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Journal articles on the topic 'Dolabriferol'

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Author: Grafiati

Published: 4 June 2021

Last updated: 19 February 2022

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1

Ciavatta, Maria Letizia, Margherita Gavagnin, Raffaella Puliti, Guido Cimino, Eugenia Martinez, Jesus Ortea, and Carlo Andrea Mattia. "Dolabriferol: A new polypropionate from the skin of the anaspidean mollusc Dolabrifera dolabrifera." Tetrahedron 52, no. 39 (September 1996): 12831–38. http://dx.doi.org/10.1016/0040-4020(96)00764-8.

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2

CIAVATTA, M. L., M. GAVAGNIN, R. PULITI, G. CIMINO, E. MARTINEZ, J. ORTEA, and C. A. MATTIA. "ChemInform Abstract: Dolabriferol: A New Polypropionate from the Skin of the Anaspidean Mollusc Dolabrifera dolabrifera." ChemInform 28, no. 4 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199704238.

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3

Lister, Troy, and Michael V. Perkins. "A Retro-Claisen Approach to Dolabriferol." Organic Letters 8, no. 9 (April 2006): 1827–30. http://dx.doi.org/10.1021/ol060347s.

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4

Currie, Russell H., and Jonathan M. Goodman. "In Silico Inspired Total Synthesis of (−)-Dolabriferol." Angewandte Chemie 124, no. 19 (March 29, 2012): 4773–75. http://dx.doi.org/10.1002/ange.201109080.

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5

Currie, Russell H., and Jonathan M. Goodman. "In Silico Inspired Total Synthesis of (−)-Dolabriferol." Angewandte Chemie International Edition 51, no. 19 (March 29, 2012): 4695–97. http://dx.doi.org/10.1002/anie.201109080.

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6

Pelchat, Nicholas, Dave Caron, and Robert Chênevert. "Enantioselective Synthesis of the Alcohol Moiety of Dolabriferol." Journal of Organic Chemistry 72, no. 22 (October 2007): 8484–88. http://dx.doi.org/10.1021/jo701524p.

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7

Laclef, Sylvain, Maris Turks, and Pierre Vogel. "Totalsynthese und Bestimmung der absoluten Konfiguration von (−)-Dolabriferol." Angewandte Chemie 122, no. 45 (September 23, 2010): 8704–6. http://dx.doi.org/10.1002/ange.201003735.

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8

Dias, Luiz C., and Márcio A. de Sousa. "Synthetic studies directed toward the total synthesis of dolabriferol." Tetrahedron Letters 44, no. 30 (July 2003): 5625–28. http://dx.doi.org/10.1016/s0040-4039(03)01351-0.

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9

Chênevert, Robert, Gabriel Courchesne, and Dave Caron. "Chemoenzymatic enantioselective synthesis of the polypropionate acid moiety of dolabriferol." Tetrahedron: Asymmetry 14, no. 17 (September 2003): 2567–71. http://dx.doi.org/10.1016/s0957-4166(03)00587-1.

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10

Laclef, Sylvain, Maris Turks, and Pierre Vogel. "Total Synthesis and Determination of the Absolute Configuration of (−)-Dolabriferol." Angewandte Chemie International Edition 49, no. 45 (September 23, 2010): 8525–27. http://dx.doi.org/10.1002/anie.201003735.

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11

Gesinski, Michael R., William E. Brenzovich, Steven T. Staben, Dianne J. Srinilta, and F. Dean Toste. "A divergent/convergent approach to dolabriferol: the Kornblum–DeLaMare enantiomeric resolution." Tetrahedron Letters 56, no. 23 (June 2015): 3643–46. http://dx.doi.org/10.1016/j.tetlet.2015.02.067.

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12

Gantasala, Naresh, Suresh Borra, and Srihari Pabbaraja. "Stereoselective Total Synthesis of the Non-Contiguous Polyketide Natural Product (-)-Dolabriferol." European Journal of Organic Chemistry 2018, no. 10 (March 14, 2018): 1230–40. http://dx.doi.org/10.1002/ejoc.201701748.

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13

Karagiannis, Athanasios, Naveen Diddi, and Dale E. Ward. "On the Origin of Dolabriferol: Total Synthesis via Its Putative Contiguous Precursor." Organic Letters 18, no. 15 (July 13, 2016): 3794–97. http://dx.doi.org/10.1021/acs.orglett.6b01798.

