1. Anti-infection
  2. Parasite
  3. Chalcone 4 hydrate

Chalcone 4 hydrate is an anti-parasitic agent. Chalcone 4 hydrate inhibits the growth and proliferation of Babesia and Theileria in vitro. Chalcone 4 hydrate reduces the viability of mammalian fibroblasts and kidney cells in vitro. Chalcone 4 hydrate can be used for the research of parasitic infections.

For research use only. We do not sell to patients.

Chalcone 4 hydrate

Chalcone 4 hydrate Chemical Structure

CAS No. : 1202866-96-3

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Description

Chalcone 4 hydrate is an anti-parasitic agent. Chalcone 4 hydrate inhibits the growth and proliferation of Babesia and Theileria in vitro. Chalcone 4 hydrate reduces the viability of mammalian fibroblasts and kidney cells in vitro. Chalcone 4 hydrate can be used for the research of parasitic infections[1].

In Vitro

Chalcone 4 hydrate (12.5-200 μM; 4 days) inhibits the in vitro growth of Babesia bovis, Babesia bigemina, Babesia divergens, Babesia caballi and Theileria equi in a dose-dependent manner, with the lowest inhibitory activity against B. bovis (IC50 = 138.4 μM) and the highest inhibitory activity against T. equi (IC50 = 19.2 μM)[1].
Chalcone 4 hydrate (0.25× IC50-4× IC50; administered daily for 4 consecutive days; regrowth monitored for 6 days after drug withdrawal) induces time-dependent morphological degeneration of Babesia bovis, Babesia bigemina, Babesia divergens, Babesia caballi and Theileria equi in vitro; at the concentration of 4× IC50, it completely eliminates Babesia bovis, Babesia bigemina, Babesia divergens and Babesia equi with no regrowth, while regrowth of Theileria equi still occurs at this concentration[1].
Chalcone 4 hydrate (0.25× IC50-4× IC50; 4 days) exhibits additive or synergistic in vitro growth inhibitory activity against Babesia bovis, Babesia bigemina, Babesia divergens, Babesia equi, and Theileria equi, with no antagonistic interactions when used in combination with Diminazene aceturate (HY-12404), Atovaquone (HY-13832), or Clofazimine (HY-B1046)[1].
Chalcone 4 hydrate (12.5-500 μM; 24 h) exhibits dose-dependent cytotoxicity in vitro against Madin-Darby bovine kidney cells, mouse embryonic fibroblasts and human foreskin fibroblast cell lines, with the highest selectivity index of 24.3 observed for Theileria equi and human foreskin fibroblasts[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cytotoxicity Assay[1]

Cell Line: Madin-Darby bovine kidney (MDBK), mouse embryonic fibroblast (NIH/3T3), human foreskin fibroblast (HFF) cell lines
Concentration: 12.5, 25, 50, 100, 200, 400, 500 μM
Incubation Time: 24 hours
Result: Exhibited dose-dependent cytotoxicity against all three cell lines.
Showed an EC50 of 252.7 μM for MDBK.
Showed an EC50 of 406.3 μM for NIH/3T3.
Showed an EC50 of 466 μM for HFF.
Had selectivity indices ranging from 1.8 (MDBK/B. bovis) to 24.3 (HFF/T. equi).
Formula

C16H13ClO3.xH2O

CAS No.
Appearance

Solid

Color

Brown to reddish brown

SMILES

O=C(C1=CC=C(Cl)C=C1)/C=C/C2=CC=C(O)C(OC)=C2.[x H2O]

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

4°C, stored under nitrogen

*In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)

Purity & Documentation
References
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Chalcone 4 hydrate
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HY-115550
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