Comparing hydrazine-derived reactive groups as inhibitors of quinone-dependent amine oxidases.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 496, doi. 10.1080/14756366.2016.1265518
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Synthesis of new N,N′-bis[1-aryl-3-(piperidine-1-yl)propylidene]hydrazine dihydrochlorides and evaluation of their cytotoxicity against human hepatoma and breast cancer cells.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 3, p. 420, doi. 10.3109/14756366.2013.795562
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SYNTHESIS AND CHARACTERISATION OF SOME PYRAZOLINE DERIVED FROM CHALCONES CONTAINING CARBAZOLE AND STUDYING THEIR EFFICACY ON LUNG, BREAST, AND COLON CANCER.
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- Oxidation Communications, 2024, v. 47, n. 3, p. 412
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MELDONIUM, THE ‘NOVEL’ DOPING IN PROFESSIONAL SPORT.
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- Oxidation Communications, 2017, v. 40, n. 2, p. 986
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Reversible Gelation System for Hydrazine Based on Polymer Absorbent.
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- Technologies (2227-7080), 2018, v. 6, n. 3, p. 80, doi. 10.3390/technologies6030080
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Synthesis and in silico studies of certain benzo[f]quinoline-based heterocycles as antitumor agents.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-64785-z
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One-Pot Synthesized Pd@N-Doped Graphene: An Efficient Catalyst for Suzuki–Miyaura Couplings.
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- Catalysts (2073-4344), 2019, v. 9, n. 5, p. 469, doi. 10.3390/catal9050469
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Iron-Doped Titanium Dioxide Nanoparticles As Potential Scaffold for Hydrazine Chemical Sensor Applications.
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- Coatings (2079-6412), 2020, v. 10, n. 2, p. 182, doi. 10.3390/coatings10020182
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Synthesis of hydrazine and azapeptide derivatives by alkylation of carbazates and semicarbazones.
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- Canadian Journal of Chemistry, 2012, v. 90, n. 11, p. 985, doi. 10.1139/v2012-070
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Enantioseparation and antioxidant activity of novel diarylpyrazoline derivatives.
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- Chirality, 2022, v. 34, n. 10, p. 1389, doi. 10.1002/chir.23493
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Design and synthesis aldehydes–thiourea and thiazolyl hydrazine derivatives as promising antifungal agents against Monilinia fructicola.
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- Pest Management Science, 2025, v. 81, n. 1, p. 170, doi. 10.1002/ps.8417
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Use of Hydrazine and Its Substitutes as Fuel.
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- Chinese Journal of Explosives & Propellants, 2022, v. 45, n. 2, p. 164, doi. 10.14077/j.issn.1007-7812.202112007
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Crystal structures and DNA-binding properties of Pr complexes derived from 8-hydroxyquinoline-2-carboxaldehyde and three aroylhydrazines.
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- Journal of Coordination Chemistry, 2014, v. 67, n. 22, p. 3689, doi. 10.1080/00958972.2014.972387
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Fluorescent "OFF–ON" Sensors for the Detection of Sn 2+ Ions Based on Amine-Functionalized Rhodamine 6G.
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- Chemosensors, 2022, v. 10, n. 2, p. 69, doi. 10.3390/chemosensors10020069
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Synthesis and Study of the Effect New Pyrazoles and Oxadiazole Linked to the 1,4-Dihydropyridine Ring on Breast Cancer.
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- Journal of Chemical Health Risks, 2023, v. 13, n. 4, p. 701, doi. 10.22034/jchr.2023.1996251.1817
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Theoretical insights into the reduction mechanism of neptunyl nitrate by hydrazine derivatives.
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- Radiochimica Acta, 2022, v. 110, n. 6-9, p. 471, doi. 10.1515/ract-2021-1120
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Synthesis of Novel Thiazolyl Hydrazine Derivatives and Their Antifungal Activity.
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- Journal of Chemistry, 2021, p. 1, doi. 10.1155/2021/6563871
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Copper(II) Anchored on Amine-Functionalized MMT: A Highly Efficient Catalytic System for the One-Pot Synthesis of Bispyrano[2,3-c]pyrazole Derivatives.
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- Journal of Chemistry, 2021, p. 1, doi. 10.1155/2021/1784142
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SYNTHESIS, ANTIMICROBIAL, AND ANTITUBERCULAR ACTIVITIES OF NOVEL N-PYRAZOLYLBENZAMIDE DERIVATIVES.
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- Rasayan Journal of Chemistry, 2022, v. 15, n. 4, p. 2407, doi. 10.31788/RJC.2022.1547092
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In-vitro ANTICANCER ACTIVITY, ANTIMICROBIAL AND In-silico STUDIES OF NAPHTHYL PYRAZOLE ANALOGUES.
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- Rasayan Journal of Chemistry, 2020, v. 13, n. 2, p. 1199, doi. 10.31788/RJC.2020.1325495
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SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF 3-(2-(5-AMINO-1H-PYRAZOL-4-YL) THIAZOL-4-YL)-2H-CHROMEN-2-ONE AND ITS DERIVATIVES.
