الرئيسية › دليل الباحثين › Hamid Morjani
Hamid Morjani
الانتماء : BioSpectroscopie Translationnelle · Université de Reims Champagne-Ardenne
- 57منشورات (انتماء فرنسي)
- 259مجموع المنشورات
- 5320الاستشهادات
- 42مؤشر h
الملف البحثي
لدى Hamid Morjani 57 منشور(ات) مفهرسة (2009–2026). تُنشر أعماله أساسًا في «Journal of Molecular Structure»، «Future Medicinal Chemistry» و«Journal of Biomolecular Structure and Dynamics». أكثر مقالاته استشهادًا هو «Thiazolidinone-linked1,2,3-triazoles with monoterpenic skeleton as new potential anticancer agents: Design, synthesis and molecular docking » (2021)، وقد استُشهد به 95 مرة. 8 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل، منهم باحثون من مؤسسات في المغرب، الجزائر، إسبانيا.
هل هذا أنت؟ عرّف بأبحاثك
أنشئ ملفك على DzCademia مجانًا وأضف مقالاتك: ستظهر بسهولة أكبر على Google وفي مساعدي الذكاء الاصطناعي مثل ChatGPT، فيقرؤها ويستشهد بها عدد أكبر من الناس.
إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Drug Transport and Resistance Mechanisms
- Synthesis and biological activity
- Synthesis and Characterization of Heterocyclic Compounds
- Spectroscopy Techniques in Biomedical and Chemical Research
- Antibiotic Resistance in Bacteria
المنشورات (57)
- Potential Anticancer Agents Based on Monoterpenic Skeleton With Mono and Bis‐Isoxazoline Derivatives: Diastereoselective Synthesis, Experimental Study, Evaluation of Biological Activity, and Molecular Docking
- Molecular hybrids based on 1,2,3-triazole and 1,3,4-thiadiazole cores: Synthesis, characterization, anticancer activity and in silico study
- Targeted synthesis via the structure-activity relationship: Biological evaluation of new 1,2,3-triazoles monoterpene as antitumor agents
- Semisynthesis of novel chalcone hybrid compounds linked by 1,2,3-triazole and evaluation of their cytotoxic effects
- New isoxazoline‐linked 1,3,4‐thiadiazole derivatives: Synthesis, antiproliferative activity, molecular docking, molecular dynamics and DFT
- Thiazolidinone-linked-1,2,3-triazoles with (R)-Carvone as new potential anticancer agents
- Semicarbazone, thiosemicarbazone tailed isoxazoline-pyrazole: synthesis, DFT, biological and computational assessment
- Novel Bis-1,2,3-triazole-thiazolidinone hybrid as anticancer agents that induce apoptosis and molecular modeling study
- Synthesis, crystal structure and evaluation of anticancer activities of some novel heterocyclic compounds based on thymol
- Synthesis, characterization and cytotoxic activity of pyrazole derivatives based on thymol
- Hybrids of thiazolidinone with 1,2,3-triazole derivatives: design, synthesis, biological evaluation, in silico studies, molecular docking, molecular dynamics simulations, and ADMET profiling
- Design, Synthesis, Cytotoxic Effect Evaluation and Molecular Docking of (R)‐Camphor‐Based Thiazolidinone‐Isoxazole and Thiazolidinone‐1,2,3‐triazole Hybrids“
- Discovery of a new Bcl-2 inhibitor through synthesis, anticancer activity, docking and MD simulations
- New (S)-verbenone-isoxazoline-1,3,4-thiadiazole Hybrids: Synthesis, Anticancer Activity and Apoptosis-Inducing Effect
- Discovery of a new Bcl-2 inhibitor through synthesis, anticancer activity, docking and MD simulations
- New 1,2,3-Triazoles from (R)-Carvone: Synthesis, DFT Mechanistic Study and In Vitro Cytotoxic Evaluation
- Design, synthesis, evaluation of new 3-acetylisoxazolines and their hybrid analogous as anticancer agents: In vitro and in silico analysis
