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Terpenoids and Glycosides

The terpenoids are a large and diverse class of naturally occurring organic chemicals, derived from five-carbon isoprene units assembled and modified in thousands of ways. Most are multicyclic structures that differ from one another not only in functional groups but also in their basic carbon skeletons. They can be classified according to the number of isoprene units used: Hemiterpenoids, Monoterpenoids, Sesquiterpenoids, Diterpenoids, Sesterterpenoids, Triterpenoids, Tetraterpenoids. These lipids can be found in all classes of living things, and are the largest group of natural products. Plant terpenoids are used extensively for their aromatic qualities and play a role in traditional herbal remedies. Terpenoids contribute to the scent of eucalyptus, the flavors of cinnamon, cloves, and ginger, the yellow color in sunflowers, and the red color in tomatoes.

Terpenoids and Glycosides (164):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-15371
    Forskolin 66575-29-9 98.60%
    Forskolin is a potent adenylate cyclase activator, with binding (IC50=41 nM) to and activation (EC50=0.5 μM) of type I adenylyl cyclase.
    Forskolin
  • HY-32735
    Triptolide 38748-32-2 99.83%
    Triptolide is an inhibitor of heat shock factor (HSF1), inhibits HSP90-CDC37 binding and induces acetylation of HSP90, and also inhibits MDM2 expression in a dose-dependent manner with IC50 values range from 47 to 73 nM.
    Triptolide
  • HY-13067
    Celastrol 34157-83-0 99.90%
    Celastrol is a proteasome inhibitor, potently and preferentially inhibits the chymotrypsin-like activity of a purified 20S proteasome (IC50=2.5 μM).
    Celastrol
  • HY-17389
    Genipin 6902-77-8 99.42%
    Genipin is a cell permeable inhibitor of uncoupling protein 2 (UCP2).
    Genipin
  • HY-N0141
    Parthenolide 20554-84-1 99.13%
    Parthenolide is an NF-κB inhibitor, reduces histone deacetylase 1 (HDAC-1) and DNA methyltransferase 1 independent of NF-κB inhibition.
    Parthenolide
  • HY-N0176
    Dihydroartemisinin 71939-50-9 >99.0%
    Dihydroartemisinin, one of the most active artemisinin derivative, exhibits anticancer activity in a number of human cancer cells.
    Dihydroartemisinin
  • HY-N0904
    Ginsenoside C-K 39262-14-1 98.06%
    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-N0603
    Ginsenoside Rg3 14197-60-5 >98.0%
    Ginsenoside Rg3 is a steroid glycoside derivative which affects endothelium relaxation in the aorta.
    Ginsenoside Rg3
  • HY-N0009
    Geniposide 24512-63-8 99.52%
    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.
    Geniposide
  • 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.
    Andrographolide
  • HY-N0431
    Astragaloside IV 84687-43-4 99.15%
    Astragaloside IV, an active component isolated from Astragalus membranaceus, suppresses the activation of ERK1/2 and JNK, and downregulates matrix metalloproteases (MMP)-2, (MMP)-9 in MDA-MB-231 breast cancer cells.
    Astragaloside IV
  • HY-N0293
    Paeoniflorin 23180-57-6 >98.0%
    Paeoniflorin is a herbal constituent extracted from the root of Paeonia albiflora Pall.
    Paeoniflorin
  • HY-10529
    Betulinic acid 472-15-1 98.58%
    Betulinic acid, a pentacyclic triterpene, selectively induces apoptosis in tumor cells, also is a inhibitor of HIV-1 with EC50 of 1.4 μ M.
    Betulinic acid
  • HY-B0719
    Ingenol Mebutate 75567-37-2 98.74%
    Ingenol Mebutate (PEP 005) is a substance found in the sap of the plant Euphorbia peplus and an inducer of cell death.
    Ingenol Mebutate
  • HY-N0045
    Ginsenoside Rg1 22427-39-0 >98.0%
    Ginsenoside Rg1 is part of a class of triterpene saponins and steroid glycosides; possess anti-inflammatory and anticancer activities.
    Ginsenoside Rg1
  • HY-N0842
    Bevirimat 174022-42-5 99.40%
    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.
    Bevirimat
  • HY-N0156
    Oleanolic Acid 508-02-1 >98.0%
    Oleanolic acid (Caryophyllin) is a natural compound from plants with anti-tumor activities.
    Oleanolic Acid
  • HY-N0039
    Ginsenoside Rb1 41753-43-9 98.10%
    Ginsenoside Rb1 is part of a class of steroid glycosides; may have properties that inhibit or prevent the growth of tumors.
    Ginsenoside Rb1
  • HY-N2312
    Mogrol 88930-15-8 98.06%
    Mogrol is a biometabolite of mogrosides, and acts via inhibition of the ERK1/2 and STAT3 pathways, or reducing CREB activation and activating AMPK signaling.
    Mogrol
  • HY-N1447
    Ganoderic acid A 81907-62-2 98.94%
    Ganoderic acid can Inhibitt of the JAK-STAT3 signaling pathway, also inhibit proliferation, viability, ROS.
    Ganoderic acid A