Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 148

2.

Halogenated metabolites from Japanese Laurencia spp.

Suzuki M, Kawamoto T, Vairappan CS, Ishii T, Abe T, Masuda M.

Phytochemistry. 2005 Dec;66(23):2787-93. Epub 2005 Sep 23.

PMID:
16183086
3.

Halogenated terpenes and a C(15)-acetogenin from the marine red alga Laurencia saitoi.

Ji NY, Li XM, Wang BG.

Molecules. 2008 Nov 20;13(11):2894-9. doi: 10.3390/molecules13112894.

4.

Proof-of-principle direct double cyclisation of a linear C15-precursor to a dibrominated bicyclic medium-ring ether relevant to Laurencia species.

Braddock DC, Sbircea DT.

Chem Commun (Camb). 2014 Oct 28;50(84):12691-3. doi: 10.1039/c4cc06402j.

PMID:
25211263
5.

Halogenated secondary metabolites from Laurencia obtusa.

Aydoğmuş Z, Imre S, Ersoy L, Wray V.

Nat Prod Res. 2004 Feb;18(1):43-9.

PMID:
14974617
6.

Nonterpenoid C15 acetogenins from Laurencia marilzae.

Gutiérrez-Cepeda A, Fernández JJ, Gil LV, López-Rodríguez M, Norte M, Souto ML.

J Nat Prod. 2011 Mar 25;74(3):441-8. doi: 10.1021/np100866g. Epub 2011 Feb 21.

PMID:
21338119
7.

Sesquiterpenes and acetogenins from the marine red alga Laurencia okamurai.

Li XD, Miao FP, Li K, Ji NY.

Fitoterapia. 2012 Apr;83(3):518-22. doi: 10.1016/j.fitote.2011.12.018. Epub 2011 Dec 30.

PMID:
22233863
8.

Halogenated diterpenoids from the red alga Laurencia nipponica.

Lyakhova EG, Kalinovsky AI, Kolesnikova SA, Vaskovsky VE, Stonik VA.

Phytochemistry. 2004 Sep;65(18):2527-32.

PMID:
15451311
9.

Laurendecumallenes A-B and laurendecumenynes A-B, halogenated nonterpenoid C(15)-acetogenins from the marine red alga Laurencia decumbens.

Ji NY, Li XM, Li K, Wang BG.

J Nat Prod. 2007 Sep;70(9):1499-502. Epub 2007 Aug 22. Erratum in: J Nat Prod. 2010 Jun 25;73(6):1192.

PMID:
17711344
10.

Halogenated metabolites with antibacterial activity from the Okinawan Laurencia species.

Vairappan CS, Suzuki M, Abe T, Masuda M.

Phytochemistry. 2001 Oct;58(3):517-23.

PMID:
11557086
11.

A general strategy for the stereocontrolled preparation of diverse 8- and 9-membered Laurencia-type bromoethers.

Snyder SA, Treitler DS, Brucks AP, Sattler W.

J Am Chem Soc. 2011 Oct 12;133(40):15898-901. doi: 10.1021/ja2069449. Epub 2011 Sep 16.

PMID:
21919540
12.

Tetrahydrofuran acetogenins from Laurencia glandulifera.

Kladi M, Vagias C, Papazafiri P, Brogi S, Tafi A, Roussis V.

J Nat Prod. 2009 Feb 27;72(2):190-3. doi: 10.1021/np800481w.

PMID:
19138151
13.

Diterpenes, sesquiterpenes, and a C15-acetogenin from the marine red alga Laurencia mariannensis.

Ji NY, Li XM, Li K, Ding LP, Gloer JB, Wang BG.

J Nat Prod. 2007 Dec;70(12):1901-5. Epub 2007 Dec 13.

PMID:
18076141
14.

A biosynthetically-inspired synthesis of the tetrahydrofuran core of obtusallenes II and IV.

Braddock DC, Bhuva R, Millan DS, Pérez-Fuertes Y, Roberts CA, Sheppard RN, Solanki S, Stokes ES, White AJ.

Org Lett. 2007 Feb 1;9(3):445-8.

PMID:
17249783
15.

Palladium-catalyzed medium-ring formation for construction of the core structure of laurencia oxacycles: synthetic study of laurendecumallene B.

Yoshimitsu Y, Inuki S, Oishi S, Fujii N, Ohno H.

Org Lett. 2013 Jun 21;15(12):3046-9. doi: 10.1021/ol401231y. Epub 2013 May 30.

PMID:
23721225
16.

Additional Insights into the Obtusallene Family: Components of Laurencia marilzae.

Gutiérrez-Cepeda A, Fernández JJ, Norte M, López-Rodríguez M, Brito I, Muller CD, Souto ML.

J Nat Prod. 2016 Apr 22;79(4):1184-8. doi: 10.1021/acs.jnatprod.5b01080. Epub 2016 Mar 11.

PMID:
26967625
17.

An integrated approach using UHPLC-PDA-HRMS and 2D HSQC NMR for the metabolic profiling of the red alga Laurencia: dereplication and tracing of natural products.

Kokkotou K, Ioannou E, Nomikou M, Pitterl F, Vonaparti A, Siapi E, Zervou M, Roussis V.

Phytochemistry. 2014 Dec;108:208-19.

PMID:
25457502
18.

Sesquiterpene and acetogenin derivatives from the marine red alga Laurencia okamurai.

Liang Y, Li XM, Cui CM, Li CS, Sun H, Wang BG.

Mar Drugs. 2012 Dec 14;10(12):2817-25. doi: 10.3390/md10122817.

19.

Bioactive C15 acetogenins from the red alga Laurencia obtusa.

Ayyad SE, Al-Footy KO, Alarif WM, Sobahi TR, Bassaif SA, Makki MS, Asiri AM, Al Halwani AY, Badria AF, Badria FA.

Chem Pharm Bull (Tokyo). 2011;59(10):1294-8. Erratum in: Chem Pharm Bull (Tokyo). 2012;60(2):283. Al Halawani, Amani Yahya [Corrected to Al Halwani, Amani Yahya].

20.

Antibacterial activity of halogenated sesquiterpenes from Malaysian Laurencia spp.

Vairappan CS, Suzuki M, Ishii T, Okino T, Abe T, Masuda M.

Phytochemistry. 2008 Oct;69(13):2490-4. doi: 10.1016/j.phytochem.2008.06.015. Epub 2008 Aug 19.

PMID:
18718619

Supplemental Content

Support Center