المؤلفون: N. I. Krasovska

المصدر: Фармацевтичний журнал, Vol 3, Pp 44-54 (2022)

مصطلحات موضوعية: heterocyclization, oxidative cyclization, ([1, 4]triazolo[1, 5-c]-quіnazolin-2-yl)benzoic acids, dimroth rearrangement, spectral characteristics, anti-inflammatory activity, Therapeutics. Pharmacology, RM1-950, Pharmacy and materia medica, RS1-441

وصف الملف: electronic resource

Relation: https://pharmj.org.ua/index.php/journal/article/view/1294/1212; https://doaj.org/toc/0367-3057; https://doaj.org/toc/2617-9628

URL الوصول: https://doaj.org/article/99213b63b6f84b3d9953fbbec410d709

المؤلفون: Wan, Yi-Hong, Nandakumar, Kutty Selva, 1965

المصدر: Acta Pharmacologica Sinica. 41(5):706-718

مصطلحات موضوعية: Dengue virus, JAK/STAT signaling pathway, RdRp inhibitor, [1, 4]triazolo[1, 5-a]pyrimidine derivative, antiviral agent, inflammation

وصف الملف: electronic

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-48357
https://doi.org/10.1038/s41401-019-0316-7
https://hh.diva-portal.org/smash/get/diva2:1702772/FULLTEXT01.pdf

المؤلفون: Seyed Sajad Sajadikhah, Fatemeh Saeedi, Hajar Dehghan

المصدر: شیمی کاربردی روز, Vol 17, Iss 62, Pp 169-178 (2022)

مصطلحات موضوعية: "organic catalyst, "p-toluenesulfonic acid monohydrate, "trityl chloride, "4, 7-dihydro[1, 4]triazolo[1, 5-a]pyrimidine, "multi-component reaction, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://chemistry.semnan.ac.ir/article_6362_f84c547748a97f0894d1c8899653a09f.pdf; https://doaj.org/toc/2981-2437

URL الوصول: https://doaj.org/article/d71fd868e4e944b8ae04714f09fb6ebe

المؤلفون: Xiang Liu (119470), Wen Li (143214), Wenxuan Jiang (6613172), Hao Lu (354247), Jiali Liu (327739), Yijun Lin (5539949), Hua Cao (123075)

مصطلحات موضوعية: Biochemistry, Cell Biology, Molecular Biology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, >]­ pyridine derivatives, triazolo ­[ 1, triazole derivatives, photoluminescence properties, good yields, free conditions, diverse 1, direct access, azomethine imines, 5 -<

Relation: https://figshare.com/articles/journal_contribution/Cu_II_-Catalyzed_C_H_Amidation_Cyclization_of_Azomethine_Imines_with_Dioxazolones_via_Acyl_Nitrenes_A_Direct_Access_to_Diverse_1_2_4-Triazole_Derivatives/17735500

الاتاحة: https://doi.org/10.1021/acs.orglett.1c04044.s001

المؤلفون: Krasovska, Nataliia, Stavytskyi, Viktor, Nosulenko, Inna, Karpenko, Oleksandr, Voskoboinik, Oleksii, Kovalenko, Serhii Ivanovych

المصدر: Acta Chimica Slovenica; Vol. 68 No. 2 (2021); 395-403 ; 1580-3155 ; 1318-0207

مصطلحات موضوعية: [1, 4]triazolo[1, 5-с]quinazolines, quinazolines, anti-inflammatory activity

Time: 2

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document; image/tiff; application/msword; application/zip

Relation: https://acsi-journal.eu/index.php/ACSi/article/view/6440/3074; https://acsi-journal.eu/index.php/ACSi/article/view/6440/8756; https://acsi-journal.eu/index.php/ACSi/article/view/6440/8757; https://acsi-journal.eu/index.php/ACSi/article/view/6440/8758; https://acsi-journal.eu/index.php/ACSi/article/view/6440/8759; https://acsi-journal.eu/index.php/ACSi/article/view/6440/8760; https://acsi-journal.eu/index.php/ACSi/article/view/6440/9014; https://acsi-journal.eu/index.php/ACSi/article/view/6440

