المؤلفون: Echevarria, A., Alkorta, I., Elguero, J.

المصدر: Afinidad. Revista de química teórica y aplicada; Vol. 73, Núm. 575 (2016)
Afinidad; Vol. 73, Núm. 575 (2016)

مصطلحات موضوعية: Aminopyrazoles, rearrangement, pyrazolo[3, 4-b]pyridines, NMR, DFT calculations.

وصف الملف: application/pdf

Relation: https://www.raco.cat/index.php/afinidad/article/view/313753/403864

URL الوصول: https://www.raco.cat/index.php/afinidad/article/view/313753

المؤلفون: Joshi, Ajit, Hussain, Nasir, Dangi, Raja, Talesara, G.

المصدر: Afinidad. Revista de química teórica y aplicada; Vol. 67, Núm. 548 (2010)
Afinidad; Vol. 67, Núm. 548 (2010)

مصطلحات موضوعية: Pyrazolo[3, 4-c]pyrazoles, nicotinohydrazide, phthalimidoxyethyl bromide, antiviral activities.

وصف الملف: application/pdf

Relation: https://www.raco.cat/index.php/afinidad/article/view/269361/356899

URL الوصول: https://www.raco.cat/index.php/afinidad/article/view/269361

المؤلفون: Abdelrazek, Fathy M., Mohamed, Ashraf M.

المصدر: Afinidad. Revista de química teórica y aplicada; Vol. 65, Núm. 533 (2008)
Afinidad; Vol. 65, Núm. 533 (2008)

مصطلحات موضوعية: Phenacylmalononitrile, 5-Diamino-4-phenacylpyrazoles, aminopyridazines and pyrazolo[3, 4-c]pyridazines.

وصف الملف: application/pdf

Relation: https://www.raco.cat/index.php/afinidad/article/view/281452/369264

URL الوصول: https://www.raco.cat/index.php/afinidad/article/view/281452

المؤلفون: ZHAI Chonggang, WANG Pengcheng, SHAN Yubao, LAN Yu, HU Rui, YANG Yunhuang

المصدر: Chinese Journal of Magnetic Resonance, Vol 40, Iss 1, Pp 1-9 (2023)

مصطلحات موضوعية: pyrazolo[3, 4-d]pyrimidin-4-one, 1h nmr, 13c nmr, mass spectrometry imaging, analgesic activity, Electricity and magnetism, QC501-766

وصف الملف: electronic resource

Relation: http://121.43.60.238/bpxzz/article/2023/1000-4556/1000-4556-40-1-1.shtml; https://doaj.org/toc/1000-4556

URL الوصول: https://doaj.org/article/9dc774b5a21f4911acdab3ad8a5607b9

المؤلفون: More, V. S. (Vishal), Chumbhale, D. C. (Deshraj), Rangari, N. T. (Nalanda), Mishra, P. A. (Pranali), Jagnar, A. B. (Annasaheb), Kadam, J. N. (Jyoti)

المصدر: International Journal of Health Sciences

مصطلحات موضوعية: analgesic, anti-inflammatory, knorr pyrazole synthesis, pyrazole, pyrazolo[3, 4-c]pyrazole, Indonesia

وصف الملف: application/pdf

Relation: https://www.neliti.com/publications/421204/synthesis-analgesic-and-anti-inflammatory-activities-of-some-pyrazolo34-cpyrazol

الاتاحة: https://www.neliti.com/publications/421204/synthesis-analgesic-and-anti-inflammatory-activities-of-some-pyrazolo34-cpyrazol

المؤلفون: Abdallah, Amira E.M., Mohareb, Rafat M.

المصدر: Pigment & Resin Technology, 2018, Vol. 48, Issue 2, pp. 89-107.

URL الوصول: http://www.emeraldinsight.com/doi/10.1108/PRT-11-2017-0085

المؤلفون: Semenenko, Olexander M., Lipson, Victoria V., Mironova, Veronika V., Budianska, Lilia V., Musatov, Vladimir I., Sofronov, Dmitro S.

