CAS 520-36-5
:Apigenin
Description:
Apigenin is a naturally occurring flavonoid found in various plants, particularly in fruits, vegetables, and herbs such as parsley, chamomile, and celery. Its chemical formula is C15H10O5, and it features a flavone structure characterized by a chromone backbone with hydroxyl groups at specific positions. Apigenin is known for its potential health benefits, including anti-inflammatory, antioxidant, and anticancer properties. It exhibits a yellow crystalline appearance and is soluble in organic solvents like ethanol and dimethyl sulfoxide, but has limited solubility in water. Apigenin interacts with various biological pathways, influencing cell signaling and gene expression, which contributes to its therapeutic potential. Additionally, it has been studied for its effects on anxiety and sleep, making it a subject of interest in both nutritional and pharmaceutical research. Its safety profile is generally favorable, but further studies are needed to fully understand its mechanisms and efficacy in clinical applications.
Formula:C15H10O5
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
InChI key:InChIKey=KZNIFHPLKGYRTM-UHFFFAOYSA-N
SMILES:O=C1C=2C(OC(=C1)C3=CC=C(O)C=C3)=CC(O)=CC2O
Synonyms:- 4',5,7-Trihydroxyflavone
- 4′,5,7-Trihydroxyflavone
- 5,7,4'-Trihydroxyflavone
- 5,7-Dihidroxi-2-(4-Hidroxifenil)-4-Benzopirona
- 5,7-Dihydroxy-2-(4-Hydroxyphenyl)-4-Benzopyrone
- 5,7-Dihydroxy-2-(4-Hydroxyphenyl)chromen-4-one
- 5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-benzopyron
- 5,7-Dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
- 5,7-Dihydroxy-2-p-hydroxyphenyl-4-chromenone
- Apegenin
- Apigenin
- Apigenine
- Apigenol
- Chamomile
- Flavone, 4',5,7-trihydroxy-
- Flavone, 4′,5,7-trihydroxy-
- Ly 080400
- Nsc 83244
- Pelargidenon 1449
- St 056301
- Uccf 031
- Versulin
- 75580
- 4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxyphenyl)-
- 5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one
- C.I. Natural Yellow 1
- See more synonyms
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Found 19 products.
Apigenin
CAS:Formula:C15H10O5Purity:>98.0%(HPLC)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:270.24Apigenin
CAS:Apigenin analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C15H10O5Purity:(HPLC) ≥99%Color and Shape:PowderMolecular weight:270.25Apigenin (5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-benzopyrone)
CAS:<p>Aromatic heterocyclic compounds with oxygen hetero-atom(s) only, nesoi</p>Formula:C15H10O5Color and Shape:Off-White Light Brown Yellow PowderMolecular weight:270.05282Apigenin
CAS:<p>Apigenin</p>Formula:C15H10O5Purity:97%Color and Shape: light beige solidMolecular weight:270.24g/molApigenin
CAS:Formula:C15H10O5Purity:≥ 98.0% (anhydrous basis)Color and Shape:Yellow or brown powderMolecular weight:270.24Apigenin
CAS:Apigenin, a naturally occurring plant flavone (4', 5, 7,-trihydroxyflavone) abundantly present in common fruits and vegetables including parsley, onions, oranges, tea, chamomile, wheat sprouts and some seasonings, has been shown to possess remarkable anti-inflammatory, antioxidant and anti-carcinogenic properties.Formula:C15H10O5Purity:95%~99%Color and Shape:Yellow powderMolecular weight:270.24Apigenin 100 µg/mL in Acetonitrile:Methanol
CAS:Controlled ProductFormula:C15H10O5Color and Shape:Single SolutionMolecular weight:270.24Apigenin
CAS:<p>Apigenin (NSC 83244) is an aromatic oil extracted from the flowers or leaves of the daisy-like plants.</p>Formula:C15H10O5Purity:97.64% - 99.66%Color and Shape:Yellow Needles From Aqueous Pyridine SolidMolecular weight:270.24Apigenin
CAS:<p>Apigenin</p>Formula:C15H10O5Purity:97%Color and Shape: faint beige powderMolecular weight:270.24g/molApigenin
CAS:Oxygen-heterocyclic compoundFormula:C15H10O5Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:270.24Apigenin
CAS:Controlled Product<p>Applications 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 tumor cells by G2/M arrest and induces morphological differentiation. Apigenin has also been reported to enhance the gap juntion intracellular communication in liver cells.uv(max)ethanol: 269, 340 nm (e= 18,800, 20,900) moderately sol. in hot alcohol<br>References Chaumontet, C., et al.: Carcinogenesis, 15, 2325 (1994); Sato, F., et al.: Biochem. Biophys. Res. Commun., 204, 578 (1994); Kuo, M.L. et al.: Biochem. Biophys. Res. Commun., 212, 767 (1995);<br></p>Formula:C15H10O5Color and Shape:Yellow To BrownMolecular weight:270.244,5,7-Trihydroxyflavone
CAS:<p>M01289 - 4,5,7-Trihydroxyflavone</p>Formula:C15H10O5Purity:95%Color and Shape:Solid, Light yellow powderMolecular weight:270.24Apigenin - 97%
CAS:<p>Apigenin - 97% is a high-purity flavonoid compound, which is primarily derived from various plant sources such as parsley, chamomile, and celery. This compound is known for its significant presence in the plant kingdom, where it functions as a secondary metabolite contributing to plant defense.</p>Formula:C15H10O5Purity:Min. 97 Area-%Color and Shape:PowderMolecular weight:270.24 g/molApigenin - 94%
CAS:<p>Apigenin - 94% is a purified form of apigenin, which is a naturally occurring flavonoid. It is primarily sourced from various plant species, including parsley, celery, and chamomile, where it is a prominent active component. The mode of action of apigenin involves multiple biochemical pathways: it acts as an anti-inflammatory agent, modulates enzyme activities, and exhibits antioxidant properties by scavenging free radicals. Additionally, apigenin interacts with cellular signaling pathways, such as the MAPK and PI3K/Akt, which contribute to its protective effects against oxidative stress and its potential in promoting apoptosis in cancerous cells.</p>Formula:C15H10O5Purity:Min. 95%Color and Shape:PowderMolecular weight:270.24 g/mol4',5,7-Trihydroxyflavone, 97%
CAS:<p>4',5,7-Trihydroxyflavone is a nonmutagenic flavonoid shown to inhibit cell proliferation, angiogenesis and protein kinase. Also induces apoptosis in breast cancer cells. It inhibit topoisomerase I-catalyzed DNA re-ligation and enhance gap junctional intercellular communication. This Thermo Scientif</p>Formula:C15H10O5Purity:97%Color and Shape:Cream to yellow to brown, PowderMolecular weight:270.24














