المؤلفون: Antonella Messore, Paolo Malune, Elisa Patacchini, Valentina Noemi Madia, Davide Ialongo, Merve Arpacioglu, Aurora Albano, Giuseppe Ruggieri, Francesco Saccoliti, Luigi Scipione, Enzo Tramontano, Serena Canton, Angela Corona, Sante Scognamiglio, Annalaura Paulis, Mustapha Suleiman, Helmi Mohammed Al-Maqtari, Fatma Mohamed A. Abid, Sarkar M. A. Kawsar, Murugesan Sankaranarayanan, Roberto Di Santo, Francesca Esposito, Roberta Costi

المصدر: Pharmaceuticals, Vol 17, Iss 5, p 650 (2024)

مصطلحات موضوعية: SARS-CoV-2, COVID-19, main protease, thiazolidinone derivatives, small molecules, docking studies, Medicine, Pharmacy and materia medica, RS1-441

Relation: https://www.mdpi.com/1424-8247/17/5/650; https://doaj.org/toc/1424-8247; https://doaj.org/article/33897d42e8a5438eb1decd73c9215d74

الاتاحة: https://doi.org/10.3390/ph17050650
https://doaj.org/article/33897d42e8a5438eb1decd73c9215d74

المؤلفون: Mostafa, Sara M., Aly, Ashraf A., Brase, Stefan, Nieger, Martin, Mohamed, Asmaa H.

المساهمون: Department of Chemistry

مصطلحات موضوعية: Chemical sciences, (Hydrazinecarbonothioyl)hydrazinecarbothioamide, dimethyl acetylenedicarboxylate, hydrazono bis-4-oxothiazolidines, X-ray structure analysis, MICROWAVE-ASSISTED SYNTHESIS, THIAZOLIDINONE DERIVATIVES, REGIOSELECTIVE SYNTHESIS, ANTIMICROBIAL ACTIVITY, ANTI-HIV, ANTIFUNGAL, POTENT, ANTIBACTERIAL, PYRAZOLINES, DESIGN, BIS HETEROCYCLES, AGENTS

وصف الملف: application/pdf

Relation: Mostafa , S M , Aly , A A , Brase , S , Nieger , M & Mohamed , A H 2022 , ' Facile synthesis of hydrazono bis-4-oxothiazolidines ' , Journal of Sulfur Chemistry , vol. 43 , no. 6 , pp. 606-619 . https://doi.org/10.1080/17415993.2022.2083454; ORCID: /0000-0003-1677-0109/work/130598628; http://hdl.handle.net/10138/358439; 25209008-9e14-4e8f-9f55-b6227c322e2d; 000807057200001

الاتاحة: http://hdl.handle.net/10138/358439

المؤلفون: Acosta, Atzel C., Cardoso, Marcos V.O., Oliveira Filho, Gevanio B., Pinheiro Junior, José W., Leite, Ana Cristina L., Mota, Rinaldo A.

المصدر: Pesquisa Veterinária Brasileira. January 2021 41

مصطلحات موضوعية: Heterocyclic compounds, clinical mastitis, thiazole derivatives, thiazolidinone derivatives, biological activity, antibacterial activity, MIC, MBC

وصف الملف: text/html

URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2021000100240

المؤلفون: M. V. Mishchenko, S. Yu. Shtrygol, R. B. Lesyk, A. V. Lozynskyi, S. M. Holota

المصدر: Zaporožskij Medicinskij Žurnal, Vol 22, Iss 6, Pp 840-846 (2020)

مصطلحات موضوعية: antiepileptic drugs, epilepsy, thiazolidinone derivatives, Medicine

وصف الملف: electronic resource

Relation: http://zmj.zsmu.edu.ua/article/view/218463/218747; https://doaj.org/toc/2306-4145; https://doaj.org/toc/2310-1210

URL الوصول: https://doaj.org/article/5c1f29dc9d994a19a144c10955d7350c

المؤلفون: Riaz, Madeeha, Abbas, Muzaffar, Khan, Arif-ullah, Nadeem, Humaira

المصدر: Molecular Medicine Communications; Vol. 2 No. 02 (2022): Molecular Medicine Communications; 121-133 ; 2790-7104 ; 2790-7090

