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Items: 1 to 20 of 108

1.

Structure, synthesis, and biological activity of a C-20 bisacetylenic alcohol from a marine sponge Callyspongia sp.

Shirouzu T, Watari K, Ono M, Koizumi K, Saiki I, Tanaka C, van Soest RW, Miyamoto T.

J Nat Prod. 2013 Jul 26;76(7):1337-42. doi: 10.1021/np400297p. Epub 2013 Jul 15.

PMID:
23855338
2.

A new C-20 polyacetylene from the sponge Callyspongia pseudoreticulata.

Braekman JC, Daloze D, Devijver C, Dubut D, van Soest RW.

J Nat Prod. 2003 Jun;66(6):871-2.

PMID:
12828480
3.

Asymmetric synthesis and biological evaluation of natural or bioinspired cytotoxic C2-symmetrical lipids with two terminal chiral alkynylcarbinol pharmacophores.

Listunov D, Fabing I, Saffon-Merceron N, Gaspard H, Volovenko Y, Maraval V, Chauvin R, Génisson Y.

J Org Chem. 2015 Jun 5;80(11):5386-94. doi: 10.1021/acs.joc.5b00494. Epub 2015 May 19.

PMID:
25961794
4.

A new diketopiperazine from South China Sea marine sponge Callyspongia sp.

Chen Y, Peng Y, Gao C, Huang R.

Nat Prod Res. 2014;28(13):1010-4. doi: 10.1080/14786419.2014.903397. Epub 2014 Apr 4.

PMID:
24697743
5.

Callyspongisines A-D: bromopyrrole alkaloids from an Australian marine sponge, Callyspongia sp.

Plisson F, Prasad P, Xiao X, Piggott AM, Huang XC, Khalil Z, Capon RJ.

Org Biomol Chem. 2014 Mar 14;12(10):1579-84. doi: 10.1039/c4ob00091a.

PMID:
24458130
6.

Sulfated meroterpenoids from the Brazilian sponge Callyspongia sp. are inhibitors of the antileishmaniasis target adenosine phosphoribosyl transferase.

Gray CA, de Lira SP, Silva M, Pimenta EF, Thiemann OH, Oliva G, Hajdu E, Andersen RJ, Berlinck RG.

J Org Chem. 2006 Nov 10;71(23):8685-90. Erratum in: J Org Chem. 2007 Feb 2;72(3):1062.

PMID:
17080994
7.

ApoE secretion modulating bromotyrosine derivative from the Australian marine sponge Callyspongia sp.

Tian LW, Feng Y, Shimizu Y, Pfeifer TA, Wellington C, Hooper JN, Quinn RJ.

Bioorg Med Chem Lett. 2014 Aug 1;24(15):3537-40. doi: 10.1016/j.bmcl.2014.05.054. Epub 2014 Jun 2.

8.

New cytotoxic metabolites from a marine sponge Homaxinella sp.

Mansoor TA, Hong J, Lee CO, Sim CJ, Im KS, Lee DS, Jung JH.

J Nat Prod. 2004 Apr;67(4):721-4.

PMID:
15104515
9.

A new 1,4-diazepine from South China Sea marine sponge Callyspongia species.

Huang RM, Ma W, Dong JD, Zhou XF, Xu T, Lee KJ, Yang X, Xu SH, Liu Y.

Molecules. 2010 Feb 10;15(2):871-7. doi: 10.3390/molecules15020871.

10.

First total synthesis of acetylenic alcohol 15-methyltricosa-2,4-diyne-1, 6-diol (strongylodiol-G) derived from marine sponge.

Gupta N, Shallu, Kad GL, Singh J.

Nat Prod Res. 2014;28(7):424-30. doi: 10.1080/14786419.2013.867855. Epub 2014 Jan 15.

PMID:
24423029
11.

Callyspongiolide, a cytotoxic macrolide from the marine sponge Callyspongia sp.

Pham CD, Hartmann R, Böhler P, Stork B, Wesselborg S, Lin W, Lai D, Proksch P.

Org Lett. 2014 Jan 3;16(1):266-9. doi: 10.1021/ol403241v. Epub 2013 Dec 13.

12.

Two new alkaloids from marine sponge Callyspongia sp.

Yang B, Tao H, Zhou X, Lin XP, Liu Y.

Nat Prod Res. 2013 Mar;27(4-5):433-7. doi: 10.1080/14786419.2012.734819. Epub 2012 Oct 16.

PMID:
23066821
13.

Six New Polyacetylenic Alcohols from the Marine Sponges Petrosia sp. and Halichondria sp.

Gabriel AF, Li Z, Kusuda R, Tanaka C, Miyamoto T.

Chem Pharm Bull (Tokyo). 2015;63(6):469-75. doi: 10.1248/cpb.c15-00203. Epub 2015 Apr 9.

14.

Structure determination of bisacetylenic oxylipins in carrots (Daucus carota L.) and enantioselective synthesis of falcarindiol.

Schmiech L, Alayrac C, Witulski B, Hofmann T.

J Agric Food Chem. 2009 Nov 25;57(22):11030-40. doi: 10.1021/jf9031475.

PMID:
19845355
15.

Callyspongenols A-C, new cytotoxic C22-polyacetylenic alcohols from a red sea sponge, Callyspongia species.

Youssef DT, van Soest RW, Fusetani N.

J Nat Prod. 2003 May;66(5):679-81.

PMID:
12762806
16.

Niphatoxin C, a cytotoxic tripyridine alkaloid from Callyspongia sp.

Buchanan MS, Carroll AR, Addepalli R, Avery VM, Hooper JN, Quinn RJ.

J Nat Prod. 2007 Dec;70(12):2040-1. Epub 2007 Nov 21.

PMID:
18027906
17.

Polyacetylene diols with antiproliferative and driving Th1 polarization effects from the marine sponge Callyspongia sp.

Umeyama A, Matsuoka N, Mine R, Nakata A, Arimoto E, Matsui M, Shoji N, Arihara S, Takei M, Hashimoto T.

J Nat Med. 2010 Jan;64(1):93-7. doi: 10.1007/s11418-009-0363-3. Epub 2009 Oct 3.

PMID:
19802655
18.

Absolute configuration of falcarinol (9Z-heptadeca-1,9-diene-4,6-diyn-3-ol) from Pastinaca sativa.

Corell M, Sheehy E, Evans P, Brunton N, Valverde J.

Nat Prod Commun. 2013 Aug;8(8):1123-6.

PMID:
24079184
19.

Acetylenic strongylodiols from a Petrosia (Strongylophora) Okinawan marine sponge.

Watanabe K, Tsuda Y, Hamada M, Omori M, Mori G, Iguchi K, Naoki H, Fujita T, Van Soest RW.

J Nat Prod. 2005 Jul;68(7):1001-5.

PMID:
16038538
20.

Antichlamydial sterol from the Red Sea sponge Callyspongia aff. implexa.

Abdelmohsen UR, Cheng C, Reimer A, Kozjak-Pavlovic V, Ibrahim AK, Rudel T, Hentschel U, Edrada-Ebel R, Ahmed SA.

Planta Med. 2015 Mar;81(5):382-7. doi: 10.1055/s-0035-1545721. Epub 2015 Mar 17.

PMID:
25782033
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