المصدر: Журнал органічної та фармацевтичної хімії; Том 18 № 1(69) (2020); 45-51 ; Journal of Organic and Pharmaceutical Chemistry; Vol. 18 No. 1(69) (2020); 45-51 ; Журнал органической и фармацевтической химии; Том 18 № 1(69) (2020); 45-51 ; 2518-1548 ; 2308-8303

مصطلحات موضوعية: pyrazolo[3, 4-b]pyridin-6-ones, 1-phenyl-3-(4-alkoxyphenyl)pyrazole-4-carbaldehydes, 3-methyl-5-aminopyrazole, 2-dimethyl-1, 3-dioxane-4, 6-dione, domino-reaction, UDC 547.859.1, тетрагидропиразоло[3, 4-b]пиридин-6-оны, 1-фенил-3-(4-алкоксифенил)пиразол-4-карбальдегиды, 3-метил-5-аминопиразол, 2-диметил-1, 3-диоксан-4, 6-дион, домино-реакции, УДК 547.859.1, тетрагідропіразоло[3, 4-b]піридин-6-они, 1-феніл-3-(4-алкоксифеніл)піразол-4-карбальдегіди, 3-метил-5-амінопіразол, 3-діоксан-4, 6-діон, доміно-реакції

Time: 2

وصف الملف: application/pdf

Relation: http://ophcj.nuph.edu.ua/article/view/ophcj.20.194936/198322; http://ophcj.nuph.edu.ua/article/view/ophcj.20.194936

الاتاحة: http://ophcj.nuph.edu.ua/article/view/ophcj.20.194936
https://doi.org/10.24959/ophcj.20.194936

المؤلفون: Trilleras, Jorge, Ríos De La Rotta, Freddy, Pedroza García, Luis-Felipe

المصدر: Revista Científica, ISSN 2344-8350, Vol. 47, Nº. 2, 2023 (Ejemplar dedicado a: May-August 2023), pags. 1-12

مصطلحات موضوعية: 5-aminopirazoles, ciclocondensación, derivados fusionados de pirazol, pirazolo[3, 4-b]piridina, síntesis por ultrasonido, 5-aminopyrazole, cyclocondensation, fused pyrazole derivatives, pyrazolo[3, 4-b]pyridine, ultrasound synthesis

وصف الملف: application/pdf

Relation: https://dialnet.unirioja.es/servlet/oaiart?codigo=9777456

الاتاحة: https://dialnet.unirioja.es/servlet/oaiart?codigo=9777456

المؤلفون: Rango E., Di Maria S., Zamperini C., Poggialini F., Crespan E., Perini C., Sabetta S., Saponara S., Fusi F., Maga G., Angelucci A., Gaudio E., Berton F., Schenone S., Botta L., Dreassi E., Botta M.

المساهمون: Rango, E., Di Maria, S., Zamperini, C., Poggialini, F., Crespan, E., Perini, C., Sabetta, S., Saponara, S., Fusi, F., Maga, G., Angelucci, A., Gaudio, E., Berton, F., Schenone, S., Botta, L., Dreassi, E., Botta, M.

مصطلحات موضوعية: diffuse large B-cell lymphoma, Src family kinases inhibitor, pyrazolo[3, 4-d]pyrimidine, hERG current, pharmacokinetics

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000952951500005; volume:56; issue:12; firstpage:1616; lastpage:1626; numberofpages:11; journal:PHARMACEUTICAL CHEMISTRY JOURNAL; https://hdl.handle.net/11365/1232445; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85150253239; https://link.springer.com/article/10.1007/s11094-023-02836-x

الاتاحة: https://hdl.handle.net/11365/1232445
https://doi.org/10.1007/s11094-023-02836-x
https://link.springer.com/article/10.1007/s11094-023-02836-x

المؤلفون: Ettahiri, Walid, Dalbouha, Amal, Elmrayej, Hajar, Adardour, Mohamed, Lahmidi, Sanae, Rais, Zakia, Baouid, Abdesselam, Essassi, El Mokhtar, Taleb, Mustapha

المصدر: Moroccan Journal of Heterocyclic Chemistry; Vol. 22 No. 04 (2023) ; Journal Marocain de Chimie Hétérocyclique; Vol. 22 No. 04 (2023) ; 2605-5996 ; 1114-7792

مصطلحات موضوعية: Synthesis, Reactivity, Medicinal agents, Pyrazolo[3, 4‐d]pyrimidine, Fused heterocycles

وصف الملف: application/pdf

Relation: https://revues.imist.ma/index.php/JMCH/article/view/41672/21429; https://revues.imist.ma/index.php/JMCH/article/view/41672

الاتاحة: https://revues.imist.ma/index.php/JMCH/article/view/41672

المؤلفون: Dipen K Sureja, Sandip P Dholakia, Kantilal R Vadalia

المصدر: Journal of Pharmacy and Bioallied Sciences, Vol 8, Iss 4, Pp 321-326 (2016)

مصطلحات موضوعية: Antimicrobial activity, conventional synthesis, microwave assisted synthesis, pyrazolo[3, 4-d] pyrimidin-4(5H)-one, Pharmacy and materia medica, RS1-441, Analytical chemistry, QD71-142

