scholarly journals Synthesis and biological evaluation of the ascidian blood-pigment halocyamine A

2017 ◽  
Vol 15 (29) ◽  
pp. 6194-6204 ◽  
Author(s):  
Hugo K. H. Fong ◽  
Jean Michel Brunel ◽  
Arlette Longeon ◽  
Marie-Lise Bourguet-Kondracki ◽  
David Barker ◽  
...  
Keyword(s):  
Natural Product ◽  
Biological Evaluation ◽  
Marine Natural Product ◽  
Synthesis And Biological Evaluation ◽  
Blood Pigment

The first synthesis of the (Z)-indolic enamide-containing antibacterial marine natural product halocyamine A is reported.

Synthesis and Biological Evaluation of a Focused Mixture Library of Analogues of the Antimitotic Marine Natural Product Curacin A

2000 ◽  
Vol 122 (39) ◽  
pp. 9391-9395 ◽  
Author(s):  
Peter Wipf ◽  
Jonathan T. Reeves ◽  
Raghavan Balachandran ◽  
Kenneth A. Giuliano ◽  
Ernest Hamel ◽  
...  
Keyword(s):  
Natural Product ◽  
Biological Evaluation ◽  
Marine Natural Product ◽  
Curacin A ◽  
Synthesis And Biological Evaluation

Synthesis and Biological Evaluation of the Antimicrobial Natural Product Lipoxazolidinone A

2018 ◽  
Author(s):  
Jonathan J. Mills ◽  
Kaylib R. Robinson ◽  
Troy E. Zehnder ◽  
Joshua G. Pierce
Keyword(s):  
Natural Products ◽  
Natural Product ◽  
Mechanism Of Action ◽  
Marine Natural Products ◽  
Biological Evaluation ◽  
Lead Compounds ◽  
Follow Up Studies ◽  
Initial Resistance ◽  
Synthesis And Biological Evaluation

The lipoxazolidinone family of marine natural products, with an unusual 4-oxazolidinone heterocycle at their core, represents a new scaffold for antimicrobial discovery; however, questions regarding their mechanism of action and high lipophilicity have likely slowed follow-up studies. Herein, we report the first synthesis of lipoxazolidinone A, 15 structural analogs to explore its active pharmacophore, and initial resistance and mechanism of action studies. These results suggest that 4-oxazolidinones are valuable scaffolds for antimicrobial development and reveal simplified lead compounds for further optimization.

Synthesis and biological evaluation of acylated oligorhamnoside derivatives structurally related to mezzettiaside-6 with cytotoxic activity

2016 ◽  
Vol 14 (28) ◽  
pp. 6691-6702 ◽  
Author(s):  
Gaopeng Song ◽  
Sumei Li ◽  
Zhiwei Lei ◽  
Yibin Li ◽  
Junhua Li ◽  
...  
Keyword(s):  
Cytotoxic Activity ◽  
Natural Product ◽  
Biological Evaluation ◽  
Synthesis And Biological Evaluation

Two partially acylated oligorhamnoside derivatives 1 and 2 structurally related to the natural product mezzettiaside-6 were synthesized via a ‘2 + 1 + 1’ convergent strategy.

Total synthesis and biological evaluation of the natural product (−)-cyclonerodiol, a new inhibitor of IL-4 signaling

2014 ◽  
Vol 12 (47) ◽  
pp. 9707-9715 ◽  
Author(s):  
Jens Langhanki ◽  
Kristina Rudolph ◽  
Gerhard Erkel ◽  
Till Opatz
Keyword(s):  
Total Synthesis ◽  
Natural Product ◽  
Specific Inhibitor ◽  
Biological Evaluation ◽  
Synthesis And Biological Evaluation

The sesquiterpene (−)-cyclonerodiol is a specific inhibitor of IL-4 induced STAT6 signaling and is readily available from (−)-linalool.

scholarly journals Synthesis and Biological Evaluation of Novel 2-Substituted ­Analogues of (–)-Pentenomycin I

Synlett ◽  
2020 ◽  
Vol 31 (05) ◽  
pp. 475-481
Author(s):  
Stavroula A. Zisopoulou ◽  
Spyridon Bousis ◽  
Jörg Haupenthal ◽  
Jennifer Herrmann ◽  
Rolf Müller ◽  
...  
Keyword(s):  
Natural Product ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Eukaryotic Cell ◽  
Biological Evaluation ◽  
Gram Positive Bacteria ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed ◽  
Synthesis And Biological Evaluation ◽  
Derivatives Of

A library of novel 2-substituted derivatives of the antibiotic natural product pentenomycin I is presented. The new collection of analogues is divided in two main classes, 2-alkynyl- and 2-aryl- derivatives, which are accessed by the appropriate type of palladium-catalyzed cross-coupling reaction of the 2-iodo-protected pentenomycin I with suitable nucleophiles. The new derivatives were tested for their activity against certain types of bacteria and one of them, compound 8h, was found to exhibit significant inhibitory activity against several Gram-positive bacteria but also displayed cytotoxic activity against eukaryotic cell lines.

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