الاتاحة: https://acsi-journal.eu/index.php/ACSi/article/view/6440

المؤلفون: Shuai Wang (109515), Sai-Qi Wang (1648441), Qiu-Xu Teng (8827559), Zi-Ning Lei (5524022), Zhe-Sheng Chen (223107), Xiao-Bing Chen (247180), Hong-Min Liu (668537), Bin Yu (14464)

مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Genetics, Neuroscience, Pharmacology, Biotechnology, Cancer, Hematology, Plant Biology, Virology, Chemical Sciences not elsewhere classified, without obvious toxicity, medicinal chemistry efforts, cytochrome p450 3a4, overcome multidrug resistance, increased ptx sensitization, based derivative ws, based abcb1 inhibitor, >]­ pyrimidine derivative, mediated ptx resistance, 50 , triazolo ­[ 1, 898 , >]­ pyrimidine, >] pyrimidine, vivo <, thus leading, shows promise, reversing paclitaxel

Relation: https://figshare.com/articles/journal_contribution/Discovery_of_the_Triazolo_1_5_i_a_i_Pyrimidine-Based_Derivative_WS-898_as_a_Highly_Efficacious_and_Orally_Bioavailable_ABCB1_Inhibitor_Capable_of_Overcoming_Multidrug_Resistance/16913341

الاتاحة: https://doi.org/10.1021/acs.jmedchem.1c01498.s001

المؤلفون: Marchi Luciano, Hugo

المساهمون: Bordeaux, Bock, Harald, Gallardo, Hugo

مصطلحات موضوعية: Luminescence, Tris(3-Aryl-[1, 4]triazolo[1, 5]triazines, Cristal liquide, Liquid crystal, 4]triazolo)[1

Time: 2, 3

Relation: http://www.theses.fr/2023BORD0037/document

الاتاحة: http://www.theses.fr/2023BORD0037/document

المؤلفون: Marchi Luciano, Hugo

المساهمون: Centre de Recherche Paul Pascal (CRPP), Université de Bordeaux (UB)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Université de Bordeaux, Harald Bock, Hugo Gallardo

المصدر: https://theses.hal.science/tel-04103862 ; Organic chemistry. Université de Bordeaux, 2023. English. ⟨NNT : 2023BORD0037⟩.

مصطلحات موضوعية: Liquid crystal, Luminescence, Tris(3-Aryl-[1, 4]triazolo)[1, 5]triazines, 4]triazolo[1, Cristal liquide, [CHIM.ORGA]Chemical Sciences/Organic chemistry

Time: 2, 3

Relation: NNT: 2023BORD0037; tel-04103862; https://theses.hal.science/tel-04103862; https://theses.hal.science/tel-04103862/document; https://theses.hal.science/tel-04103862/file/MARCHI_LUCIANO_HUGO_2023.pdf

الاتاحة: https://theses.hal.science/tel-04103862
https://theses.hal.science/tel-04103862/document
https://theses.hal.science/tel-04103862/file/MARCHI_LUCIANO_HUGO_2023.pdf

المؤلفون: Martynenko, Yulya Victorivna, Antypenko, Oleksii Mykolayovich, Brazhko, Olexandr Anatolievich, Labenska, Irina Borisivna, Kovalenko, Sergii Ivanovich

المصدر: Acta Chimica Slovenica; Vol. 66 No. 1 (2019); 145-154 ; 1580-3155 ; 1318-0207

مصطلحات موضوعية: (3Н-quinazoline-4-ylidene)hydrazides of N-carboxyalkyl-(aralkyl-aryl-)-isoindoline-1, 3-diones, 2-([1, 4]triazolo[1, 5-c]quinazoline-2-yl-)alkyl-(alkaryl-, aryl-)-hydroisoindole-1, 3(2H)-diones, directed search, physico-chemical properties, spectral featu

Time: 2

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document; application/zip; image/jpeg; application/x-rar; application/octet-stream