- Novel isoxazoline‐linked 1,3,4‐thiadiazole hybrids as anticancer agents: Design, synthesis, biological evaluation, molecular docking, and molecular dynamics simulation
- Design, synthesis, in vitro anticancer activity, and molecular docking studies of new (R)-carvone-pyrazole-1,2,3-triazoles
- Design, Synthesis, Biological and Computational Assessment of New Thiazolidin‐4‐one Derivatives as Potential Anticancer Agents Through the Apoptosis Pathway
- Synthesis, characterization, molecular docking, and anticancer activities of new 1,3,4-oxadiazole-5-fluorocytosine hybrid derivatives
- Cytotoxic and apoptotic effects of some (R)-carvone-isoxazoline derivatives on human fibrosarcoma and carcinoma cells: experimental evaluation for cytotoxicity, molecular docking and molecular dynamics studies
- Convenient route to benzo[1,2,3]selenadiazole–isoxazole hybrids and evaluation of their in vitro cytotoxicity
- Novel Hydrazono‐2‐Iminothiazolidin‐4‐Ones Based on a Monoterpenic Skeleton as Potential Antitumor Agents: Synthesis, DFT Studies, in Vitro Cytotoxicity, Apoptosis Inducing Properties and Molecular Docking
- Synthesis and Biological Evaluation of Novel Thiazole Analogs with Both Anti‐Proliferative and Mechanistic Analyses and Molecular Docking Studies
- New 1,3,4-thiadiazoles Derivatives: Synthesis, Antiproliferative Activity, Molecular Docking and Molecular Dynamics
- Chemical profiling, cytotoxic activities through apoptosis induction in human fibrosarcoma and carcinoma cells, and molecular docking of some 1,2,3-triazole-isoxazoline hybrids using the eugenol as a precursors
- New gem‑dichlorocyclopropane-pyrazole hybrids with monoterpenic skeleton: Synthesis, crystal structure, cytotoxic evaluation, molecular dynamics and theoretical study
- Diastereomerically pure (S)‐ verbenone‐isoxazoline hybrids: Synthesis, molecular structure, Hirshfeld surface analysis, density functional theory, cytotoxic effect, and apoptosis induction
- Thymoquinone induces G2/M cell cycle phase arrest and apoptosis through inhibition of JNK phosphorylation and induction of p53 and p21 expression in HT-1080 fibrosarcoma cells
- NMR 800Hz characterization, mass spectrometry discussion and anti-proliferative effects of flavonoids, senecic acid and caffeic acid isolated from Senecio leucanthemifolius poiret growing in Morocco
- Thiazolidinone-linked1,2,3-triazoles with monoterpenic skeleton as new potential anticancer agents: Design, synthesis and molecular docking studies
- Newly synthesized (R)-carvone-derived 1,2,3-triazoles: structural, mechanistic, cytotoxic and molecular docking studies
- Design, Hemiysnthesis, crystal structure and anticancer activity of 1, 2, 3-triazoles derivatives of totarol
- Discovery of novel furo[2,3‐d]pyrimidin‐2‐one–1,3,4‐oxadiazole hybrid derivatives as dual antiviral and anticancer agents that induce apoptosis
- New enaminone sesquiterpenic: TiCl4-catalyzed synthesis, spectral characterization, crystal structure, Hirshfeld surface analysis, DFT studies and cytotoxic activity
- Hybrid of the 1,2,3‐triazole nucleus and sesquiterpene skeleton as a potential antitumor agent: Hemisynthesis, molecular structure, Hirshfeld surface analysis, density functional theory, and in vitro cytotoxic and apoptotic effects
- Click Synthesis, Anticancer Activity, and Molecular Docking Investigation of some Functional 1,2,3-triazole Derivatives
