Literature DB >> 17067167

Phenolic marine natural products as aldose reductase inhibitors.

Sonia Manzanaro1, Javier Salva, Jesús Angel de la Fuente.   

Abstract

Four different types of marine natural compounds isolated from tunicates were found to inhibit human aldose reductase. They all are characterized by a heterocyclic system, and at least two phenolic groups are present in the structure. Two of the compounds tested showed an inhibitory potency 5/6-fold higher than that of the known AR inhibitor sorbinil. One notable structural feature of these active compounds is the lack of either the carboxylic acid or the spiro-hydantoin commonly present in the principal classes of currently used inhibitors.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 17067167     DOI: 10.1021/np0503698

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  13 in total

Review 1.  Advancements in tetronic acid chemistry. Part 2: Use as a simple precursor to privileged heterocyclic motifs.

Authors:  Moaz M Abdou; Rasha A El-Saeed; Khaled M Elattar; Zeynel Seferoğlu; John Boukouvalas
Journal:  Mol Divers       Date:  2016-06-27       Impact factor: 2.943

2.  Antimicrobial rubrolides from a South African species of Synoicum tunicate.

Authors:  Justyna Sikorska; Shirley Parker-Nance; Michael T Davies-Coleman; Oliver B Vining; Aleksandra E Sikora; Kerry L McPhail
Journal:  J Nat Prod       Date:  2012-10-02       Impact factor: 4.050

Review 3.  Lamellarins and related pyrrole-derived alkaloids from marine organisms.

Authors:  Hui Fan; Jiangnan Peng; Mark T Hamann; Jin-Feng Hu
Journal:  Chem Rev       Date:  2007-12-21       Impact factor: 60.622

Review 4.  Marine pharmacology in 2005-6: Marine compounds with anthelmintic, antibacterial, anticoagulant, antifungal, anti-inflammatory, antimalarial, antiprotozoal, antituberculosis, and antiviral activities; affecting the cardiovascular, immune and nervous systems, and other miscellaneous mechanisms of action.

Authors:  Alejandro M S Mayer; Abimael D Rodríguez; Roberto G S Berlinck; Mark T Hamann
Journal:  Biochim Biophys Acta       Date:  2009-03-19

5.  2-(N-Phenyl-methane-sulfonamido)-ethyl 1H-pyrrole-2-carboxyl-ate.

Authors:  Salman Tariq Khan; Peng Yu; Aisha Nelofar; Zaheer Ahmed; Suchada Chantrapromma
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-04-13

6.  Molecular Insight into Gene Response of Diorcinol- and Rubrolide-Treated Biofilms of the Emerging Pathogen Stenotrophomonas maltophilia.

Authors:  Mirja Gudzuhn; Ifey Alio; Raphael Moll; Jessica de Vries; Jacob Boehlich; Maik Assmann; Jasmin Janneschütz; Nina Schützenmeister; Axel Himmelbach; Anja Poehlein; Rolf Daniel; Wolfgang R Streit
Journal:  Microbiol Spectr       Date:  2022-04-26

7.  Esculetin, a Coumarin Derivative, Inhibits Aldose Reductase Activity in vitro and Cataractogenesis in Galactose-Fed Rats.

Authors:  Chan-Sik Kim; Junghyun Kim; Yun Mi Lee; Eunjin Sohn; Jin Sook Kim
Journal:  Biomol Ther (Seoul)       Date:  2016-03-01       Impact factor: 4.634

8.  Gold-catalyzed formation of pyrrolo- and indolo-oxazin-1-one derivatives: The key structure of some marine natural products.

Authors:  Sultan Taskaya; Nurettin Menges; Metin Balci
Journal:  Beilstein J Org Chem       Date:  2015-05-28       Impact factor: 2.883

Review 9.  Natural Products Diversity of Marine Ascidians (Tunicates; Ascidiacea) and Successful Drugs in Clinical Development.

Authors:  Satheesh Kumar Palanisamy; N M Rajendran; Angela Marino
Journal:  Nat Prod Bioprospect       Date:  2017-01-17

10.  Inhibitory effects of Colocasia esculenta (L.) Schott constituents on aldose reductase.

Authors:  Hong Mei Li; Seung Hwan Hwang; Beom Goo Kang; Jae Seung Hong; Soon Sung Lim
Journal:  Molecules       Date:  2014-08-27       Impact factor: 4.411

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.