1. Natural Products
  2. Terpenoids and Glycosides

Terpenoids and Glycosides

Terpenoids and Glycosides (136):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-N0141
    Parthenolide 20554-84-1
    Parthenolide is an NF-κB inhibitor, reduces histone deacetylase 1 (HDAC-1) and DNA methyltransferase 1 independent of NF-κB inhibition.
  • HY-N0603
    Ginsenoside Rg3 14197-60-5
    Ginsenoside Rg3 is a steroid glycoside derivative which affects endothelium relaxation in the aorta.
    Ginsenoside Rg3
  • HY-N0176
    Dihydroartemisinin 71939-50-9
    Dihydroartemisinin, one of the most active artemisinin derivative, exhibits anticancer activity in a number of human cancer cells.
  • HY-N0904
    Ginsenoside C-K 39262-14-1
    Ginsenoside C-K(Ginsenoside compound K) is an intestinal microbiota metabolite of ginsenoside Rb1; possessing anti-proliferative and anti-inflammatory activities.
    Ginsenoside C-K
  • HY-N0009
    Geniposide 24512-63-8
    Geniposide is an iridoid glucoside extracted from Gardenia jasminoides Ellis fruits; exhibits a varity of biological activities such as anti-diabetic, antioxidative, antiproliferative and neuroprotective activities.
  • HY-N0191
    Andrographolide 5508-58-7
    Andrographolide(Andrographis) is an irreversible antagonist of NF-κB and prevents in vitro T cell activation; displays antiviral, antiinflammatory, antiapoptotic, and antihyperglycemic properties.
  • HY-N0201
    Atractylenolide I 73069-13-3
    Atractylenolide I is a natural compound extracted from largehead atractylodes rhizome; induce apoptosis and bring about cytotoxicity of human promyeloleukemic HL-60 cells; TLR4-antagonizing agent.
    Atractylenolide I
  • HY-N0842
    Bevirimat 174022-42-5
    Bevirimat(YK FH312; FH11327; MPC-4326) is an anti-HIV drug derived from a betulinic acid-like compound; is believed to inhibit HIV by a novel mechanism, so-called maturation inhibition.
  • HY-N0797
    (20S)-Protopanaxadiol 30636-90-9
    protopanaxadiol-type ginseng saponin; apoptosis inducer.
  • HY-N0835
    (20S)-Protopanaxatriol 34080-08-5
    (20S)-Protopanaxatriol(g-PPT) is a metabolites of ginsenoside, protopanaxatriol (g-PPT), could modulate endothelial cell functions through the glucocorticoid receptor (GR) and oestrogen receptor (ER).
  • HY-N0156
    Oleanolic Acid 508-02-1
    Oleanolic acid (Caryophyllin) is a natural compound from plants with anti-tumor activities.
    Oleanolic Acid
  • HY-N0836
    Jervine 469-59-0
    Jervine(11-Ketocyclopamine) is a naturally occuring steroidal alkaloid that causes cyclopia by blocking sonic hedgehog(Shh) signaling; Jervine is an inhibitor of Smo.
  • HY-N0039
    Ginsenoside Rb1 41753-43-9
    Ginsenoside Rb1 is part of a class of steroid glycosides; may have properties that inhibit or prevent the growth of tumors.
    Ginsenoside Rb1
  • HY-N0045
    Ginsenoside Rg1 22427-39-0
    Ginsenoside Rg1 is part of a class of triterpene saponins and steroid glycosides; possess anti-inflammatory and anticancer activities.
    Ginsenoside Rg1
  • HY-N0668
    Rubusoside 64849-39-4
    Rubusoside is a natural sweetener and a solubilizing agent with antiangiogenic and antiallergic properties.
  • HY-N0890
    Tubeimoside I 102040-03-9
    Tubeimoside I(Lobatoside-H) is an extract from Chinese herbal medicine Bolbostemma paniculatum (MAXIM.) FRANQUET (Cucurbitaceae) has been shown as a potent anti-tumor agent for a variety of human cancers.
    Tubeimoside I
  • HY-N0038
    Alantolactone 546-43-0
    Alantolactone(Alant camphor) is a sesquiterpene lactone; has potential activity against triple-negative breast cancer MDA-MB-231 cells by suppressing the signal transducer and activator of transcription 3 (STAT3) signaling pathway.
  • HY-N0560
    Oroxylin A 480-11-5
    Oroxylin A is a natural active flavonoid with strong anticancer effects.
    Oroxylin A
  • HY-N0410
    Daucosterol 474-58-8
    Daucosterol is a natural sterolin.
  • HY-N0865
    Ingenol 30220-46-3
    Ingenol is an extremely weak PKC (protein kinase C) activator; has been found to induce apoptosis and act as an anticancer agent.