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1

Shaala, Lamiaa, Hani Asfour, Diaa Youssef, et al. "New Source of 3D Chitin Scaffolds: The Red Sea Demosponge Pseudoceratina arabica (Pseudoceratinidae, Verongiida)." Marine Drugs 17, no. 2 (2019): 92. http://dx.doi.org/10.3390/md17020092.

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The bioactive bromotyrosine-derived alkaloids and unique morphologically-defined fibrous skeleton of chitin origin have been found recently in marine demosponges of the order Verongiida. The sophisticated three-dimensional (3D) structure of skeletal chitinous scaffolds supported their use in biomedicine, tissue engineering as well as in diverse modern technologies. The goal of this study was the screening of new species of the order Verongiida to find another renewable source of naturally prefabricated 3D chitinous scaffolds. Special attention was paid to demosponge species, which could be far
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2

Duminis, Tomas, Marcin Heljak, Wojciech Święszkowski, et al. "On the Mechanical Properties of Microfibre-Based 3D Chitinous Scaffolds from Selected Verongiida Sponges." Marine Drugs 21, no. 9 (2023): 463. http://dx.doi.org/10.3390/md21090463.

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Skeletal constructs of diverse marine sponges remain to be a sustainable source of biocompatible porous biopolymer-based 3D scaffolds for tissue engineering and technology, especially structures isolated from cultivated demosponges, which belong to the Verongiida order, due to the renewability of their chitinous, fibre-containing architecture focused attention. These chitinous scaffolds have already shown excellent and promising results in biomimetics and tissue engineering with respect to their broad diversity of cells. However, the mechanical features of these constructs have been poorly stu
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3

Lever, James, Robert Brkljača, Colin Rix, and Sylvia Urban. "Application of Networking Approaches to Assess the Chemical Diversity, Biogeography, and Pharmaceutical Potential of Verongiida Natural Products." Marine Drugs 19, no. 10 (2021): 582. http://dx.doi.org/10.3390/md19100582.

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This study provides a review of all isolated natural products (NPs) reported for sponges within the order Verongiida (1960 to May 2020) and includes a comprehensive compilation of their geographic and physico-chemical parameters. Physico-chemical parameters were used in this study to infer pharmacokinetic properties as well as the potential pharmaceutical potential of NPs from this order of marine sponge. In addition, a network analysis for the NPs produced by the Verongiida sponges was applied to systematically explore the chemical space relationships between taxonomy, secondary metabolite an
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4

Gómez, Patricia, Bárbara González-Acosta, Carlos Sánchez-Ortíz, Zvi Hoffman, and Claudia J. Hernández-Guerrero. "Amended definitions for Aplysinidae and Aplysina (Porifera, Demospongiae, Verongiida): on three new species from a remarkable population in the Gulf of California." Zootaxa 4455, no. 2 (2018): 322–42. https://doi.org/10.11646/zootaxa.4455.2.4.

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Gómez, Patricia, González-Acosta, Bárbara, Sánchez-Ortíz, Carlos, Hoffman, Zvi, Hernández-Guerrero, Claudia J. (2018): Amended definitions for Aplysinidae and Aplysina (Porifera, Demospongiae, Verongiida): on three new species from a remarkable population in the Gulf of California. Zootaxa 4455 (2): 322-342, DOI: 10.11646/zootaxa.4455.2.4
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5

Klinger, Christine, Sonia Żółtowska-Aksamitowska, Marcin Wysokowski, et al. "Express Method for Isolation of Ready-to-Use 3D Chitin Scaffolds from Aplysina archeri (Aplysineidae: Verongiida) Demosponge." Marine Drugs 17, no. 2 (2019): 131. http://dx.doi.org/10.3390/md17020131.

