• ChemicalBook
    Chinese Japanese Germany Korea

    Apigenin

    Chemical Properties Occurance Preparation Health Benifits Description References
    Apigenin
    Apigenin structure
    CAS No.
    520-36-5
    Chemical Name:
    Apigenin
    Synonyms
    Apig;75580;75590;apigenol;Apegenin;UCCF 031;APIGENIN;Versulin;apigenine;Versuline
    CBNumber:
    CB1384541
    Molecular Formula:
    C15H10O5
    Formula Weight:
    270.24
    MOL File:
    520-36-5.mol

    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
    InChIKey
    KZNIFHPLKGYRTM-UHFFFAOYSA-N
    CAS DataBase Reference
    520-36-5(CAS DataBase Reference)
    EWG's Food Scores
    1
    FDA UNII
    7V515PI7F6
    NCI Dictionary of Cancer Terms
    chamomile
    NCI Drug Dictionary
    chamomile
    SAFETY
    • Risk and Safety Statements
    Symbol(GHS) 
    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

    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 25 mg $138 2021-12-16 Buy
    Sigma-Aldrich 01760595 Apigenin primary pharmaceutical reference standard 520-36-5 10mg $376 2021-12-16 Buy
    Sigma-Aldrich 1040683 Apigenin United States Pharmacopeia (USP) Reference Standard 520-36-5 30mg $439 2021-12-16 Buy
    TCI Chemical A1514 Apigenin >98.0%(HPLC) 520-36-5 100mg $133 2021-12-16 Buy
    Alfa Aesar L15041 4',5,7-Trihydroxyflavone, 97% 520-36-5 100mg $127 2021-12-16 Buy

    Apigenin Chemical Properties,Uses,Production

    Chemical Properties

    Apigenin (C15H10O5, CAS registry No. 520-36-5) is also called 4’,5,7-trihydroxyflavone, which is a pale yellow crystalline solid. Its melting point is 345-350 oC, and flash point is 217 oC. The solubility of apigenin is 27 g/L in DMSO. Apigenin has a very low solubility in water (1.35 μg/mL) and high permeability. Taking into consideration its high permeability, apigenin is categorized as a Class II drug according to Biopharmaceutics Classification System (BCS), whose characteristics are low solubility and high permeability. Pure apigenin is generally regarded as unstable for long term storage at room temperature, and thus it requires storage at -20°C..

    Occurance

    Apigenin 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. 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.

    Preparation

    Biogenetically, apigenin is a product of the phenylpropanoid pathway and may be obtained from both phenylalanine and tyrosine, two shikimate-derived precursors. From phenylalanine, cinnamic acid is formed by non-oxidative deamination and then by oxidation at C-4, which is then converted to p-coumaric acid, whereas from tyrosine p-coumaric acid is formed directly by deamination. After activation with CoA, p-coumarate is condensed with three malonyl-CoA residues and then subjected to aromatization by chalcone synthase to form chalcone, which is further isomerized by chalcone isomerase to form naringenin; finally, a flavanone synthase oxidizes naringenin to apigenin.

    Health Benifits

    A high number of studies carried out over the years have indicated that apigenin has many interesting pharmacological activities and nutraceutical potential. As an example, its properties as an antioxidant are well known, and it can also be a therapeutic agent to overcome diseases like inflammation, autoimmune, neurodegenerative disease, and even several types of cancers. It has a low intrinsic toxicity on normal versus cancerous cells, compared with other structurally related flavonoids.

    Description

    Apigenin (chemically known as 4′, 5, 7-trihydroxyflavone, with molecular formula C15H10O5) is with molecular weight of 270.24. It is a naturally occurring plant flavone and is abundantly present in common fruits such as grapefruit, plant-derived beverages, and vegetables such as parsley, onions, oranges, tea, chamomile, wheat sprouts and in some seasonings.
    Apigenin has gained particular interest in recent years as a beneficial and health promoting agent owing to its low intrinsic toxicity and its striking effects on normal versus cancer cells, compared with other structurally-related flavonoids. It has been increasingly recognized as a cancer and tumor  chemopreventive agent (for breast cancer, cervical cancer, colon cancer, hematologic cancer, lung cancer, ovaria cancer, prostate cancer, skin cancer, thyroid cancer, endometrial cancer, gastric cancer, liver cancer, adrenal cortical cancer, leukemia, and neuroblastoma) owing to its anti-inflammatory, antioxidant and anticancer properties.

    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/

    Chemical Properties

    Pale Yellow Crystalline Solid

    Occurrence

    Chamomile is a perennial found in Europe.

    Uses

    antispasmodic, antineoplastic, topoisomerase I inhibitor

    Uses

    Induces the reversion of transformed phenotypes of v-H-ras-transformed NIH 3T3 cells at low concentration (12.5 uM) by inhibiting MAP kinase activity. Also inhibits the proliferation of malignant tum or cells by G2/M arrest and induces morphological differentiation. Apigenin has also been reported to enhance the gap juntion intracellular communication in liver cells.

    Uses

    Has been used to dye Cr mordanted wool yellow. The color is fast to soap.

