Ying Yao
Shanghai Jiao Tong University
8 Papers
36 Citations
Ying Yao is an academic researcher from Shanghai Jiao Tong University. The author has contributed to research in topics: Chemistry & Medicine. The author has an hindex of 1, co-authored 1 publications.
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Papers
Synthesis of glycoconjugated poly(amindoamine) dendrimers for targeting human liver cancer cells
Rui Guo,Ying Yao,Guangcun Cheng,Su He Wang,Yong Li,Mingwu Shen,Yuehua Zhang,James R. Baker,Jianhua Wang,Xiangyang Shi +9 more
TL;DR: Amine-terminated generation 5 poly(amidoamine) dendrimers were utilized as a platform to conjugate fluorescein isothiocyanate and lactobionic acid, which enabled effective targeting to human liver cancer cells (HepG2) in vitro.
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The structural pathology for hypophosphatasia caused by malfunctional tissue non-specific alkaline phosphatase
Kewei Rong,Deqiang Yao,Qing Zhang,Xiankun Cao,Bing Rao,Ying Xia,Yi Lu,Yafeng Shen,Ying Yao,Hongtao Xu,Peixiang Ma,Yu Cao,An Qin +12 more
TL;DR: In this article , the crystal structures of human non-specific alkaline phosphatase (TNAP) were determined at near-atomic resolution and mapped the major pathogenic mutations onto the structure.
Metal‐Free and Open‐Air Arylation Reactions of Diaryliodonium Salts for DNA‐Encoded Library Synthesis (Adv. Sci. 26/2022)
Hongtao Xu,Tingting Tan,Yi-Ying Zhang,Yan Wang,Kangyin Pan,Ying Yao,Shuning Zhang,Yuang Gu,Wanting Chen,Jie Li,Hewei Dong,Yu Meng,Peixiang Ma,Wei Hou,Guangsheng Yang +14 more
TL;DR: Xu et al. as discussed by the authors developed the first on-DNA meeting diaryliodonium salts (DAI) chemistry and realized the selective arylation of phenols and oximes with both high yield and DNA fidelity via substrate activation strategy.
Metal‐Free and Open‐Air Arylation Reactions of Diaryliodonium Salts for DNA‐Encoded Library Synthesis
Hongtao Xu,Tingting Tan,Yi-Ying Zhang,Yan Wang,Kangyin Pan,Ying Yao,Shuning Zhang,Yuang Gu,Wanting Chen,Jie Li,Hewei Dong,Yu Meng,Peixiang Ma,Wei Hou,Guang Yang +14 more
TL;DR: The use of “substrate activation” approach to address the arylation of DNA‐conjugated phenols is described and the new on‐DNA diaryliodonium salts chemistry affords a greater flexibility in DEL design and synthesis.
A Small Molecule Selected from a DNA‐Encoded Library of Natural Products That Binds to TNF‐α and Attenuates Inflammation In Vivo (Adv. Sci. 21/2022)
Shuyue Wang,Xiaojie Shi,Jie Li,Qianping Huang,Qun Ji,Ying Yao,Tao Wang,Lili Liu,Min Ye,Yun Deng,Peixiang Ma,Hongtao Xu,Guang Yang +12 more
TL;DR: The nDEL hit, kaempferol, represents a novel chemical scaffold capable of specifically recognizing TNF‐α and blocking its signal transduction, a promising starting point for the development of a small molecule TNF-α inhibitor for use in the clinical setting.