Online Database of Chemicals from Around the World

Luteolin
[CAS# 491-70-3]

List of Suppliers
Shaanxi Scidoor Hi-Tech Biology Co., Ltd. China Inquire  
+86 (29) 6296-0300
6296-0309
6296-0305
sales@scidoor.com
Chemical manufacturer
chemBlink standard supplier since 2006
Xi'an App-Chem Bio (Tech) Co., Ltd. China Inquire  
+86 (29) 8831-8908 ex 805
400-6699-003
sales@appchem.cn
Chemical manufacturer
chemBlink standard supplier since 2007
Shaanxi Sciphar Biotechnology Co., Ltd. China Inquire  
+86 (29) 8835-3228
8838-9752
8300-6195
sales@sciphar.com
Chemical manufacturer
chemBlink standard supplier since 2007
Simagchem Corporation China Inquire  
+86 13806087780
sale@simagchem.com
Chemical manufacturer since 2002
chemBlink standard supplier since 2008
Extrasynthese Chemical S.A.S. France Inquire  
+33 (47) 898-2034
info@extrasynthese.com
Chemical manufacturer
chemBlink standard supplier since 2009
Hangzhou Skyherb Technologies Co., Ltd. China Inquire  
+86 (571) 8805-3319
sales@skyherb.cn
Chemical manufacturer since 2003
chemBlink standard supplier since 2009
Shanghai Standard Biotech Co., Ltd. China Inquire  
+86 (21) 5132-0033
wangxinliang@nature-standard.com
sales@nature-standard.com
Chemical manufacturer
chemBlink standard supplier since 2009
Wilshire Technologies, Inc. USA Inquire  
+1 (609) 683-1117
Wilshire-info@evonik.com
Chemical manufacturer since 1997
chemBlink standard supplier since 2010
Complete supplier list of Luteolin
Identification
Classification API >> Respiratory medication >> Antitussive
Name Luteolin
Synonyms 3',4',5,7-Tetrahydroxyflavone; 5,7,3',4'-Tetrahydroxyflavone
Molecular Structure CAS # 491-70-3, Luteolin, 3',4',5,7-Tetrahydroxyflavone, 5,7,3',4'-Tetrahydroxyflavone
Molecular Formula C15H10O6
Molecular Weight 286.24
CAS Registry Number 491-70-3
EC Number 207-741-0
SMILES C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O
Properties
Solubility 35 mg/mL (DMSO)
Density 1.7±0.1 g/cm3, Calc.*
Melting point 330 ºC
Index of Refraction 1.768, Calc.*
Boiling Point 616.1±55.0 ºC (760 mmHg), Calc.*
Flash Point 239.5±25.0 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
Eye irritationEye Irrit.2AH319
Specific target organ toxicity - single exposureSTOT SE3H336
SDS Available
up Discovory and Applicatios
Luteolin is a naturally occurring flavonoid that has attracted considerable interest in the fields of nutrition, pharmacology, and biochemistry. Discovered in the early 19th century, luteolin was first isolated from the leaves of the plant species *Reseda luteola*, from which it derives its name. Over the years, researchers have identified luteolin in various other plant sources, including fruits, vegetables, and herbs, making it an important component of the human diet.

The chemical structure of luteolin is characterized by its flavone backbone, which consists of a 15-carbon skeleton with a chromone ring. This structural configuration is significant as it contributes to luteolin's diverse biological activities. The compound exhibits strong antioxidant properties, which are attributed to its ability to scavenge free radicals and chelate metal ions. These properties are critical in mitigating oxidative stress, a condition associated with various chronic diseases.

One of the primary applications of luteolin lies in its potential therapeutic benefits. Numerous studies have demonstrated its anti-inflammatory effects, making it a candidate for treating various inflammatory conditions such as arthritis and asthma. The mechanism behind this anti-inflammatory activity involves the inhibition of pro-inflammatory cytokines and enzymes, such as cyclooxygenase and lipoxygenase, which play crucial roles in the inflammatory response.

In addition to its anti-inflammatory properties, luteolin has been investigated for its neuroprotective effects. Research suggests that luteolin can cross the blood-brain barrier and exert protective effects on neuronal cells. It has shown promise in preventing neurodegenerative diseases such as Alzheimer’s and Parkinson’s by reducing neuroinflammation and oxidative damage. This neuroprotective potential has made luteolin a focus of interest in developing functional foods and nutraceuticals aimed at enhancing cognitive health.

Luteolin's anticancer properties are another area of significant research. Studies have indicated that luteolin can inhibit the proliferation of various cancer cell lines, including breast, colon, and prostate cancers. The compound induces apoptosis (programmed cell death) in cancer cells while sparing normal cells, which is a desirable trait in cancer therapeutics. Moreover, luteolin has been shown to enhance the effectiveness of conventional chemotherapy agents, making it a potential adjunct therapy in cancer treatment.

In addition to its therapeutic applications, luteolin is commonly used as a dietary supplement due to its health benefits. As an ingredient in herbal formulations and nutritional supplements, luteolin is marketed for its antioxidant, anti-inflammatory, and immune-modulating effects. Its presence in a variety of fruits and vegetables underscores the importance of a diet rich in flavonoids for maintaining health and preventing disease.

Recent advancements in nanotechnology have also paved the way for innovative delivery systems for luteolin, enhancing its bioavailability and therapeutic efficacy. Nanoparticle formulations have been developed to improve the solubility and stability of luteolin, facilitating its application in targeted drug delivery systems for various health conditions.

In summary, luteolin is a multifaceted flavonoid with a rich history and diverse applications in health and medicine. Its discovery has contributed significantly to our understanding of the role of dietary phytochemicals in human health, and ongoing research continues to explore its potential as a therapeutic agent in various health conditions.

References

2007. Luteolin sensitizes the anticancer effect of cisplatin via c-Jun NH2-terminal kinase-mediated p53 phosphorylation and stabilization. Molecular Cancer Therapeutics, 6(4).
DOI: 17431112

2005. Flavonoids: from cell cycle regulation to biotechnology. Biotechnology Letters, 27(6).
DOI: 15834800

2000. Flavonoids Inhibit Cell Growth and Induce Apoptosis in B16 Melanoma 4A5 Cells. Bioscience, Biotechnology, and Biochemistry, 64(9).
DOI: 11055382
Market Analysis Reports
List of Reports Available for Luteolin
Related Products
LY-2584702  LY 2603618  LY 2608204  LY 2784544  LY 2811376  Lurasidone Impurity A  Lurasidone Impurity 4 DiHCl  Lurbinectedin  Luseogliflozin  Lusutrombopag  Luteolin 6-C-alpha-L-arabinopyranosyl-8-C-beta-D-glucopyranoside  Luteolin 7,3'-di-O-glucuronide  Luteolin 3'-O-galacturonide  Luteolin 7-O-galacturonide  Luteolin glucoside  Luteolin 5-glucoside  Luteolin-7-beta-D-glucuronide  Luteolin 3'-O-beta-D-glucuronide  Luteolin 5-methyl ether  Luteolin 7-sulfate