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PLEUROTUS CORNUCOPIAE EXTRACT.

Insufficient Data CAS - / SKIN CONDITIONING

Pleurotus Cornucopiae Extract, derived from the Golden Oyster mushroom, is a multifunctional ingredient demonstrating significant antioxidant capacity and a potential role in skin brightening. Its documented actions suggest benefits for overall skin conditioning and addressing uneven tone.

Skin Conditioning Antioxidant Brightening

Science

This extract actively neutralizes harmful free radicals through mechanisms such as DPPH radical scavenging and superoxide anion radical scavenging, protecting skin from oxidative stress. It further targets hyperpigmentation by inhibiting tyrosinase, a key enzyme in melanin synthesis, and demonstrates xanthine oxidase inhibitory activity. Categorized as a skin conditioning agent, it aims to enhance overall skin health and appearance. However, it is noteworthy that certain beta-glucans from this species have been reported to exert a proinflammatory effect on macrophage action in some studies.


Research

Low confidence
Effective range N/A
Optimal

N/A


Transparency

Not commonly dusted

The Formula

Solubility
Water
Optimal pH N/A
0 7 14

Stability

Specific optimal pH ranges for cosmetic formulation stability are not documented in the available research, with pH information primarily pertaining to extraction processes or enzymatic activity.


Safety

CIR Status
Not reviewed
Sensitization risk Unknown

The Cosmetic Ingredient Review (CIR) has not assessed Pleurotus Cornucopiae Extract for safety. While the Golden Oyster mushroom is edible, this status does not translate to formal cosmetic ingredient safety approval by regulatory bodies such as CIR or SCCS. Comprehensive safety references from industry sources like The Good Scents Company are also currently unavailable.


Your Skin

No Normal
No Dry
No Oily
No Sensitive
Irritancy Unknown
Comedogenicity Unknown

Our Assessment

Insufficient Data

While in vitro studies suggest promising antioxidant and brightening effects, the current lack of comprehensive safety assessments and in vivo efficacy data necessitates further research before widespread inclusion.


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