Relation: https://acsi-journal.eu/index.php/ACSi/article/view/4731/2202; https://acsi-journal.eu/index.php/ACSi/article/view/4731/6998; https://acsi-journal.eu/index.php/ACSi/article/view/4731/6999; https://acsi-journal.eu/index.php/ACSi/article/view/4731/7000; https://acsi-journal.eu/index.php/ACSi/article/view/4731/7001; https://acsi-journal.eu/index.php/ACSi/article/view/4731/7002; https://acsi-journal.eu/index.php/ACSi/article/view/4731/7201; https://acsi-journal.eu/index.php/ACSi/article/view/4731/7202; https://acsi-journal.eu/index.php/ACSi/article/view/4731/7203; https://acsi-journal.eu/index.php/ACSi/article/view/4731/7204; https://acsi-journal.eu/index.php/ACSi/article/view/4731/7205; https://acsi-journal.eu/index.php/ACSi/article/view/4731

الاتاحة: https://acsi-journal.eu/index.php/ACSi/article/view/4731

المؤلفون: Boshi Huang, Ye Tian, Peng Zhan, Dirk Daelemans, Dongwei Kang, Erik De Clercq, Christophe Pannecouque, Xinyong Liu

المصدر: Chemical Biology & Drug Design. 97:67-76

مصطلحات موضوعية: Etravirine, Chemistry, Medicinal, anti-HIV-1 potency, 01 natural sciences, Biochemistry, chemistry.chemical_compound, Drug Discovery, Pharmacology & Pharmacy, DRUG, Cytotoxicity, Biological evaluation, Chemistry, reduced cytotoxicity, HIV Reverse Transcriptase, Molecular Docking Simulation, Reverse Transcriptase Inhibitors, Molecular Medicine, Life Sciences & Biomedicine, medicine.drug, Biochemistry & Molecular Biology, Pyrimidine, Anti-HIV Agents, Cell Survival, Stereochemistry, Cell Line, Structure-Activity Relationship, reverse transcriptase, medicine, Humans, Potency, OPTIMIZATION, EC50, Pharmacology, Science & Technology, Binding Sites, 010405 organic chemistry, Organic Chemistry, BEARING BRIDGEHEAD NITROGEN, molecular docking, Triazoles, DIARYLPYRIMIDINES, Reverse transcriptase, 0104 chemical sciences, 010404 medicinal & biomolecular chemistry, Pyrimidines, 4]Triazolo[1, Design synthesis, DISCOVERY, Drug Design, 5-a]pyrimidines, HIV-1, POTENCY, [1, HIV-1 NNRTIS, INHIBITORS

وصف الملف: Print-Electronic

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53aef6531ee5d1fff895b5697bf34d60
https://doi.org/10.1111/cbdd.13760

المؤلفون: Romeo Romagnoli, Paola Oliva, Filippo Prencipe, Stefano Manfredini, Federica Budassi, Andrea Brancale, Salvatore Ferla, Ernest Hamel, Diana Corallo, Sanja Aveic, Lorenzo Manfreda, Elena Mariotto, Roberta Bortolozzi, Giampietro Viola

المصدر: Pharmaceuticals; Volume 15; Issue 8; Pages: 1031
Pharmaceuticals

مصطلحات موضوعية: 4]triazolo[1, Drug Discovery, [1,2,4]triazolo[1,5-a]pyrimidine, antitumor activity, apoptosis, colchicine binding site, microtubule-targeting agents, Pharmaceutical Science, Molecular Medicine, [1, 5-a]pyrimidine

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c08dcd9c99600c2e0ad2a7d35ddf5c1
https://hdl.handle.net/11577/3474772

المؤلفون: Omar A. Miqdad, Nadia G. Kandile, Hamdi M. Hassaneen, Nada M. Abunada

المصدر: Molecules, Vol 13, Iss 7, Pp 1501-1517 (2008)

مصطلحات موضوعية: Hydrazonyl bromides, pyrazolo[3, 4-d]pyrimidine, pyrazolo[4, 3-e][1, 4]- triazolo[1, 5-c]pyrimidine, antimicrobial activity., Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: http://www.mdpi.com/1420-3049/13/7/1501/; https://doaj.org/toc/1420-3049

URL الوصول: https://doaj.org/article/b45b488de1ad4bb591d8414348550f47

المؤلفون: Martynenko, Yu. V., Kazunin, M. S., Selivanova, E. А., Kovalenko, S. I.

