Chemodex

Curcumin

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CDX-C0158-G01010 gCHF 54.00
CDX-C0158-G05050 gCHF 177.00

Specifications / Handling

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Product Details
Synonyms (E,E)-1,7-bis(4-Hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione; Diferuloylmethane; Diferulylmethane; Diferuloylmethane; Natural Yellow 3
Product Type Chemical
Properties
Formula

C21H20O6

MW 368.38
CAS 458-37-7
RTECS MI5230000
Source/Host Chemicals Plant
Purity Chemicals ≥95%
Appearance Yellow to orange solid.
Solubility Soluble in DMSO (25mg/ml) or ethanol (10mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key VFLDPWHFBUODDF-FCXRPNKRSA-N
Smiles OC1=CC=C(/C=C/C(CC(/C=C/C2=CC(OC)=C(O)C=C2)=O)=O)C=C1OC
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
MSDS Download PDF Download PDF
Product Specification Sheet
Datasheet Download PDF Download PDF

Scientific Background Information

Product Description

Curcumin is the major yellow pigment in turmeric and curry and has antioxidant, anti-inflammatory, neuroprotective, cardioprotective, antidiabetic, antiviral, antibacterial, antifungal, chemopreventive and antitumor activities. It interferes with multiple cell signaling pathways, including cell cycle (cyclin D1 and cyclin E), apoptosis (activation of caspases and down-regulation of anti-apoptotic gene products), proliferation (HER-2, EGFR and AP-1), survival (PI3K/AKT pathway), invasion (MMP-9 and adhesion molecules), angiogenesis (VEGF), metastasis (CXCR-4), tumorigenesis and development (Shh, Gli), metabolism (PPARγ, Nrf2), epigenetics (HDACs, HATs, DNA methyltransferase I and microRNAs) and inflammation (NLRP3, TLR4, NF-κB, TNF, IL-6, IL-1, COX-2 and 5-LOX).

Product-specific References

(1) R.K. Maheshwari, et al.; Life Sci. 78, 2081 (2006) (Review) | (2) V.P. Menon & A.R. Sudheer; Adv. Exp. Med. Biol. 595, 105 (2007) (Review) | (3) G. Kuttan, et al.; Adv. Exp. Med. Biol. 595, 173 (2007) (Review) | (4) B.B. Aggarwal & K.B. Harikumar; Int. J. Biochem. Cell Biol. 41, 40 (2009) (Review) | (5) S. Fu & R. Kurzrock; Cancer 116, 4670 (2010) (Review) | (6) L. Alappat & A.B. Awad; Nutr. Rev. 68, 729 (2010) (Review) | (7) R.B. Mythri & M.M. Bharath; Curr. Pharm. Des. 18, 91 (2012) (Review) | (8) A.A. Momtazi, et al.; Rev. Physiol. Biochem. Pharmacol. 171, 1 (2016) (Review) | (9) S.S. Soflaei, et al.; Curr. Pharm. Des. 24, 123 (2018) (Review) | (10) M. Boozari, et al.; J. Cell Physiol. 234, 12471 (2019) (Review) | (11) K.R. Kahkhaie, et al.; Inflammopharmacol. 27, 885 (2019) (Review) | (12) D.J.Den Hartogh, et al.; Nutrients 12, 118 (2020) (Review) | (13) D.J.Den Hartogh, et al.; Nutrients 12, 58 (2020) (Review) | (14) M.A. Panaro, et al.; Int. J. Mol. Sci. 21, 2299 (2020) (Review) | (15) M.R. Jennings & R.J. Parks; Viruses 12, 1242 (2020) (Review) | (16) A.Saeedi-Boroujeni, et al.; Basic. Clin. Pharmacol. Toxicol. 128, 37 (2021) (Review)

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