المؤلفون: Guendouzi, Abdelmadjid, Belkhiri, Lotfi, Djelti, Farah, Mohamed Zendaoui, Zineddine, Brahim, Houari, Guendouzi, Abdelkrim, Djekoun, Abdelhamid, Boucekkine, Abdou

المساهمون: École normale supérieure - Constantine (ENS Constantine), Université Frères Mentouri – Constantine 1 = Constantine 1 – Frères Mentouri University (UMC), Université Aboubekr Belkaid - University of Belkaïd Abou Bekr Tlemcen, Université de Saïda Dr. Moulay Tahar, Institut des Sciences Chimiques de Rennes (ISCR), Université de Rennes (UR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), The authors are grateful to the Frères Mentouri University of Constantine 1 (Algeria) and the Pharmaceutical Sciences Research Center (CRSP) for providing computing facilities. Are also acknowledged, the General Directorate of Scientific Research and Technological Development (DGRSDT) for the PRFU project (2022-2024: Grant No. B00L01EN250120220001) and the Thematic Research Agency in Health and Life Sciences – ATRSSV for the PNR (Grant 2022-2024).

المصدر: ISSN: 0892-7022.

مصطلحات موضوعية: Furoxan derivatives, multi-target, anti-cancer, QSAR, molecular docking, dynamics, ADMET, [CHIM.THER]Chemical Sciences/Medicinal Chemistry, [CHIM.CHEM]Chemical Sciences/Cheminformatics

Relation: hal-04506398; https://hal.science/hal-04506398; https://hal.science/hal-04506398/document; https://hal.science/hal-04506398/file/Manuscript.pdf

الاتاحة: https://hal.science/hal-04506398
https://hal.science/hal-04506398/document
https://hal.science/hal-04506398/file/Manuscript.pdf
https://doi.org/10.1080/08927022.2024.2326180

المؤلفون: Abdelmadjid Guendouzi, Lotfi Belkhiri, Farah Djelti, Zineddine Mohamed Zendaoui, Houari Brahim, Abdelkrim Guendouzi, Abdelhamid Djekoun, Abdou Boucekkine

مصطلحات موضوعية: Biophysics, Biochemistry, Genetics, Molecular Biology, Pharmacology, Biotechnology, Cancer, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, Furoxan derivatives, multi-target, anti-cancer, QSAR, molecular docking, dynamics, ADMET

Relation: https://figshare.com/articles/journal_contribution/In-silico_design_novel_phenylsulfonyl_furoxan_and_phenstatin_derivatives_as_multi-target_anti-cancer_inhibitors_based_on_2D-QSAR_molecular_docking_dynamics_and_ADMET_approaches/25404096

الاتاحة: https://doi.org/10.6084/m9.figshare.25404096.v1

المؤلفون: Qi Wan, Yan Deng, Yaoqing Huang, Zhihui Yu, Chunli Wang, Ke Wang, Assoc. Prof. Jibin Dong, Prof. Ying Chen

المصدر: ChemistryOpen, Vol 9, Iss 2, Pp 176-182 (2020)

مصطلحات موضوعية: apoptosis, estradiol, nitric oxide, furoxan derivatives, anticancer drugs, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2191-1363

URL الوصول: https://doaj.org/article/8fce184bc5fc49848dad720fac87920e

المؤلفون: de Almeida, Letícia, Passalacqua, Thaís Gaban, Dutra, Luiz Antonio, Fonseca, Jéssica N. Varonez da, Nascimento, Rhayanne F. Queiroz, Imamura, Kely Braga, de Andrade, Cleverton Roberto, dos Santos, Jean Leandro, Graminha, Márcia A.S.

المساهمون: Universidade Estadual Paulista (UNESP)

مصطلحات موضوعية: Furoxan derivatives, In vivo antileishmanial activity, L. infantum, NO-donor, Semi-quantitative histopathological analysis, Visceral leishmaniasis

وصف الملف: 536-547

Relation: Biomedicine and Pharmacotherapy; 0,951; http://dx.doi.org/10.1016/j.biopha.2017.08.096; Biomedicine and Pharmacotherapy, v. 95, p. 536-547.; http://hdl.handle.net/11449/170081; 2-s2.0-85028556866; 2-s2.0-85028556866.pdf; 2402682969776875; orcid:0000-0001-7015-7175

الاتاحة: http://hdl.handle.net/11449/170081
https://doi.org/10.1016/j.biopha.2017.08.096

المؤلفون: Henning Hopf, Aboul-fetouh E. Mourad, Peter G. Jones

المصدر: Beilstein Journal of Organic Chemistry, Vol 6, Iss 1, p 68 (2010)

مصطلحات موضوعية: cinnamyl alcohol, furoxan derivatives, isoxazole derivatives, X-ray diffraction, Science, Organic chemistry, QD241-441

Relation: https://doi.org/10.3762/bjoc.6.68; https://doaj.org/toc/1860-5397; https://doaj.org/article/be82cea3cb5a45e9a2ec512c199b9e73

الاتاحة: https://doi.org/10.3762/bjoc.6.68
https://doaj.org/article/be82cea3cb5a45e9a2ec512c199b9e73

المؤلفون: Yan Deng, Jibin Dong, Zhihui Yu, Ke Wang, Qi Wan, Ying Chen, Yaoqing Huang, Chunli Wang

المصدر: ChemistryOpen
ChemistryOpen, Vol 9, Iss 2, Pp 176-182 (2020)

