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Apigenin

CAS No.
520-36-5
Chemical Name:
Apigenin
Synonyms
CHAMOMILE;5,7-Dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one;apigenol;apigenine;5,7-dihydroxy-2-(4-hydroxyphenyl)-4-benzopyrone;Apig;75580;75590;Apegenin;UCCF 031
CBNumber:
CB1384541
Molecular Formula:
C15H10O5
Molecular Weight:
270.24
MDL Number:
MFCD00006831
MOL File:
520-36-5.mol
MSDS File:
SDS
Last updated:2024-11-19 15:53:33

Apigenin Properties

Melting point >300 °C (lit.)
Boiling point 333.35°C (rough estimate)
Density 1.2319 (rough estimate)
refractive index 1.6000 (estimate)
storage temp. 2-8°C
solubility DMSO: 27 mg/mL
form powder
pka 6.53±0.40(Predicted)
color yellow
Merck 14,730
BRN 262620
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 1 month.
InChI InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)13-7-12(19)15-11(18)5-10(17)6-14(15)20-13/h1-7,16-18H
InChIKey KZNIFHPLKGYRTM-UHFFFAOYSA-N
SMILES C1(C2=CC=C(O)C=C2)OC2=CC(O)=CC(O)=C2C(=O)C=1
LogP 3.020
CAS DataBase Reference 520-36-5(CAS DataBase Reference)
EWG's Food Scores 1
NCI Dictionary of Cancer Terms chamomile
FDA UNII 7V515PI7F6
NCI Drug Dictionary chamomile

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
RTECS  LK9276000
10
HS Code  29329985
Hazardous Substances Data 520-36-5(Hazardous Substances Data)
NFPA 704
1
2 0

Apigenin price More Price(83)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHL89159 Apigenin phyproof? Reference Substance 520-36-5 25mg $344 2024-03-01 Buy
Sigma-Aldrich 1040683 Apigenin United States Pharmacopeia (USP) Reference Standard 520-36-5 30mg $527 2024-03-01 Buy
Sigma-Aldrich 01760595 Apigenin primary pharmaceutical reference standard 520-36-5 10mg $463 2023-06-20 Buy
TCI Chemical A1514 Apigenin >98.0%(HPLC) 520-36-5 100mg $151 2024-03-01 Buy
Alfa Aesar L15041 4',5,7-Trihydroxyflavone, 97% 520-36-5 25mg $59.2 2024-03-01 Buy
Product number Packaging Price Buy
PHL89159 25mg $344 Buy
1040683 30mg $527 Buy
01760595 10mg $463 Buy
A1514 100mg $151 Buy
L15041 25mg $59.2 Buy

Apigenin Chemical Properties,Uses,Production

Description

Apigenin(520-36-5) is one of the most widespread flavonoids in plants and formally belongs to the flavone sub-class. Of all the flavonoids, apigenin is one of the most widely distributed in the plant kingdom, and one of the most studied phenolics. Apigenin is present principally as glycosylated in significant amount in vegetables (parsley, celery, onions) fruits (oranges), herbs (chamomile, thyme, oregano, basil), and plant-based beverages (tea, beer, and wine). Plants belonging to the Asteraceae, such as those belonging to Artemisia, Achillea, Matricaria, and Tanacetum genera, are the main sources of this compound. 

Chemical Properties

Pale Yellow Crystalline Solid

Uses

Apigenin has been shown to possess antibacterial, antiviral, antifungal, and antiparasitic activities. Although it can’t stop all types of bacteria on its own, it can be combined with other antibiotics to increase their effects.

Uses

Apigenin is a promising reagent for cancer therapy. Apigenin appears to have the potential to be developed either as a dietary supplement or as an adjuvant chemotherapeutic agent for cancer therapy.

Uses

Apigenin is an active antioxidant, anti-inflammatory, anti-amyloidogenic, neuroprotective and cognitive enhancing substance with interesting potential in the treatment/prevention of Alzheimer's disease.

