Helichrysetin

CAS No. 62014-87-3

Helichrysetin( —— )

Catalog No. M22912 CAS No. 62014-87-3

Helichrysetin has mild anti-HIV-1 PR activity. Helichrysetin has great potentials for development as an anticancer agent, it has cytotoxic effect on four selected cancer cell lines, A549, MCF-7, Ca Ski, and HT-29.Searching for anti-HIV-1 protease (PR) inhibitors of Thai medicinal plants led to the isolation of a new cyclohexenyl chalcone named panduratin C and chalcone derivatives (2-6) from the methanol extract of Boesenbergia pandurata rhizomes.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Helichrysetin
  • Note
    Research use only, not for human use.
  • Brief Description
    Helichrysetin has mild anti-HIV-1 PR activity. Helichrysetin has great potentials for development as an anticancer agent, it has cytotoxic effect on four selected cancer cell lines, A549, MCF-7, Ca Ski, and HT-29.Searching for anti-HIV-1 protease (PR) inhibitors of Thai medicinal plants led to the isolation of a new cyclohexenyl chalcone named panduratin C and chalcone derivatives (2-6) from the methanol extract of Boesenbergia pandurata rhizomes.
  • Description
    Helichrysetin has mild anti-HIV-1 PR activity. Helichrysetin has great potentials for development as an anticancer agent, it has cytotoxic effect on four selected cancer cell lines, A549, MCF-7, Ca Ski, and HT-29.Searching for anti-HIV-1 protease (PR) inhibitors of Thai medicinal plants led to the isolation of a new cyclohexenyl chalcone named panduratin C and chalcone derivatives from the methanol extract of Boesenbergia pandurata rhizomes. The known compounds were identified to be panduratin A, hydroxypanduratin A, Helichrysetin, 2',4',6'-trihydroxyhydrochalcone, and uvangoletin . The structures of all compounds were elucidated on the basis of chemical and spectroscopic methods.
  • In Vitro
    Cell Viability AssayCell Line:HT-29, A549, MCF-7, and Ca SkiConcentration:1.56, 3.13, 6.25, 12.5, 25, 50, 100 μg/mL Incubation Time:72 h Result:Inhibited cell growth in a dose-dependent manner.IC50 for A549, Ca Ski, HT29, MCF-7 was 50.72 ± 1.26 μM (14.52 ± 0.36 μg/mL), 31.02 ± 0.45 μM (8.88 ± 0.13 μg/mL), 102.94 ± 2.20 μM (29.47 ± 0.63 μg/mL) and 97.35 ± 1.71 μM (27.87 ± 0.49 μg/mL).Apoptosis Analysis Cell Line:A549 Concentration:5, 15, 20 μg/mL Incubation Time:24-72 h Result:The population of early apoptotic cells increased from 2.65 ± 0.31% (control) to 2.78 ± 0.21%, 14.98 ± 0.79%, and 28.55 ±1.19%.Caused accumulation of cells in S phase, occurring simultaneously with the significant reduction of cell percentage in G0/G1 phase with 15 and 20 μg/mL.Western Blot Analysis Cell Line:MGC803 Concentration:10, 20 40 μM Incubation Time:24 h Result:Increased the protein expression of cleaved caspase 3 (20 and 40 μM) and reduced protein expression of Bcl-2 (40 μM), but had no significant effect on the protein expression of Bax.RT-PCR Cell Line:MGC803 Concentration:10, 20 40 μM Incubation Time:24 h Result:Reduced the mRNA and protein expression of PDHK1 and LDHA but only decreased the mRNA level of LDHB.
  • In Vivo
    Animal Model:MGC803 cell-xenografted mouse model Dosage:3, 10, 30 mg/kg Administration:i.p.Result:Decreased the tumor size and weight without an obvious effect on body weight in nude mice.Reduced the expression of Ki67 and increased the number of apoptotic cells in tumor tissues.
  • Synonyms
    ——
  • Pathway
    Microbiology/Virology
  • Target
    HIV
  • Recptor
    HIV
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    62014-87-3
  • Formula Weight
    286.3
  • Molecular Formula
    C16H14O5
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (174.65 mM)
  • SMILES
    O=C(C1=C(OC)C=C(O)C=C1O)/C=C/C2=CC=C(O)C=C2
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Anti-HIV-1 protease activity of compounds from Boesenbergia pandurata.Bioorg Med Chem. 2006 Mar 15;14(6):1710-4.
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