Podophyllotoxone

CAS No. 477-49-6

Podophyllotoxone( —— )

Catalog No. M21508 CAS No. 477-49-6

Podophyllotoxinone a natural compound found in Dysosma versipellis shows inhibitory activity against L1210 leukemia and KB cells in vitro.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 57 In Stock
2MG 29 In Stock
5MG 46 In Stock
10MG 73 In Stock
25MG 124 In Stock
50MG 182 In Stock
100MG 271 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Podophyllotoxone
  • Note
    Research use only, not for human use.
  • Brief Description
    Podophyllotoxinone a natural compound found in Dysosma versipellis shows inhibitory activity against L1210 leukemia and KB cells in vitro.
  • Description
    Podophyllotoxinone a natural compound found in Dysosma versipellis shows inhibitory activity against L1210 leukemia and KB cells in vitro.
  • In Vitro
    Podophyllotoxone inhibits human prostate cancer cells PC3 and DU145 growth with IC50 values of 14.7 and 20.6 μM.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    477-49-6
  • Formula Weight
    412.4
  • Molecular Formula
    C22H20O8
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (242.49 mM)
  • SMILES
    COc1cc([C@@H]([C@H]([C@@H]2CO3)C3=O)c(cc3OCOc3c3)c3C2=O)cc(OC)c1OC
  • Chemical Name
    Furo(3'4':67)naphtho(23-d)-13-dioxole-58-dione 5a68a9-tetrahydro-9-(345-trimethoxyphenyl)- (5aR-(5aalpha8abeta9alpha))-

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • Eprodisate disodium

    Eprodisate Disodium is the orally available disodium salt form of Eprodisate, a negatively charged sulfonated inhibitor of fibrillogenesis, that can be used in the treatment of amyloid A (AA) amyloidosis.

  • D3-βArr

    D3-βArr is a positive allosteric modulator for thyrotropin receptor (TSHR) which initiates translocation of β-Arr 1 (EC50: 11.6 μM) by direct TSHR activation.

  • Angiotensin I

    Des-Leu10-angiotensin I is a nonapeptide that inhibits rabbit lung angiotensin-converting enzyme peptidyl-dipeptide hydrolase with a Ki value of 31 μM, which is generated from angiotensin I by the action of carboxypeptidase-like activities residing in the human platelet and mast cell.