Preparation

4-hydroxybenzaldehyde (1.22 g, 9.97 mmol, 1.0 equiv) was added to asolution of 50% KOH (aq.) (6.72 g, 59.82 mmol, 6.0 equiv) and ethanol (3 mL) andstirred for 10 min. Then compound 9 (2.02g, 9.97 mmol, 1.0 equiv) was added to the reaction mixture and heated to 60 °C and stirred for 4 h. After cooled toroom temperature, the mixture was poured into ice water and acidified withconcentrated hydrochloric acid to pH = 3. Then the suspension was filtrated, washed and the residue was dried toafford Apigenin(2.43 g, 90%) as a red solid. 520-36-5.png

Definition

ChEBI: Apigenin is a trihydroxyflavone that is flavone substituted by hydroxy groups at positions 4', 5 and 7. It induces autophagy in leukaemia cells. It has a role as a metabolite and an antineoplastic agent. It is a conjugate acid of an apigenin-7-olate.

benefits

Apigenin has various beneficial health effects such as antioxidant, anti-inflammatory, and chemoprevention. Apigenin can downregulate the expression of IL-1β and TNF-α in LPS-stimulated mouse macrophages and human monocytes. preclinical studies have suggested that apigenin may improve outcomes in multiple health states, including anxiety, brain function, oxidative stress, inflammation, and hormonal regulation (testosterone, estrogen, and cortisol

Mechanism of action

Apigenin exerts anxiolytic effects at high doses by inhibiting NMDA receptors; it also has affinity to GABA-A receptors. Apigenin also exerts potent antioxidant activities by scavenging free radicals and upregulating glutathione levels; it also exerts anti-inflammatory effects. Apigenin is most studied for its potential anti-cancer properties.

Anticancer Research

It induces apoptosis by targeting leptin/leptin receptor pathway and by targeting caspase-dependent extrinsic pathway aswell as STAT3 signaling pathway in lung adenocarcinoma and BT-474 breast cancercells, respectively.
It shows antitumor activity against breastcancer MCF-7 cells and colon cancer HCT 116 cells and is a mediator of cancerchemoprevention and an inducer of autophagy. It can be used to treat colon canceras it induces apoptosis in colon cancer cells. It also increase melanogenesis in B16cells by activating the p38 MAPK pathway.

Safety

Apigenin is considered safe when consumed in normal amounts through a diet rich in fruits, vegetables, and herbs. However, supplement doses tend to deliver a significantly higher amount of apigenin than would be generally consumed via dietary means. Higher doses of apigenin can cause stomach discomfort, and people should cease using it immediately and consult medical professionals. At high doses, it can trigger muscle relaxation and sedation[1]. Allergic reactions can also occur as a response to chamomile tea or apigenin.

Source

Apigenin (4′,5,7-trihydroxyflavone) is one of the most widespread flavonoids in plants and formally belongs to the flavone sub-class. Plants belonging to the Asteraceae, such as those belonging to Artemisia, Achillea, Matricaria, and Tanacetum genera, are the main sources of this compound. However, species belonging to other families, such as the Lamiaceae, for instance, Sideritis and Teucrium, or species from the Fabaceae, such as Genista, showed the presence of apigenin in the aglycone form and/or its C- and O-glucosides, glucuronides, O-methyl ethers, and acetylated derivatives. In gymnosperms, apigenin derivatives are mostly present in dimeric forms, with apigenin residues variously coupled, e.g., with C?C linkage as in cupressuflavone and amentoflavone (I-8, II-8″ and I-3′, II-8″, respectively), or C—O linkage (I-4′, II-6″) as in hinokiflavone.

storage

+4°C

Purification Methods

The current method for the purification of apigenin is crude-solvent extraction method by using solvent in small quantity and also time saving. Apigenin that was isolated from Symphyotrichum novae-angliae was obtained in large quantity and directly from extract.

References

[1] Sanjeev Shukla, Sanjay Gupta (2010) Apigenin: a promising molecule for cancer prevention, 27, 962-978.
[2] https://en.wikipedia.org/wiki/Apigenin
[3] http://bodynutrition.org/apigenin/

References

[1] Bahare Salehi, et al. “The Therapeutic Potential of Apigenin.” Int J Mol Sci. 2019 Mar; 20(6): 1305.

