Suzuki coupling-based synthesis of VATPase inhibitor archazolid natural product derived fragments
Author:
Affiliation:
1. Department of Chemistry
2. Western Washington University
3. Bellingham
4. USA 98229
5. Department of Biology
Abstract
An archazolid natural product fragment that displays dose-dependent inhibition of the vacuolar-type ATPase (VATPase) has been synthesized by a high-yielding Suzuki coupling of two complex subunits.
Funder
Camille and Henry Dreyfus Foundation
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/RA/C9RA07050H
Reference35 articles.
1. Synthesis of the C1–C23 Fragment of the Archazolids and Evidence for V-ATPase but not COX Inhibitory Activity
2. V-ATPase inhibition overcomes trastuzumab resistance in breast cancer
3. Up-regulation of cholesterol associated genes as novel resistance mechanism in glioblastoma cells in response to archazolid B
4. Anti-leukemic effects of the V-ATPase inhibitor Archazolid A
5. Vacuolar-ATPase Inhibition Blocks Iron Metabolism to Mediate Therapeutic Effects in Breast Cancer
Cited by 2 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. Modular Total Synthesis of iso-Archazolids and Archazologs;The Journal of Organic Chemistry;2021-07-23
2. Correction: Suzuki coupling-based synthesis of VATPase inhibitor archazolid natural product derived fragments;RSC Advances;2019
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