Literature DB >> 26521648

Marine Bi-, Bis-, and Trisindole Alkaloids.

Clinton G L Veale1, Michael T Davies-Coleman2.   

Abstract

This chapter, covering the chemistry literature up until June 2013 and comprising 142 references, records the chemical structures of 130 bi-, bis-, and trisindole alkaloids isolated from a plethora of marine phyla including bacteria, algae, bryozoans, sponges, mollusks, hard corals, and ascidians. While the vast majority of bisindoles have been isolated from marine sponges, biindoles are more commonly found in red algae species than sponges. Trisindoles are far less common than bisindoles in the marine environment and have been limited to two species of sponge and a single species of marine microbe. Antimicrobial activity and cytotoxicity dominate the bioactivities explored for selected members of this family of alkaloids. Synthetic approaches to 28 natural products are presented in 33 schemes, and in the absence of any in vivo biosynthetic studies, the putative biosyntheses of eight bisindole metabolites are presented.
© 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Alkaloids; Aplysinopsin; Biindole; Bisindole; Caulerpin; Marine; Trisindole

Year:  2013        PMID: 26521648     DOI: 10.1016/B978-0-12-411565-1.00001-9

Source DB:  PubMed          Journal:  Alkaloids Chem Biol        ISSN: 1099-4831


  1 in total

1.  A Mild and General Larock Indolization Protocol for the Preparation of Unnatural Tryptophans.

Authors:  Kangway V Chuang; Madeleine E Kieffer; Sarah E Reisman
Journal:  Org Lett       Date:  2016-09-06       Impact factor: 6.005

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.