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

QW-5-70 targets the colchicine site and demonstrates antitumor activity in P-gp-overexpressing cancer models

QW-5-70靶向秋水仙碱结合位点,并在P-gp过表达的癌症模型中表现出抗肿瘤活性。

Xie, Yang; Hou, Ruida; Albadari, Najah; Chen, Hao; Miller, Darcie J; Quadrozzi Gruntz, Judith; Oldham, Michael L; Kamal, Mir Shahriar; Jiang, Jianxiong; Wu, Zhongzhi; Miller, Duane D; Li, Wei

Gazania rigens (L.) gaertn leaf extract-inspired innovative synthesis of silver nanoparticles and promising applications as antibacterial and cytotoxic agents

受非洲菊(Gazania rigens (L.) gaertn)叶提取物启发,创新性地合成了银纳米粒子,并探索了其作为抗菌剂和细胞毒性剂的潜在应用。

Mohammed, Afrah E; Aldahasi, Reham M; Aldraiwiesh, Hessa O; Rahman, Ishrat; Alhammadi, Munirah M; Albadari, Najah; Bin Break, Mohammed Khaled; Alghamdi, Sahar S; Aabed, Kawther

Design and synthesis of novel 4-aryl-2-benzoyl-imidazoles as colchicine binding site inhibitors.

设计和合成新型 4-芳基-2-苯甲酰基咪唑类化合物作为秋水仙碱结合位点抑制剂

Albadari Najah, Xie Yang, Wang Qinghui, Miller Darcie J, Gruntz Judith Quadrozzi, Oldham Michael L, Chen Hao, Ma Dejian, Wu Zhongzhi, Miller Duane D, Li Wei

Synthesis, in vitro and in silico studies of a novel chrysin-ferrocene Schiff base with potent anticancer activity via G1 arrest, caspase-dependent apoptosis and inhibition of topoisomerase II

本文合成了一种新型的芹菜素-二茂铁席夫碱,并通过体外和计算机模拟研究证实其具有强效抗癌活性,其作用机制包括G1期阻滞、caspase依赖性细胞凋亡以及拓扑异构酶II抑制。

Break, Mohammed Khaled Bin; Ansari, Siddique Akber; Katamesh, Ahmed A; Albadari, Najah; Alshammari, Maali D; Alkahtani, Hamad M

Targeting the MYCN-MDM2 pathways for cancer therapy: Are they druggable?

以 MYCN-MDM2 通路为靶点进行癌症治疗:它们是否可成药?

Wang, Wei; Du, Yi; Datta, Sayantap; Fowler, Josef F; Sang, Hannah T; Albadari, Najah; Li, Wei; Foster, Jennifer; Zhang, Ruiwen

MDM2 Inhibitors for Cancer Therapy: The Past, Present, and Future

MDM2抑制剂在癌症治疗中的应用:过去、现在和未来

Wang, Wei; Albadari, Najah; Du, Yi; Fowler, Josef F; Sang, Hannah T; Xian, Wa; McKeon, Frank; Li, Wei; Zhou, Jia; Zhang, Ruiwen

An MDM2 degrader shows potent cytotoxicity to MDM2-overexpressing acute lymphoblastic leukemia cells with minimal toxicity to normal cells/tissues

MDM2 降解剂对 MDM2 过表达的急性淋巴细胞白血病细胞表现出强效细胞毒性,而对正常细胞/组织的毒性极小

Tao Liu, Lubing Gu, Anna Mui, Zhongzhi Wu, Najah Albadari, Wei Li, Muxiang Zhou

Synthesis and biological evaluation of dual MDM2/XIAP inhibitors based on the tetrahydroquinoline scaffold

基于四氢喹啉骨架的双重 MDM2/XIAP 抑制剂的合成及生物学评价

Najah Albadari, Yang Xie, Tao Liu, Rui Wang, Lubing Gu, Muxiang Zhou, Zhongzhi Wu, Wei Li

Deciphering treatment resistance in metastatic colorectal cancer: roles of drug transports, EGFR mutations, and HGF/c-MET signaling

揭示转移性结直肠癌的治疗耐药机制:药物转运、EGFR突变和HGF/c-MET信号通路的作用

Albadari, Najah; Xie, Yang; Li, Wei

MYCN mRNA degradation and cancer suppression by a selective small-molecule inhibitor in MYCN-amplified neuroblastoma

MYCN 扩增神经母细胞瘤中选择性小分子抑制剂可降解 MYCN mRNA 并抑制癌症

Tao Liu, Lubing Gu, Zhongzhi Wu, Najah Albadari, Wei Li, Muxiang Zhou