Orthogonal Chemistry for the Synthesis of Thiocoraline–Triostin Hybrids. Exploring their Structure–Activity Relationship-Reference-Cited by-同舟云学术

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Orthogonal Chemistry for the Synthesis of Thiocoraline–Triostin Hybrids. Exploring their Structure–Activity Relationship

Published:2013-06-19 Issue:13 Volume:56 Page:5587-5600
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Tulla-Puche Judit¹²,Auriemma Sara¹,Falciani Chiara¹,Albericio Fernando¹²³⁴

Affiliation:

1. Institute for Research in Biomedicine Barcelona, Baldiri Reixac 10, 08028 Barcelona, Spain

2. CIBER-BBN, Networking Centre on Bioengineering, Biomaterials, and Nanomedicine, Baldiri Reixac 10, 08028 Barcelona

3. Department of Organic Chemistry, University of Barcelona, Martí i Franquès 1, 08028 Barcelona, Spain

4. University of KwaZulu Natal, 4001 Durban, South Africa

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm4006093

Reference46 articles.

1. Bisintercalator natural products with potential therapeutic applications: isolation, structure determination, synthetic and biological studies

2. Recent developments in bisintercalator natural products

3. BBM-928, a new antitumor antibiotic complex I. Production, isolation, characterization and antitumor activity.

4. BBM-928, a new antitumor antibiotic complex II. Taxonomic studies on the producing organism.

5. Quinoxapeptins: Novel Chromodepsipeptide Inhibitors of HIV-1 and HIV-2 Reverse Transcriptase. I. The Producing Organism and Biological Activity.

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5. Solid-Phase Synthesis of Biaryl Cyclic Lipopeptides Derived from Arylomycins;ACS Omega;2020-09-04

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