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Sponges are a valuable source of natural compounds and biomaterials for many biotechnological applications. Marine sponges belonging to the order Verongiida are known to contain both chitin and biologically active bromotyrosines. Aplysina archeri (Aplysineidae: Verongiida) is well known to contain bromotyrosines with relevant bioactivity against human and animal diseases. The aim of this study was to develop an express method for the production of naturally prefabricated 3D chitin and bromotyrosine-containing extracts simultaneously. This new method is based on microwave irradiation (MWI) toge
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6

Sinane, Maha, Colin Grunberger, Lucile Gentile, et al. "Potential of Marine Sponge Metabolites against Prions: Bromotyrosine Derivatives, a Family of Interest." Marine Drugs 22, no. 10 (2024): 456. http://dx.doi.org/10.3390/md22100456.

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The screening of 166 extracts from tropical marine organisms (invertebrates, macroalgae) and 3 cyclolipopeptides from microorganisms against yeast prions highlighted the potential of Verongiida sponges to prevent the propagation of prions. We isolated the known compounds purealidin Q (1), aplysamine-2 (2), pseudoceratinine A (3), aerophobin-2 (4), aplysamine-1 (5), and pseudoceratinine B (6) for the first time from the Wallisian sponge Suberea laboutei. We then tested compounds 1–6 and sixteen other bromotyrosine and bromophenol derivatives previously isolated from Verongiida sponges against y
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7

GÓMEZ, PATRICIA, BÁRBARA GONZÁLEZ-ACOSTA, CARLOS SÁNCHEZ-ORTÍZ, ZVI HOFFMAN, and CLAUDIA J. HERNÁNDEZ-GUERRERO. "Amended definitions for Aplysinidae and Aplysina (Porifera, Demospongiae, Verongiida): on three new species from a remarkable population in the Gulf of California." Zootaxa 4455, no. 2 (2018): 322. http://dx.doi.org/10.11646/zootaxa.4455.2.4.

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Verongiid sponges inhabiting the La Paz region, Gulf of California are described herein as new species. Although morphological evidence was sufficient to determine the identity between species, we have confirmed their uniqueness and relationships with molecular (CO1 and ITS1 and 2), and ecological studies. An amended definition of family Aplysinidae and genus Aplysina is presented to highlight a novel skeletal trait for the latter, clearly described herein as a complex of dendritic fibers sustained by anastomosed fibers deep in the choanosome. This novel fiber arrangement combination is a cons
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8

Dai, Jingqiu, Stephen M. Parrish, Wesley Y. Yoshida, et al. "Bromotyrosine-derived metabolites from an Indonesian marine sponge in the family Aplysinellidae (Order Verongiida)." Bioorganic & Medicinal Chemistry Letters 26, no. 2 (2016): 499–504. http://dx.doi.org/10.1016/j.bmcl.2015.11.086.

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9

Youssef, Diaa T. A., and Lamiaa A. Shaala. "Psammaplysins: Insights from Natural Sources, Structural Variations, and Pharmacological Properties." Marine Drugs 20, no. 11 (2022): 663. http://dx.doi.org/10.3390/md20110663.

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Marine natural products (MNPs) continue to be in the spotlight in the global drug discovery endeavor. Currently, more than 32,000 structurally diverse secondary metabolites from marine sources have been isolated, making MNPs a vital source for researchers to look for novel drug candidates. The marine-derived psammaplysins possess the rare and unique 1,6-dioxa-2-azaspiro [4.6] undecane backbone and are represented by 44 compounds in the literature, mostly from sponges of the order Verongiida. Compounds with 1,6-dioxa-2-azaspiro [4.6] undecane moiety exist in the literature under five names, inc
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10

Díaz, Maria C., Robert W. Thacker, Niamh E. Redmond, Thierry Perez, and Allen G. Collins. "Vansoestia caribensis gen. nov., sp. nov.: first report of the family Ianthellidae (Verongida, Demospongiae) in the Caribbean." Zootaxa 3956, no. 3 (2015): 403–12. https://doi.org/10.11646/zootaxa.3956.3.5.

