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Luteolin(491-70-3)C15H10O6

  • Chemical Name: Luteolin
  • CAS No.:491-70-3
  • MF:C15H10O6
  • MW:286.24
  • Purity:≥98% or according to customer requirements
  • Color: Yellow
  • Product Categories: Inhibitors;Pharmaceuticals;Intermediates & Fine Chemicals;Plant extract;pharmaceutical intermediate
  • Test method: HPLC
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What is Luteolin?

Luteolin is a tetrahydroxyflavone in which the four hydroxy groups are located at positions 3', 4', 5 and 7. It is thought to play an important role in the human body as an antioxidant, a free radical scavenger, an anti-inflammatory agent and an immune system modulator as well as being active against several cancers. It has a role as an EC 2.3.1.85 (fatty acid synthase) inhibitor, an antineoplastic agent, a vascular endothelial growth factor receptor antagonist, a plant metabolite, a nephroprotective agent, an angiogenesis inhibitor, a c-Jun N-terminal kinase inhibitor, an anti-inflammatory agent, an apoptosis inducer, a radical scavenger and an immunomodulator. It is a 3'-hydroxyflavonoid and a tetrahydroxyflavone. It is a conjugate acid of a 2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate(1-). (Source: ChEBI)

Basic information
           
Product Name: Luteolin
Synonyms: Digitoflavoe; Luteolol ; Flacitran; Luteoline; Salifazide; 
CAS: 491-70-3
MF: C15H10O6
MW: 286.24
EINECS: 207-741-0
Chemical Structure

Luteolin            

Luteolin Chemical Properties
          
Melting point  ~330 °C(lit.)
Boiling point  348.61°C (rough estimate)
density  1.2981 (rough estimate)
refractive index  1.4413 (estimate)
storage temp.  2-8°C
pka 6.50±0.40(Predicted)
form  powder
color  yellow
Water Solubility  Soluble in aqueous alkaline solutions (1.4 mg/ml), ethanol (~5 mg/ml), dimethyl sulfoxide (7 mg/ml), 1eq. Sodium hydroxide (5 mM), dimethylformamide (~20 mg/ml), water (1 mg/ml) at 25°C and methanol.
Merck  14,5614
BRN  292084
InChIKey IQPNAANSBPBGFQ-UHFFFAOYSA-N
Usage And Synthesis

Natural Luteolin:  Luteolin is a very typical kind of natural flavonoid and belongs to weak acidic tetrahydroxy flavonoids. It is widely distributed in the plant kingdom and is mainly presented in honeysuckle, chrysanthemum, Nepeta, Herba Ajuga and some other drugs as well as many kinds of vegetables such as thyme, Brussels sprouts, cabbage, cauliflower, beets, broccoli and carrots. Moreover, it is also distributed in the form of glycosides in celery, green pepper, and basil leaves as well as the fruit shell of the legume plant Arachis hypogaea, Ajuga decumbus, Lonicera japonica Thunb, Gentianaceae plant Gentianopsis paludosa, and Valerianaceae plant Valeriana amurensis Smir. The pure product of Luteolin appears as yellow crystalline powder.

luteolin

Synthetic Luteolin: 

In addition to extracting from natural products, luteolin can also be obtained by synthetic methods.

1. Semi-synthetic route: Taking the biologically active hesperidin extracted from orange peel as raw material, luteolin is obtained through a three-step reaction, and the total yield of the product is about 40~47%.

2. Total synthesis route: Synthesize luteolin with phloroglucinol as raw material, and the total product yield is about 34%.


Luteolin Uses:

1. Anti-inflammatory

2. Anti-tumor

3. Anti-allergic

4. Anti-inflammatory demyelinating diseases

5. Anti-fibrosis

6. Anti-fertility and hormone effects

7. It also has effect on blood vessels


Technical Support & Resources

Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

MSDS: MSDS available.

COA: COA can be available if you send us inquiry.

Email us at: info@maxmedchem.com for more details.            

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