المصدر: Zaporozhye мedical journal; No. 4 (2016): Zaporozhye medical journal ; Запорожский медицинский журнал; № 4 (2016): Запорізький медичний журнал ; Запорізький медичний журнал; № 4 (2016): Запорізький медичний журнал ; 2310-1210 ; 2306-4145

مصطلحات موضوعية: Aminoacіds, (1, 3-dioxo-1, 3-dihydro-2H-isoindol-2-yl)alkyl-(alkaryl-, aryl-)carboxylic acids, (3Н-quinazolin-4-yliden)hydrazides, 2-substituted [1, 4]triazolo[1, 5-c]quinazolines, Antimicrobial And Antifungal Activity, аминокислоты, 3-диоксо-1, 3-дигидро-2H-изоиндол-2-ил)алкил-(алкарил-, арил-)карбоновые кислоты, (3Н-хиназолин-4-илиден)гидразиды, 2-замещённые [1, 4]триазол[1, 5-c]хиназолины, противомикробная и противогрибковая активность, амінокислоти, 3-діоксо-1, 3-дигідро-2H-ізоіндол-2-іл)алкіл(алкарил-, арил-)карбонові кислоти, (3Н-хіназолін-4-іліден)гідразиди, 2-заміщені [1, 5-c]хіназоліни, протимікробна та протигрибкова активність

Time: 2

وصف الملف: application/pdf

Relation: http://zmj.zsmu.edu.ua/article/view/79709/77609; http://zmj.zsmu.edu.ua/article/view/79709

الاتاحة: http://zmj.zsmu.edu.ua/article/view/79709

المؤلفون: Kholodnyak, S. V., Voskoboynik, O. Yu., Kovalenko, S. I., Sergeieva, T. Yu., Okovytyy, S. I., Shishkina, S. V.

المصدر: Journal of Organic and Pharmaceutical Chemistry; Vol. 14 No. 2(54) (2016); 47-52 ; Журнал органической и фармацевтической химии; Том 14 № 2(54) (2016); 47-52 ; Журнал органічної та фармацевтичної хімії; Том 14 № 2(54) (2016); 47-52 ; 2518-1548 ; 2308-8303

مصطلحات موضوعية: 2-aryl-5-trichloromethyl-5, 6-dihydro[1, 4]triazolo[1, 5-c]quinazolines, [5 1]-cyclocondensation, N-nucleophiles, elimination, UDC 547.792’856.057, 2-арил-5-трихлорометил-5, 6-дигидро-[1, 4]триазоло[1, 5-с]хиназолины, [5 1]-циклоконденсации, N-нуклеофилы, элиминация, УДК 547.792’856.057, 6-дигідро-[1, 5-с]хіназоліни, [5 1]-циклоконденсація, N-нуклеофіли, елімінація

Time: 2

وصف الملف: application/pdf

Relation: https://ophcj.nuph.edu.ua/article/view/ophcj.16.879/85598; https://ophcj.nuph.edu.ua/article/view/ophcj.16.879

الاتاحة: https://ophcj.nuph.edu.ua/article/view/ophcj.16.879
https://doi.org/10.24959/ophcj.16.879

المؤلفون: Kholodnyak, S. V., Schabelnyk, K. P., Voskoboynik, O. Yu., Antypenko, O. M., Kovalenko, S. I., Palchykov, V. O., Okovytyy, S. I., Shishkina, S. V.

المصدر: Journal of Organic and Pharmaceutical Chemistry; Vol. 14 No. 3(55) (2016); 24-31 ; Журнал органической и фармацевтической химии; Том 14 № 3(55) (2016); 24-31 ; Журнал органічної та фармацевтичної хімії; Том 14 № 3(55) (2016); 24-31 ; 2518-1548 ; 2308-8303

مصطلحات موضوعية: 2’-aryl-6’H-spiro[1, 4]triazolo[1, 5-c]quinazolines, synthesis, spectral characteristics, UDC 547.792’856.057, 2-арил-6’H-спиро[1, 4]триазоло[1, 5-c]хиназолины, синтез, спектральные характеристики, УДК 547.792’856.057, 2-арил-6’H-спіро[1, 5-c]хіназоліни, спектральні характеристики

Time: 2

وصف الملف: application/pdf

Relation: https://ophcj.nuph.edu.ua/article/view/ophcj.16.897/85602; https://ophcj.nuph.edu.ua/article/view/ophcj.16.897