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Díaz, Maria C., Thacker, Robert W., Redmond, Niamh E., Perez, Thierry, Collins, Allen G. (2015): Vansoestia caribensis gen. nov., sp. nov.: first report of the family Ianthellidae (Verongida, Demospongiae) in the Caribbean. Zootaxa 3956 (3): 403-412, DOI: 10.11646/zootaxa.3956.3.5
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11

Schubert, Mario, Björn Binnewerg, Alona Voronkina, et al. "Naturally Prefabricated Marine Biomaterials: Isolation and Applications of Flat Chitinous 3D Scaffolds from Ianthella labyrinthus (Demospongiae: Verongiida)." International Journal of Molecular Sciences 20, no. 20 (2019): 5105. http://dx.doi.org/10.3390/ijms20205105.

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Marine sponges remain representative of a unique source of renewable biological materials. The demosponges of the family Ianthellidae possess chitin-based skeletons with high biomimetic potential. These three-dimensional (3D) constructs can potentially be used in tissue engineering and regenerative medicine. In this study, we focus our attention, for the first time, on the marine sponge Ianthella labyrinthus Bergquist & Kelly-Borges, 1995 (Demospongiae: Verongida: Ianthellidae) as a novel potential source of naturally prestructured bandage-like 3D scaffolds which can be isolated simultaneo
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12

Lever, James, Florian Kreuder, Jason Henry, et al. "Targeted Isolation of Antibiotic Brominated Alkaloids from the Marine Sponge Pseudoceratina durissima Using Virtual Screening and Molecular Networking." Marine Drugs 20, no. 9 (2022): 554. http://dx.doi.org/10.3390/md20090554.

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Many targeted natural product isolation approaches rely on the use of pre-existing bioactivity information to inform the strategy used for the isolation of new bioactive compounds. Bioactivity information can be available either in the form of prior assay data or via Structure Activity Relationship (SAR) information which can indicate a potential chemotype that exhibits a desired bioactivity. The work described herein utilizes a unique method of targeted isolation using structure-based virtual screening to identify potential antibacterial compounds active against MRSA within the marine sponge
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13

Dziedzic, Izabela, Alona Voronkina, Martyna Pajewska-Szmyt, et al. "The Loss of Structural Integrity of 3D Chitin Scaffolds from Aplysina aerophoba Marine Demosponge after Treatment with LiOH." Marine Drugs 21, no. 6 (2023): 334. http://dx.doi.org/10.3390/md21060334.

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Aminopolysaccharide chitin is one of the main structural biopolymers in sponges that is responsible for the mechanical stability of their unique 3D-structured microfibrous and porous skeletons. Chitin in representatives of exclusively marine Verongiida demosponges exists in the form of biocomposite-based scaffolds chemically bounded with biominerals, lipids, proteins, and bromotyrosines. Treatment with alkalis remains one of the classical approaches to isolate pure chitin from the sponge skeleton. For the first time, we carried out extraction of multilayered, tube-like chitin from skeletons of
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14

Kovalchuk, Valentine, Alona Voronkina, Björn Binnewerg, et al. "Naturally Drug-Loaded Chitin: Isolation and Applications." Marine Drugs 17, no. 10 (2019): 574. http://dx.doi.org/10.3390/md17100574.

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Naturally occurring three-dimensional (3D) biopolymer-based matrices that can be used in different biomedical applications are sustainable alternatives to various artificial 3D materials. For this purpose, chitin-based structures from marine sponges are very promising substitutes. Marine sponges from the order Verongiida (class Demospongiae) are typical examples of demosponges with well-developed chitinous skeletons. In particular, species belonging to the family Ianthellidae possess chitinous, flat, fan-like fibrous skeletons with a unique, microporous 3D architecture that makes them particul
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15

Andreakis, Nikos, Heidi M. Luter, and Nicole S. Webster. "Cryptic speciation and phylogeographic relationships in the elephant ear sponge Ianthella basta (Porifera, Ianthellidae) from northern Australia." Zoological Journal of the Linnean Society 166, no. 2 (2012): 225–35. https://doi.org/10.1111/j.1096-3642.2012.00848.x.

