Search Results - "Jiang, Hualiang"

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    Identification of pyrogallol as a warhead in design of covalent inhibitors for the SARS-CoV-2 3CL protease by Su, Haixia, Yao, Sheng, Zhao, Wenfeng, Zhang, Yumin, Liu, Jia, Shao, Qiang, Wang, Qingxing, Li, Minjun, Xie, Hang, Shang, Weijuan, Ke, Changqiang, Feng, Lu, Jiang, Xiangrui, Shen, Jingshan, Xiao, Gengfu, Jiang, Hualiang, Zhang, Leike, Ye, Yang, Xu, Yechun

    Published in Nature communications (15-06-2021)
    “…The ongoing pandemic of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) urgently needs an effective…”
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    Structural basis for inhibition of the SARS-CoV-2 RNA polymerase by suramin by Yin, Wanchao, Luan, Xiaodong, Li, Zhihai, Zhou, Ziwei, Wang, Qingxing, Gao, Minqi, Wang, Xiaoxi, Zhou, Fulai, Shi, Jingjing, You, Erli, Liu, Mingliang, Wang, Qingxia, Jiang, Yi, Jiang, Hualiang, Xiao, Gengfu, Zhang, Leike, Yu, Xuekui, Zhang, Shuyang, Eric Xu, H.

    Published in Nature structural & molecular biology (01-03-2021)
    “…The COVID-19 pandemic caused by nonstop infections of SARS-CoV-2 has continued to ravage many countries worldwide. Here we report that suramin, a 100-year-old…”
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    Rhodium(III)-Catalyzed Site-Selective C–H Alkylation and Arylation of Pyridones Using Organoboron Reagents by Peng, Panfeng, Wang, Jiang, Jiang, Hualiang, Liu, Hong

    Published in Organic letters (21-10-2016)
    “…In this study we developed a method for the pyridine-directed, rhodium-catalyzed, site-selective C–H alkylation and arylation of pyridones using commercially…”
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    Full-length human GLP-1 receptor structure without orthosteric ligands by Wu, Fan, Yang, Linlin, Hang, Kaini, Laursen, Mette, Wu, Lijie, Han, Gye Won, Ren, Qiansheng, Roed, Nikolaj Kulahin, Lin, Guangyao, Hanson, Michael A., Jiang, Hualiang, Wang, Ming-Wei, Reedtz-Runge, Steffen, Song, Gaojie, Stevens, Raymond C.

    Published in Nature communications (09-03-2020)
    “…Glucagon-like peptide-1 receptor (GLP-1R) is a class B G protein-coupled receptor that plays an important role in glucose homeostasis and treatment of type 2…”
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    Structural basis for allosteric, substrate-dependent stimulation of SIRT1 activity by resveratrol by Cao, Duanfang, Wang, Mingzhu, Qiu, Xiayang, Liu, Dongxiang, Jiang, Hualiang, Yang, Na, Xu, Rui-Ming

    Published in Genes & development (15-06-2015)
    “…Sirtuins with an extended N-terminal domain (NTD), represented by yeast Sir2 and human SIRT1, harbor intrinsic mechanisms for regulation of their NAD-dependent…”
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    Structural basis of leukotriene B4 receptor 1 activation by Wang, Na, He, Xinheng, Zhao, Jing, Jiang, Hualiang, Cheng, Xi, Xia, Yu, Eric Xu, H., He, Yuanzheng

    Published in Nature communications (03-03-2022)
    “…Leukotriene B4 receptor 1 (BLT1) plays crucial roles in the acute inflammatory responses and is a valuable target for anti-inflammation treatment, however, the…”
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    Crystal Structures of Membrane Transporter MmpL3, an Anti-TB Drug Target by Zhang, Bing, Li, Jun, Yang, Xiaolin, Wu, Lijie, Zhang, Jia, Yang, Yang, Zhao, Yao, Zhang, Lu, Yang, Xiuna, Yang, Xiaobao, Cheng, Xi, Liu, Zhijie, Jiang, Biao, Jiang, Hualiang, Guddat, Luke W., Yang, Haitao, Rao, Zihe

