Literature DB >> 16753777

Manoalide derivatives from a sponge, Luffariella sp.

Guang-Xiong Zhou1, Tadeusz F Molinski.   

Abstract

A new derivative of manoalide, 24-n-propyl-O-manoalide (1) together with manoalide (4) and four known derivatives (2, 3, 5, 6) were isolated from the methanolic extract of a sponge. Their structures were elucidated on the basis of spectroscopic method. All the compounds showed significant cytotoxicity against HCT-116 cell line by MTS assay. Secomanoalide indicated antifungal activity on fungal lines Candida glabrata,Candida krusei and Candida albicans by invitro antibiotic assay.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16753777     DOI: 10.1080/10286020500246022

Source DB:  PubMed          Journal:  J Asian Nat Prod Res        ISSN: 1028-6020            Impact factor:   1.569


  4 in total

Review 1.  Marine pharmacology in 2005-2006: antitumour and cytotoxic compounds.

Authors:  Alejandro M S Mayer; Kirk R Gustafson
Journal:  Eur J Cancer       Date:  2008-08-11       Impact factor: 9.162

Review 2.  Targeting cancer with sesterterpenoids: the new potential antitumor drugs.

Authors:  Caiguo Zhang; Yan Liu
Journal:  J Nat Med       Date:  2015-04-19       Impact factor: 2.343

3.  Cacolides: Sesterterpene Butenolides from a Southern Australian Marine Sponge, Cacospongia sp.

Authors:  Shamsunnahar Khushi; Laizuman Nahar; Angela A Salim; Robert J Capon
Journal:  Mar Drugs       Date:  2018-11-20       Impact factor: 5.118

4.  24-O-ethylmanoalide, a manoalide-related sesterterpene from the marine sponge Luffariella cf. variabilis.

Authors:  Anne Gauvin-Bialecki; Maurice Aknin; Jacqueline Smadja
Journal:  Molecules       Date:  2008-12-15       Impact factor: 4.411

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.