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Andreakis, Nikos, Luter, Heidi M., Webster, Nicole S. (2012): Cryptic speciation and phylogeographic relationships in the elephant ear sponge Ianthella basta (Porifera, Ianthellidae) from northern Australia. Zoological Journal of the Linnean Society 166 (2): 225-235, DOI: 10.1111/j.1096-3642.2012.00848.x, URL: http://dx.doi.org/10.1111/j.1096-3642.2012.00848.x
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16

Manconi, R., A. Padiglia, B. M. Padedda, and R. Pronzato. "Invasive green algae in a western Mediterranean Marine Protected Area: interaction of photophilous sponges with Caulerpa cylindracea." Journal of the Marine Biological Association of the United Kingdom 100, no. 3 (2020): 361–73. http://dx.doi.org/10.1017/s0025315420000193.

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AbstractWe report on the relationships between some conspicuous Mediterranean photophilous sponge species and Caulerpa cylindracea, a non-indigenous species. A diversification of defence strategies and behaviour is highlighted in target species belonging to different orders of Demospongiae from a western Mediterranean Marine Protected Area (NW Sardinian Sea). Caulerpa cylindracea displays a strongly invasive behaviour during body colonization of the Irciniidae Sarcotragus spinosulus and Ircinia retidermata (order Dictyoceratida). These sponges possess pre-adaptive defensive morpho-functional a
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17

Fromont, Jane, Sonia Żółtowska-Aksamitowska, Roberta Galli, et al. "New family and genus of a Dendrilla-like sponge with characters of Verongiida. Part II. Discovery of chitin in the skeleton of Ernstilla lacunosa." Zoologischer Anzeiger 280 (May 2019): 21–29. http://dx.doi.org/10.1016/j.jcz.2019.03.002.

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18

Abdul Wahab, Muhammad Azmi, Rocky de Nys, Ross Holzman, Caroline Luise Schneider, and Steve Whalan. "Patterns of reproduction in two co-occurring Great Barrier Reef sponges." Marine and Freshwater Research 68, no. 7 (2017): 1233. http://dx.doi.org/10.1071/mf16272.

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Reproduction is a key biological process that underpins the persistence and maintenance of populations. However, information on the reproductive biology of Great Barrier Reef (GBR) sponges is depauperate. The present study established the reproductive biology of two co-occurring GBR sponges, namely Ianthella basta (Verongida) and Ircinia sp. (Dictyoceratida). Sponges were haphazardly sampled (monthly) over a period of 1 year. Histological analysis of samples established the sexuality, development, seasonality, gametogenesis and fecundity of the two species, as well as the effects of temperatur
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19

Carballeira, Néstor M., and Carlos R. Bou. "The sterol composition of the marine sponge Aplysina (= Verongia) archeri: A comparative study of the verongidae." Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 93, no. 1 (1989): 175–79. http://dx.doi.org/10.1016/0305-0491(89)90232-0.

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20

Gugel, Jochen, Marit Wagler, and Franz Brümmer. "Porifera, one new species Suberea purpureaflava n. sp. (Demospongiae, Verongida, Aplysinellidae) from northern Red Sea coral reefs, with short descriptions of Red Sea Verongida and known Suberea species." Zootaxa 2994 (December 31, 2011): 60–68. https://doi.org/10.5281/zenodo.278410.

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Gugel, Jochen, Wagler, Marit, Brümmer, Franz (2011): Porifera, one new species Suberea purpureaflava n. sp. (Demospongiae, Verongida, Aplysinellidae) from northern Red Sea coral reefs, with short descriptions of Red Sea Verongida and known Suberea species. Zootaxa 2994: 60-68, DOI: 10.5281/zenodo.278410
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Vacelet, Jean, Dirk Erpenbeck, Cristina Diaz, Hermann Ehrlich, and Jane Fromont. "New family and genus for Dendrilla-like sponges with characters of Verongiida. Part I redescription of Dendrilla lacunosa Hentschel 1912, diagnosis of the new family Ernstillidae and Ernstilla n. g." Zoologischer Anzeiger 280 (May 2019): 14–20. http://dx.doi.org/10.1016/j.jcz.2019.03.001.

