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Journal articles on the topic 'Peribysin'

Author: Grafiati

Published: 6 September 2023

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1

Danishefsky, S., A. Angeles, D. Dorn, C. Kou, and M. Moore. "Synthesis of ent-Peribysin E." Synfacts 2007, no. 7 (July 2007): 0678. http://dx.doi.org/10.1055/s-2007-968601.

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2

Angeles, Angie R., Stephen P. Waters, and Samuel J. Danishefsky. "Total Syntheses of (+)- and (−)-Peribysin E." Journal of the American Chemical Society 130, no. 41 (October 15, 2008): 13765–70. http://dx.doi.org/10.1021/ja8048207.

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3

Lee, Hung-Yi, and Chin-Kang Sha. "Stereoselective Total Synthesis of (±)-Peribysin E." Journal of Organic Chemistry 77, no. 1 (November 30, 2011): 598–605. http://dx.doi.org/10.1021/jo2021604.

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4

Kalmode, Hanuman P., Kishor L. Handore, Raveena Rajput, Samir R. Shaikh, Rajesh G. Gonnade, Kiran A. Kulkarni, and D. Srinivasa Reddy. "Total Synthesis and Biological Evaluation of Cell Adhesion Inhibitors Peribysin A and B: Structural Revision of Peribysin B." Organic Letters 20, no. 22 (October 26, 2018): 7003–6. http://dx.doi.org/10.1021/acs.orglett.8b02838.

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5

Inose, Kota, Kazuaki Tanaka, Takeshi Yamada, Hiroyuki Koshino, and Masaru Hashimoto. "Isolation of Peribysins O, P, and Q from Periconia macrospinosa KT3863 and Configurational Reinvestigation of Peribysin E Diacetate from Periconia byssoides OUPS-N133." Journal of Natural Products 82, no. 4 (February 15, 2019): 911–18. http://dx.doi.org/10.1021/acs.jnatprod.8b01001.

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6

Athawale, Paresh R., Hanuman P. Kalmode, Zenia Motiwala, Kiran A. Kulkarni, and D. Srinivasa Reddy. "Overturning the Peribysin Family Natural Products Isolated from Periconia byssoides OUPS-N133: Synthesis and Stereochemical Revision of Peribysins A, B, C, F, and G." Organic Letters 22, no. 8 (April 7, 2020): 3104–9. http://dx.doi.org/10.1021/acs.orglett.0c00857.

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7

Handore, Kishor L., and D. Srinivasa Reddy. "A Diverted Total Syntheses of Potent Cell Adhesion Inhibitor Peribysin E Analogues." Organic Letters 15, no. 8 (April 4, 2013): 1894–97. http://dx.doi.org/10.1021/ol400555m.

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8

Angeles, Angie R, David C Dorn, Cynthia A Kou, Malcolm A S. Moore, and Samuel J Danishefsky. "Total Synthesis of Peribysin E Necessitates Revision of the Assignment of its Absolute Configuration." Angewandte Chemie 119, no. 9 (February 19, 2007): 1473–76. http://dx.doi.org/10.1002/ange.200604308.

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9

Angeles, Angie R, David C Dorn, Cynthia A Kou, Malcolm A S. Moore, and Samuel J Danishefsky. "Total Synthesis of Peribysin E Necessitates Revision of the Assignment of its Absolute Configuration." Angewandte Chemie International Edition 46, no. 9 (February 19, 2007): 1451–54. http://dx.doi.org/10.1002/anie.200604308.

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10

Azhari, Azmi, and Unang Supratman. "The Chemistry and Pharmacology of Fungal Genus Periconia: A Review." Scientia Pharmaceutica 89, no. 3 (July 29, 2021): 34. http://dx.doi.org/10.3390/scipharm89030034.

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Abstract:

Periconia is filamentous fungi belonging to the Periconiaceae family, and over the last 50 years, the genus has shown interest in natural product exploration for pharmacological purposes. Therefore, this study aims to analyze the different species of Periconia containing natural products such as terpenoids, polyketides, cytochalasan, macrosphelides, cyclopentenes, aromatic compounds, and carbohydrates carbasugar derivates. The isolated compound of this kind, which was reported in 1969, consisted of polyketide derivatives and their structures and was determined by chemical reaction and spectroscopic methods. After some years, 77 compounds isolated from endophytic fungus Periconia were associated with eight plant species, 28 compounds from sea hare Aplysia kurodai, and ten from endolichenic fungi Parmelia sp. The potent pharmacological agents from this genus are periconicin A, which acts as an antimicrobial, pericochlorosin B as an anti-human immunodeficiency virus (HIV), peribysin D, and pericosine A as cytotoxic agents, and periconianone A as an anti-inflammatory agent. Furthermore, information about taxol and piperine from Periconia producing species was also provided. Therefore, this study supports discovering new drugs produced by the Periconia species and compares them for future drug development.

