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

Novel spirooxindole-triazole derivatives: unveiling [3+2] cycloaddition reactivity through molecular electron density theory and investigating their potential cytotoxicity against HepG2 and MDA-MB-231 cell lines

新型螺吲哚三唑衍生物:通过分子电子密度理论揭示 [3+2] 环加成反应性并研究其对 HepG2 和 MDA-MB-231 细胞系的潜在细胞毒性

Ihab Shawish, Samha Al Ayoubi, Ayman El-Faham, Ali Aldalbahi, Fardous F El-Senduny, Farid A Badria, Mar Ríos-Gutiérrez, Hassan H Hammud, Sajda Ashraf, Zaheer Ul-Haq, Assem Barakat

Discovery of Cell-Permeable Allosteric Inhibitors of Liver Pyruvate Kinase: Design and Synthesis of Sulfone-Based Urolithins

发现可穿透细胞的肝丙酮酸激酶变构抑制剂:砜基尿石素的设计和合成

Shazia Iqbal, Md Zahidul Islam, Sajda Ashraf, Woonghee Kim, Amal A Al-Sharabi, Mehmet Ozcan, Essam Hanashalshahaby, Cheng Zhang, Mathias Uhlén, Jan Boren, Hasan Turkez, Adil Mardinoglu

New spiro-indeno[1,2- b]quinoxalines clubbed with benzimidazole scaffold as CDK2 inhibitors for halting non-small cell lung cancer; stereoselective synthesis, molecular dynamics and structural insights

新型螺茚并[1,2- b]喹喔啉与苯并咪唑骨架结合作为 CDK2 抑制剂用于阻止非小细胞肺癌;立体选择性合成、分子动力学和结构洞察

Assem Barakat, Saeed Alshahrani, Abdullah Mohammed Al-Majid, Abdullah Saleh Alamary, Matti Haukka, Marwa M Abu-Serie, Luis R Domingo, Sajda Ashraf, Zaheer Ul-Haq, Mohamed S Nafie, Mohamed Teleb

Synthesis, crystal structure, DFT, Hirshfeld surface analysis, energy frameworks and in-Silico drug-targeting PFKFB3 kinase of novel triazolequinoxalin derivative (TZQ) as a therapeutic Strategy against cancer

新型三唑喹喔啉衍生物 (TZQ) 的合成、晶体结构、DFT、Hirshfeld 表面分析、能量框架和硅药物靶向 PFKFB3 激酶作为抗癌治疗策略

Nadeem Abad, Fares Hezam Al-Ostoot, Sajda Ashraf, Karim Chkirate, Majed S Aljohani, Hussam Y Alharbi, Shafeek Buhlak, Mohamed El Hafi, Luc Van Meervelt, Basheer M Al-Maswari, El Mokhtar Essassi, Youssef Ramli

Designing Functionally Substituted Pyridine-Carbohydrazides for Potent Antibacterial and Devouring Antifungal Effect on Multidrug Resistant (MDR) Strains

设计功能取代的吡啶-碳酰肼,对多重耐药 (MDR) 菌株产生强效抗菌和吞噬抗真菌作用

Farooq-Ahmad Khan, Sana Yaqoob, Shujaat Ali, Nimra Tanveer, Yan Wang, Sajda Ashraf, Khwaja Ali Hasan, Shaden A M Khalifa, Qiyang Shou, Zaheer Ul-Haq, Zi-Hua Jiang, Hesham R El-Seedi

A Gene Co-Expression Network-Based Drug Repositioning Approach Identifies Candidates for Treatment of Hepatocellular Carcinoma

基于基因共表达网络的药物重新定位方法可识别治疗肝细胞癌的候选药物

Meng Yuan, Koeun Shong, Xiangyu Li, Sajda Ashraf, Mengnan Shi, Woonghee Kim, Jens Nielsen, Hasan Turkez, Saeed Shoaie, Mathias Uhlen, Cheng Zhang, Adil Mardinoglu

Phenylpyrazalopyrimidines as Tyrosine Kinase Inhibitors: Synthesis, Antiproliferative Activity, and Molecular Simulations

苯基吡唑并嘧啶作为酪氨酸激酶抑制剂:合成、抗增殖活性和分子模拟

Bhupender S Chhikara, Sajda Ashraf, Saghar Mozaffari, Nicole St Jeans, Dindyal Mandal, Rakesh Kumar Tiwari, Zaheer Ul-Haq, Keykavous Parang

Synthesis of a New Class of Spirooxindole-Benzo[ b]Thiophene-Based Molecules as Acetylcholinesterase Inhibitors

一类新型螺吲哚-苯并[ b]噻吩类分子作为乙酰胆碱酯酶抑制剂的合成

Assem Barakat, Saeed Alshahrani, Abdullah Mohammed Al-Majid, M Ali, Mezna Saleh Altowyan, Mohammad Shahidul Islam, Abdullah Saleh Alamary, Sajda Ashraf, Zaheer Ul-Haq

Synthesis and dynamics studies of barbituric acid derivatives as urease inhibitors

巴比妥酸衍生物作为脲酶抑制剂的合成及动力学研究

Assem Barakat #, Abdullah Mohammed Al-Majid #, Gehad Lotfy #, Fiza Arshad #, Sammer Yousuf #, M Iqbal Choudhary #, Sajda Ashraf #, Zaheer Ul-Haq #