    General Description

    The herb known as chamomile is derived from the plants Matricaria chamomilla (German, Hungarian, or genuine chamomile) and Anthemis nobilis (English, Roman, or common chamomile). Plants from the two genera have similar activities. The medicinal components are obtained from the flowering tops. The flowers are dried and used for chamomile teas and extracts. Chamomile has been used medicinally for at least 2,000 years. The Romans used the herb for its medicinal properties, which they knew were antispasmodic and sedative.
    The herb also has a long history in the treatment of digestive and rheumatic disorders. The activity of chamomile is found in a light blue essential oil that composes only 0.5% of the flower. The blue color is caused by chamazulene, 7-ethyl-1,4-dimethylazulene . This compound is actually a byproduct of processing the herb. The major component of the oil is the sesquiterpene (-)-α-bisabolol. Also present are apigenin, angelic acid, tiglic acid, the terpene precursors (farnesol, nerolidol, and germacranolide) coumarin, scopoletin-7-glucoside, umbelliferone, and herniarin. Much of the effect of chamomile is caused by bisabolol . Bisabolol is a highly active anti-inflammatory agent in various rodent inflammation and arthritis tests.

    Biological Activity

    Protein kinase inhibitor. Suppresses tumor-promoting effects of TPA and exhibits antiproliferative activity in human breast cancer cells (IC 50 values are 59.44 and 31.15 μ M at 24 and 72 hrs respectively). Activates both the intrinsic and extrinsic apoptotic pathways and displays anti-inflammatory, hypotensive, antispasmodic and antioxidant properties in vivo .

    Biochem/physiol Actions

    A plant flavonoid that has been found to inhibit cell proliferation by arresting the cell cycle at the G2/M phase. Inhibition of growth through cell cycle arrest and induction of apoptosis appear to be related to induction of p53. Inhibits PMA-mediated tumor promotion by inhibiting protein kinase C and the resulting suppression of oncogene expression. It has also been reported to inhibit topoisomerase I-catalyzed DNA re-ligation and enhance gap junctional intercellular communication.

    Anticancer Research

    It is a flavone compound found in many fruits and vegetables and abundant in chamomiletea, parsley, celeriac, and celery. 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 (Singh et al. 2016b). 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 (Wang et al. 2012).

    Purification Methods

    Crystallise it from aqueous pyridine or aqueous EtOH. It dyes wool yellow when mixed with Cr ions. [Beilstein 18 H 181, 18 I 396, 18 II 178, 18 III/IV 2682, 18/4 V 574.]

    Apigenin Preparation Products And Raw materials

    Raw materials

    Preparation Products


    Apigenin Suppliers

    Global( 509)Suppliers
    Supplier Tel Fax Email Country ProdList Advantage
    Xi'an Kono chem co., Ltd.,
    13289246953 029-86107037
    info@konochemical.com CHINA 3000 58
    Shaanxi Pioneer Biotech Co., Ltd .
    86-13259417953(Whatsapp/Wechat) 86-13259417953(Whatsapp)
    029-84385017 sales@pioneerbiotech.com CHINA 3001 58
    Aktin Chemicals, Inc.
    028-85159085
    86-28-85159085 Ex:604 info@aktinchem.com CHINA 1026 58
    Sinoway Industrial co., ltd.
    13806035118
    0592-5854960 xie@china-sinoway.com CHINA 311 58
    Capot Chemical Co.,Ltd.
    +86(0)13336195806 +86-571-85586718
    +86-571-85864795 sales@capotchem.com China 20012 60
    Henan DaKen Chemical CO.,LTD.
    +86-371-66670886
    info@dakenchem.com China 15427 58
    Henan Tianfu Chemical Co.,Ltd.
    0371-55170693
    0371-55170693 info@tianfuchem.com China 22607 55
    Hangzhou FandaChem Co.,Ltd.
    008615858145714
    +86-571-56059825 fandachem@gmail.com CHINA 9128 55
    Nanjing Finetech Chemical Co., Ltd.
    025-85710122 17714198479
    025-85710122 sales@fine-chemtech.com CHINA 890 55
    ATK CHEMICAL COMPANY LIMITED
    +86 21 5161 9050/ 5187 7795
    +86 21 5161 9052/ 5187 7796 ivan@atkchemical.com CHINA 26782 60

    Related articles


    View Lastest Price from Apigenin manufacturers

    Image Release date Product Price Min. Order Purity Supply Ability Manufacturer
    2022-01-20 Apigenin;Versulin
    520-36-5
    US $1.00 / g 10g 98% HPLC 1000kg Guangzhou Biocar Biotechnology Co.,Ltd.
    2022-01-19 Apigenin
    520-36-5
    US $9.80 / KG 1KG 99% 100KG Hong Kong Tiansheng New Material Trading Co., Ltd
    2022-01-19 Apigenin
    520-36-5
    US $9.80 / KG 1KG 99% 10kg Hong Kong Tiansheng New Material Trading Co., Ltd

    Apigenin Spectrum


    520-36-5(Apigenin)Related Search:


    Copyright 2017 ? ChemicalBook. All rights reserved