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22

Pinheiro, Ulisses Dos S., Eduardo Hajdu, and Márcio R. Custódio. "Aplysina Nardo (Porifera, Verongida, Aplysinidae) from the Brazilian coast with description of eight new species." Zootaxa 1609 (December 31, 2007): 1–51. https://doi.org/10.5281/zenodo.178878.

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Pinheiro, Ulisses Dos S., Hajdu, Eduardo, Custódio, Márcio R. (2007): Aplysina Nardo (Porifera, Verongida, Aplysinidae) from the Brazilian coast with description of eight new species. Zootaxa 1609: 1-51, DOI: 10.5281/zenodo.178878
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23

Diaz, M.C., Van Soest, K. Rützler, and H. M. Guzman. "Aplysina chiriquiensis, a new pedunculate sponge from the Gulf of Chiriquí, Panamá, Eastern Pacific (Aplysinidae, Verongida)." Zootaxa 1012, no. 1 (2005): 1–12. https://doi.org/10.11646/zootaxa.1012.1.1.

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Diaz, M.C., Soest, Van, Rützler, K., Guzman, H. M. (2005): Aplysina chiriquiensis, a new pedunculate sponge from the Gulf of Chiriquí, Panamá, Eastern Pacific (Aplysinidae, Verongida). Zootaxa 1012 (1): 1-12, DOI: 10.11646/zootaxa.1012.1.1, URL: https://biotaxa.org/Zootaxa/article/view/zootaxa.1012.1.1
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24

Graham, Sharna K., Lynette K. Lambert, Gregory K. Pierens, John N. A. Hooper, and Mary J. Garson. "Psammaplin Metabolites New and Old: An NMR Study Involving Chiral Sulfur Chemistry." Australian Journal of Chemistry 63, no. 6 (2010): 867. http://dx.doi.org/10.1071/ch09617.

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The new metabolite psammaplin N (8) that contains a sulfoxide moiety has been isolated together with psammaplins A (1), I (4a), and J (2) from a specimen of the marine sponge Aplysinella rhax (order Verongida family Aplysinidae) collected in South East Queensland. An NMR study on psammaplin J reveals its facile conversion to psammaplins A and I when exposed to methanol.
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25

Ferreira Montenegro, Paula, Giang Nam Pham, Fatouma Mohamed Abdoul-Latif, Elisabeth Taffin-de-Givenchy, and Mohamed Mehiri. "Marine Bromotyrosine Derivatives in Spotlight: Bringing Discoveries and Biological Significance." Marine Drugs 22, no. 3 (2024): 132. http://dx.doi.org/10.3390/md22030132.

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The Verongida order comprises several sponge families, such as Aplysinellidae, Aplysinidae, Ianthellidae, and Pseudoceratinidae, reported for producing bromotyrosine-derived compounds. First identified in 1913, bromotyrosine derivatives have since captivated interest notably for their antitumor and antimicrobial properties. To date, over 360 bromotyrosine derivatives have been reported. Our review focuses specifically on bromotyrosine derivatives newly reported from 2004 to 2023, by summarizing current knowledge about their chemical diversity and their biological activities.
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26

Diaz, M. C., R. W. Thacker, N. E. Redmond, K. O. Matterson, and A. G. Collins. "Phylogenetic Novelties and Geographic Anomalies among Tropical Verongida." Integrative and Comparative Biology 53, no. 3 (2013): 482–94. http://dx.doi.org/10.1093/icb/ict033.

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27

GUGEL, JOCHEN, MARIT WAGLER, and FRANZ Brümmer. "Porifera, one new species Suberea purpureaflava n. sp. (Demospongiae, Verongida, Aplysinellidae) from northern Red Sea coral reefs, with short descriptions of Red Sea Verongida and known Suberea species." Zootaxa 2994, no. 1 (2011): 60. http://dx.doi.org/10.11646/zootaxa.2994.1.5.

