Chemistry:Fascaplysin
From HandWiki
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| IUPAC name
13-Oxo-12,13-dihydrobenzo[2,3]indolizino[8,7-b]indol-5-ium
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| Other names
LSM-4272
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C18H11N2O+ | |
| Molar mass | 271.298 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Fascaplysin is a marine alkaloid based on 12H-pyrido[1–2-a:3,4-b′]diindole ring system.[1] It was first isolated as a red pigment from the marine sponge Fascaplysinopsis bergquist collected in the South Pacific near Fiji in 1988.[2] Fascaplysin possesses a broad range of in vitro biological activities including analgesic,[3] antimicrobial, antifungal, antiviral, antimalarial, anti-angiogenic, and antiproliferative activity against numerous cancer cell lines.[1]
Synthesis
The first total synthesis of fascaplysin was performed in seven steps from indole in 1990.[4] Fascaplysin and its derivatives can be synthesized from tryptamine,[5][6][7][8] beta-carboline,[9] indoleketones,[10][11] and indigo.[12]
References
- ↑ 1.0 1.1 B. Bharate, S.; Manda, S.; Mupparapu, N.; Battini, N.; A. Vishwakarma, R. (1 May 2012). "Chemistry and Biology of Fascaplysin, a Potent Marine-Derived CDK-4 Inhibitor". Mini-Reviews in Medicinal Chemistry 12 (7): 650–664. doi:10.2174/138955712800626719. PMID 22512549.
- ↑ Roll, D. (1988). "Fascaplysin, an unusual antimicrobial pigment from the marine sponge Fascaplysinopsis sp". J. Org. Chem. 53 (14): 3276–3278. doi:10.1021/jo00249a025. https://pubs.acs.org/doi/10.1021/jo00249a025.
- ↑ Johnson, Tyler A.; Milan-Lobo, Laura; Che, Tao; Ferwerda, Madeline; Lambu, Eptisam; McIntosh, Nicole L.; Li, Fei; He, Li et al. (2016-11-22). "Identification of the First Marine-Derived Opioid Receptor "Balanced" Agonist with a Signaling Profile That Resembles the Endorphins". ACS Chemical Neuroscience (American Chemical Society (ACS)) 8 (3): 473–485. doi:10.1021/acschemneuro.6b00167. ISSN 1948-7193. PMID 27744679.
- ↑ Pelcman, Benjamin; Gribble, Gordon (1990). "Total synthesis of the marine sponge pigment fascaplysin". Tetrahedron Letters 31 (17): 2381–2384. doi:10.1016/S0040-4039(00)97367-2.
- ↑ Radchenko, Oleg S.; Novikov, Vyacheslav L.; Elyakov, George B. (1997). "A simple and practical approach to the synthesis of the marine sponge pigment fascaplysin and related compounds". Tetrahedron Letters (Elsevier BV) 38 (30): 5339–5342. doi:10.1016/s0040-4039(97)01167-2. ISSN 0040-4039.
- ↑ Zhu, Yan-Ping; Liu, Mei-Cai; Cai, Qun; Jia, Feng-Cheng; Wu, An-Xin (2013-06-20). "A Cascade Coupling Strategy for One-Pot Total Synthesis of β-Carboline and Isoquinoline-Containing Natural Products and Derivatives". Chemistry - A European Journal (Wiley) 19 (31): 10132–10137. doi:10.1002/chem.201301734. ISSN 0947-6539. PMID 23788489.
- ↑ Dighe, Shashikant U.; Samanta, Surya K.; Kolle, Shivalinga; Batra, Sanjay (2017). "Iodine-mediated oxidative Pictet-Spengler reaction using terminal alkyne as the 2-oxoaldehyde surrogate for the synthesis of 1-aroyl-β-carbolines and fused-nitrogen heterocycles". Tetrahedron (Elsevier BV) 73 (17): 2455–2467. doi:10.1016/j.tet.2017.03.031. ISSN 0040-4020.
- ↑ Bharate, Sandip B.; Manda, Sudhakar; Joshi, Prashant; Singh, Baljinder; Vishwakarma, Ram A. (2012). "Total synthesis and anti-cholinesterase activity of marine-derived bis-indole alkaloid fascaplysin". MedChemComm (Royal Society of Chemistry (RSC)) 3 (9): 1098. doi:10.1039/c2md20076g. ISSN 2040-2503.
- ↑ Zhidkov, Maxim E.; Kaminskii, Vladimir A. (2013). "A new method for the synthesis of the marine alkaloid fascaplysin based on the microwave-assisted Minisci reaction". Tetrahedron Letters (Elsevier BV) 54 (27): 3530–3532. doi:10.1016/j.tetlet.2013.04.113. ISSN 0040-4039.
- ↑ Dubovitskii, Sergey (1996). "Method for synthesis of 12H-pyrido[1,2-a:3,4-b']diindoles. Total synthesis of homofascaplysin C". Tetrahedron Letters 37 (29): 5207–5208. doi:10.1016/0040-4039(96)01052-0.
- ↑ Zhidkov, M. (2010). "A new method for the synthesis of the marine alkaloid fascaplysin". Tetrahedron Letters 51 (50): 6498–6499. doi:10.1016/j.tetlet.2010.09.120.
- ↑ Zhidkov, M. (2018). "Syntheses of the marine alkaloids 6-oxofascaplysin, fascaplysin and their derivatives". Tetrahedron Letters 59 (8): 708–711. doi:10.1016/j.tetlet.2018.01.023.
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