مصطلحات موضوعية: Buprenorphine, Neuroinflammation, Interleukin-1β, Thiazolidinone derivatives, Mice

Relation: http://rootspress.org/journals/index.php/MMC/article/view/131/372; http://rootspress.org/journals/index.php/MMC/article/view/131

الاتاحة: http://rootspress.org/journals/index.php/MMC/article/view/131
https://doi.org/10.55627/mmc.002.002.0131

المؤلفون: Atzel C. Acosta, Marcos V.O. Cardoso, Gevanio B. Oliveira Filho, José W. Pinheiro Junior, Ana Cristina L. Leite, Rinaldo A. Mota

المصدر: Pesquisa Veterinária Brasileira, Vol 41 (2021)

مصطلحات موضوعية: Heterocyclic compounds, clinical mastitis, thiazole derivatives, thiazolidinone derivatives, biological activity, antibacterial activity, MIC, MBC, Veterinary medicine, SF600-1100

وصف الملف: electronic resource

Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2021000100240&tlng=en; https://doaj.org/toc/1678-5150

URL الوصول: https://doaj.org/article/5ba8afd3fa4f4ad48870b485fe03965e

المؤلفون: Nawel Rekiba, Abdelmadjid Benmohammed, Sofiane Khanoussi, Ayada Djafri, Jérôme Thibonnet

المصدر: Molbank, Vol 2021, Iss 4, p M1284 (2021)

مصطلحات موضوعية: indole, thiosemicarbazone derivatives, thiazolidinone derivatives, thioxothiazolidinone derivatives, Inorganic chemistry, QD146-197

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-8599/2021/4/M1284; https://doaj.org/toc/1422-8599

URL الوصول: https://doaj.org/article/589179aa2e774eb0be6df32d4498f599

المؤلفون: Mishchenko , M. V., Shtrygol’ , S. Yu., Lozynskyi , A. V., Lesyk , R. B.

المصدر: Вісник фармації; № 2(102) (2021); 96-103 ; News of Pharmacy; No. 2(102) (2021); 96-103 ; Вестник фармации; № 2(102) (2021); 96-103 ; 2415-8844

مصطلحات موضوعية: производные тиазолидинона, психотропные свойства, противосудорожные средства, похідні тіазолідинону, психотропні властивості, протисудомні засоби, thiazolidinone derivatives, psychotropic properties, anticonvulsants

وصف الملف: application/pdf

Relation: http://nphj.nuph.edu.ua/article/view/225651/240998; http://nphj.nuph.edu.ua/article/view/225651

الاتاحة: http://nphj.nuph.edu.ua/article/view/225651
https://doi.org/10.24959/nphj.21.53

المؤلفون: Guerraoui, Amal, Goudjil, Meriem, Direm, Amani, Guerraoui, Abdenour, Şengün, İlkin Yücel, Parlak, Cemal, Djedouani, Amel

مصطلحات موضوعية: Rhodanine single crystal, Fluorescence microscopy, DFT, Hirshfeld surface analysis, In silico anticancer and antibacterial , inhibitory activity, ADMET properties, Polo-Like Kinases, Drug Discovery, Thiazolidinone Derivatives, Prediction, Classification, Inhibitors, Toxicity, Scaffold, Design, Binary

Relation: Journal of Molecular Structure; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://doi.org/10.1016/j.molstruc.2023.135025; https://hdl.handle.net/11454/82748; 1280; WOS:000932002700001; 2-s2.0-85150911746

الاتاحة: https://hdl.handle.net/11454/82748
https://doi.org/10.1016/j.molstruc.2023.135025

المؤلفون: Sara M. Mostafa, Ashraf A. Aly, Stefan Bräse, Martin Nieger, Asmaa H. Mohamed

