 Enol form
| |
 Keto form
| |
 | |
 | |
| Names | |
|---|---|
| Pronunciation | /ˈkɜːrkjʊmɪn/ |
| Preferred IUPAC name
(1E,6E)-1,7-Bis(4-hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione | |
Other names
| |
| Identifiers | |
3D model (JSmol)
|
|
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.006.619 |
| E number | E100 (colours) |
| KEGG | |
PubChem CID
|
|
| UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
| Properties | |
| C21H20O6 | |
| Molar mass | 368.385 g·mol−1 |
| Appearance | Bright yellow-orange powder |
| Melting point | 183 °C (361 °F; 456 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Curcumin is a bright yellow chemical produced by plants of the Curcuma longa species. It is the principal curcuminoid of turmeric (Curcuma longa), a member of the ginger family, Zingiberaceae. It is sold as an herbal supplement, cosmetics ingredient, food flavoring, and food coloring.[1]
Chemically, curcumin is a polyphenol, more particularly a diarylheptanoid, belonging to the group of curcuminoids, which are phenolic pigments responsible for the yellow color of turmeric.[2]
Extensive studies have consistently failed to show any medical value for curcumin. It is difficult to study because it is both unstable and poorly bioavailable. It is unlikely to produce useful leads for drug development as a lead compound.[3]
History
Curcumin was named in 1815 when Henri Auguste Vogel and Pierre Joseph Pelletier reported the first isolation of a "yellow coloring-matter" from the rhizomes of turmeric.[4] Later, it was found to be a mixture of resin and turmeric oil. In 1910, Milobedzka and Lampe reported the chemical structure of curcumin to be as diferuloylmethane.[5] Later in 1913, the same group accomplished the synthesis of the compound.
Although used in traditional medicine, the possible therapeutic properties of turmeric or curcumin remain undetermined.[3][6][7]
Uses
The most common applications are as an ingredient in dietary supplement, in cosmetics, as flavoring for foods, such as turmeric-flavored beverages in South and Southeast Asia,[1] and as coloring for foods, such as curry powders, mustards, butters, and cheeses. As a food additive for orange-yellow coloring in prepared foods, its E number is E 100 in the European Union.[8][9] It is also approved by the U.S. FDA to be used as a food coloring in US.[10]
Chemistry
Curcumin incorporates a seven carbon linker and three major functional groups: an α,β-unsaturated β-diketone moiety and an aromatic O-methoxy-phenolic group.[2][5] The aromatic ring systems, which are phenols, are connected by two α,β-unsaturated carbonyl groups.[2][11] It is a diketone tautomer, existing in enolic form in organic solvents and in keto form in water.[12] The diketones form stable enols and are readily deprotonated to form enolates, which bind metal ions to form acetylacetonate-like complexes.[13] Its complexing properties are manifesting in its reaction with boric acid to give a red-colored rosocyanine.[2][14]
Because of its hydrophobic nature, curcumin is poorly soluble in water[2] but is easily soluble in organic solvents.[5]
Biosynthesis
The biosynthetic route of curcumin is uncertain. In 1973, Peter J. Roughley and Donald A. Whiting proposed two mechanisms for curcumin biosynthesis. The first mechanism involves a chain extension reaction by cinnamic acid and 5 malonyl-CoA molecules that eventually arylize into a curcuminoid. The second mechanism involves two cinnamate units coupled together by malonyl-CoA. Both use cinnamic acid as their starting point, which is derived from the amino acid phenylalanine.[15]
Plant biosynthesis starting with cinnamic acid is rare compared to the more common p-coumaric acid.[15] Only a few identified compounds, such as anigorufone and pinosylvin, build from cinnamic acid.[16][17]
Pharmacology
Curcumin, which shows positive results in most drug discovery assays, is regarded as a false lead that medicinal chemists include among "pan-assay interference compounds". This attracts undue experimental attention while failing to advance as viable therapeutic or drug leads,[3][6][18] although some derivatives of curcumin such as EF-24 have been well-studied.[19]
Factors that limit the bioactivity of curcumin or its analogs include chemical instability, water insolubility, absence of potent and selective target activity, low bioavailability, limited tissue distribution, and extensive metabolism.[3] Very little curcumin escapes the GI tract and most is excreted in feces unchanged.[20] If curcumin enters plasma in reasonable amounts, there is a high risk of toxicity since it is promiscuous, and interacts with several proteins known to increase the risk of adverse effects, including hERG, cytochrome P450s, and glutathione S-transferase.[3]
