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Relevant bibliographies by topics / Microsclerodermin / Journal articles

Journal articles on the topic 'Microsclerodermin'

To see the other types of publications on this topic, follow the link: Microsclerodermin.

Author: Grafiati

Published: 4 June 2021

Last updated: 20 February 2023

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1

Zhu, Jidong, and Dawei Ma. "Total Synthesis of Microsclerodermin E." Angewandte Chemie 115, no. 43 (November 10, 2003): 5506–9. http://dx.doi.org/10.1002/ange.200352423.

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2

Zhu, Jidong, and Dawei Ma. "Total Synthesis of Microsclerodermin E." Angewandte Chemie International Edition 42, no. 43 (November 10, 2003): 5348–51. http://dx.doi.org/10.1002/anie.200352423.

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3

Melikhova, Ekaterina Y., Robert D. C. Pullin, Christian Winter, and Timothy J. Donohoe. "Dehydromicrosclerodermin B and Microsclerodermin J: Total Synthesis and Structural Revision." Angewandte Chemie International Edition 55, no. 33 (July 15, 2016): 9753–57. http://dx.doi.org/10.1002/anie.201604764.

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4

Melikhova, Ekaterina Y., Robert D. C. Pullin, Christian Winter, and Timothy J. Donohoe. "Dehydromicrosclerodermin B and Microsclerodermin J: Total Synthesis and Structural Revision." Angewandte Chemie 128, no. 33 (July 15, 2016): 9905–9. http://dx.doi.org/10.1002/ange.201604764.

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5

Winter, Christian, Robert D. C. Pullin, and Timothy J. Donohoe. "Diastereoselective synthesis of the 5-hydroxy-pyrrolidinone amino acid of the microsclerodermins and model studies for an end-game strategy for microsclerodermin B." Tetrahedron Letters 58, no. 7 (February 2017): 602–5. http://dx.doi.org/10.1016/j.tetlet.2016.12.045.

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6

Bewley, Carole A., Cecile Debitus, and D. John Faulkner. "Microsclerodermins A and B. Antifungal Cyclic Peptides from the Lithistid Sponge Microscleroderma sp." Journal of the American Chemical Society 116, no. 17 (August 1994): 7631–36. http://dx.doi.org/10.1021/ja00096a020.

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7

Shuter, Emily C., Hung Duong, Craig A. Hutton, and Malcolm D. McLeod. "The enantioselective synthesis of APTO and AETD: polyhydroxylated β-amino acid constituents of the microsclerodermin cyclic peptides." Organic & Biomolecular Chemistry 5, no. 19 (2007): 3183. http://dx.doi.org/10.1039/b707891a.

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8

Qureshi, Asfia, Patrick L. Colin, and D. John Faulkner. "Microsclerodermins F–I, Antitumor and Antifungal Cyclic Peptides from the Lithistid Sponge Microscleroderma sp." Tetrahedron 56, no. 23 (June 2000): 3679–85. http://dx.doi.org/10.1016/s0040-4020(00)00286-6.

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9

BEWLEY, C. A., C. DEBITUS, and D. J. FAULKNER. "ChemInform Abstract: Microsclerodermins A and B. Anifungal Cyclic Peptides from the Lithistid Sponge Microscleroderma sp." ChemInform 26, no. 15 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199515241.

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10

Schmidt, Eric W., and D. John Faulkner. "Microsclerodermins C - E, antifungal cyclic peptides from the lithistid marine sponges Theonella sp. and Microscleroderma sp." Tetrahedron 54, no. 13 (March 1998): 3043–56. http://dx.doi.org/10.1016/s0040-4020(98)00054-4.

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11

Qureshi, Asfia, Patrick L. Colin, and D. John Faulkner. "ChemInform Abstract: Microsclerodermins F-I, Antitumor and Antifungal Cyclic Peptides from the Lithistid Sponge Microscleroderma sp." ChemInform 31, no. 41 (October 10, 2000): no. http://dx.doi.org/10.1002/chin.200041159.

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12

SCHMIDT, E. W., and D. J. FAULKNER. "ChemInform Abstract: Microsclerodermins C-E, Antifungal Cyclic Peptides from the Lithistid Marine Sponges Theonella sp. and Microscleroderma sp." ChemInform 29, no. 26 (June 21, 2010): no. http://dx.doi.org/10.1002/chin.199826240.

