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  4. Vitex trifolia L.

Vitex trifolia L.

Vitex trifolia L. (13):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-N0439
    Asiaticoside 16830-15-2 99.84%
    Asiaticoside, a trisaccaride triterpene from Centella asiatica, suppresses TGF-β/Smad signaling through inducing Smad7 and inhibiting TGF-βRI and TGF-βRII in keloid fibroblasts; Asiaticoside shows antioxidant, anti-inflammatory, and anti-ulcer properties.
    Asiaticoside
  • HY-N0194
    Asiatic acid 464-92-6 99.40%
    Asiatic acid, a pentacyclic triterpene found in Centella asiatica (Centella asiatica), has anticancer activity. Asiatic acid induces apoptosis in melanoma cells and has barrier protective effects on human aortic endothelial cells (HAEC). Asiatic acid also has anti-inflammatory activity and inhibits tumor necrosis factor (TNF)-α-induced endothelial barrier dysfunction. Asiatic acid also inhibits NLRP3 inflammasome activation and NF-κB pathway, effectively inhibits inflammation in rats, and has neuroprotective effects in rat spinal cord injury (SCI) model.
    Asiatic acid
  • HY-N0568
    Madecassoside 34540-22-2 99.86%
    Madecassoside is a pentacyclic triterpene isolated from Centella asiatica and has anti-inflammatory properties. Antioxidant and anti-aging effects. Madecassoside is a pentacyclic triterpene isolated from Centella asiatica. Madecassoside is orally active and has inhibitory properties against inflammation, oxidation, apoptosis and autophagy. Madecassosid inhibits activities of p38 MAPK and NF-kB[5][6], exhibits an anti-apopototic property, activates Nrf2 expression to reduce the neurotoxicity. Madecassoside can be used in endocrine diseases, cardiovascular diseases, skin diseases and other diseases.
    Madecassoside
  • HY-N0569
    Madecassic acid 18449-41-7 99.23%
    Madecassic acid is isolated from Centella asiatica (Umbelliferae). Madecassic acid has anti-inflammatory properties caused by iNOS, COX-2, TNF-alpha, IL-1beta, and IL-6 inhibition via the downregulation of NF-κB activation in RAW 264.7 macrophage cells.
    Madecassic acid
  • HY-N5052
    Asiaticoside B 125265-68-1 99.32%
    Asiaticoside B is a triterpene glycoside isolated from Actaea asiatica, with anti-cancer activity.
    Asiaticoside B
  • HY-N0569R
    Madecassic acid (Standard) 18449-41-7
    Madecassic acid (Standard) is the analytical standard of Madecassic acid. This product is intended for research and analytical applications. Madecassic acid is isolated from Centella asiatica (Umbelliferae). Madecassic acid has anti-inflammatory properties caused by iNOS, COX-2, TNF-alpha, IL-1beta, and IL-6 inhibition via the downregulation of NF-κB activation in RAW 264.7 macrophage cells.
    Madecassic acid (Standard)
  • HY-N10783
    (-)-Toddanol 77715-99-2
    (-)-Toddanol, a coumarin, can be isolated from the root of Toddalia asiatica.
    (-)-Toddanol
  • HY-N10785
    Toddanone 77636-08-9
    Toddanone, a coumarin, can be isolated from the root of Toddalia asiatica.
    Toddanone
  • HY-N10803
    (+)-6-(3-Chloro-2-hydroxy-3-methylbutyl)-5,7-dimethoxycoumarin 15575-50-5
    (+)-6-(3-Chloro-2-hydroxy-3-methylbutyl)-5,7-dimethoxycoumarin is a nature product that could be isolated form the root bark of Toddalia asiatica (L.) LAM.
    (+)-6-(3-Chloro-2-hydroxy-3-methylbutyl)-5,7-dimethoxycoumarin
  • HY-N10842
    6-Formyllimetin 88140-31-2
    6-Formyllimetin is a natural product isolated from the root bark of T. asiatica LAM.
    6-Formyllimetin
  • HY-N12190
    Centellasaponin A 261767-77-5
    Centellasaponin A (compound 10) is a pentacyclic triterpene saponin isolated from the methanolic extract of Centella asiatica.
    Centellasaponin A
  • HY-N12225
    Isoasiaticoside 948827-09-6
    Isoasiaticoside is a pentacyclic triterpene saponin that can be isolated from Centella asiatica. Isoasiaticoside has potential neuroprotective effects in the 6-OHDA (HY-B1081)-induced PC12 cell model.
    Isoasiaticoside
  • HY-N7990
    Scheffoleoside A 160669-23-8
    Scheffoleoside A is a neuroprotective agent can be derived from Centella asiatica. Scheffoleoside A exhibits moderate activity in inhibiting 6-OHDA-induced cytotoxicity.
    Scheffoleoside A