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
Size | Price / USD | Stock | Quantity |
5MG | 222 | In Stock |
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10MG | 331 | In Stock |
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25MG | 536 | In Stock |
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100MG | Get Quote | In Stock |
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200MG | Get Quote | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameHelichrysetin
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NoteResearch use only, not for human use.
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Brief DescriptionHelichrysetin 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.
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DescriptionHelichrysetin 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.
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In VitroCell 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.
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In VivoAnimal 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.
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Synonyms——
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PathwayMicrobiology/Virology
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TargetHIV
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RecptorHIV
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Research Area——
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Indication——
Chemical Information
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CAS Number62014-87-3
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Formula Weight286.3
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Molecular FormulaC16H14O5
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (174.65 mM)
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SMILESO=C(C1=C(OC)C=C(O)C=C1O)/C=C/C2=CC=C(O)C=C2
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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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