3-Oxo-16β-acetoxy-14,15β-epoxy-5β-bufa-20,22-dienolide

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3-Oxo-16β-acetoxy-14,15β-epoxy-5β-bufa-20,22-dienolide Basic information
Product Name:3-Oxo-16β-acetoxy-14,15β-epoxy-5β-bufa-20,22-dienolide
Synonyms:16β-Acetyloxy-14,15β-epoxy-3-oxo-5β-bufa-20,22-dienolide;3-Ketocinobufagin;3-Oxo-16β-acetoxy-14,15β-epoxy-5β-bufa-20,22-dienolide;3-Oxocinobufagin;Cinobufagone
CAS:6869-66-5
MF:C26H32O6
MW:440.52868
EINECS:
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Mol File:6869-66-5.mol
3-Oxo-16β-acetoxy-14,15β-epoxy-5β-bufa-20,22-dienolide Structure
3-Oxo-16β-acetoxy-14,15β-epoxy-5β-bufa-20,22-dienolide Chemical Properties
Safety Information
MSDS Information
3-Oxo-16β-acetoxy-14,15β-epoxy-5β-bufa-20,22-dienolide Usage And Synthesis
Uses3-Oxo-cinobufagin (compound 8) is a potential anticancer compound that can be isolated from the broth of M. spinosus by high-performance liquid chromatography. Compared to other isolated compounds, the hydroxyl group at the C-5 position of 3-Oxo-cinobufagin is further oxidized or isomerized, significantly reducing its cytotoxic activity against most cell lines (except HEL), while increasing its activity against the BEL cell line. The IC50 values of 3-Oxo-cinobufagin's cytotoxicity against cancer cells are: 71.3 μM (HepG2), 90.2 μM (SMMC-7221), 0.11 μM (BEL-7402), 72.5 μM (K562), 5.3 μM (HL-60), and 12 nM (HEL)[1].
References[1] He X, Tang J, Qiao A, et al. Cytotoxic biotransformed products from cinobufagin by Mucor spinosus and Aspergillus Niger[J]. Steroids, 2006, 71(5): 392-402.
3-Oxo-16β-acetoxy-14,15β-epoxy-5β-bufa-20,22-dienolide Preparation Products And Raw materials
Tag:3-Oxo-16β-acetoxy-14,15β-epoxy-5β-bufa-20,22-dienolide(6869-66-5) Related Product Information
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