المساهمون: Department of Chemistry

مصطلحات موضوعية: POTENT, 116 Chemical sciences, ANTI-HIV, General Chemistry, hydrazono bis-4-oxothiazolidines, REGIOSELECTIVE SYNTHESIS, BIS HETEROCYCLES, X-ray structure analysis, DESIGN, ANTIFUNGAL, MICROWAVE-ASSISTED SYNTHESIS, dimethyl acetylenedicarboxylate, PYRAZOLINES, ANTIBACTERIAL, THIAZOLIDINONE DERIVATIVES, AGENTS, (Hydrazinecarbonothioyl)hydrazinecarbothioamide, ANTIMICROBIAL ACTIVITY

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ed9a100ef87f493a281d072475ef9b5
http://hdl.handle.net/10138/358439

المؤلفون: Patel, VI¹, Patel, RG, Patel, NG, Panchal, SR, Bhardia, PD

المصدر: Asian Journal of Research in Chemistry 3(2):468-471. 2010

المؤلفون: ÖZSAVCI, DERYA, KÜÇÜKGÜZEL, İLKAY, KULABAŞ, NECLA, BİNGÖL ÖZAKPINAR, ÖZLEM

المساهمون: Kulabas, Necla, Ozakpinar, Ozlem Bingol, Ozsavci, Derya, Leyssen, Pieter, Neyts, Johan, Kucukguzel, Ilkay

مصطلحات موضوعية: Acylthioureas, anticancer, antiviral, tautomerism, thiourea, 2-amino-1,3-thiazol-4-one, 2-imino-1,3-thiazolidin-4-one, DRUG DISCOVERY, N,N-DISUBSTITUTED THIOUREAS, THIAZOLIDINONE DERIVATIVES, NONNUCLEOSIDE INHIBITORS, ANTITUBERCULOSIS AGENTS, ANTIMICROBIAL ACTIVITY, CYTOTOXIC ACTIVITIES, ACYL THIOUREAS, ANALOGS, MOIETY

وصف الملف: application/pdf

Relation: MARMARA PHARMACEUTICAL JOURNAL; https://hdl.handle.net/11424/241685; WOS:000411289700022

الاتاحة: https://hdl.handle.net/11424/241685
https://doi.org/10.12991/marupj.300913

المؤلفون: Roman Lesyk, S. Yu. Shtrygol, Serhii Holota, Andrii Lozynskyi, Mariia Mishchenko

المصدر: Zaporožskij Medicinskij Žurnal, Vol 22, Iss 6, Pp 840-846 (2020)

مصطلحات موضوعية: 0303 health sciences, Chemistry, medicine.medical_treatment, lcsh:R, 030311 toxicology, lcsh:Medicine, Carbamazepine, Pharmacology, Effective dose (pharmacology), 03 medical and health sciences, Maximal electroshock, 0302 clinical medicine, Anticonvulsant, medicine, epilepsy, antiepileptic drugs, thiazolidinone derivatives, Pentylenetetrazol, 030217 neurology & neurosurgery, Screening study, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ea86ecf6d82f5d5b23b4fcd01d1c484
http://zmj.zsmu.edu.ua/article/view/218463/218747

المصدر: Вісник фармації; № 2(102) (2021); 96-103
News of Pharmacy; No. 2(102) (2021); 96-103
Вестник фармации; № 2(102) (2021); 96-103

مصطلحات موضوعية: похідні тіазолідинону, психотропні властивості, протисудомні засоби, производные тиазолидинона, психотропные свойства, противосудорожные средства, thiazolidinone derivatives, psychotropic properties, anticonvulsants

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=scientific_p::330e104af3d75f51fc0ae6178b624b09
http://nphj.nuph.edu.ua/article/view/225651

المؤلفون: Mishchenko, M. V., Shtrygol, S. Yu., Lesyk, R. B., Lozynskyi, A. V., Holota, S. M.