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14

Laclef, Sylvain, Maris Turks, and Pierre Vogel. "ChemInform Abstract: Total Synthesis and Determination of the Absolute Configuration of (-)-Dolabriferol." ChemInform 42, no. 10 (February 10, 2011): no. http://dx.doi.org/10.1002/chin.201110207.

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15

Jiménez-Romero, Carlos, Karilys González, and Abimael D. Rodríguez. "Dolabriferols B and C, non-contiguous polypropionate esters from the tropical sea hare Dolabrifera dolabrifera." Tetrahedron Letters 53, no. 49 (December 2012): 6641–45. http://dx.doi.org/10.1016/j.tetlet.2012.09.068.

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16

Bandaru, Anandaraju, Debjani Si, and Krishna P. Kaliappan. "Synthesis of C 1 −C 9 and C 10 −C 21 Fragments of (−)‐Dolabriferol." Asian Journal of Organic Chemistry 9, no. 7 (June 8, 2020): 1045–52. http://dx.doi.org/10.1002/ajoc.202000255.

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17

Clark, Kathryn E., Angela Capper, Gina Della Togna, Valerie J. Paul, Luz I. Romero, Timothy Johns, Luis Cubilla-Rios, and Todd L. Capson. "Ecology- and Bioassay-Guided Drug Discovery for Treatments of Tropical Parasitic Disease: 5α,8α-Epidioxycholest-6-en-3β-ol Isolated from the Mollusk Dolabrifera dolabrifera Shows Significant Activity against Leishmania donovani." Natural Product Communications 8, no. 11 (November 2013): 1934578X1300801. http://dx.doi.org/10.1177/1934578x1300801109.

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An ecology- and bioassay-guided search employed to discover compounds with activity against tropical parasitic diseases and cancer from the opisthobranch mollusk, Dolabrifera dolabrifera, led to the discovery of antileishmanial properties in the known compound, 5α,8α-epidioxycholest-6-en-3β-ol (1). Compound 1 was identified through nuclear magnetic resonance spectroscopy (1H, 13C) and mass spectrometry. The compound was concentrated in the digestive gland of D. dolabrifera, but was not detected in other body parts, fecal matter or mucus. Compound 1 showed an IC50 of 4.9 μM towards the amastigote form of Leishmania donovani compared with an IC50 of 281 μM towards the control Vero cell line, a 57.3-fold difference, and demonstrated no measurable activity against Plasmodium falciparum, Trypanosoma cruzi, and the breast cancer cell line, MCF-7.

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18

Padula, Vinicius, Peter Wirtz, and Michael Schrödl. "Heterobranch sea slugs (Mollusca: Gastropoda) from Ascension Island, South Atlantic Ocean." Journal of the Marine Biological Association of the United Kingdom 97, no. 4 (May 16, 2014): 743–52. http://dx.doi.org/10.1017/s0025315414000575.

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The small volcanic island of Ascension is situated in the middle of the South Atlantic Ocean, more than 1500 km from the coast of Africa, its nearest continental area. To date, eight ‘opisthobranch’ species were reported from the island. As a result of a recent survey, 10 species were found. Seven species are new records from Ascension: Platydoris angustipes (Mörch, 1863), Diaulula sp., Dolabrifera dolabrifera (Rang, 1828), Aplysia parvula Guilding in Mörch, 1863 and Caliphylla mediterranea A. Costa, 1867, and two new species: Phidiana mimica sp. nov.; and Felimida atlantica sp. nov. Half of the species found have a wide geographical distribution, being not restricted to the Atlantic Ocean. However, traditional taxonomy based on few characters is probably masking complexes of species.

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19

Assing, Volker. "On the Turkish species of Sunius. V. New species, additional records, a new synonymy, and an updated key to species (Coleoptera: Staphylinidae, Paederinae)." Beiträge zur Entomologie = Contributions to Entomology 55, no. 1 (July 1, 2005): 109–21. http://dx.doi.org/10.21248/contrib.entomol.55.1.109-121.

