AMENTOFLAVONE
Bis-Apigenin ; 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)- .
AMENTOFLAVONE is listed in the EU CosIng inventory, but no direct annex records are linked on this page yet.
Regulatory evidence by market
No rule for this ingredient has been imported for any of the 13 markets tracked here.
That describes this inventory, not the law. No imported rule is not evidence that an ingredient is permitted: a rule may exist under another name or identifier, or in a dataset not yet imported here.
Chemical identity and properties

Amentoflavone
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 an antiviral agent, an angiogenesis inhibitor, a P450 inhibitor, a cathepsin B inhibitor and a plant metabolite. It is a hydroxyflavone, a ring assembly and a biflavonoid. — ChEBI
- IUPAC name
- 8-[5-(5,7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenyl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
- Molecular formula
- C30H18O10
- Molecular weight
- 538.5 g/mol
- Exact mass
- 538.08999677 Da
- XLogP3
- 5.0
- Topological polar surface area
- 174.0 Ų
- Hydrogen-bond donors
- 6
- Hydrogen-bond acceptors
- 10
- Covalent units
- 1
- Defined stereocentres
- 0
Also known as
16 more reported names
External database identifiers
- ChEBI:CHEBI:2631
- ChEMBL:CHEMBL63354
- EPA DTXSID:DTXSID20167225
- PubMed:41524907
- PubMed:40915523
- PubMed:38225072
- PubMed:34599948
- PubMed:32421801
- PubMed:29470958
- PubMed:28185818
- PubMed:26456343
- PubMed:22445328
- PubMed:19775597
- PubMed:17473463
- PubMed:17003167
Retrieved from NIH PubChem on 2026-08-31 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.
Inventory details for AMENTOFLAVONE
INCI name
AMENTOFLAVONE
Description
Bis-Apigenin ;
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)- .
Record provenance
- Inventory reference
- 88262
- Imported identity
- AMENTOFLAVONE
- Source update
- 30/11/2011
Annex records for AMENTOFLAVONE
Key data
- ANTIOXIDANT
- Inhibiting reactions promoted by oxygen, thus avoiding oxidation and rancidity.
- BLEACHING
- Bleaching or lightening the shade of hair and/or skin.
Official EU ingredient-name evidence
The ingredient name exactly matches the official 2025 EU glossary of common ingredient names.
Related inventory evidence
Ingredients with overlapping formulation functions
Additional official and scientific sources
11 external databases to check this identity in
Each link searches that source for this identity. What each source is, and its legal weight
How AMENTOFLAVONE appears in the CosIng inventory
The CosIng inventory lists AMENTOFLAVONE as a cosmetic ingredient and this page links it to 0 annex records. The inventory entry captures names and identifiers, while the annex records show where the substance is prohibited, restricted or positively listed in EU cosmetics law.
AMENTOFLAVONE is also tagged with 2 cosmetic functions in the official data. Function labels describe intended use, but they do not replace regulatory review of linked annex records before formulation or labelling work.
Frequently asked questions
Source note for AMENTOFLAVONE
This page reproduces the CosIng inventory entry for AMENTOFLAVONE from public European Commission cosmetic ingredient materials and shows linked identifiers even when no direct annex match is currently attached.
Use this inventory page to research AMENTOFLAVONE and compare linked records, but verify restrictions and legal status against the current official source text and law before making regulatory decisions.
Tools & next steps
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