Synthesis and evaluation of 9-O-substituted berberine derivatives containing aza-aromatic terminal group as highly selective telomeric G-quadruplex stabilizing ligands-Reference-Cited by-同舟云学术

Synthesis and evaluation of 9-O-substituted berberine derivatives containing aza-aromatic terminal group as highly selective telomeric G-quadruplex stabilizing ligands

Published:2009-07 Issue:13 Volume:19 Page:3414-3417
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Ma Yan,Ou Tian-Miao,Tan Jia-Heng,Hou Jin-Qiang,Huang Shi-Liang,Gu Lian-Quan,Huang Zhi-Shu

Publisher

Elsevier BV

Subject

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

Reference25 articles.

1. Specific Association of Human Telomerase Activity with Immortal Cells and Cancer

2. Tri- and tetra-substituted naphthalene diimides as potent G-quadruplex ligands

3. Telomerase Maintains Telomere Structure in Normal Human Cells

4. The structure of telomeric DNA

5. 5-N-Methylated Quindoline Derivatives as Telomeric G-Quadruplex Stabilizing Ligands: Effects of 5-NPositive Charge on Quadruplex Binding Affinity and Cell Proliferation

Cited by 73 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Current development and structure–activity relationship study of berberine derivatives;Bioorganic & Medicinal Chemistry;2024-10

2. Recent advances in glycoside hydrolase family 20 and 84 inhibitors: Structures, inhibitory mechanisms and biological activities;Bioorganic Chemistry;2024-01

3. RhIII-catalyzed synthesis and investigation of the DNA-binding properties of 11- and 13-substituted berberine derivatives;Arkivoc;2023-12-23

4. Design and Synthesis of Xanthone Analogues Conjugated with Aza‐aromatic Substituents as Promising G‐Quadruplex Stabilizing Ligands and their Selective Cancer Cell Cytotoxic Action;ChemBioChem;2023-01-17

5. Structural modifications of berberine and their binding effects towards polymorphic deoxyribonucleic acid structures: A review;Frontiers in Pharmacology;2022-08-09