المصدر: Запорожский медицинский журнал; Том 22 № 6 (2020)
Zaporozhye Medical Journal; Vol. 22 No. 6 (2020)

مصطلحات موضوعية: протиепілептичні засоби, похідні тіазолідинону, производные тиазолидинона, эпилепсия, epilepsy, противоэпилептические средства, antiepileptic drugs, thiazolidinone derivatives, епілепсія

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=scientific_p::a936a3f568716a688fc510e7f4fee84a
http://zmj.zsmu.edu.ua/article/view/218463

المؤلفون: Sofiane Khanoussi, Ayada Djafri, Abdelmadjid Benmohammed, Nawel Rekiba, Jérôme Thibonnet

المصدر: Molbank, Vol 2021, Iss M1284, p M1284 (2021)

مصطلحات موضوعية: Indole test, Organic Chemistry, thioxothiazolidinone derivatives, Ring (chemistry), Biochemistry, Combinatorial chemistry, thiosemicarbazone derivatives, chemistry.chemical_compound, indole, chemistry, Biological property, Moiety, thiazolidinone derivatives, Physical and Theoretical Chemistry, Semicarbazone, Heterocyclic derivatives, Inorganic chemistry, QD146-197

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcb285603f0db8c2ef7a9c493e3352a9
https://doi.org/10.3390/m1284

المؤلفون: R. M. ABDEL-RAHMAN, Z. EL-GENDY, M. M. FAWZY, M. B. MAHMOUD

المصدر: Journal of Indian Chemical Society, Vol. 68(Nov 1991), 628-630, (1991-11-30)

مصطلحات موضوعية: thiazolidinone derivatives, Acylation, Antifungal activity, Heterocyclic

Relation: https://doi.org/10.5281/zenodo.6155394; https://doi.org/10.5281/zenodo.6155395; oai:zenodo.org:6155395

الاتاحة: https://doi.org/10.5281/zenodo.6155395

المؤلفون: Kulabas, Necla, Ozakpinar, Ozlem Bingol, Ozsavci, Derya, Leyssen, Pieter, Neyts, Johan, Kucukguzel, Ilkay

مصطلحات موضوعية: N,N-DISUBSTITUTED THIOUREAS, Science & Technology, ANALOGS, 2-imino-1,3-thiazolidin-4-one, Acylthioureas, ACYL THIOUREAS, anticancer, 2-amino-1,3-thiazol-4-one, antiviral, DRUG DISCOVERY, tautomerism, CYTOTOXIC ACTIVITIES, ANTITUBERCULOSIS AGENTS, Pharmacology & Pharmacy, NONNUCLEOSIDE INHIBITORS, MOIETY, THIAZOLIDINONE DERIVATIVES, Life Sciences & Biomedicine, thiourea, ANTIMICROBIAL ACTIVITY

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1131::3479a287e660cf68783a3e100487bcd5
https://lirias.kuleuven.be/handle/123456789/623977

المؤلفون: Savukynaitė, Lina

المساهمون: Petrikaitė, Vilma

مصطلحات موضوعية: 2,5-substituted thiazolidinone derivatives, anticancer activity, pharmacokinetic properties, toxicity

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2888::f9cda95609332ffe6a219d64ca99d4ea
https://library.lsmuni.lt/LSMU:ELABAETD16669867&prefLang=en_US

المؤلفون: Stefano Fiore, Francesco La Torre, Elias Maccioni, Cristina Faggi, Roberto Cirilli, Daniela Secci, Maria Luisa Sanna

المصدر: Chirality. 22:56-62

مصطلحات موضوعية: Models, Molecular, Magnetic Resonance Spectroscopy, Molecular Conformation, Crystallography, X-Ray, Chiral stationary phase, High-performance liquid chromatography, Catalysis, Analytical Chemistry, Drug Discovery, absolute configuration, anti-inflammatory agents, chiral stationary phase, chiralpak ia, chiroptical properties, cox-2-inhibitors, hplc, sulfonamide derivatives, thiazolidinone derivatives, Cyclooxygenase Inhibitors, Chromatography, High Pressure Liquid, Spectroscopy, Pharmacology, Chromatography, biology, Chemistry, Organic Chemistry, Absolute configuration, Stereoisomerism, Enantiopure drug, Cyclooxygenase 2, biology.protein, Spectrophotometry, Ultraviolet, Cyclooxygenase, Enantiomer, Chirality (chemistry)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23329cb383416e2aea03b15b9e3c0ff5
https://doi.org/10.1002/chir.20705