2. Apoptosis
  3. Apoptosis
  4. Silybin

Silybin is a flavonolignan isolated from milk thistle (Silybum marianum) seeds. Silybin induces apoptosis and exhibits hepatoprotective, antioxidant, anti-inflammatory, anti-cancer activity.

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Silybin Chemical Structure

Silybin Chemical Structure

CAS No. : 802918-57-6

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Customer Review

Based on 2 publication(s) in Google Scholar

Other Forms of Silybin:

Silybin Related Antibodies

Top Publications Citing Use of Products

  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

Silybin is a flavonolignan isolated from milk thistle (Silybum marianum) seeds. Silybin induces apoptosis and exhibits hepatoprotective, antioxidant, anti-inflammatory, anti-cancer activity[1][2].

In Vitro

Silybin (0-200 mM; for 72 hours) has growth inhibition in a time- and dose-dependent manner[1].
Silybin (68 μM; for 72 hours) induces apoptosis and increases the cells in G1-phase of ~22%[1].
Silybin (68 μM; for 72 hours) induces AKT activity inhibition[1].

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

Silybin Related Antibodies

Cell Viability Assay[1]

Cell Line: HepG2 cell growth
Concentration: 0-200 mM
Incubation Time: For 72 hours
Result: Had growth inhibition in a time- and dose-dependent manner with an IC50 of 68 μM.

Apoptosis Analysis[1]

Cell Line: HepG2 cell growth
Concentration: 68 μM
Incubation Time: For 72 hours
Result: Induced apoptosis in a higher number of cells (60%) when compared to untreated cells.

Cell Cycle Analysis[1]

Cell Line: HepG2 cell growth
Concentration: 68 μM
Incubation Time: For 72 hours
Result: Increased the cells in G1-phase of ~22% and decreased of 47% the cells in S-phase.

Western Blot Analysis[1]

Cell Line: HepG2 cell growth
Concentration: 68 μM
Incubation Time: For 72 hours
Result: Induced AKT activity inhibition.
In Vivo

Silybin (50, 100 mg/kg/day; given intragastrically for the last 4 weeks) significantly lowers both serum and hepatic lipid accumulation[2].

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

Animal Model: Male C57BL/6J mice (6-8 weeks old) with nonalcoholic fatty liver disease (NAFLD)[2]
Dosage: 50, 100 mg/kg
Administration: Given intragastrically; daily; for the last 4 weeks
Result: Significantly lowered both serum and hepatic lipid accumulation.
Clinical Trial
Molecular Weight

482.44

Formula

C25H22O10
CAS No.
Appearance

Solid

Color

White to off-white

SMILES

O=C1[C@H](O)[C@@H](C2=CC=C(OC(CO)C(C3=CC=C(O)C(OC)=C3)O4)C4=C2)OC5=CC(O)=CC(O)=C15
Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Solvent & Solubility
In Vitro: 

DMSO : 25 mg/mL (51.82 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.0728 mL 10.3640 mL 20.7280 mL
5 mM 0.4146 mL 2.0728 mL 4.1456 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

  • Molarity Calculator

  • Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass
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Concentration
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Volume
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Molecular Weight *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

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Volume (start)

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C2

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V2

In Vivo:

Select the appropriate dissolution method based on your experimental animal and administration route.

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

  • Protocol 1

    Add each solvent one by one:  10% Tween-80 in Saline

    Solubility: 10 mg/mL (20.73 mM); Suspended solution; Need ultrasonic

  • Protocol 2

    Add each solvent one by one:  15% Cremophor EL    85% Saline

    Solubility: 10 mg/mL (20.73 mM); Suspended solution; Need ultrasonic

In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
%
DMSO +
% 
+
%
Tween-80 +
%
Saline
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Calculation results:
Working solution concentration: mg/mL
Method for preparing stock solution: mg drug dissolved in μL  DMSO (Stock solution concentration: mg/mL).

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only. If necessary, please contact MedChemExpress (MCE).
Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline.
 If the continuous dosing period exceeds half a month, please choose this protocol carefully.
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Purity & Documentation

Purity: 99.91%

COA (248 KB) HNMR (281 KB) LCMS (260 KB)

Handling Instructions (2659 KB)
References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.0728 mL 10.3640 mL 20.7280 mL 51.8199 mL
5 mM 0.4146 mL 2.0728 mL 4.1456 mL 10.3640 mL
10 mM 0.2073 mL 1.0364 mL 2.0728 mL 5.1820 mL
15 mM 0.1382 mL 0.6909 mL 1.3819 mL 3.4547 mL
20 mM 0.1036 mL 0.5182 mL 1.0364 mL 2.5910 mL
25 mM 0.0829 mL 0.4146 mL 0.8291 mL 2.0728 mL
30 mM 0.0691 mL 0.3455 mL 0.6909 mL 1.7273 mL
40 mM 0.0518 mL 0.2591 mL 0.5182 mL 1.2955 mL
50 mM 0.0415 mL 0.2073 mL 0.4146 mL 1.0364 mL
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Silybin Related Classifications

Help & FAQs
  • 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.

Keywords:

Silybin802918-57-6SilibininApoptosismilkthistlehepatoprotectiveantioxidantanti-inflammatoryanti-cancerHepG2G1-phaseS-phaseAKTInhibitorinhibitorinhibit

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