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- Rasayan Journal of Chemistry, 2019, v. 12, n. 4, p. 1810, doi. 10.31788/RJC.2019.1245375
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SYNTHETIC STUDIES OF 1-TETRA-O-BENZOYL- -DGLUCOPYRANOSYL- 3-(2)-SUBSTITUTED HYDRAZINO-1, 3- BENZOTHIAZOLYL THIOCARBAMIDES.
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- Rasayan Journal of Chemistry, 2016, v. 9, n. 1, p. 52
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In‐situ Immobilization of a Polyoxometalate Metal‐Organic Framework (NENU‐3) on Functionalized Reduced Graphene Oxide for Hydrazine Sensing.
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- Chinese Journal of Chemistry, 2021, v. 39, n. 10, p. 2889, doi. 10.1002/cjoc.202100314
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Comparative Study of Polymethyl Acrylate, its Hydrazide Derivative with Commercial Surfactants for Flow Improvements in Waxy Crude Oil.
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- Petroleum & Coal, 2020, v. 62, n. 1, p. 11
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Synthesis, characterization, and in vitro antibacterial activity of some new pyridinone and pyrazole derivatives with some in silico ADME and molecular modeling study.
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- Journal of the Iranian Chemical Society, 2022, v. 19, n. 9, p. 3899, doi. 10.1007/s13738-022-02575-y
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Tetramethylguanidine-functionalized nanosize γ-Al2O3 as a novel and efficient catalyst for the four-component synthesis of pyrazolopyranopyrimidine derivatives.
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- Journal of the Iranian Chemical Society, 2021, v. 18, n. 6, p. 1419, doi. 10.1007/s13738-020-02123-6
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Comparative electroanalytical performance of poly o‐toulidine and polyaniline towards hydrazine oxidation supplemented by DFT.
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- Journal of Applied Polymer Science, 2023, v. 140, n. 31, p. 1, doi. 10.1002/app.54112
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Muricazine, a new hydrazine derivative from Ranunculus muricatus L. with antioxidant, lipoxygenase and urease inhibitory activities.
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- Natural Product Research, 2022, v. 36, n. 4, p. 961, doi. 10.1080/14786419.2020.1855169
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Synthesis and Characterization of Graphene Oxide (GO) and Reduced Graphene Oxide (rGO) for Gas Sensing Application.
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- Macromolecular Symposia, 2017, v. 376, n. 1, p. n/a, doi. 10.1002/masy.201700006
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The Effect of Environmental and Chemical Approach on rGO Structure.
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- Suleyman Demirel University Faculty of Arts & Science Journal of Science / Süleyman Demirel Üniversitesi Fen Edebiyat Fakültesi Fen Dergisi, 2021, v. 16, n. 1, p. 216, doi. 10.29233/sdufeffd.891066
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Synthesis, antileishmanial, antimalarial evaluation and molecular docking study of some hydrazine-coupled pyrazole derivatives.
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- BMC Chemistry, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s13065-023-01111-0
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Ethyl Aceto Acetate as starting material for preparation pyrazol ring Derivatives.
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- Journals Kufa for Chamical, 2021, v. 2, n. 7, p. 1
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Synthesis, Anticonvulsant, and Molecular Docking Studies of (3,5-disubstituted-4,5-dihydro-1H-pyrazol-1-yl) (4-chlorophenyl) Methanone Derivatives.
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- Indian Journal of Pharmaceutical Education & Research, 2023, v. 57, n. 1, p. 202, doi. 10.5530/001954641727
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Design, Synthesis, Characterization, and Anti-Cancer Activity Evaluation of Novel Thiosemicarbazide Analogs.
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- Indian Journal of Pharmaceutical Education & Research, 2023, v. 57, n. 1, p. 210, doi. 10.5530/001954641768
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DESIGN AND SYNTHESIS OF NOVEL TRIAZOLYL/OXADIAZOLYL/THIADIAZOLYL-CARBAZOLES AS POTENT ANTICONVULSANT AGENTS.
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- Indian Drugs, 2020, v. 57, n. 7, p. 19, doi. 10.53879/id.57.07.12123
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Synthesis and Biological Evaluation of 1-(6-bromobenzo [d]thiazol-2-yl)-2- (disubstituted methylene) hydrazine derivatives.
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- Journal of Drug Delivery & Therapeutics, 2019, v. 9, n. 4A, p. 577, doi. 10.22270/jddt.v9i4-A.3520
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Synthesis and Biological Evaluation of 1-(6-chlorobenzo [d]thiazol-2-yl)-2- (disubstituted methylene) hydrazine derivatives.
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- Journal of Drug Delivery & Therapeutics, 2019, v. 9, n. 4A, p. 561, doi. 10.22270/jddt.v9i4-A.3515
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Synthesis and Biological Evaluation of 1-(6-bromobenzo [d]thiazol-2-yl)-2-(disubstituted methylene) hydrazine derivatives.
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- Journal of Drug Delivery & Therapeutics, 2019, v. 9, p. 577, doi. 10.22270/jddt.v9i4-A.3520
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Synthesis and Biological Evaluation of 1-(6-chlorobenzo [d]thiazol-2-yl)-2-(disubstituted methylene) hydrazine derivatives.
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- Journal of Drug Delivery & Therapeutics, 2019, v. 9, p. 561, doi. 10.22270/jddt.v9i4-A.3515
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