Dihydrotanshinone I

CAS No. 87205-99-0

Dihydrotanshinone I ( DHTS; Dihydrotanshinone I )

Catalog No. M16341 CAS No. 87205-99-0

Dihydrotanshinone I (DHTS) was previously reported to exhibit the most potent anti-Y activity among several tanshinones in colon Y cells.

Purity : >98%(HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 46 In Stock
10MG 83 In Stock
25MG 172 In Stock
50MG 249 In Stock
100MG 412 In Stock
500MG 888 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Dihydrotanshinone I
  • Note
    Research use only, not for human use.
  • Brief Description
    Dihydrotanshinone I (DHTS) was previously reported to exhibit the most potent anti-Y activity among several tanshinones in colon Y cells.
  • Description
    Dihydrotanshinone I (DHTS) was previously reported to exhibit the most potent anti-Y activity among several tanshinones in colon Y cells. Its cytotoxic action was reactive oxygen species (ROS) dependent but p53 independent.
  • Synonyms
    DHTS; Dihydrotanshinone I
  • Pathway
    Immunology/Inflammation
  • Target
    ROS
  • Recptor
    ROS
  • Research Area
    Cardiovascular Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    87205-99-0
  • Formula Weight
    278.31
  • Molecular Formula
    C18H14O3
  • Purity
    >98%(HPLC)
  • Solubility
    Soluble in Chloroform
  • SMILES
    CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3C=CC=C4C
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Wang L, et al.Phytomedicine. 2015 Nov 15;22(12):1079-87.;
molnova catalog
related products
  • Topiroxostat

    Topiroxostat(FYX-051) is a novel and potent xanthine oxidoreductase (XOR) inhibitor with IC50 value of 5.3 nM.

  • Emeramide

    Emeramide is a thiol-redox antioxidant. It is also a heavy metal chelator.

  • 5-Hydroxyoxindole

    5-Hydroxyoxindole has been identified as a urinary metabolite of indole, which is produced from tryptophane via the tryptophanase activity of gut bacteria.