وصف الملف: electronic resource

Relation: http://www.jpbsonline.org/article.asp?issn=0975-7406;year=2016;volume=8;issue=4;spage=321;epage=326;aulast=Sureja; https://doaj.org/toc/0975-7406

URL الوصول: https://doaj.org/article/c71652b164804b37aad5b914ea5da4b0

المؤلفون: El-Kashef, Hussein, El-Emary, Talaat, Verhaeghe, Pierre, Vanelle, P., Samy, Maha

المساهمون: Chemistry Department, Faculty of Science, Assiut University, Assiut University, Laboratoire de chimie de coordination (LCC), Institut de Chimie de Toulouse (ICT), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT), Institut de Chimie Radicalaire (ICR), Aix Marseille Université (AMU)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)

المصدر: ISSN: 1420-3049 ; Molecules ; https://hal.science/hal-01954194 ; Molecules, 2018, 23 (10), pp.2657. ⟨10.3390/molecules23102657⟩.

مصطلحات موضوعية: Pyrazolo[3 4-b]pyrazines, o-aminonitrosopyrazole, Anticancer, Anti-inflammatory, Anti-breast cancer, [CHIM.COOR]Chemical Sciences/Coordination chemistry

Relation: hal-01954194; https://hal.science/hal-01954194; https://hal.science/hal-01954194/document; https://hal.science/hal-01954194/file/molecules-23-02657.pdf

الاتاحة: https://hal.science/hal-01954194
https://hal.science/hal-01954194/document
https://hal.science/hal-01954194/file/molecules-23-02657.pdf
https://doi.org/10.3390/molecules23102657

المؤلفون: Zemlyana, N. I., Karnozhitska, T. M., Pavlovska, T. L., Mazepa, O. V., Musatov, V. I., Lipson, V. V.

المصدر: Журнал органічної та фармацевтичної хімії; Том 16 № 4(64) (2018); 3-10 ; Journal of Organic and Pharmaceutical Chemistry; Vol. 16 No. 4(64) (2018); 3-10 ; Журнал органической и фармацевтической химии; Том 16 № 4(64) (2018); 3-10 ; 2518-1548 ; 2308-8303

مصطلحات موضوعية: pyrazolo[3, 4-b]pyridine-4-spiroindolinones, 3-(5-aminopyrazol-4-yl)-3-hydroxy-2-oxindolines, isatins, 5-aminopyrazoles, 2-dimethyl-1, 3-dioxane-4, 6-dione, domino-reactions, UDC, 547.859.1, пиразоло[3, 4-b]пиридин-4-спироиндолиноны, 3-(5-аминопиразол-4-ил)-3-гидрокси-2-оксиндолины, изатины, 5-аминопиразолы, 2-диметил-1, 3-диоксан-4, 6-дион, домино-реакции, УДК, піразоло[3, 4-b]піридин-4-спіроіндолінони, 3-(5-амінопіразол-4-іл)-3-гідрокси-2-оксіндоліни, ізатини, 5-амінопіразоли, 3-діоксан-4, 6-діон, доміно-реакції

Time: 2

وصف الملف: application/pdf

Relation: http://ophcj.nuph.edu.ua/article/view/ophcj.18.950/150323; http://ophcj.nuph.edu.ua/article/view/ophcj.18.950

الاتاحة: http://ophcj.nuph.edu.ua/article/view/ophcj.18.950
https://doi.org/10.24959/ophcj.18.950

المؤلفون: Singh, S.¹, Sharma, P. K., Dudhe, R., Kumar, N.

المصدر: Asian Journal of Research in Chemistry 4(10):1594-1599. 2011

المؤلفون: Ilaria Laurenzana, Antonella Caivano, Francesco La Rocca, Stefania Trino, Luciana De Luca, Francesca D'Alessio, Silvia Schenone, Geppino Falco, Maurizio Botta, Luigi Del Vecchio, Pellegrino Musto

المصدر: Frontiers in Pharmacology, Vol 7 (2016)

مصطلحات موضوعية: hematological malignancies, targeted therapies, Src kinase inhibitor, Fyn tyrosine kinase, pyrazolo[3 4-d]pyrimidine compound, Therapeutics. Pharmacology, RM1-950

وصف الملف: electronic resource

Relation: http://journal.frontiersin.org/Journal/10.3389/fphar.2016.00416/full; https://doaj.org/toc/1663-9812

URL الوصول: https://doaj.org/article/626a72154ca342d08cd52f8c8fcfe89b

المؤلفون: Di Maria, Salvatore, Picarazzi, Francesca, Mori, Mattia, Cianciusi, Annarita, Carbone, Anna, Crespan, Emmanuele, Perini, Cecilia, Sabetta, Samantha, Deplano, Serenella, Poggialini, Federica, Molinari, Alessio, Aronne, Rossella, Maccioni, Elias, Maga, Giovanni, Angelucci, Adriano, Schenone, Silvia, Musumeci, Francesca, Dreassi, Elena