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A new verongid sponge (Suberea purpureaflava n. sp.) is described from Dahab, Gulf of Aqaba, in the northern Red Sea. It has a pronounced colour change (a dark red ectosome with whitish pore sieves and a light yellow choanosome in the living specimen changes to a uniform dark violet in the fixed state) and rather rare dendritic fibres with pith and bark and a diameter of about 110–165µm, with the pith occupying 80–90 % of the fibre. Especially the pore sieves were very striking in situ. The new species is compared to all verongid sponges so far recorded from the Red Sea and to all known and ac
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28

Evan, Tamar, Amira Rudi, Micha Ilan, and Yoel Kashman. "Aplyzanzine A, a New Dibromotyrosine Derivative from a Verongida Sponge." Journal of Natural Products 64, no. 2 (2001): 226–27. http://dx.doi.org/10.1021/np000383e.

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29

Freckelton, Marnie L., Heidi M. Luter, Nikos Andreakis, Nicole S. Webster, and Cherie A. Motti. "Qualitative variation in colour morphotypes of Ianthella basta (Porifera: Verongida)." Hydrobiologia 687, no. 1 (2011): 191–203. http://dx.doi.org/10.1007/s10750-011-0818-x.

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Rigby, J. Keith, Stephen B. Church, and Nicolle K. Anderson. "Middle Cambrian sponges from the Drum Mountains and House Range in western Utah." Journal of Paleontology 84, no. 1 (2010): 66–78. http://dx.doi.org/10.1666/08-046.1.

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A diverse assemblage of Middle Cambrian sponges, recently collected from the Wheeler and Marjum Formations of western Millard County, Utah, includes a variety of demosponges and hexactinellids. This collection includes the verongiid Vauxia bellula Walcott, 1920, and the protomonaxonids Choia carteri and Choia ridleyi Walcott, 1920, Hamptonia bowerbanki Walcott, 1920, and Hamptonia parva n. sp. Hexactinellids in the collection include the reticulosid protospongioids Diagoniella hindei Walcott, 1920, and Diagoniella magna n. sp.; the dierespongioid hydnodictyid Valospongia? gigantus Rigby, 1973;
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Santalova, Elena A. "Base-mediated Transformations of 3,5-Dibromoverongiaquinol from the Sponge Aplysina sp. to Cavernicolins-1, -2 and a Subereatensin Analogue." Natural Product Communications 7, no. 5 (2012): 1934578X1200700. http://dx.doi.org/10.1177/1934578x1200700519.

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Treatment of 3,5-dibromoverongiaquinol (1) with NaHCO3-MeOH at room temperature gave cavernicolin-1 (2), cavernicolin-2 (3), the 4,7-dimethoxy analogue of subereatensin (4) and dimethyl ketal (5). These transformations may clarify the origin of the cavernicolins and subereatensin isolated from the extracts of some verongid sponges.
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Ramirez-Garcia, Jennie L., Hannah Lee-Harwood, David Ackerley, et al. "Purpuramine R, a New Bromotyrosine Isolated from Pseudoceratina cf. verrucosa Collected in the Kingdom of Tonga." Marine Drugs 23, no. 5 (2025): 186. https://doi.org/10.3390/md23050186.

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Sponges in the verongiid genus Pseudoceratina Carter are well-known producers of bioactive secondary metabolites. Chemical screening of a Tongan P. cf. verrucosa Bergquist using NMR highlighted the presence of aromatic natural products. Subsequent extraction and purification of P. cf. verrucosa yielded a new bromotyrosine, purpuramine R (1), that exhibits moderate (MIC 16 µg/mL) antibacterial activity against Gram-positive Staphylococcus aureus. The E-geometry of the oxime was confirmed using a combination of NMR and computational approaches. Additionally, computational conformational analysis
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33

Ehrlich, Hermann, Lamiaa A. Shaala, Diaa T. A. Youssef, et al. "Discovery of chitin in skeletons of non-verongiid Red Sea demosponges." PLOS ONE 13, no. 5 (2018): e0195803. http://dx.doi.org/10.1371/journal.pone.0195803.