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13

Guzmán, Esther A., Kelly Maers, Jill Roberts, Hilaire V. Kemami-Wangun, Dedra Harmody, and Amy E. Wright. "The marine natural product microsclerodermin A is a novel inhibitor of the nuclear factor kappa B and induces apoptosis in pancreatic cancer cells." Investigational New Drugs 33, no. 1 (November 23, 2014): 86–94. http://dx.doi.org/10.1007/s10637-014-0185-3.

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14

Gómez, Patricia, Fernando Calderón-Gutiérrez, Carlos González-Gándara, and María De Los Angeles Rojas-Terán. "New species of Microscleroderma and Amphibleptula (Demospongiae, Tetractinellida, Scleritodermidae) from two contrasting marine environments." Journal of the Marine Biological Association of the United Kingdom 101, no. 2 (March 2021): 241–51. http://dx.doi.org/10.1017/s0025315421000114.

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Abstract:

AbstractWe record for the first time a nominal species of the genus Microscleroderma in the Western Atlantic, and the first record of the genus Amphibleptula in Mexico. Two new species of ‘lithistid’ Tetractinellida are described: Microscleroderma mexica sp. nov. from crevices of two reefs in Veracruz, Mexico, and Amphibleptula aaktun sp. nov. from the anchialine cave El Aerolito, Cozumel Island, Mexico. Microscleroderma mexica sp. nov. is characterized by its tubular and cup-shaped to wavy laminar habitus, hirsute surface and two size categories of oxea diactines. Amphibleptula aaktun sp. nov. is characterized by its ficiform or lobular habitus with an exhalant area at the flat top of the body, divided into numerous vertical septa-like structures; its desmas have thinner epirhabds, and thinner oxea than those of Amphibleptula madrepora. This is the second species of Amphibleptula that has been described; hence, we propose the redefinition of the genus. Both species described have a shallow distribution (≤21 m depth); they are differentiated from each other by the disjunction between their habitats as well as by their morphology.

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15

Shioiri, Takayuki, Shigekazu Sasaki, and Yasumasa Hamada. "Synthetic approach to microsclerodermins: construction of three building blocks." Arkivoc 2003, no. 2 (March 5, 2003): 103–22. http://dx.doi.org/10.3998/ark.5550190.0004.213.

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16

Sasaki, Shigekazu, Yasumasa Hamada, and Takayuki Shioiri. "Construction of Three Building Blocks for the Total Synthesis of Microsclerodermins." Synlett 1999, no. 4 (April 1999): 453–55. http://dx.doi.org/10.1055/s-1999-2651.

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17

Costantino, Valeria, Ernesto Fattorusso, Alfonso Mangoni, Maurice Aknin, and Emil M. Gaydou. "Novel 3-β-methoxysteroids from the senegalse sponge Microscleroderma spirophora." Steroids 59, no. 3 (March 1994): 181–84. http://dx.doi.org/10.1016/0039-128x(94)90025-6.

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18

Pullin, Robert D. C., Akshat H. Rathi, Ekaterina Y. Melikhova, Christian Winter, Amber L. Thompson, and Timothy J. Donohoe. "Tethered Aminohydroxylation: Synthesis of the β-Amino Acid of Microsclerodermins A and B." Organic Letters 15, no. 21 (October 16, 2013): 5492–95. http://dx.doi.org/10.1021/ol402638n.

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19

Hoffmann, Thomas, Stefan Müller, Suvd Nadmid, Ronald Garcia, and Rolf Müller. "Microsclerodermins from Terrestrial Myxobacteria: An Intriguing Biosynthesis Likely Connected to a Sponge Symbiont." Journal of the American Chemical Society 135, no. 45 (November 2013): 16904–11. http://dx.doi.org/10.1021/ja4054509.

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20

Chandrasekhar, S., and S. Shameem Sultana. "Stereoselective synthesis of the C1–C20 segment of the microsclerodermins A and B." Tetrahedron Letters 47, no. 40 (October 2006): 7255–58. http://dx.doi.org/10.1016/j.tetlet.2006.07.107.

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21

Mayasundari, Anand, Ulf Peters, and David G. J. Young. "Synthesis of a model bicyclic core related to Microscleroderma spirophora steroids." Tetrahedron Letters 44, no. 13 (March 2003): 2633–36. http://dx.doi.org/10.1016/s0040-4039(03)00378-2.

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22

Hjelmgaard, Thomas, Sophie Faure, Pascale Lemoine, Bernard Viossat, and David J. Aitken. "Rapid Assembly of the Polyhydroxylated β-Amino Acid Constituents of Microsclerodermins C, D, and E." Organic Letters 10, no. 5 (March 2008): 841–44. http://dx.doi.org/10.1021/ol702962z.