5631-70-9
520-36-5
Synthesis of Apigenin from 4',5,7-TRIMETHOXYFLAVONE

Apigenin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 708)Suppliers
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Bonerge(Hunan) Lifescience Co., Ltd.
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Related articles

  • What is apigenin?
  • Apigenin is a flavonoid of low toxicity and multiple beneficial bioactivities.
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Related Qustion

  • Q:Is Apigenin a dietary supplement?
  • A:Yes, apigenin can be used as a dietary supplement in everyday life, in fact, it is found in fruits, vegetables, herbs and beve....
  • Nov 23,2023

View Lastest Price from Apigenin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Apigenin pictures 2024-12-20 Apigenin
520-36-5
US $10.00 / kg 1kg 95% 95% 98%HPLC Changsha Staherb Natural Ingredients Co., Ltd.
chamomile extract apigenin pictures 2024-12-20 chamomile extract apigenin
520-36-5
US $15.00-1350.00 / kg 1kg 0.6%-98% 10000 Changsha Staherb Natural Ingredients Co., Ltd.
Apigenin; Celery extract  pictures 2024-12-20 Apigenin; Celery extract
520-36-5
US $0.00 / KG 1KG 40%; 98% HPLC 1000KG Changsha Staherb Natural Ingredients Co., Ltd.
  • Apigenin pictures
  • Apigenin
    520-36-5
  • US $10.00 / kg
  • 95%
  • Changsha Staherb Natural Ingredients Co., Ltd.
4,5,7-Trihydroxyflavone (apigenin) APIGENIN CRYSTALLINE APIGENIN FROM PARSLEY Matricaria chamomilla flower Versuline Pelargidenon 1449 4’,5,7-trihydroxyflavaone 4’,5,7-trihydroxy-flavon 5,7-dihydroxy-2-(4-hydroxyphenyl)-4h-1-benzopyran-4-on c.i.naturalyellow1 Apigenin (30 mg) LY 080400 Pelargidenone Apegenin NSC 83244 UCCF 031 APIGENIN >= 95.0% (HPLC) 4',5,7-Trihydroxyflavone, 5,7-Dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one Chinese Taxillus Herb Apigenin/Celery seed extract Chinese Taxillus Herb Extract 4',5,7-Trihydroxyflavone 5,7-dihydroxy-2-(4-hydroxyphenyl)-4h-1-benzopyran-4-on 5,7,4'-Trihydroxyflavone APIGENIN 4',5,7-TRIHYDROXYFLAVONE 4,5,7-TRIHYDROXYFLAVONE 4',5,7-TRIHYROXYFLAVONE 5,7,4'-TRIHYDROXYFLAVONE 5,7-DIHYDROXY-2-(4-HYDROXYPHENYL)-4H-1-BENZOPYRAN-4-ONE 7,4',5-TRIHYDROXYFLAVONE APIGENIN / 4'',5,7-TRIHYDROXYFLAVONE 2-(p-hydroxyphenyl)-5,7-dihydroxychromone 4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxyphenyl)- 5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one APIGENIN(P) APIGENIN WITH HPLC APIGENIN hplc 4H-1-Benzopyran-4-one,5,7-dihydroxy-2- Versulin APIGENIN(RG)(PLEASE CALL) Chinese Taxillus Twing 75580 75590 Nano Liposomal Apigenin AS CUSTOMERS' REQUIREMENTS Mulberry parasitic extract 7-hydroxy-2-(4-hydroxyphenyl)-4-oxo-1-benzopyran-5-olate Apigenin 520-36-5 Apigenin, ≥95% (HPLC) Apigenin, ≥97% (HPLC) Apigenin, ≥98.0% (HPLC) Apigenin - CAS 520-36-5 - Calbiochem Apigenin/ 4′,5,7-Trihydroxyflavone, 5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-benzopyrone Apigenin 97+% Talxilli Herba。 Apigenin 98% Apigenin > Apig hot selling Apigenin