مصطلحات موضوعية: MAPK/ERK pathway, MAP Kinase Signaling System, Antineoplastic Agents, furoxan derivatives, 010402 general chemistry, Nitric Oxide, 01 natural sciences, Nitric oxide, HeLa, lcsh:Chemistry, chemistry.chemical_compound, Structure-Activity Relationship, Cell Line, Tumor, Humans, Cell Proliferation, Mitogen-Activated Protein Kinase Kinases, Oxadiazoles, biology, Estradiol, Full Paper, 010405 organic chemistry, Furoxan, apoptosis, General Chemistry, Cell cycle, Full Papers, biology.organism_classification, In vitro, 0104 chemical sciences, anticancer drugs, chemistry, Biochemistry, lcsh:QD1-999, Apoptosis, Cell culture, Steroids, Drug Screening Assays, Antitumor

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8382ba5ba6ce035de46f44401e78bb07
https://pubmed.ncbi.nlm.nih.gov/32025462

المؤلفون: Jean Leandro dos Santos, Rhayanne F. Queiroz Nascimento, Thais Gaban Passalacqua, Jéssica N. Varonez da Fonseca, Kely Braga Imamura, Leticia de Almeida, Cleverton Roberto de Andrade, Luiz Antonio Dutra, Marcia A. S. Graminha

المساهمون: Universidade Estadual Paulista (Unesp)

المصدر: Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP

مصطلحات موضوعية: 0301 basic medicine, Male, 030106 microbiology, Antiprotozoal Agents, Spleen, Pharmacology, Kidney, Nitric Oxide, Parasite load, 03 medical and health sciences, chemistry.chemical_compound, Mice, In vivo, Amphotericin B, Cricetinae, medicine, Animals, Leishmania infantum, Amastigote, Visceral leishmaniasis, Benzoxazoles, biology, Macrophages, Furoxan, General Medicine, medicine.disease, biology.organism_classification, In vitro, L. infantum, 030104 developmental biology, medicine.anatomical_structure, Treatment Outcome, chemistry, Liver, Furoxan derivatives, Leishmaniasis, Visceral, NO-donor, In vivo antileishmanial activity, Semi-quantitative histopathological analysis, Biomarkers

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdd04f5e858d7feeab99587556897c8d
https://pubmed.ncbi.nlm.nih.gov/28866421

المؤلفون: Peter G. Jones, Aboul-Fetouh E. Mourad, Henning Hopf

المصدر: Beilstein Journal of Organic Chemistry, Vol 6, Iss 1, p 68 (2010)
Beilstein Journal of Organic Chemistry

مصطلحات موضوعية: Cinnamyl alcohol, Chemistry, Organic Chemistry, Nanotechnology, furoxan derivatives, Preliminary Communication, cinnamyl alcohol, isoxazole derivatives, X-ray diffraction, lcsh:QD241-441, Acetic acid, chemistry.chemical_compound, lcsh:Organic chemistry, Yield (chemistry), X-ray crystallography, Nitro, lcsh:Q, Sodium nitrite, lcsh:Science, Nuclear chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6454450993078899d196f041108ef39c
https://doaj.org/article/be82cea3cb5a45e9a2ec512c199b9e73

المؤلفون: BERTINARIA, Massimo

المساهمون: M. BERTINARIA

مصطلحات موضوعية: H3-antagonist, NO-donor, Furoxan derivatives

Relation: volume:58; firstpage:279; lastpage:283; journal:IL FARMACO; http://hdl.handle.net/2318/2738

الاتاحة: http://hdl.handle.net/2318/2738
https://doi.org/10.1016/S0014-827X(03)00023-5

المؤلفون: Massimo Bertinaria

مصطلحات موضوعية: Stereochemistry, Antagonist, Histamine Antagonists, H3-antagonist, NO-donors, Furoxan derivatives, Pharmaceutical Science, General Medicine, Furazan, Ligands, Chemical synthesis, In vitro, No donors, chemistry.chemical_compound, Muscle relaxation, chemistry, Drug Discovery, Imidazole, Animals, Humans, Receptors, Histamine H3, Nitric Oxide Donors, Histamine H3 receptor, Derivative (chemistry)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d595617067de81b64fbbbbe8c0074d6
http://hdl.handle.net/2318/2738

المؤلفون: Mu, L., Feng, S.-S., Go, M.L.

المساهمون: CHEMICAL & ENVIRONMENTAL ENGINEERING, PHARMACY

المصدر: Scopus

مصطلحات موضوعية: Furoxan derivatives, Hypertension, Nitric oxide, NO- donor, Synthesis, Vasodilation

Relation: Mu, L.,Feng, S.-S.,Go, M.L. (2000-06). Study of synthesis and cardiovascular activity of some furoxan derivatives as potential NO-donors. Chemical and Pharmaceutical Bulletin 48 (6) : 808-816. ScholarBank@NUS Repository.; http://scholarbank.nus.edu.sg/handle/10635/92355; NOT_IN_WOS

الاتاحة: http://scholarbank.nus.edu.sg/handle/10635/92355

المؤلفون: Chenlu Dong (11575410), Xufeng Zhao (8355906), Yuki Katsuragi (11575413), Hojin Kim (462672), Masahiko Hayashi (1320954), Ryosuke Matsubara (2142895)

مصطلحات موضوعية: Biophysics, Biochemistry, Genetics, Molecular Biology, Biotechnology, Infectious Diseases, Chemical Sciences not elsewhere classified, containing functional groups, concise synthetic route, alkylated furoxan derivatives, resultant furoxan ring, furoxan ring, furoxan incorporation, various types, various nitrogen, efficient strategy, also provides

Relation: https://figshare.com/articles/journal_contribution/Furoxan_Incorporation_into_C_H_Bonds_Enabling_Nitrogen-Containing_Functional_Group_Installation_into_the_Same/16825377

الاتاحة: https://doi.org/10.1021/acs.joc.1c01950.s001