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23

Burnett, Cameron M., and Robert M. Williams. "Asymmetric synthesis of the core of AMPTD, the key amino acid of microsclerodermins F-I." Tetrahedron Letters 50, no. 39 (September 2009): 5449–51. http://dx.doi.org/10.1016/j.tetlet.2009.06.144.

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24

Davies, Stephen G., Ai M. Fletcher, Emma M. Foster, James A. Lee, Paul M. Roberts, and James E. Thomson. "Asymmetric Syntheses of APTO and AETD: the β-Amino Acid Fragments within Microsclerodermins C, D, and E." Journal of Organic Chemistry 78, no. 6 (February 21, 2013): 2500–2510. http://dx.doi.org/10.1021/jo302731m.

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25

Tian, Tian, Kentaro Takada, Yuji Ise, Susumu Ohtsuka, Shigeru Okada, and Shigeki Matsunaga. "Microsclerodermins N and O, cytotoxic cyclic peptides containing a p-ethoxyphenyl moiety from a deep-sea marine sponge Pachastrella sp." Tetrahedron 76, no. 10 (March 2020): 130997. http://dx.doi.org/10.1016/j.tet.2020.130997.

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26

Tarrade-Matha, Aurélie, Marcelo Siqueira Valle, Pierre Tercinier, Philippe Dauban, and Robert H. Dodd. "Enantiospecific Synthesis of a Protected Equivalent of APTO, the β-Amino Acid Fragment of Microsclerodermins C and D, by Aziridino-γ-lactone Methodology." European Journal of Organic Chemistry 2009, no. 5 (February 2009): 673–86. http://dx.doi.org/10.1002/ejoc.200801000.

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27

SASAKI, S., Y. HAMADA, and T. SHIOIRI. "ChemInform Abstract: Synthetic Studies of Microsclerodermins. A Stereoselective Synthesis of a Core Building Block for (2S,3R,4S,5S,6S,11E)-3-Amino-6-methyl-12- (4-methoxyphenyl)-2,4,5-Trihydroxydodec-11-enoic Acid (AMMTD)." ChemInform 28, no. 32 (August 3, 2010): no. http://dx.doi.org/10.1002/chin.199732167.

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28

Sasaki, Shigekazu, Yasumasa Hamada, and Takayuki Shioiri. "The efficient stereoselective synthesis of (2S,3R,4S,5S,6S,11E)-3-amino-6-methyl-12-(4-methoxyphenyl)-2,4,5-trihydroxydodec-11-enoic acid (AMMTD), a component of microsclerodermins of marine sponge origin, as its protected form." Tetrahedron Letters 40, no. 16 (April 1999): 3187–90. http://dx.doi.org/10.1016/s0040-4039(99)00411-6.

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29

Sasaki, Shigekazu, Yasumasa Hamada, and Takayuki Shioiri*. "Sunthetic Studies of Microsclerodermins. A Stereoselective Synthesis of a Core Building Block for (2 S,3 R, 4 S,5 S,6 S, 11 E)-3-Amino-6-methyl-12-(4-methoxyphenyl)-2,4,5-trihydroxydodec-11-enoic Acid (AMMTD)." Tetrahedron Letters 38, no. 17 (April 1997): 3013–16. http://dx.doi.org/10.1016/s0040-4039(97)00522-4.

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30

Zhu, Jidong, and Dawei Ma. "Total Synthesis of Microsclerodermin E." ChemInform 35, no. 11 (March 16, 2004). http://dx.doi.org/10.1002/chin.200411172.

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31

Li, Xing-Cong, Zhang, Jacob, Rao, Wang, Agarwal, Newman, Khan, and Clark. "Antifungal cyclic peptides from the marine sponge Microscleroderma herdmani." Research and Reports in Medicinal Chemistry, May 2012, 7. http://dx.doi.org/10.2147/rrmc.s30895.

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32

Zhang, X., MR Jacob, RR Rao, YH Wang, A. Agarwal, IA Khan, A. Clark, and XC Li. "Antifungal Cyclic Peptides from the Marine Sponge Microscleroderma sp." Planta Medica 78, no. 05 (March 7, 2012). http://dx.doi.org/10.1055/s-0032-1307625.

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33

Li, Xing-Cong, Zhang, Jacob, Rao, Wang, Agarwal, Newman, Khan, and Clark. "Antifungal cyclic peptides from the marine sponge Microscleroderma herdmani [Corrigendum]." Research and Reports in Medicinal Chemistry, March 2013, 9. http://dx.doi.org/10.2147/rrmc.s44029.

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