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34

Ciminiello, P., E. Fattorusso, S. Magno, and M. Pansini. "Chemistry of Verongida Sponges, III. Constituents of a Caribbean Verongula sp." Journal of Natural Products 57, no. 11 (1994): 1564–69. http://dx.doi.org/10.1021/np50113a016.

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35

Hamann, Mark T., and Paul J. Scheuer. "Cyanopuupehenol, an antiviral metabolite of a sponge of the order Verongida." Tetrahedron Letters 32, no. 41 (1991): 5671–72. http://dx.doi.org/10.1016/s0040-4039(00)93525-1.

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36

Schmitt, Susanne, Ute Hentschel, Sven Zea, Thomas Dandekar, and Matthias Wolf. "ITS-2 and 18S rRNA Gene Phylogeny of Aplysinidae (Verongida, Demospongiae)." Journal of Molecular Evolution 60, no. 3 (2005): 327–36. http://dx.doi.org/10.1007/s00239-004-0162-0.

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Schmitt, Susanne, Ute Hentschel, Sven Zea, Thomas Dandekar, and Matthias Wolf. "ITS-2 and 18S rRNA gene phylogeny of Aplysinidae (Verongida, Demospongiae)." Journal of Molecular Evolution 61, no. 1 (2005): 148–50. http://dx.doi.org/10.1007/s00239-005-6111-8.

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38

Ciminiello, Patrizia, Carmela Dell'Aversano, Ernesto Fattorusso, Silvana Magno, and Maurizio Pansini. "Chemistry of Verongida Sponges. 10.1Secondary Metabolite Composition of the Caribbean SpongeVerongulagigantea." Journal of Natural Products 63, no. 2 (2000): 263–66. http://dx.doi.org/10.1021/np990343e.

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39

Shaala, Lamiaa A., and Diaa T. A. Youssef. "Pseudoceratonic Acid and Moloka’iamine Derivatives from the Red Sea Verongiid Sponge Pseudoceratina arabica." Marine Drugs 18, no. 11 (2020): 525. http://dx.doi.org/10.3390/md18110525.

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During an investigation of the chemistry of the Red Sea Verongiid sponge Pseudoceratina arabica, we discovered a small molecule, pseudoceratonic acid (1), along with the new moloka’iamine derivatives, ceratinines N (2), O (3), and the previously reported compounds moloka’iamine (4), hydroxymoloka’iamine (5) and ceratinamine (6). The structural assignments of 1–6 were accomplished by interpretation of their NMR and HRESIMS spectral data. Pseudoceratonic acid possesses a dibrominated hydrazine-derived functional group not found in any reported chemical compound. Pseudoceratonic acid selectively
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40

Silva, Michelli M., Juliana Bergamasco, Simone P. Lira, et al. "Dereplication of Bromotyrosine-derived Metabolites by LC-PDA-MS and Analysis of the Chemical Profile of 14 Aplysina Sponge Specimens from the Brazilian Coastline." Australian Journal of Chemistry 63, no. 6 (2010): 886. http://dx.doi.org/10.1071/ch09616.

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In order to investigate the chemical profile of 14 specimens of Aplysina spp. marine sponges, we have developed a method based on LC-PDA-MS for the detection of bromotyrosine-derived metabolites. The method enabled the dereplication of three distinct chemotypes of bromotyrosine-derived compounds based on UV absorptions, which were further refined by electrospray ionization-mass spectrometry analysis of the brominated quasi-molecular ion clusters. This procedure led to either a single compound assignment, or a maximum of two possible isobaric compounds. The dereplication study indicated that th
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41

Erpenbeck, Dirk, Ratih Aryasari, John N. A. Hooper, and Gert Wörheide. "A Mitochondrial Intron in a Verongid Sponge." Journal of Molecular Evolution 80, no. 1 (2014): 13–17. http://dx.doi.org/10.1007/s00239-014-9653-9.

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42

Pawlik, J. R., and L. K. Deignan. "Cowries graze verongid sponges on Caribbean reefs." Coral Reefs 34, no. 2 (2015): 663. http://dx.doi.org/10.1007/s00338-015-1279-x.

