1. Natural Products
  2. Plants
  3. Caprifoliaceae
  4. Lonicera japonica Thunb.

Lonicera japonica Thunb.

Synonyms: honeysuckle

Lonicera japonica Thunb. (7):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-N0055
    Chlorogenic acid 327-97-9 99.55%
    Chlorogenic acid is a major phenolic compound in coffee and tea. It plays several important and therapeutic roles such as antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension.
    Chlorogenic acid
  • HY-N0056
    Isochlorogenic acid A 2450-53-5 99.54%
    Isochlorogenic acid A (3,5-Dicaffeoylquinic acid) is a natural phenolic acid with antioxidant and anti-inflammatory activities .
    Isochlorogenic acid A
  • HY-N0722
    Neochlorogenic acid 906-33-2 99.07%
    Neochlorogenic acid is a natural polyphenolic compound found in dried fruits and other plants. Neochlorogenic acid inhibits the production of TNF-α and IL-1β. Neochlorogenic acid suppresses iNOS and COX-2 protein expression. Neochlorogenic acid also inhibits phosphorylated NF-κB p65 and p38 MAPK activation.
    Neochlorogenic acid
  • HY-N2008
    Luteolin 5-O-glucoside 20344-46-1 ≥98.0%
    Luteolin 5-O-glucoside, a major flavonoidfrom Cirsium maackii, possesses anti-inflammatory activity. Luteolin 5-O-glucoside inhibits LPS-induced NO production and t-BHP-induced ROS generation. Luteolin 5-O-glucoside suppresses the expression of iNOS and COX-2 in macrophages.
    Luteolin 5-O-glucoside
  • HY-N7199
    (Rac)-Hydnocarpin 51419-48-8 98.84%
    (Rac)-Hydnocarpin is a flavonoid isolated from Hydnocarpus wightiana Blume, and exhibits moderate cytotoxic on cancer cells.
  • HY-N0358
    1,4-Dicaffeoylquinic acid 1182-34-9 99.80%
    1,4-Dicaffeoylquinic acid (1,4-DCQA) is a phenylpropanoid from Xanthii fructus, inhibits LPS-stimulated TNF-α production.
    1,4-Dicaffeoylquinic acid
  • HY-125598
    Secologanin 19351-63-4
    Secologanin, a secoiridoid glucoside, is a pivotal terpenoid intermediate in the biosynthesis of biologically active monoterpenoid indole alkaloids such as reserpine, ajmaline, and vinblastine. Secologanin synthase (cytochrome P450 isoform CYP72A1) catalyzes the oxidative cleavage of loganin into Secologanin.