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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
89 Results for "
flavanone
" in MedChemExpress (MCE) Product Catalog:
Products (89)
89 Results for "flavanone" in MCE Product Catalog:
Cat. No.: HY-N18207
CAS No.: 117160-67-5
Category:
Flavonoids Monophenols Labiatae Phenols Plants Medicago truncatula Gaertn. Other Flavonoids
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Cat. No.: HY-N19665
CAS No.: 74175-75-0
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Cat. No.: HY-N20673
CAS No.: 117160-68-6
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Cat. No.: HY-N18363
CAS No.: 72704-06-4
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Cat. No.: HY-N18304
CAS No.: 1162664-57-4
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Cat. No.: HY-N21599
CAS No.: 1619976-99-6
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Cat. No.: HY-N21977
CAS No.: 20194-60-9
Synonyms: Stepposide
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Cat. No.: HY-N17719
CAS No.: 103617-12-5
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Cat. No.: HY-N18016
CAS No.: 1203675-19-7
Synonyms: Hesperitin-5,7-dimethyl-ether
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Cat. No.: HY-N21601
CAS No.: 1619976-97-4
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Cat. No.: HY-N21600
CAS No.: 1619976-98-5
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Cat. No.: HY-N21598
CAS No.: 1619977-00-2
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Cat. No.: HY-N17732
CAS No.: 109469-87-6
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Cat. No.: HY-E70104A
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α-Rhamnosidase, Penicillium sp. is a kind of glycoside hydrolase. α-Rhamnosidase, Penicillium sp. exhibits activity against Naringin (HY-N0153), 4-NRP, flavonoid glycosides and flavanone rhamnosides, and can hydrolyze the corresponding glycosidic bonds to release L-Rhamnose (Rhamnose) (HY-N1420) and other products. α-Rhamnosidase, Penicillium sp. promotes the release of total flavonoids, ginkgolides and aroma components from ginkgo tea, while also enhancing the free radical scavenging capacity of the leachate, inhibiting inflammatory cell activation and increasing its cytotoxicity against tumor cells. α-Rhamnosidase, Penicillium sp. can be used in research related to bacillary dysentery and cancer .
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Cat. No.: HY-L068
583 compounds
Flavonoids are an important class of natural products; particularly, they belong to a class of plant secondary metabolites having a polyphenolic structure, widely found in fruits, vegetables and certain beverages. Flavonoids can be subdivided into different subgroups depending on the carbon of the C ring on which the B ring is attached and the degree of unsaturation and oxidation of the C ring. These subgroups are: flavones, flavonols, flavanones, flavanonols, flavanols or catechins, anthocyanins and chalcones. Flavonoids are now considered as an indispensable component in a variety of nutraceutical, pharmaceutical, medicinal and cosmetic applications. This is attributed to their anti-oxidative, anti-inflammatory, anti-mutagenic and anti-carcinogenic properties coupled with their capacity to modulate key cellular enzyme function. Naturally occurring flavonoids are known to have biological activities for use as drugs, for example, in diseases like cancer, Alzheimer’s disease (AD), atherosclerosis, etc.
MCE offers a unique collection of 583 natural flavonoid compounds which is a useful tool for drug discovery as an important source of lead compounds.
Cat. No.: HY-E71565
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2-Hydroxyisoflavanone synthase (EC 1.14.13.136) requires cytochrome P-450; the reaction involves the migration of the 2-phenyl group of the flavanone to the 3-position of the isoflavanone.
Cat. No.: HY-N16888
CAS No.: 450407-31-5
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Cat. No.: HY-N0377S
Synonyms: 4',7-Dihydroxyflavanone-d4
Cat. No.: HY-N21978
CAS No.: 247031-40-9
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
