Design, synthesis and in vitro activity of phidianidine B derivatives as novel PTP1B inhibitors with specific selectivity-Reference-Cited by-同舟云学术

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Design, synthesis and in vitro activity of phidianidine B derivatives as novel PTP1B inhibitors with specific selectivity

Published:2016-02 Issue:3 Volume:26 Page:778-781
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Zhang Li,Jiang Cheng-Shi,Gao Li-Xin,Gong Jing-Xu,Wang Zhong-Hua,Li Jing-Ya,Li Jia,Li Xu-Wen,Guo Yue-Wei

Funder

National Marine “863” Projects

Natural Science Foundation of China

SCTSM Project

NSFC Shandong Joint Fund

SKLDR/SIMM Projects

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference20 articles.

1. Protein kinases and phosphatases: The Yin and Yang of protein phosphorylation and signaling

2. Regulation of receptor tyrosine kinase signaling by protein tyrosine phosphatases

3. Protein tyrosine phosphatases: their role in insulin action and potential as drug targets

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1. Design and synthesis of some new imidazole-morpholine-1,2,4-oxadiazole hybrids as EGFR targeting in vitro anti-breast cancer agents;Journal of Molecular Structure;2024-08

2. Structural and molecular insights of protein tyrosine phosphatase 1B (PTP1B) and its inhibitors as anti-diabetic agents;Journal of Molecular Structure;2023-12

3. Synthesis of Indole-1,3,4-oxadiazole Based Sulfonyl 1,2,4-Oxadiazole Derivatives as EGFR Targeting Anticancer Agents;Russian Journal of General Chemistry;2023-11

4. Discovery of marine phidianidine-based Nrf2 activators and their potential against oxLDL- and HG-induced injury in HUVECs;Bioorganic & Medicinal Chemistry Letters;2023-10

5. Anti-Proliferative, Anti-EGFR and In Silico Studies of a Series of New Imidazole Tethered 1,2,4-Oxadiazoles;Polycyclic Aromatic Compounds;2023-09-19

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