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| Names | |
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| IUPAC name
(E)-5-[(1R,4aR,8aR)-5,5,8a-Trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoic acid
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| Other names
(-)-Copalic acid
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C20H32O2 | |
| Molar mass | 304.474 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Copalic acid is a chemical compound that is a constituent of copaiba oil, an oleoresin extracted from trees in the genus Copaifera.[1] It is a diterpenoid of the labdane class.[2]
Because copaiba oil has some uses in traditional herbal medicine, there has been scientific interest in investigating the potential pharmacology of its constituents, including copalic acid.[2][3] In addition, synthetic derivatives of copalic acid have been investigated for their potential pharmacology as well.[4]
Several laboratory syntheses of copalic acid have been reported.[5][6]
References
- ^ Souza, Ariana Borges; Moreira, Monique Rodrigues; Borges, Carly Henrique Gambeta; Simão, Marília Rodrigues; Bastos, Jairo Kenupp; Sousa, João Paulo Barreto; Ambrosio, Sérgio Ricardo; Veneziani, Rodrigo Cassio Sola (2012). "Development and validation of a rapid RP-HPLC method for analysis of (−)-copalic acid in copaíba oleoresin". Biomedical Chromatography. 27 (3): 280–283. doi:10.1002/bmc.2788. PMID 22847230.
- ^ a b Medeiros, Vanessa Gonçalves; Durán, Fernando Javier; Lang, Karen Luise (2021). "Copalic Acid: Occurrence, Chemistry, and Biological Activities". Revista Brasileira de Farmacognosia. 31 (4): 375–386. doi:10.1007/s43450-021-00173-2. S2CID 258704922.
- ^ Nakamura, Marcela; Endo, Eliana; De Sousa, João Paulo; Callejon, Daniel; Ueda-Nakamura, Tânia; Dias Filho, Benedito; De Freitas, Osvaldo; Nakamura, Celso; Lopes, Norberto (2016). "Copaiba Oil and Its Constituent Copalic Acid as Chemotherapeutic Agents against Dermatophytes". Journal of the Brazilian Chemical Society. doi:10.21577/0103-5053.20160309.
- ^ Idippily, Nethrie D.; Zheng, Qiaoyun; Gan, Chunfang; Quamine, Aicha; Ashcraft, Morgan M.; Zhong, Bo; Su, Bin (2017). "Copalic acid analogs down-regulate androgen receptor and inhibit small chaperone protein". Bioorganic & Medicinal Chemistry Letters. 27 (11): 2292–2295. doi:10.1016/j.bmcl.2017.04.046. PMID 28442254.
- ^ Fujii, Mikio; Ishii, Sadayuki; Saito, Ryota; Akita, Hiroyuki (2009). "Enzymatic resolution of albicanol and its application to the synthesis of (−)-copalic acid". Journal of Molecular Catalysis B: Enzymatic. 59 (4): 254–260. doi:10.1016/j.molcatb.2008.07.004.
- ^ Xin, Zhengyuan; Lu, Yunlong; Xing, Xiaolan; Long, Jingjie; Li, Jiabin; Xue, Xiaowen (2016). "Synthesis of (−)-agathic acid and (−)-copalic acid from andrographolide via a regioselective Barton-McCombie reaction". Tetrahedron. 72 (4): 555–562. doi:10.1016/j.tet.2015.12.022.
This page was last edited on 8 November 2023, at 11:16