الاتاحة: https://ophcj.nuph.edu.ua/article/view/ophcj.16.897
https://doi.org/10.24959/ophcj.16.897

المؤلفون: Ping Gong, Ding Wang, Hai-Sheng Song, Shu-Chun Guo, Yan-Fang Zhao, Xiang-Lin Zhao

المصدر: Molecules, Vol 12, Iss 5, Pp 1136-1146 (2007)

مصطلحات موضوعية: [1, 4]Triazolo[1, 5-a]pyrimidines, Synthesis, antitumor activities, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: http://www.mdpi.com/1420-3049/12/5/1136/; https://doaj.org/toc/1420-3049

URL الوصول: https://doaj.org/article/7169f695ae644bad85d331e45c65093e

المؤلفون: Milan Potacek, Jiri Verner

المصدر: Molecules, Vol 11, Iss 1, Pp 34-42 (2006)

مصطلحات موضوعية: Criss-cross cycloaddition, ketazines, cyclohexanone azine, cyclopentanone azine, cycloheptanone azine, substituted perhydro[1, 4]triazolo[1, 2-a][1, 4]triazole-1, 5- diones, 5-dithiones, spiro compounds., Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: http://www.mdpi.com/1420-3049/11/1/34/; https://doaj.org/toc/1420-3049

URL الوصول: https://doaj.org/article/22ac0db29ecc429698ca6bd14786334e

المؤلفون: Kholodnyak, S. V., Schabelnyk, K. P., Shernova, G. A., Sergeieva, T. Yu., Ivchuk, V. V., Voskoboynik, O. Yu., Kovalenko, S. I., Trzhetsinskiy, S. D., Okovytyy, S. I., Shishkina, S. V.

المصدر: News of Pharmacy; No. 3(83) (2015); 9-17 ; Вестник фармации; № 3(83) (2015); 9-17 ; Вісник фармації; № 3(83) (2015); 9-17 ; 2415-8844

مصطلحات موضوعية: 2-aryl-[1, 4]triazolo[1, 5-c]quinazolines, hydrolytic cleavage, hypoglycemic activity, UDC 615.31, 547.792’856.03/.04.057, 615.27.015, 2-арил-[1, 4]триазоло[1, 5-c]хиназолины, гидролитическое расщепление, гипогликемическая активность, УДК 615.31, 5-c]хіназолини, гідролітичне розщеплення, гіпоглікемічна активність

Time: 2

وصف الملف: application/pdf

Relation: http://nphj.nuph.edu.ua/article/view/nphj.15.2054/85958; http://nphj.nuph.edu.ua/article/view/nphj.15.2054

الاتاحة: http://nphj.nuph.edu.ua/article/view/nphj.15.2054
https://doi.org/10.24959/nphj.15.2054

المؤلفون: A. H. Bedair, A. H. Fakery, N. A. El-Hady, M. S. Abd El-Latif, A. M. El-Agrody

المصدر: Molecules, Vol 6, Iss 6, Pp 519-527 (2001)

مصطلحات موضوعية: Pyrano[3, 2-c][1]benzopyrans, Pyrano[2, 3-d]pyrimidines, [1, 4]-triazolo- [1, 5-c]pyrimidines, Pyrimido[1, 6-b][1, 4]triazine, antimicrobial activities, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: http://www.mdpi.com/1420-3049/6/6/519/; https://doaj.org/toc/1420-3049

URL الوصول: https://doaj.org/article/07aac133da9d4fb68017c1f7d01b8a0c

المؤلفون: MAGDI E. A. ZAKI, OSAMA I. ABD EL-SALAM, SAMIRA A. SWELAM

المصدر: Journal of the Serbian Chemical Society, Vol 64, Iss 11, Pp 655-662 (1999)

مصطلحات موضوعية: pyrazolo[3, 4-d]pyrimidine, m-thiazine, rearragnement, triazolo[1, 5-c]-pyrimidine, tetrazolo[1, 5-c]pyrimidine, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: http://www.shd.org.yu/HtDocs/SHD/Vol64/No11-Pdf/V64-no11-02.zip; https://doaj.org/toc/0352-5139

URL الوصول: https://doaj.org/article/7b33e27aeb3943cda051ba09fa8ac0f8