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ACS Medicinal Chemistry Letters
|
February 18, 2026
Design, Synthesis, and Structure-Activity Relationship Studies of 7<i>H</i>‑Pyrrolo[2,3‑<i>d</i>]pyrimidine Derivatives as Potent Casein Kinase 1α (CK1α) Inhibitors
Meiying Liu, Yutong Tu, Wangyang Xu, et al.
Organic Letters
|
February 12, 2026
Construction of PROTAC Library via Liquid-Phase Synthesis Enabled by a Hydrophobic Tag
Yifeng Zhou, Wei He, Zehui Zhou, et al.
Talanta
|
April 17, 2026
Applications of bioorthogonal reactions in bioimaging
Weihua Zhuang, Yanfei Xu, Xiyong Zhuo, et al.
International Immunopharmacology
|
December 14, 2025
Targeting Cbl-b by a small molecular inhibitor potentiates T cell receptor signaling and suggests rational combination strategies
Yuantong Li, Haotian Tang, Wenhao Shi, et al.
Lab on a Chip
|
January 30, 2026
Lab-on-a-chip for biomarker detection: advances, practical applications, and future perspectives
Tianfeng Xu, Hao Bai, Jie Hu, et al.
Gland Surgery
|
April 13, 2026
Novel triple-drug regimen for preoperative optimization in giant Graves' disease: a prospective efficacy and safety trial
Tianfeng Xu, Xun Zheng, Yujie Zhang, et al.
Journal of Medicinal Chemistry
|
October 16, 2013
Design, synthesis, and biological evaluation of 2-oxo-3,4-dihydropyrimido[4,5-d]pyrimidinyl derivatives as new irreversible epidermal growth factor receptor inhibitors with improved pharmacokinetic properties
Shilin Xu, Tianfeng Xu, Lianwen Zhang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
August 11, 2025
M2c Macrophages Mediate YAP1 to Promote Vascularized Bone Regeneration in Distraction Osteogenesis
Haifeng Liu, Kai Liu, Yinyv Shang, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 20, 2022
Design, synthesis and structure-activity relationship studies of pyrido[2,3-d]pyrimidin-7-ones as potent Janus Kinase 3 (JAK3) covalent inhibitors
Wenhong Su, Zhiwen Chen, Meiying Liu, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 7, 2024
Design, synthesis, and bioevaluation of SOS1 PROTACs derived from pyrido[2,3-d]pyrimidin-7-one-based SOS1 inhibitor
Kun Wang, Zehui Zhou, Xinyi Ma, et al.
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Showing results (21-30 of 51) with videos related to
Sort By:
Page
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ACS Medicinal Chemistry Letters
|
February 18, 2026
Design, Synthesis, and Structure-Activity Relationship Studies of 7<i>H</i>‑Pyrrolo[2,3‑<i>d</i>]pyrimidine Derivatives as Potent Casein Kinase 1α (CK1α) Inhibitors
Meiying Liu, Yutong Tu, Wangyang Xu, et al.
Organic Letters
|
February 12, 2026
Construction of PROTAC Library via Liquid-Phase Synthesis Enabled by a Hydrophobic Tag
Yifeng Zhou, Wei He, Zehui Zhou, et al.
Talanta
|
April 17, 2026
Applications of bioorthogonal reactions in bioimaging
Weihua Zhuang, Yanfei Xu, Xiyong Zhuo, et al.
International Immunopharmacology
|
December 14, 2025
Targeting Cbl-b by a small molecular inhibitor potentiates T cell receptor signaling and suggests rational combination strategies
Yuantong Li, Haotian Tang, Wenhao Shi, et al.
Lab on a Chip
|
January 30, 2026
Lab-on-a-chip for biomarker detection: advances, practical applications, and future perspectives
Tianfeng Xu, Hao Bai, Jie Hu, et al.
Gland Surgery
|
April 13, 2026
Novel triple-drug regimen for preoperative optimization in giant Graves' disease: a prospective efficacy and safety trial
Tianfeng Xu, Xun Zheng, Yujie Zhang, et al.
Journal of Medicinal Chemistry
|
October 16, 2013
Design, synthesis, and biological evaluation of 2-oxo-3,4-dihydropyrimido[4,5-d]pyrimidinyl derivatives as new irreversible epidermal growth factor receptor inhibitors with improved pharmacokinetic properties
Shilin Xu, Tianfeng Xu, Lianwen Zhang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
August 11, 2025
M2c Macrophages Mediate YAP1 to Promote Vascularized Bone Regeneration in Distraction Osteogenesis
Haifeng Liu, Kai Liu, Yinyv Shang, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 20, 2022
Design, synthesis and structure-activity relationship studies of pyrido[2,3-d]pyrimidin-7-ones as potent Janus Kinase 3 (JAK3) covalent inhibitors
Wenhong Su, Zhiwen Chen, Meiying Liu, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 7, 2024
Design, synthesis, and bioevaluation of SOS1 PROTACs derived from pyrido[2,3-d]pyrimidin-7-one-based SOS1 inhibitor
Kun Wang, Zehui Zhou, Xinyi Ma, et al.
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of 6