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11

Athawale, Paresh R., Vishal M. Zade, Gamidi Rama Krishna, and D. Srinivasa Reddy. "Tuning of α-Silyl Carbocation Reactivity into Enone Transposition: Application to the Synthesis of Peribysin D, E-Volkendousin, and E-Guggulsterone." Organic Letters 23, no. 17 (August 13, 2021): 6642–47. http://dx.doi.org/10.1021/acs.orglett.1c02173.

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12

Koshino, Hiroyuki, Hiroko Satoh, Takeshi Yamada, and Yasuaki Esumi. "Structural revision of peribysins C and D." Tetrahedron Letters 47, no. 27 (July 2006): 4623–26. http://dx.doi.org/10.1016/j.tetlet.2006.04.139.

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13

Yamada, Takeshi, Masashi Iritani, Katsuhiko Minoura, Kenzo Kawai, and Atsushi Numata. "Peribysins A–D, potent cell-adhesion inhibitors from a sea hare-derived culture of Periconia species." Org. Biomol. Chem. 2, no. 14 (2004): 2131–35. http://dx.doi.org/10.1039/b404459b.

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14

Yamada, Takeshi, Mitsunobu Doi, Atsuko Miura, Waka Harada, Mika Hiramura, Katsuhiko Minoura, Reiko Tanaka, and Atsushi Numata. "Absolute Stereostructures of Cell-adhesion Inhibitors, Peribysins A, E, F and G, Produced by a Sea Hare-derived Periconia sp." Journal of Antibiotics 58, no. 3 (March 2005): 185–91. http://dx.doi.org/10.1038/ja.2005.21.

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15

"Synthesis of (±)-Peribysin E." Synfacts 8, no. 03 (February 20, 2012): 0236. http://dx.doi.org/10.1055/s-0031-1290239.

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16

Angeles, Angie R., Stephen P. Waters, and Samuel J. Danishefsky. "ChemInform Abstract: Total Syntheses of (+)- and (-)-Peribysin E." ChemInform 40, no. 7 (February 17, 2009). http://dx.doi.org/10.1002/chin.200907193.

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17

Angeles, Angie R., David C. Dorn, Cynthia A. Kou, Malcolm A. S. Moore, and Samuel J. Danishefsky. "Total Synthesis of Peribysin E Necessitates Revision of the Assignment of Its Absolute Configuration." ChemInform 38, no. 25 (June 19, 2007). http://dx.doi.org/10.1002/chin.200725180.

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18

Yamada, Takeshi, Katsuhiko Minoura, Reiko Tanaka, and Atsushi Numata. "Cell-Adhesion Inhibitors Produced by a Sea Hare-Derived Periconia sp. Part 3. Absolute Stereostructures of Peribysin J and Macrosphelide M." ChemInform 38, no. 50 (December 11, 2007). http://dx.doi.org/10.1002/chin.200750214.

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19

Koshino, Hiroyuki, Hiroko Satoh, Takeshi Yamada, and Yasuaki Esumi. "Structural Revision of Peribysins C and D." ChemInform 37, no. 41 (October 10, 2006). http://dx.doi.org/10.1002/chin.200641183.

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20

Kanehara, Ryuhi, Kazuaki Tanaka, Takeshi Yamada, Hiroyuki Koshino, and Masaru Hashimoto. "Termination of the Chirality Confusion of Peribysins." Bulletin of the Chemical Society of Japan, February 28, 2023. http://dx.doi.org/10.1246/bcsj.20230025.

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21

Yamada, Takeshi, Masashi Iritani, Katsuhiko Minoura, Kenzo Kawai, and Atsushi Numata. "Peribysins A—D, Potent Cell-Adhesion Inhibitors from a Sea Hare-Derived Culture of Periconia Species." ChemInform 35, no. 48 (November 30, 2004). http://dx.doi.org/10.1002/chin.200448153.

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22

Yamada, Takeshi, Misunobu Doi, Atsuko Miura, Waka Harada, Mika Hiramura, Katsuhiko Minoura, Reiko Tanaka, and Atsushi Numata. "Absolute Stereostructures of Cell-Adhesion Inhibitors, Peribysins A, E, F and G, Produced by a Sea Hare-Derived Periconia sp." ChemInform 36, no. 39 (September 27, 2005). http://dx.doi.org/10.1002/chin.200539190.

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23

Yamada, Takeshi, Katsuhiko Minoura, Reiko Tanaka, and Atsushi Numata. "Cell-Adhesion Inhibitors Produced by a Sea Hare-Derived Periconia sp. Part 2. Absolute Stereostructures of Peribysins H (I) and I (II)." ChemInform 37, no. 50 (December 12, 2006). http://dx.doi.org/10.1002/chin.200650216.

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