Safety
Although curcumin has been assessed in numerous laboratory and clinical studies, it has no medical uses.[21] Its instability, reactivity, and poor bioavailability, make curcumin an unlikely drug candidate.[3] Curcumin exhibits numerous interference properties which may lead to misinterpretation of results.[3][6][22]
Between 1995 and 2017, the US government funded US$150 million in biomedical research into curcumin through the National Center for Complementary and Integrative Health. No support was found for curcumin as a medical treatment.[3] As a component of turmeric, curcumin may interact with prescription drugs and dietary supplements.[23] In high amounts, it may be unsafe for women during pregnancy.[23] It may cause side effects, such as nausea, diarrhea, hives, or dizziness.[23] Between 2004 and 2022 there were ten cases of liver injury caused by curcumin herbal and dietary supplements.[24] Curcumin is a contact allergen.[25]
The intended use of curcumin as a food additive is generally recognized as safe by the U.S. Food and Drug Administration.[26]
Research fraud
Bharat Aggarwal, a former cancer researcher at the University of Texas MD Anderson Cancer Center, had 29 papers retracted due to research fraud as of July 2021[update].[27][28][29] Aggarwal's research had focused on potential anti-cancer properties of herbs and spices, particularly curcumin, and according to a March 2016 article in the Houston Chronicle, "attracted national media interest and laid the groundwork for ongoing clinical trials".[30][31][32]
Aggarwal cofounded a company in 2004 called Curry Pharmaceuticals based in Research Triangle Park, North Carolina, which planned to develop drugs based on synthetic analogs of curcumin.[31][33] SignPath Pharma, a company seeking to develop liposomal formulations of curcumin, licensed three patents by Aggarwal related to that approach from MD Anderson in 2013.[34]
Warnings about dietary supplements
Between 2018 and 2023, the U.S. FDA issued 29 warning letters to American manufacturers of dietary supplements for making false claims of anti-disease effects from using products containing curcumin.[35] In each letter, the FDA stated that the supplement product was not an approved new drug because the "product is not generally recognized as safe and effective" for the advertised uses, that "new drugs may not be legally introduced or delivered for introduction into interstate commerce without prior approval from FDA", and that the "FDA approves a new drug on the basis of scientific data and information demonstrating that the drug is safe and effective".[35]
Alternative medicine
Though there is no evidence for the safety or efficacy of using curcumin as a therapy,[3][6] some alternative medicine practitioners give it intravenously, supposedly as a treatment for numerous diseases.[36][37][38] In 2017, two serious cases of adverse events were reported from curcumin or turmeric products—one severe allergic reaction and one death[36]—that were caused by administration of a curcumin-polyethylene glycol (PEG40) emulsion product by a naturopath.[38] One treatment caused anaphylaxis leading to death.[36][38]
Stability
In 2016, laboratory research established and compared the radiosensitivity of three organic food colorants including curcumin, carmine, and annatto to create data to be used for application whenever food products containing these food colors were to undergo the radiation process.[39] The researchers used spectrophotometry and capillary electrophoresis to establish radiosensitivity of the three organic food colorants. Carmine samples were quite stable against radiation treatment, annatto showed limited stability, and curcumin was found to be unstable, particularly when diluted.[39]
References
- ^ a b Majeed S (28 December 2015). "The State of the Curcumin Market". Natural Products Insider. Archived from the original on October 17, 2017. Retrieved February 29, 2016.
- ^ a b c d e CID 969516 from PubChem
- ^ a b c d e f g h i Nelson KM, Dahlin JL, Bisson J, Graham J, Pauli GF, Walters MA (March 2017). "The Essential Medicinal Chemistry of Curcumin". Journal of Medicinal Chemistry. 60 (5): 1620–1637. doi:10.1021/acs.jmedchem.6b00975. PMC 5346970. PMID 28074653.
