Onychium japonicum (Thunb.) Kunze

Onychium japonicum (Thunb.) Kunze (7):

Cat. No.	Product Name	CAS No.	Purity	Chemical Structure

Herbacetin-3-sophoroside-8--glucoside	77298-68-1
Herbacetin-3-sophoroside-8--glucoside is a natural product that can be isolated from Equisetum hyemale.

Lavandoside	117405-51-3	99.98%
Lavandoside is an ABTS^?+ free radical scavenger and a moderate inhibitor of xanthine oxidase (XO), with an IC₅₀ of 71.6 μM for inhibiting NO production in LPS-induced macrophages. Lavandoside exerts its antioxidant and potential anti-inflammatory effects by directly scavenging free radicals and inhibiting XO activity, a mechanism related to the hydroxyl groups in its molecular structure. Lavandoside can be isolated from lavender and can be used in the development of natural antioxidants and in research on oxidative stress-related diseases and inflammation-related diseases.

Gossypetin 3-sophoroside-8-glucoside	77306-93-5
Gossypetin 3-sophoroside-8-glucoside is a flavonol glycoside, which can be isolated from the aerial parts of Equisetum hyemale L..

N-Cinnamoylpyrrole	252248-89-8
N-Cinnamoylpyrrole is a amide.

Onitisin 2'-O-glucoside	62043-53-2
Onitisin 2'-O-glucoside is a Sesquiterpenoids product that can be isolated from the herbs of Onychium japonicum.

Onitin 2'-O-glucoside	76947-60-9
Onitin 2'-O-glucoside is a Sesquiterpenoids product that can be isolated from the herbs of Onychium japonicum.

3-(β-D-Glucopyranosyloxy)-2-hydroxybenzoic acid methyl ester	53827-68-2
3-(β-D-Glucopyranosyloxy)-2-hydroxybenzoic acid methyl ester is a Phenols product that can be isolated from the herbs of Onychium japonicum.

BODIPY 493/503 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 1;16(1):1241. [Abstract]

MedchemExpress Validation 01
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature. Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature. Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.

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