Isobromotopsentin: a New Bis(indole) Alkaloid From a Deep-Water Marine Sponge Spongosorites sp.

1995 ◽  
Vol 48 (12) ◽  
pp. 2053 ◽  
Author(s):  
LM Murray ◽  
TK Lim ◽  
JNA Hooper ◽  
RJ Capon
Keyword(s):  
Deep Water ◽  
Marine Sponge ◽  
Indole Alkaloid ◽  
Spectroscopic Methods

Isobromotopsentin (16) is a new brominated bis(indole) alkaloid isolated from a deep-water marine sponge Spongosorites sp. collected off the southern Australian coast. The structure for (16) was determined by spectroscopic methods.

ChemInform Abstract: Isobromotopsentin (I): A New Bis(indole) Alkaloid from a Deep-Water Marine Sponge Spongosorites sp.

ChemInform ◽  
2010 ◽  
Vol 27 (18) ◽  
pp. no-no
Author(s):  
L. M. MURRAY ◽  
T. K. LIM ◽  
J. N. A. HOOPER ◽  
R. J. CAPON
Keyword(s):  
Deep Water ◽  
Marine Sponge ◽  
Indole Alkaloid

Dragmacidin, a new cytotoxic bis(indole) alkaloid from a deep water marine sponge, Dragmacidon sp

1988 ◽  
Vol 53 (13) ◽  
pp. 3116-3118 ◽  
Author(s):  
Shigeo Kohmoto ◽  
Yoel Kashman ◽  
Oliver J. McConnell ◽  
Kenneth L. Rinehart ◽  
Amy Wright ◽  
...  
Keyword(s):  
Deep Water ◽  
Marine Sponge ◽  
Indole Alkaloid

A new bis-(indole) alkaloid from a deep-water marine sponge of the genus Spongosorites

1992 ◽  
Vol 57 (17) ◽  
pp. 4772-4775 ◽  
Author(s):  
Amy E. Wright ◽  
Shirley A. Pomponi ◽  
Sue S. Cross ◽  
Peter McCarthy
Keyword(s):  
Deep Water ◽  
Marine Sponge ◽  
Indole Alkaloid

ChemInform Abstract: Dragmacidin, a New Cytotoxic Bis(indole) Alkaloid from a Deep Water Marine Sponge, Dragmacidon sp.

ChemInform ◽  
1988 ◽  
Vol 19 (51) ◽  
Author(s):  
S. KOHMOTO ◽  
Y. KASHMAN ◽  
O. J. MCCONNELL ◽  
K. L. JUN. RINEHART ◽  
A. WRIGHT ◽  
...  
Keyword(s):  
Deep Water ◽  
Marine Sponge ◽  
Indole Alkaloid

scholarly journals Cytotoxic Sesterterpenes from Thai Marine Sponge Hyrtios erectus

Marine Drugs ◽  
2018 ◽  
Vol 16 (12) ◽  
pp. 474 ◽  
Author(s):  
Wirongrong Kaweetripob ◽  
Chulabhorn Mahidol ◽  
Pittaya Tuntiwachwuttikul ◽  
Somsak Ruchirawat ◽  
Hunsa Prawat
Keyword(s):  
Methyl Ether ◽  
Marine Sponge ◽  
Indole Alkaloids ◽  
Cytotoxic Activities ◽  
Spectroscopic Methods ◽  
The Absolute ◽  
Modified Mosher’S Method

Four sesterterpenes, erectusolides B, C, D, and seco-manoalide-25-methyl ether, two 2-furanone derivatives, erectusfuranones A and B, together with thirteen known sesterterpenes, (6Z)-neomanoalide-24-acetate, two diastereomers of 24-O-methylmanoalide, luffariolide B, manoalide, (6E)- and (6Z)-neomanoalide, seco-manoalide, scalarafuran, 12-acetylscalarolide, 12-epi-O-deacetyl-19-deoxyscalarin, 12-epi-scalarin, and 12-O-deacetyl-12-epi-scalarin, three indole alkaloids, 5-hydroxy-1H-indole-3-carbaldehyde, hyrtiosine A, and variabine B, and one norterpene, cavernosine were isolated from the marine sponge Hyrtios erectus. Their structures were determined by means of spectroscopic methods and the absolute configurations of the asymmetric centers were determined using the modified Mosher’s method. The cytotoxic activities for the isolated compounds have been reported.

(–)-Agelasidine A from Agelas clathrodes

2006 ◽  
Vol 61 (7-8) ◽  
pp. 472-476 ◽  
Author(s):  
Maria Augusta Medeiros ◽  
Ana Lourenço ◽  
Maria Regina Tavares ◽  
Maria João Marcelo Curto ◽  
Sónia Savluchinske Feio ◽  
...  
Keyword(s):  
Staphylococcus Aureus ◽  
Marine Sponge ◽  
Methanol Extract ◽  
Spectroscopic Methods ◽  
Antifungal Activities ◽  
Antibacterial And Antifungal Activities ◽  
Bacteriostatic Agent ◽  
Antibacterial And Antifungal ◽  
First Time

(-)-Agelasidine A was identified from the methanol extract of the marine sponge Agelas clathrodes for the first time together with zooanemonin, 1-carboxymethylnicotinic acid, hymenidin, mukanadins A and C, monobromodispacamide, agelasidine D, 2-amide-4-bromopyrrole, O-methyltryptophan and an agelasines mixture. The structures were characterized by spectroscopic methods. (-)-Agelasidine A was tested for antibacterial and antifungal activities and shown to act as a bacteriostatic agent as it inhibited the growth of Staphylococcus aureus and partially the growth of other bacteria.

The Constituents of Marine Sponges. V. The Isolation From Chelonaplysilla violacea (Dendroceratida) of Aplyviolene and Other Diterpenes, and the Determination of the Crystal Structure of Aplyviolene

1990 ◽  
Vol 43 (11) ◽  
pp. 1861 ◽  
Author(s):  
TW Hambley ◽  
A Poiner ◽  
WC Taylor
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Marine Sponge ◽  
Marine Sponges ◽  
Spectroscopic Methods ◽  
Orthorhombic Space Group ◽  
Space Group ◽  
X Ray ◽  
Deep Violet

From the deep violet, encrusting marine sponge Chelonaplysilla violacea, two rearranged spongian diterpenes, aplyviolene, (1R*,1′S*,3?aR*,5R*,6R*,8R*,8′aS*)-3-oxo-8-(1′,4′,4′-trimethyl-8′-methylenedecahydroazulen-1′-yl)-2,7-dioxabicyclo[3.2.1]oct-6-yl acetate (1), the acetoxy derivative, aplyviolacene (2), (5R*,8S*,9S*,10R*,13S*,14R* ,15S*,16R*)-spongian-15,16-diyl diacetate (3) and (5R*,8S*,9S*,10R*,13S*,14R*)-spongian-16-one (4) were isolated. The structures were determined by spectroscopic methods, and the structure of aplyviolene was confirmed by a single-crystal X-ray determination. The crystal structure was refined to a residual of 0.036 for 1125 independent observed reflections. The crystals were orthorhombic, space group P212121 with a 8.098(1), b 11.628(1), c 21.774(3)Ǻ.

Sign in / Sign up

Export Citation Format

Share Document