Synthesis and Biological Activities of Aplyronine A Analogues toward the Development of Antitumor Protein–Protein Interaction Inducers between Actin and Tubulin: Conjugation of the C1–C9 Macrolactone Part and the C24–C34 Side Chain
Author:
Affiliation:
1. Graduate School of Pure and Applied Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8571, Japan
2. Graduate School of Bioagricultural Sciences, Nagoya University, Furo-cho, Chikusa, Nagoya 464-8601, Japan
Funder
Naito Foundation
Program on Open Innovation Platform with Enterprises, Research Institute and Academia
Japan Society for the Promotion of Science
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acsomega.9b01099
Reference59 articles.
1. Bovens, S.; Ottmann, C. In Chemical Biology: Learning through Case Studies; Waldmann, H., Jannig, P., Eds. Wiley-VCH Verlag GmbH: Weinheim, 2009; pp 105–119.
2. Marine natural products that interfere with multiple cytoskeletal protein interactions
3. Aplyronine A, a potent antitumor substance and the congeners aplyronines B and C isolated from the sea hare Aplysia kurodai
4. Further studies on aplyronine A, an antitumor substance isolated from the sea hare Aplysia kurodai
5. Studies on the stereochemistry of aplyronine A: Determination of the stereochemistry of the C21C34 fragment
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