Lonicera caerulea L.

Lonicera caerulea L. (4):

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

HY-N17920

6α-Methoxygeniposide	135383-98-1
6α-Methoxygeniposide is a geniposide-type iridoid compound present in the leaves of Gardenia jasminoides cv. fortuneana HARA. 6α-Methoxygeniposide induces neurite outgrowth in pheochromocytoma cells.

HY-N17920A

6β-Methoxygeniposide	655225-30-2
6β-Methoxygeniposide is a geniposide-type iridoid compound. 6β-Methoxygeniposide induces neurite outgrowth in PC12h cells.

HY-N17690

7-Ketologanic acid	170382-11-3
7-Ketologanic acid is an iridoid glucoside. 7-Ketologanic acid is an efficient precursor for 8-epi-kingisidic acid. 7-Ketologanic acid can be extracted from dry leaves of P. azorica.

HY-N12543

Peonidin 3-rutinoside	27539-32-8
Peonidin 3-rutinoside is a natural product that can be isolated from Lonicera caerulea L.

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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