See also: Nelson KM, Dahlin JL, Bisson J, Graham J, Pauli GF, Walters MA (May 2017). "Curcumin May (Not) Defy Science". ACS Medicinal Chemistry Letters. 8 (5): 467–470. doi:10.1021/acsmedchemlett.7b00139. PMC 5430405. PMID 28523093. - ^ Vogel, A; Pelletier, J (July 1815). "Examen chimique de la racine de Curcuma" [Chemical examination of turmeric root]. Journal de Pharmacie et des Sciences Accessoires (in French). 1: 289–300. available at Gallica.
- ^ a b c Farooqui, Tahira; Farooqui, Akhlaq A. (2019). "Curcumin: Historical Background, Chemistry, Pharmacological Action, and Potential Therapeutic Value". Curcumin for Neurological and Psychiatric Disorders. pp. 23–44. doi:10.1016/B978-0-12-815461-8.00002-5. ISBN 978-0-12-815461-8. S2CID 146070671.
- ^ a b c d Baker M (January 2017). "Deceptive curcumin offers cautionary tale for chemists". Nature. 541 (7636): 144–145. Bibcode:2017Natur.541..144B. doi:10.1038/541144a. PMID 28079090.
- ^ "Turmeric". US National Center for Complementary and Integrative Health, National Institutes of Health. April 2020. Retrieved 24 October 2023.
- ^ European Commission. "Food Additives". Archived from the original on October 8, 2022. Retrieved February 15, 2014.
- ^ "Curcumin, E 100, page 9". Specifications for food additives listed in Annexes II and III to Regulation (EC) No 1333/2008 of the European Parliament. March 9, 2012. Retrieved July 24, 2019.
- ^ "CFR – Code of Federal Regulations Title 21". www.accessdata.fda.gov.
- ^ Miłobȩdzka J, van Kostanecki S, Lampe V (1910). "Zur Kenntnis des Curcumins" [Knowing about curcumin]. Berichte der Deutschen Chemischen Gesellschaft (in German). 43 (2): 2163–2170. doi:10.1002/cber.191004302168.
- ^ Manolova Y, Deneva V, Antonov L, Drakalska E, Momekova D, Lambov N (November 2014). "The effect of the water on the curcumin tautomerism: a quantitative approach" (PDF). Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 132: 815–820. Bibcode:2014AcSpA.132..815M. doi:10.1016/j.saa.2014.05.096. PMID 24973669.
- ^ Pham, Chien Thang; Pham, Thu Thuy; Nguyen, Hung Huy; Trieu, Thi Nguyet (2020). "Syntheses, Structures, and Bioactivities Evaluation of some Transition Metal Complexes with 4,4'-Diacetylcurcumin". Zeitschrift für Anorganische und Allgemeine Chemie. 646 (11–12): 495–499. Bibcode:2020ZAACh.646..495P. doi:10.1002/zaac.202000088.
- ^ National Exposure Research Laboratory (EPA-NERL) (1974). "EPA-NERL: 212.3: Boron by Colorimetry – Boron (Colorimetric, Curcumin)". National Environmental Methods Index. Archived from the original on 2017-02-03. Retrieved 2024-02-18.
- ^ a b c Kita T, Imai S, Sawada H, Kumagai H, Seto H (July 2008). "The biosynthetic pathway of curcuminoid in turmeric (Curcuma longa) as revealed by 13C-labeled precursors". Bioscience, Biotechnology, and Biochemistry. 72 (7): 1789–1798. doi:10.1271/bbb.80075. PMID 18603793.
- ^ Schmitt B, Hölscher D, Schneider B (February 2000). "Variability of phenylpropanoid precursors in the biosynthesis of phenylphenalenones in Anigozanthos preissii". Phytochemistry. 53 (3): 331–337. Bibcode:2000PChem..53..331S. doi:10.1016/S0031-9422(99)00544-0. PMID 10703053.
- ^ Gehlert R, Schoeppner A, Kindl H (1990). "Stilbene Synthase from Seedlings of Pinus sylvestris: Purification and Induction in Response to Fungal Infection" (PDF). Molecular Plant-Microbe Interactions. 3 (6): 444–449. Bibcode:1990MPMI....3..444G. doi:10.1094/MPMI-3-444.
