Structure–activity relationship in the antitumor activity of 6-, 8- or 6,8-substituted 3-benzylamino-β-carboline derivatives-Reference-Cited by-同舟云学术

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Structure–activity relationship in the antitumor activity of 6-, 8- or 6,8-substituted 3-benzylamino-β-carboline derivatives

Published:2012-05 Issue:10 Volume:22 Page:3506-3515
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Ikeda Reiko,Kimura Takanori,Tsutsumi Tatsuya,Tamura Syunsuke,Sakai Norio,Konakahara Takeo

Publisher

Elsevier BV

Subject

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

Reference15 articles.

1. β-Carboline Alkaloids: Biochemical and Pharmacological Functions

2. Human monoamine oxidase is inhibited by tobacco smoke: β-carboline alkaloids act as potent and reversible inhibitors

3. In vitro bioactivation of N -hydroxy-2-amino-α-carboline

4. Novel N-(3-carboxyl-9-benzylcarboline-1-yl)ethylamino acids: synthesis, anti-proliferation activity and two-step-course of intercalation with calf thymus DNA

5. Synthesis and biological evaluation of DNA targeting flexible side-chain substituted β-carboline derivatives

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