المساهمون: Di Maria, Salvatore, Picarazzi, Francesca, Mori, Mattia, Cianciusi, Annarita, Carbone, Anna, Crespan, Emmanuele, Perini, Cecilia, Sabetta, Samantha, Deplano, Serenella, Poggialini, Federica, Molinari, Alessio, Aronne, Rossella, Maccioni, Elia, Maga, Giovanni, Angelucci, Adriano, Schenone, Silvia, Musumeci, Francesca, Dreassi, Elena

مصطلحات موضوعية: 4-d]pyrimidines, Abl, Chronic myeloid leukemia, Kinase inhibitors, Pyrazolo[3, Src

Relation: info:eu-repo/semantics/altIdentifier/pmid/35932498; info:eu-repo/semantics/altIdentifier/wos/WOS:000878032800008; volume:128; journal:BIOORGANIC CHEMISTRY; https://hdl.handle.net/11584/424225

الاتاحة: https://hdl.handle.net/11584/424225
https://doi.org/10.1016/j.bioorg.2022.106071

المؤلفون: Salvatore, Di Maria, Francesca, Picarazzi, Mattia, Mori, Annarita, Cianciusi, Anna, Carbone, Emmanuele, Crespan, Cecilia, Perini, Samantha, Sabetta, Serenella, Deplano, Federica, Poggialini, Alessio, Molinari, Rossella, Aronne, Elias, Maccioni, Giovanni, Maga, Adriano, Angelucci, Silvia, Schenone, Francesca, Musumeci, Elena, Dreassi

مصطلحات موضوعية: Organic Chemistry, Abl, Chronic myeloid leukemia, Fusion Proteins, bcr-abl, Antineoplastic Agents, Biochemistry, Piperazines, Pyrimidines, Drug Resistance, Neoplasm, Kinase inhibitors, Leukemia, Myelogenous, Chronic, BCR-ABL Positive, 4-d]pyrimidines, Benzamides, Drug Discovery, Pyrazolo[3, Imatinib Mesylate, Humans, Protein Kinase Inhibitors, Molecular Biology, Src

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46b7e6e1b26e009186124e9325bd1b70
https://hdl.handle.net/11697/203582

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: VIRESH H. SHAH, SHAILESH J. VAGHASIA, SAMIR H. JARSANIA, AMIT R. TRIVEDI, DIPTI K. DODIYA

المصدر: Journal of the Serbian Chemical Society, Vol 73, Iss 7, Pp 683-690 (2008)

مصطلحات موضوعية: pyrazolo[3’, 4’:4, 5]thieno[2, 3-d]pyrimidin-8-ones, carbonitrile, Gewald reaction, antimicrobial activity, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: http://www.shd.org.rs/JSCS/Vol73/No7/JSCS-3751.pdf; https://doaj.org/toc/0352-5139

URL الوصول: https://doaj.org/article/5e03c57e42564ca1a2331caacee5efaf

المؤلفون: Ferrari, Silvia Martina, LA MOTTA, CONCETTINA, SARTINI, STEFANIA, Baldini, Enke, MATERAZZI, GABRIELE, Politti, Ugo, Ruffilli, Ilaria, Ulisse, Salvatore, MICCOLI, PAOLO, ANTONELLI, ALESSANDRO, Fallahi, Poupak

المساهمون: Ferrari, Silvia Martina, LA MOTTA, Concettina, Sartini, Stefania, Baldini, Enke, Materazzi, Gabriele, Politti, Ugo, Ruffilli, Ilaria, Ulisse, Salvatore, Miccoli, Paolo, Antonelli, Alessandro, Fallahi, Poupak

مصطلحات موضوعية: Antiangiogenic inhibitors, CLM29, CLM3, PP1, PP2, pyrazolo[3, 4-d]pyrimidine, RET inhibitors, tyrosine kinase inhibitors

Relation: info:eu-repo/semantics/altIdentifier/pmid/26471970; info:eu-repo/semantics/altIdentifier/wos/WOS:000365468300002; volume:16; issue:2; firstpage:86; lastpage:93; numberofpages:8; journal:MINI-REVIEWS IN MEDICINAL CHEMISTRY; http://hdl.handle.net/11568/763608; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84949845294; http://www.eurekaselect.com/135842/article

الاتاحة: http://hdl.handle.net/11568/763608
https://doi.org/10.2174/1389557515666151016124208
http://www.eurekaselect.com/135842/article