- ^ Bisson J, McAlpine JB, Friesen JB, Chen SN, Graham J, Pauli GF (March 2016). "Can Invalid Bioactives Undermine Natural Product-Based Drug Discovery?". Journal of Medicinal Chemistry. 59 (5): 1671–1690. doi:10.1021/acs.jmedchem.5b01009. PMC 4791574. PMID 26505758.
- ^ He, Yonghan; Li, Wen; Hu, Guangrong; Sun, Hui; Kong, Qingpeng (11 December 2018). "Bioactivities of EF24, a Novel Curcumin Analog: A Review". Frontiers in Oncology. 8 614. doi:10.3389/fonc.2018.00614. PMC 6297553. PMID 30619754.
- ^ Metzler M, Pfeiffer E, Schulz SI, Dempe JS (2013). "Curcumin uptake and metabolism". BioFactors. 39 (1): 14–20. doi:10.1002/biof.1042. PMID 22996406. S2CID 8763463.
- ^ "Curcumin". Micronutrient Information Center; Phytochemicals. Linus Pauling Institute, Oregon State University, Corvallis. 2016. Retrieved June 18, 2016.
- ^ Lowe, Derek (12 January 2017). "Curcumin Will Waste Your Time". Science Blogs.
- ^ a b c "Turmeric". Drugs.com. December 6, 2017. Retrieved November 28, 2018.
- ^ Chaudhari SP, Tam AY, Barr JA (November 2015). "Curcumin: A Contact Allergen". J Clin Aesthet Dermatol. 8 (11): 43–48. PMC 4689497. PMID 26705440.
- ^ "GRAS Notice (GRN) No. 822". U.S. Food & Drug Administration. GRAS Notice Inventory. Archived from the original on December 3, 2020.
- ^ "The Retraction Watch Leaderboard". Retraction Watch. 16 June 2015. Retrieved 28 July 2021.
- ^ Ackerman T (February 29, 2012). "M.D. Anderson professor under fraud probe". Houston Chronicle. Retrieved March 8, 2016.
- ^ "Caught Our Notice: Researcher who once threatened to sue Retraction Watch now up to 19 retractions". Retraction Watch. April 10, 2018.
- ^ Ackerman T (March 2, 2016). "M.D. Anderson scientist, accused of manipulating data, retires". Houston Chronicle.
- ^ a b Stix G (February 2007). "Spice Healer". Scientific American. 296 (2): 66–69. Bibcode:2007SciAm.296b..66S. doi:10.1038/scientificamerican0207-66. PMID 17367023.
- ^ Ackerman T (July 11, 2005). "In cancer fight, a spice brings hope to the table". Houston Chronicle. Retrieved March 24, 2015.
- ^ Singh S (September 2007). "From exotic spice to modern drug?". Cell. 130 (5): 765–768. doi:10.1016/j.cell.2007.08.024. PMID 17803897. S2CID 16044143.
- ^ Baum S (March 26, 2013). "Biotech startup raises $1M for lung cancer treatment using component of tumeric". Med City News.
- ^ a b "Warning Letters: Curcumin (search term)". US Food and Drug Administration. 23 April 2023. Archived from the original on April 28, 2019. Retrieved 23 April 2023.
- ^ a b c "FDA investigates two serious adverse events associated with ImprimisRx's compounded curcumin emulsion product for injection". Food and Drug Administration. August 4, 2017. Archived from the original on November 2, 2017.
- ^ Hermes BM (March 27, 2017). "Naturopathic Doctors Look Bad After California Woman Dies From Turmeric Injection". Forbes. Retrieved May 12, 2017.
- ^ a b c Hermes BM (April 10, 2017). "Confirmed: Licensed Naturopathic Doctor Gave Lethal 'Turmeric' Injection". Forbes. Retrieved December 9, 2017.
- ^ a b Cosentino, Helio M.; Takinami, Patricia Y.I.; del Mastro, Nelida L. (2016). "Comparison of the ionizing radiation effects on cochineal, annatto and turmeric natural dyes". Radiation Physics and Chemistry. 124: 208–211. Bibcode:2016RaPC..124..208C. doi:10.1016/j.radphyschem.2015.09.016.