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Drei ungeflügelte und wahrscheinlich lokalendemische Arten der Gattung Sunius Curtis, 1829 werden aus der Südtürkei beschrieben, abgebildet und von ähnlichen Arten unterschieden: S. goektepensis sp. n. (Mersin), S. amanensis sp. n. (Antakya) und S. hatayanus sp. n. (Antakya). Sunius rastrifer Assing, 2001, syn. n. wird mit S. dolabrifer Assing, 2001 synonymisiert. Für vier Arten werden weitere Nachweise aus der Türkei gemeldet. Für sieben Arten werden Verbreitungskarten erstellt. 17 Sunius-Arten sind derzeit aus der Türkei bekannt, darunter ein bisher nicht zu deutender Name. Eine aktualisierte Bestimmungstabelle wird vorgelegt.StichwörterColeoptera, Staphylinidae, Paederinae, Sunius, Palaearctic region, Turkey, taxonomy, new species, new records, new synonym, distribution, endemism.Nomenklatorische Handlungenamanensis Assing, 2005 (Sunius), spec. n.goektepensis Assing, 2005 (Sunius), spec. n.hatayanus Assing, 2005 (Sunius), spec. n.rastrifer Assing, 2001 (Sunius), syn. n. of Sunius dolabrifer Assing, 2001

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20

Prince, Jeffrey S., and Paul Micah Johnson. "Ultrastructural Comparison of Processing of Protein and Pigment in the Ink Gland of Four Species of Sea Hares." Journal of Marine Biology 2015 (2015): 1–13. http://dx.doi.org/10.1155/2015/847961.

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The ink glands of four sea hare species (Aplysia californica,A. parvula,A. juliana, andDolabrifera dolabrifera) were compared to determine where ink protein is synthesized, how it is incorporated into protein storage vesicles, and the degree of variation in the structure of the ink gland. Ink protein was synthesized in RER cells and stored in amber and white vesicles. Lack of competent RER cells in the ink gland ofD. dolabriferawas correlated with the absence of ink protein. Ink protein had similar characteristics in all threeAplysiaspecies but, again, it was absent inD. dolabrifera. Its uptake involved pinocytosis by protein vesicle cell membranes. Granulate cells showed little variation in structure among the four species, the opposite was the case for RER cells. The conversion of the red algal pigment, phycoerythrin, to phycoerythrobilin (PEB) occurs in the digestive gland but the change of PEB to aplysioviolin (APV), the form of pigment released by the ink gland, occurs in the ink gland itself by both granulate cells and pigment vesicles. The literature describes five types of vesicles based upon color and contents in the ink gland of these four species. We report only three types of vesicle: colored (purple), protein (white and amber), and transparent (includes clear vesicles).

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21

Clarke, Cathryn L., and Annette Klussmann-Kolb. "Parasitic copepods in the sea hare Dolabrifera brazieri (Gastropoda: Opisthobranchia: Anaspidea)." Journal of the Marine Biological Association of the United Kingdom 83, no. 4 (August 2003): 793–96. http://dx.doi.org/10.1017/s0025315403007823h.

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The parasitic copepod, Alimeda orientalis, is recorded from the gill of the sea hare, Dolabrifera brazieri (Gastropoda: Opisthobranchia: Anaspidea). Ten specimens of D. brazieri from a population on the coast of New South Wales, Australia were examined for the incidence of parasitism. Histological techniques and scanning electron microscopy were utilized to determine the feeding mode of A. orientalis and its effect on the host. Alimeda orientalis is a tissue feeder on the gill tissue, and damage caused by feeding and attachment is minimal.

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22

Valdés, Ángel, Eric Breslau, Vinicius Padula, Michael Schrödl, Yolanda Camacho, Manuel António E. Malaquias, Jennifer Alexander, et al. "Molecular and morphological systematics of Dolabrifera Gray, 1847 (Mollusca: Gastropoda: Heterobranchia: Aplysiomorpha)." Zoological Journal of the Linnean Society 184, no. 1 (December 29, 2017): 31–65. http://dx.doi.org/10.1093/zoolinnean/zlx099.

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23

Prince, Jeffrey S., and Paul Micah Johnson. "Ultrastructural comparison of Aplysia and Dolabrifera ink glands suggests cellular sites of anti-predator protein production and algal pigment processing." Journal of Molluscan Studies 72, no. 4 (September 26, 2006): 349–57. http://dx.doi.org/10.1093/mollus/eyl017.

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24

Lister, Troy, and Michael V. Perkins. "A Retro-Claisen Approach to Dolabriferol (I)." ChemInform 37, no. 37 (September 12, 2006). http://dx.doi.org/10.1002/chin.200637178.

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