Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Miaobo Pan"'
Autor:
Miaobo Pan, Gabriela Morán Cruz, Chloé Grazon, Djamila Kechkeche, Ludivine Houel Renault, Gilles Clavier, Rachel Méallet-Renault
Publikováno v:
ACS Applied Polymer Materials. 4:5482-5492
Autor:
Ananya Sathanikan, Jorge Bañuls-Ciscar, Fadwa Kamal, Damien Prim, Frédéric Guittard, Anne Gaucher, Talia Bsaibess, Giacomo Ceccone, Rachel Méallet-Renault, Sonia Amigoni, Thierry Darmanin, Miaobo Pan, Pascal Colpo
Publikováno v:
Journal of Colloid and Interface Science
Journal of Colloid and Interface Science, Elsevier, 2022, 606, pp.236-247. ⟨10.1016/j.jcis.2021.08.013⟩
Journal of Colloid and Interface Science, Elsevier, 2022, 606, pp.236-247. ⟨10.1016/j.jcis.2021.08.013⟩
Hypothesis In this original work, we aim to control both the surface wetting and fluorescence properties of extremely ordered and porous conducting polymer nanotubes prepared by soft template electropolymerization and post-grafting. For reaching this
Autor:
Davy-Louis Versace, Thi-Thanh-Tam Nguyen, Daniel Grande, Annalisa Chiapionne, Steffen Jockusch, Pauline Sautrot-Ba, Rachel Méallet-Renault, Samir Abbad-Andaloussi, Miaobo Pan
Publikováno v:
European Polymer Journal
European Polymer Journal, Elsevier, 2020, 138, pp.109936. ⟨10.1016/j.eurpolymj.2020.109936⟩
European Polymer Journal, Elsevier, 2020, 138, pp.109936. ⟨10.1016/j.eurpolymj.2020.109936⟩
International audience; A new photoactivable material based on polyethylene imine with allyl functions (A-PEI monomer) was synthesized to develop new hydrogel. The water-based photoinitiating system consisting of anthraquinone-2-sulfonic acid (AQS) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::798ee5f6936781d0a60056cb3dc40f00
https://hal.archives-ouvertes.fr/hal-02925552/file/VERSACE_Eur_Polym_J_28072020_SJ_DLV_Final.pdf
https://hal.archives-ouvertes.fr/hal-02925552/file/VERSACE_Eur_Polym_J_28072020_SJ_DLV_Final.pdf
Autor:
Huilan Li, Xinzhou Bi, Wenlong Huang, Yuxuan Dai, Xin Su, Cai Xingguang, Miaobo Pan, Hai Qian, Wei Shi, Haiyan Lin
Publikováno v:
Amino Acids. 49:1601-1610
Host defense peptides have been demonstrated to exhibit prominent advantages in cancer therapy with selective binding ability toward tumor cells via electrostatic attractions, which can overcome the limitations of traditional chemotherapy drugs, such
Autor:
Zheng Li, Jian Cui, Wei Shi, Hai Qian, Qianqian Qiu, Miaobo Pan, Yuxuan Dai, Wenlong Huang, Bo Zhang
Publikováno v:
Journal of Medicinal Chemistry. 60:2930-2943
Overexpression of the ATP-binding cassette (ABC) transport proteins, like ABCB1, commonly referred to as P-glycoprotein (P-gp), initiates active efflux of a broad spectrum of unrelated chemotherapeutic drugs in structure and function, leading to chem
Publikováno v:
Chemical Biology & Drug Design. 90:167-174
A novel mitochondria-targeting fluorescent probe compound S-N3 for hydrogen sulfide (H2S) in living cells has been designed and synthesized in this study. This article contained the chemosynthesis and some studies on bioactivity of the target compoun
Autor:
Qianqian Qiu, Mutta Kairuki, Qifei Li, Hai Qian, Wenlong Huang, Hesham Ghaleb, Miaobo Pan, Jiaqi Zhou, Cheng Jiang
Publikováno v:
Bioorganicmedicinal chemistry. 27(15)
Multidrug resistance (MDR) refers to the cross-resistance of cancer cells to one drug, accompanied by other drugs with different mechanisms and structures, which is one of the main obstacles of clinical chemotherapy. Overexpression of P-glycoprotein
Autor:
Yuxuan Dai, Hai Qian, Jian Cui, Qianqian Qiu, Wenlong Huang, Miaobo Pan, Baomin Liu, Wu Yuxiang, Wei Shi
Publikováno v:
Bioorganic & Medicinal Chemistry. 24:2287-2297
A novel series of P-glycoprotein (P-gp)-mediated multidrug resistance (MDR) inhibitors with triazol-N-phenethyl-tetrahydroisoquinoline or triazol-N-ethyl-tetrahydroisoquinoline scaffold were designed and synthesized via click chemistry. Most of the s
Autor:
Wenlong Huang, Cai Xingguang, Wei Shi, Miaobo Pan, Xin Su, Mian Fu, Yuxuan Dai, Zheng Li, Hai Qian
Publikováno v:
Bioorganic & Medicinal Chemistry. 24:1981-1987
The free fatty acid receptor 1 (FFA1) has gained significant interest as a novel antidiabetic target. Most of FFA1 agonists reported in the literature bearing a common biphenyl scaffold, which was crucial for toxicity verified by the researchers of D
Autor:
Yuxuan Dai, Hai Qian, Miaobo Pan, Bo Zhang, Jie Zhou, Wenlong Huang, Qianqian Qiu, Tianxiao Zhao
Publikováno v:
RSC Advances. 6:25819-25828
We designed and synthesized a novel series of P-glycoprotein (P-gp)-mediated multidrug resistance (MDR) inhibitors bearing a triazolphenethyl–tetrahydroisoquinoline scaffold through click chemistry. Then those synthesized compounds were tested on d