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S
Silong Zhang
H-index:17
Citation Count:795
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Design of fibroblast growth factor receptor (FGFR) inhibitors containing a 3,4-dihydropyrido[4,3-d]pyrimidin-2(1H)-one motif
含3,4-二氢吡啶并[4,3-d]嘧啶-2(1H)-酮基序的成纤维细胞生长因子受体(FGFR)抑制剂的分子设计
Development of a Scalable Manufacturing Process for Kv1.3 Antagonist LY3972406 Hemiglutarate Hemihydrate
Kv1.3拮抗剂LY3972406半戊二酸盐半水合物可扩展制造工艺的开发
Dual inhibition of ERα/NF-κB pathways coupled with sonodynamic therapy via a multifunctional AIEgen
通过多功能AIEgen实现ERα/NF-κB通路的协同抑制与声动力疗法的耦合。
Effect of Ti layer on deformation ability and damage mechanism of diamond-like carbon coated aluminum alloy
Ti层对类金刚石碳涂层铝合金的变形能力及损伤机制的影响
Vacuum
IF3.9
Design of pyrrolo[2; 3-d]pyrimidine-endoperoxide hybrids as first-in-class dual degraders of cyclin D1/3 and CDK4/6 with potent antiproliferative effects
设计作为第一类细胞周期蛋白D1/3和CDK4/6双降解剂的吡咯并[2; 3-d]嘧啶-内过氧化物杂合物的抗增殖效应研究
Org. Biomol. Chem.
IF2.7
Design of photoactivatable methylene blue-bufalin conjugate for GPX4-targeted degradation to induce ferroptosis-like death in breast cancer therapy
设计一种光激活亚甲蓝-华法林偶联物，用于GPX4靶向降解以诱导乳腺癌治疗中的铁死亡样细胞死亡
Bioorganic Chemistry
IF4.7
Design and synthesis of stilbene analogs based on resveratrol as NF-κB inhibitors for the treatment of breast cancer
基于白藜芦醇的 stilbene 类似物的设计与合成，作为 NF-κB 抑制剂用于乳腺癌治疗
MOLECULAR DIVERSITY
IF3.8
