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Amentoflavone

Amentoflavone structure

Amentoflavone 

structure
  • CAS No:

    1617-53-4

  • Formula:

    C30H18O10

  • Chemical Name:

    Amentoflavone

  • Synonyms:

    4H-1-Benzopyran-4-one,8-[5-(5,7-dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2-hydroxyphenyl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-;3′′′,8-Biflavone,4′,4′′′,5,5′′,7,7′′-hexahydroxy-;Ginkgetin,didemethyl-;8-[5-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2-hydroxyphenyl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one;Amentoflavone;Tridemethylsciadopitysin;I3′,II8-Biapigenin;Amenthoflavone;NSC 295677;79596-89-7

  • Categories:

    Cosmetic Ingredient  >  Bleaching Agent

Description

Amentoflavone is a natural biflavone compound with many biological properties, including anti-inflammatory, antioxidative, and neuroprotective effects.IC50 value:Target:In vitro: In irradiated v79 cells, Pretreatment with amentoflavone 24 hours prior to 8 Gy 60Co γ-ray irradiation significantly inhibited apoptosis, promoted the G2 phase, decreased the concentration of ROS and mitochondrial mass [2]. Amentoflavone dose-dependently inhibited the viability of SW480 cells, and a high concent


Solid


Amentoflavone is a biflavonoid that is obtained by oxidative coupling of two molecules of apigenin resulting in a bond between positions C-3 of the hydroxyphenyl ring and C-8 of the chromene ring. A natural product found particularly in Ginkgo biloba and Hypericum perforatum. It has a role as a cathepsin B inhibitor, an antiviral agent, an angiogenesis inhibitor, a P450 inhibitor and a plant metabolite. It is a biflavonoid, a hydroxyflavone and a ring assembly.

Amentoflavone Basic Attributes

538.46

538.46

9I1VC79L77

295677

DTXSID20167225

29329990

Characteristics

174

5

Odourless Whitish Solid

1.656±0.06 g/cm3(Predicted)

245-250 °C (decomp)

910.5°C at 760 mmHg

308.5±27.8 °C

1.793

0.03344 mg/L @ 25 °C (est)

2-8°C

2.79E-35mmHg at 25°C

230.16 Ų [M+H]+ [CCS Type: DT, Method: stepped-field]|217.23 Ų [M-H]- [CCS Type: DT, Method: stepped-field]|216.5 Ų [M-H]-

Safety Information

NONH for all modes of transport

3

22-24/25

Drug Information

Drugs and compounds which inhibit or antagonize the biosynthesis or actions of CYTOCHROME P-450 CYP3A. (See all compounds classified as Cytochrome P-450 CYP3A Inhibitors.)|Drugs and compounds which inhibit or antagonize the biosynthesis or actions of CYTOCHROME P-450 CYP2C9. (See all compounds classified as Cytochrome P-450 CYP2C9 Inhibitors.)

amentoflavone

Amentoflavone Use and Manufacturing

Polyketides [PK] -> Flavonoids [PK12] -> Biflavonoids and polyflavonoids [PK1204]

Computed Properties

Molecular Weight:538.5
XLogP3:5
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:3
Exact Mass:538.08999677
Monoisotopic Mass:538.08999677
Topological Polar Surface Area:174
Heavy Atom Count:40
Complexity:1050
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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