    Published in Cell (24-01-2019)
    “…Despite intensive efforts to discover highly effective treatments to eradicate tuberculosis (TB), it remains as a major threat to global human health. For this…”
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    SHAFTS: A Hybrid Approach for 3D Molecular Similarity Calculation. 1. Method and Assessment of Virtual Screening by Liu, Xiaofeng, Jiang, Hualiang, Li, Honglin

    “…We developed a novel approach called SHAFTS (SHApe-FeaTure Similarity) for 3D molecular similarity calculation and ligand-based virtual screening. SHAFTS…”
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    Low dose of hydroxychloroquine reduces fatality of critically ill patients with COVID-19 by Yu, Bo, Li, Chenze, Chen, Peng, Zhou, Ning, Wang, Luyun, Li, Jia, Jiang, Hualiang, Wang, Dao-Wen

    Published in Science China. Life sciences (01-10-2020)
    “…Coronavirus disease 2019 (COVID-19) is a pandemic with no specific drugs and high fatality. The most urgent need is to find effective treatments. We sought to…”
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    Discovery of Highly Potent, Selective, and Orally Efficacious p300/CBP Histone Acetyltransferases Inhibitors by Yang, Yaxi, Zhang, Rukang, Li, Zhaojun, Mei, Lianghe, Wan, Shili, Ding, Hong, Chen, Zhifeng, Xing, Jing, Feng, Huijin, Han, Jie, Jiang, Hualiang, Zheng, Mingyue, Luo, Cheng, Zhou, Bing

    Published in Journal of medicinal chemistry (13-02-2020)
    “…p300 and CREB-binding protein (CBP) are ubiquitously expressed pleiotropic lysine acetyltransferases and play a key role as transcriptional co-activators that…”
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    Discovery of the First-in-Class Agonist-Based SOS1 PROTACs Effective in Human Cancer Cells Harboring Various KRAS Mutations by Zhou, Chuan, Fan, Zisheng, Zhou, Zehui, Li, Yupeng, Cui, Rongrong, Liu, Chaoyi, Zhou, Guizhen, Diao, Xingxing, Jiang, Hualiang, Zheng, Mingyue, Zhang, Sulin, Xu, Tianfeng

    Published in Journal of medicinal chemistry (10-03-2022)
    “…Regulating SOS1 functions may result in targeted pan-KRAS therapies. Small-molecule SOS1 inhibitors showed promising anticancer potential, and the most…”
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    Molecular basis for allosteric agonism and G protein subtype selectivity of galanin receptors by Duan, Jia, Shen, Dan-Dan, Zhao, Tingting, Guo, Shimeng, He, Xinheng, Yin, Wanchao, Xu, Peiyu, Ji, Yujie, Chen, Li-Nan, Liu, Jinyu, Zhang, Huibing, Liu, Qiufeng, Shi, Yi, Cheng, Xi, Jiang, Hualiang, Eric Xu, H., Zhang, Yan, Xie, Xin, Jiang, Yi

    Published in Nature communications (15-03-2022)
    “…Peptide hormones and neuropeptides are complex signaling molecules that predominately function through G protein-coupled receptors (GPCRs). Two unanswered…”
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    Two disparate ligand-binding sites in the human P2Y1 receptor by Zhang, Dandan, Gao, Zhan-Guo, Zhang, Kaihua, Kiselev, Evgeny, Crane, Steven, Wang, Jiang, Paoletta, Silvia, Yi, Cuiying, Ma, Limin, Zhang, Wenru, Han, Gye Won, Liu, Hong, Cherezov, Vadim, Katritch, Vsevolod, Jiang, Hualiang, Stevens, Raymond C., Jacobson, Kenneth A., Zhao, Qiang, Wu, Beili

    Published in Nature (London) (16-04-2015)
    “…In response to adenosine 5′-diphosphate, the P2Y 1 receptor (P2Y 1 R) facilitates platelet aggregation, and thus serves as an important antithrombotic drug…”
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