日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Design, synthesis, and apoptotic antiproliferative action of new 1,2,3-triazole/1,2,4-oxadiazole hybrids as dual EGFR/VEGFR-2 inhibitors

新型1,2,3-三唑/1,2,4-恶二唑杂合物作为双重EGFR/VEGFR-2抑制剂的设计、合成及其凋亡抗增殖作用

期刊:Journal of Enzyme Inhibition and Medicinal Chemistry
影响因子:5.4
doi:10.1080/14756366.2024.2305856
Mahmoud, Mohamed A; Mohammed, Anber F; Salem, Ola I A; Almutairi, Tahani Mazyad; Bräse, Stefan; Youssif, Bahaa G M
EGFR
凋亡
EGF
表观遗传
VEGF
发表日期：2024
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Neuroprotective effects of rutin against cuprizone-induced multiple sclerosis in mice

芦丁对小鼠铜宗诱发的多发性硬化症的神经保护作用

期刊:Inflammopharmacology
影响因子:4.6
doi:10.1007/s10787-024-01442-x
Mariam A Nicola, Abdelraheim H Attaai, Mahmoud H Abdel-Raheem, Anber F Mohammed, Yasmin F Abu-Elhassan
神经
多发性硬化症
发表日期：2024
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Design, synthesis, biological evaluation and docking study of some new aryl and heteroaryl thiomannosides as FimH antagonists

一些新的芳基和杂芳基硫甘露糖苷作为FimH拮抗剂的设计、合成、生物学评价及对接研究

期刊:Bioorganic Chemistry
影响因子:4.5
doi:10.1016/j.bioorg.2024.107258
Anber F Mohammed, Shimaa A Othman, Ola F Abou-Ghadir, Ahmed A Kotb, Yaser A Mostafa, Mohamed A El-Mokhtar, Hajjaj H M Abdu-Allah
信号转导
发表日期：2024
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Design, synthesis, and apoptotic antiproliferative action of new benzimidazole/1,2,3-triazole hybrids as EGFR inhibitors

新型苯并咪唑/1,2,3-三唑杂合物作为EGFR抑制剂的设计、合成及其凋亡抗增殖作用

期刊:Frontiers in Chemistry
影响因子:4.2
doi:10.3389/fchem.2024.1541846
Ahmed, Alshimaa A Y; Mohammed, Anber F; Almarhoon, Zainab M; Bräse, Stefan; Youssif, Bahaa G M
表观遗传
EGFR
EGF
凋亡
发表日期：2024
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Design, synthesis, apoptotic, and antiproliferative effects of 5-chloro-3- (2-methoxyvinyl)-indole-2-carboxamides and pyrido[3,4-b]indol-1-ones as potent EGFR(WT/)EGFR(T790M) inhibitors

5-氯-3-(2-甲氧基乙烯基)-吲哚-2-甲酰胺和吡啶并[3,4-b]吲哚-1-酮作为强效EGFR(WT/)EGFR(T790M)抑制剂的设计、合成、凋亡和抗增殖作用

期刊:Journal of Enzyme Inhibition and Medicinal Chemistry
影响因子:5.4
doi:10.1080/14756366.2023.2218602
Al-Wahaibi, Lamya H; Mohammed, Anber F; Abdel Rahman, Fatema El-Zahraa S; Abdelrahman, Mostafa H; Gu, Xuyuan; Trembleau, Laurent; Youssif, Bahaa G M
表观遗传
凋亡
EGFR
EGF
发表日期：2023
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Design, Synthesis, and Biological Evaluation of Indole-2-carboxamides as Potential Multi-Target Antiproliferative Agents

吲哚-2-甲酰胺类化合物作为潜在多靶点抗增殖剂的设计、合成及生物学评价

期刊:Pharmaceuticals
影响因子:4.8
doi:10.3390/ph16071039
Al-Wahaibi, Lamya H; Mohammed, Anber F; Abdelrahman, Mostafa H; Trembleau, Laurent; Youssif, Bahaa G M
发表日期：2023
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Design, Synthesis, and Antiproliferative Activity of New 5-Chloro-indole-2-carboxylate and Pyrrolo[3,4-b]indol-3-one Derivatives as Potent Inhibitors of EGFR(T790M)/BRAF(V600E) Pathways

新型5-氯吲哚-2-羧酸酯和吡咯并[3,4-b]吲哚-3-酮衍生物作为EGFR(T790M)/BRAF(V600E)通路强效抑制剂的设计、合成及抗增殖活性

期刊:Molecules
影响因子:4.6
doi:10.3390/molecules28031269
Al-Wahaibi, Lamya H; Mohammed, Anber F; Abdelrahman, Mostafa H; Trembleau, Laurent; Youssif, Bahaa G M
信号转导
BRAF
EGFR
EGF
发表日期：2023
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Discovery of new 5-substituted-indole-2-carboxamides as dual epidermal growth factor receptor (EGFR)/cyclin dependent kinase-2 (CDK2) inhibitors with potent antiproliferative action

发现新型5-取代吲哚-2-甲酰胺类化合物作为双重表皮生长因子受体（EGFR）/细胞周期蛋白依赖性激酶-2（CDK2）抑制剂，具有强效抗增殖作用

期刊:RSC Medicinal Chemistry
影响因子:3.6
doi:10.1039/d3md00038a
Mohamed, Fatma A M; Alakilli, Saleha Y M; El Azab, Eman Fawzy; Baawad, Faris A M; Shaaban, Esraa Ibrahim A; Alrub, Heba Abu; Hendawy, Omnia; Gomaa, Hesham A M; Bakr, Adel G; Abdelrahman, Mostafa H; Trembleau, Laurent; Mohammed, Anber F; Youssif, Bahaa G M
EGFR
细胞生物学
EGF
CDK2
信号转导
发表日期：2023
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New Cytotoxic Natural Products from the Red Sea Sponge Stylissa carteri

来自红海海绵 Stylissa carteri 的新型细胞毒性天然产物

期刊:Marine Drugs
影响因子:5.4
doi:10.3390/md18050241
Abdelhameed, Reda F A; Habib, Eman S; Eltahawy, Nermeen A; Hassanean, Hashim A; Ibrahim, Amany K; Mohammed, Anber F; Fayez, Shaimaa; Hayallah, Alaa M; Yamada, Koji; Behery, Fathy A; Al-Sanea, Mohammad M; Alzarea, Sami I; Bringmann, Gerhard; Ahmed, Safwat A; Abdelmohsen, Usama Ramadan
细胞生物学
毒理研究
发表日期：2020
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