- Degradation of p53 by HPV16-E6 variants isolated from cervical cancer specimens of Moroccan women
- Design, synthesis, biological evaluation and molecular docking of new uracil analogs-1,2,4-oxadiazole hybrids as potential anticancer agents
- Synthesis, characterization, and biological evaluation of new heterocyclic systems 1, 2, 3-triazole-isoxazoline from eugenol by the mixed condensation reactions
- Synthesis and Antitumor Activity of Novel Heterocyclic Systems with Monoterpenic Skeleton Combining Dichlorocyclopropane and 1,3,4‐Thiadiazole Nucleus
- Design, synthesis, biological evaluation and molecular docking of new 1,3,4-oxadiazole homonucleosides and their double-headed analogs as antitumor agents
- Synthesis, characterization and in vitro anticancer activity of thiabendazole-derived 1,2,3-triazole derivatives
- Effects of the Tumor Environment on Ion Channels: Implication for Breast Cancer Progression
- Diastereoselective synthesis and cytotoxic evaluation of new isoxazoles and pyrazoles with monoterpenic skeleton
- Triterpenes from Salvia argentea var. aurasiaca and their antibacterial and cytotoxic activities
- Triterpenoid saponins from Scabiosa stellata collected in North-eastern Algeria
- Two new bis-iridoids isolated from Scabiosa stellata and their antibacterial, antioxidant, anti-tyrosinase and cytotoxic activities
- Oleanane-type triterpene saponins from Calendula stellata
- Antibacterial, antioxidant and cytotoxic activities of triterpenes and flavonoids from the aerial parts of Salvia barrelieri Etl.
- Isolation and characterisation of cytotoxic compounds from Euphorbia clementei Boiss.
- A new 2-alkylhydroquinone glucoside from Phagnalon saxatile (L.) Cass
- Tomentosin Induces Telomere Shortening and Caspase‐Dependant Apoptosis in Cervical Cancer Cells
- Inula ViscosaExtracts Induces Telomere Shortening and Apoptosis in Cancer Cells and Overcome Drug Resistance
- Antiproliferative Effect and Induction of Apoptosis by Inula viscosa L. and Retama monosperma L. Extracts in Human Cervical Cancer Cells
- Antiproliferative Effects of Withanolides from Withania adpressa
مجلات النشر
- Journal of Molecular Structure × 11
- Future Medicinal Chemistry × 5
- Journal of Biomolecular Structure and Dynamics × 5
- ChemistrySelect × 4
- Journal of Heterocyclic Chemistry × 3
- Bioorganic Chemistry × 3
المنشورات حسب السنة
- 20261
- 20247
- 20237
- 202216
- 20218
- 20206
- 20192
- 20181
- 20175
- 20162
التعاون العلمي
المؤسسات الشريكة : Centre National de la Recherche Scientifique · Institut de Chimie Moléculaire de Reims · Matrice Extracellulaire et Dynamique Cellulaire MEDyC · Biomatériaux et Inflammation en Site Osseux · Cadi Ayyad University
بلدان المؤلفين المشاركين : المغرب · الجزائر · إسبانيا
المؤلفون المشاركون
- Abdelkhalek Riahi
- Anthony Robert
- Abdulmagid Alabdul Magid
- Laurence Voutquenne‐Nazabadioko
- Meryem Lehbili
- Amin Abedini
- Sophie C. Gangloff
- Hassan El Btaouri
- Olivier Mentré
- Ahmad Mehdi
- Claudie Madoulet
- Chantal Trentesaux
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
لماذا تختارون Dzcademia؟
ملفات أكاديمية ومقالات ومداخلات علمية: امنحوا أبحاثكم حضوراً عاماً منظماً. تساعد البيانات الوصفية المدمجة محركات البحث ومساعدات الذكاء الاصطناعي على التعرف على أعمالكم وفهم مراجعها.
علّق عبر Google
سجّل الدخول عبر Google للتعليق مباشرة على هذه الصفحة.