Chemistry:Hopeanol
From HandWiki
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| Names | |
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| IUPAC name
Methyl (1'S,9'R)-3',5',11',13'-tetrahydroxy-9'-(4-hydroxyphenyl)-6,8'-dioxospiro[cyclohexa-1,4-diene-3,16'-tetracyclo[7.6.1.02,7.010,15]hexadeca-2(7),3,5,10(15),11,13-hexaene]-1'-carboxylate[1]
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
PubChem CID
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| Properties | |
| C29H20O9 | |
| Molar mass | 512.470 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 | |
Hopeanol is a highly cytotoxic resveratrol-derivative with the molecular formula C29H20O9 which has been isolated from the bark of the tree Hopea exalata.[2][1][3][4]
References
- ↑ 1.0 1.1 "Hopeanol" (in en). https://pubchem.ncbi.nlm.nih.gov/compound/Hopeanol#section=Names-and-Identifiers.
- ↑ Ge, Hui Ming; Xu, Chen; Wang, Xiao Ting; Huang, Bo; Tan, Ren Xiang (December 2006). "Hopeanol: A Potent Cytotoxin with A Novel Skeleton fromHopea exalata". European Journal of Organic Chemistry 2006 (24): 5551–5554. doi:10.1002/ejoc.200600661.
- ↑ Gupta, Ajai Prakash; Pandotra, Pankaj; Sharma, Rajni; Kushwaha, Manoj; Gupta, Suphla (25 June 2013) (in en). Studies in Natural Products Chemistry: Chapter 8. Marine Resource: A Promising Future for Anticancer Drugs. Elsevier Inc. Chapters. ISBN 978-0-12-808473-1.
- ↑ (in en) Issues in Chemistry and General Chemical Research: 2011 Edition. ScholarlyEditions. 9 January 2012. ISBN 978-1-4649-6329-2.
Further reading
- Nicolaou, K. C.; Wu, T. Robert; Kang, Qiang; Chen, David Y.-K. (27 April 2009). "Total Synthesis of Hopeahainol A and Hopeanol". Angewandte Chemie International Edition 48 (19): 3440–3443. doi:10.1002/anie.200900438. PMID 19280619.
- "Synthesis of ()-Hopeanol". Synfacts 2009 (11): 1194. 22 October 2009. doi:10.1055/s-0029-1218028.
- Zografos, Alexandros L. (17 March 2016) (in en). From Biosynthesis to Total Synthesis: Strategies and Tactics for Natural Products. John Wiley & Sons. p. 371. ISBN 978-1-118-75356-9.
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