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43

Uemura, Daisuke, Tomoyuki Koyama, Osamu Ohno, Kaoru Yamada, and Norihito Maru. "Sunabedine, a Novel Toxic Bromotyrosine-derivative Alkaloid from Okinawan Sponge, Order Verongida." HETEROCYCLES 82, no. 1 (2010): 371. http://dx.doi.org/10.3987/com-10-s(e)7.

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Albrizio, Stefania, Patrizia Ciminiello, Ernesto Fattorusso, Silvana Magno, and Maurizio Pansini. "Chemistry of Verongida sponges. I. Constituents of the Caribbean sponge Pseudoceratina crassa." Tetrahedron 50, no. 3 (1994): 783–88. http://dx.doi.org/10.1016/s0040-4020(01)80793-6.

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Ciminiello, Patrizia, Carmela Dell'Aversano, Ernesto Fattorusso, Silvana Magno, Lucia Carrano, and Maurizio Pansini. "Chemistry of Verongida sponges. VII bromocompounds from the caribbean sponge Aplysina archeri." Tetrahedron 52, no. 29 (1996): 9863–68. http://dx.doi.org/10.1016/0040-4020(96)00518-2.

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46

Ciminiello, Patrizia, Carmela Dell'Aversano, Ernesto Fattorusso, Silvana Magno, and Maurizio Pansini. "Chemistry of Verongida Sponges. 9.1Secondary Metabolite Composition of the Caribbean SpongeAplysina cauliformis." Journal of Natural Products 62, no. 4 (1999): 590–93. http://dx.doi.org/10.1021/np9805138.

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47

Trejo, Alejandra, José Luis Carballo, and Johanna Segovia. "New records and checklist of sponges from El Salvador (Eastern Tropical Pacific)." Zootaxa 5613, no. 1 (2025): 99–125. https://doi.org/10.11646/zootaxa.5613.1.4.

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Trejo, Alejandra, Carballo, José Luis, Segovia, Johanna (2025): New records and checklist of sponges from El Salvador (Eastern Tropical Pacific). Zootaxa 5613 (1): 99-125, DOI: 10.11646/zootaxa.5613.1.4, URL: https://doi.org/10.11646/zootaxa.5613.1.4
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Van, Soest Rob W.M. "Typification of Porifera described in the 10 edition of Linnaeus' Systema Naturae, volume II, 1759." Zootaxa 5638, no. 1 (2025): 1–65. https://doi.org/10.11646/zootaxa.5638.1.1.

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Van Soest, Rob W.M. (2025): Typification of Porifera described in the 10 edition of Linnaeus' Systema Naturae, volume II, 1759. Zootaxa 5638 (1): 1-65, DOI: 10.11646/zootaxa.5638.1.1, URL: https://doi.org/10.11646/zootaxa.5638.1.1
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El-Demerdash, Amr, Atanas G. Atanasov, Olaf K. Horbanczuk, et al. "Chemical Diversity and Biological Activities of Marine Sponges of the Genus Suberea: A Systematic Review." Marine Drugs 17, no. 2 (2019): 115. http://dx.doi.org/10.3390/md17020115.

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Marine natural products (MNPs) continue to be in the spotlight in the global drug discovery endeavor. Currently, more than 30,000 structurally diverse secondary metabolites from marine sources have been isolated, making MNPs a profound, renewable source to investigate novel drug compounds. Marine sponges of the genus Suberea (family: Aplysinellidae) are recognized as producers of bromotyrosine derivatives, which are considered distinct chemotaxonomic markers for the marine sponges belonging to the order Verongida. This class of compounds exhibits structural diversity, ranging from simple monom
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Weiss, Beate, Rainer Ebel, Malte Elbrächter, Marianna Kirchner, and Peter Proksch. "Defense metabolites from the marine sponge Verongia aerophoba." Biochemical Systematics and Ecology 24, no. 1 (1996): 1–12. http://dx.doi.org/10.1016/0305-1978(95)00101-8.

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