副教授
当前位置: 首页 >> 师资队伍 >> 教师队伍 >> 副教授 >> 正文
郭传龙
发布时间:2019-07-11    作者:      审核人:    点击:[]

化工学院教师介绍:郭传龙

                                               

个人简介

工作职位:化工学院药物化学教研室,副教授,硕士生导师

办公地址:青岛科技大学 CCF1021/1023(青岛市市北区郑州路53号)

招生专业:药学1007/1055

联系方式:gcl_cpu@126.comguochuanlong@qust.edu.cn

2019年获中国科学院海洋研究所海洋生物学专业博士学位,主要从事新型抗肿瘤药物研制与开发、活性化合物筛选及新型药物递送系统构建及应用。作为项目负责人,主持国家自然科学基金1项,山东省自然科学基金2项,参与国家自然科学基金项目3项。近五年,其中第一或通讯作者在J Med ChemEur J Med Chem等期刊发表SCI论文20余篇。

代表性论文(通讯或第一作者)

[1] Gao, Xintao et al. Regulation of Eukaryotic Translation Initiation Factor 4E as a Potential Anticancer Strategy. J Med Chem, 2023. (一区,通讯作者)

[2] Zhang, Qin et al. Design, synthesis and SAR of novel 7-azaindole derivatives as potential Erk5 kinase inhibitor with anticancer activity. Bioorg Med Chem, 2023. (二区,通讯作者)

[3] Gao, Xintao et al. Fucoidan-proanthocyanidins nanoparticles protect against cisplatin-induced acute kidney injury by activating mitophagy and inhibiting mtDNA-cGAS/STING signaling pathway. Int J Biol Macromol, 2023. (一区,通讯作者)

[4] Liu, Shuai et al. Silk fibroin peptide self-assembled nanofibers delivered naringenin to alleviate cisplatin-induced acute kidney injury by inhibiting mtDNA-cGAS-STING pathway. Food Chem Toxicol, 2023 (一区,通讯作者)

[5] Qi, Xueju et al. EGPI-1, a novel eIF4E/eIF4G interaction inhibitor, inhibits lung cancer cell growth and angiogenesis through Ras/MNK/ERK/eIF4E signaling pathway. Chem Biol Interact, 2022 (二区,通讯作者)

[6] Gao, Xintao et al. Fucoidan-ferulic acid nanoparticles alleviate cisplatin-induced acute kidney injury by inhibiting the cGAS-STING pathway. Int J Biol Macromol, 2022.(一区,通讯作者)

[7] Wu, Xiaochen et al. Novel poly (ADP-ribose) polymerases inhibitor DHC-1 exhibits in vitro and in vivo anticancer activity on BRCA-deficient pancreatic cancer cells. Food Chem Toxicol, 2021 (一区,通讯作者)

[8] Guo, Chuanlong et al. The ERK-MNK-eIF4F signaling pathway mediates TPDHT-induced A549 cell death in vitro and in vivo. Food Chem Toxicol, 2020(一区,第一作者)

[9] Guo, Chuanlong et al. BTH-8, a novel poly (ADP-ribose) polymerase-1 (PARP-1) inhibitor, causes DNA double-strand breaks and exhibits anticancer activities in vitro and in vivo. Int J Biol Macromol, 2020(一区,第一作者)

[10] Wang, Jun et al. Novel eIF4E/eIF4G protein-protein interaction inhibitors DDH-1 exhibits anti-cancer activity in vivo and in vitro. Int J Biol Macromol, 2020(一区,通讯作者)

[11] Guo, Chuanlong et al. Discovery of Novel Bromophenol-Thiosemicarbazone Hybrids as Potent Selective Inhibitors of Poly(ADP-ribose) Polymerase-1 (PARP-1) for Use in Cancer. J Med Chem, 2019(一区,第一作者)

[12] Wang, Lijun et al. Design, synthesis and biological evaluation of bromophenol-thiazolylhydrazone hybrids inhibiting the interaction of translation initiation factors eIF4E/eIF4G as multifunctional agents for cancer treatment. Eur J Med Chem, 2019(一区,第一作者)

承担的主要科研项目

[1] 2024.1-2026.12国家自然科学基金青年基金,主持,在研

[2] 2021.1-2023.12山东省自然科学基金青年基金,主持,在研。

[3] 2019.9-2024.8青岛科技大学人才启动经费。主持,在研

[4] 2023.1-2024.12中国科学院暨山东省实验海洋生物学重点实验室开放课题。主持,在研。

[5] 2015.7-2016.12山东省自然科学基金, ZR2015PH06。主持,已结题。



上一条:夏力
下一条:杜姗姗

Copyright 2019 版权所有:青岛科技大学化工学院   
鲁ICP备05001948号-1 鲁公网安备 37021202000007号 E-mail:jingcai@qust.edu.cn