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Bengenin

SKU: orb1224989

Description

Bergenin, a polyphenol, is a potent antinarcotic agent with antioxidant action. (In Vitro):Bergenin (7.5-30μM; 24 hours) decreases the viability of HeLa cervical cancer cells (IC50=15 μM).Bergenin (7.5-30 μM; 24 hours) induces apoptosis in HeLa cervical cancer cells.(In Vivo):Pretreatment with Bergenin (12.5-100 mg/kg; i.p.; once) produces a dose-related inhibition of acetic acid-induced writhing in mice.

Images & Validation

Key Properties

CAS Number477-90-7
MW328.27
Purity>98% (HPLC)
FormulaC14H16O9
SMILESCOC1=C(C=C2C(=C1O)[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)OC2=O)O
TargetIL Receptor
SolubilityDMSO: 66 mg/mL (201.05 mM)

Bioactivity

In Vivo
Pretreatment with Bergenin (12.5-100 mg/kg; i.p.; once) produces a dose-related inhibition of acetic acid-induced writhing in mice. Animal model: Male Swiss Webster C57BL/6 mice. Dosage: 12.5, 25, 50, 100 mg/kg. Administration: i.p.; Once. Result: Produced a dose-related inhibition of acetic acid-induced writhing in mice.
In Vitro
Bergenin (7.5-30 μM; 24 hours) decreases the viability of HeLa cervical cancer cells (IC50 = 15 μM). Bergenin (7.5-30 μM; 24 hours) induces apoptosis in HeLa cervical cancer cells. Cell Viability Assay Cell line: HeLa cervical cancer cells. Concentration: 7.5, 15, 30 μM Incubation time: 24 hours. Result: Decreased the viability of HeLa cervical cancer cells. Cell Viability Assay Cell line: HeLa cervical cancer cells. Concentration: 7.5, 15, 30 μM Incubation time: 24 hours. Result: Induced apoptosis in HeLa cervical cancer cells.

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

(–)-Bergenin | Cuscutin | NSC 661749

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    99.01% (May vary between batches)

    477-90-7

    328.27

    C14H16O9

    50 mg, 1 ml x 10 mM (in DMSO)
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Bengenin (orb1224989)

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Step 1: Enter information below

(Recommended: An additional animal making an allowance for loss during the experiment)

Step 2: Enter the in vivo formulation

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