1. MAPK/ERK Pathway PI3K/Akt/mTOR Apoptosis Autophagy NF-κB Metabolic Enzyme/Protease Immunology/Inflammation
  2. JNK Akt Apoptosis Autophagy Reactive Oxygen Species
  3. Actein

Actein, a triterpene glycoside, shows an inhibitory effect on cancer cells, which is isolated from the rhizomes of Cimicifuga foetida. Actein suppresses cell proliferation, induces autophagy and apoptosis through promoting ROS/JNK activation, and blunting AKT pathway in bladder cancer. Actein has little toxicity in vivo.

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

Actein Chemical Structure

Actein Chemical Structure

CAS No. : 18642-44-9

Size Price Stock Quantity
1 mg In-stock
5 mg In-stock
10 mg   Get quote  
50 mg   Get quote  

* Please select Quantity before adding items.

This product is a controlled substance and not for sale in your territory.

Customer Review

Based on 1 publication(s) in Google Scholar

Other Forms of Actein:

Top Publications Citing Use of Products

View All JNK Isoform Specific Products:

View All Akt Isoform Specific Products:

  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

Actein, a triterpene glycoside, shows an inhibitory effect on cancer cells, which is isolated from the rhizomes of Cimicifuga foetida. Actein suppresses cell proliferation, induces autophagy and apoptosis through promoting ROS/JNK activation, and blunting AKT pathway in bladder cancer. Actein has little toxicity in vivo[1][2][3].

Cellular Effect
Cell Line Type Value Description References
HCC1806 IC50
> 20 μM
Compound: 1
Antiproliferative activity against human HCC1806 cells assessed as inhibition of cell growth incubated for 36 hrs by SRB assay
Antiproliferative activity against human HCC1806 cells assessed as inhibition of cell growth incubated for 36 hrs by SRB assay
[PMID: 37121522]
HeLa IC50
> 10 μM
Compound: 11
Cytotoxicity against human HeLa cells after 48 hrs by MTT assay
Cytotoxicity against human HeLa cells after 48 hrs by MTT assay
[PMID: 25136911]
HL-60 IC50
> 10 μM
Compound: 11
Cytotoxicity against human HL60 cells after 48 hrs by MTT assay
Cytotoxicity against human HL60 cells after 48 hrs by MTT assay
[PMID: 25136911]
MCF7 IC50
> 10 μM
Compound: 11
Cytotoxicity against human MCF7 cells after 48 hrs by MTT assay
Cytotoxicity against human MCF7 cells after 48 hrs by MTT assay
[PMID: 25136911]
MCF7 IC50
14 μM
Compound: 1
Antiproliferative activity against human MCF7 cells assessed as inhibition of cell growth incubated for 96 hrs by coulter counter analysis
Antiproliferative activity against human MCF7 cells assessed as inhibition of cell growth incubated for 96 hrs by coulter counter analysis
[PMID: 37121522]
MDA-MB-231 IC50
> 20 μM
Compound: 1
Antiproliferative activity against human MDA-MB-231 cells assessed as inhibition of cell growth incubated for 36 hrs by SRB assay
Antiproliferative activity against human MDA-MB-231 cells assessed as inhibition of cell growth incubated for 36 hrs by SRB assay
[PMID: 37121522]
MDA-MB-231 IC50
74 μM
Compound: 1
Antiproliferative activity against human MDA-MB-231 cells overexpressing ERnegative and Her2 assessed as inhibition of cell growth incubated for 96 hrs by coulter counter analysis
Antiproliferative activity against human MDA-MB-231 cells overexpressing ERnegative and Her2 assessed as inhibition of cell growth incubated for 96 hrs by coulter counter analysis
[PMID: 37121522]
NCI-H460 IC50
> 10 μM
Compound: 11
Cytotoxicity against human H460 cells after 48 hrs by MTT assay
Cytotoxicity against human H460 cells after 48 hrs by MTT assay
[PMID: 25136911]
Oocyte EC50
36 μM
Compound: 1
Allosteric modulation of alpha1beta2gamma2S GABAA receptor expressed in Xenopus laevis oocytes assessed as stimulation of GABA-induced chloride current by electrophysiology
Allosteric modulation of alpha1beta2gamma2S GABAA receptor expressed in Xenopus laevis oocytes assessed as stimulation of GABA-induced chloride current by electrophysiology
[PMID: 21082802]
SMMC-7721 IC50
> 10 μM
Compound: 11
Cytotoxicity against human SMMC-7721 cells after 48 hrs by MTT assay
Cytotoxicity against human SMMC-7721 cells after 48 hrs by MTT assay
[PMID: 25136911]
In Vitro

Actein (0-30 µM, 24 h) significantly suppress cell proliferation and induce cell apoptosis of gastric cancer cells via Caspase-3 and p53 signaling pathway combined with tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)[1].
Actein (0-40 μM, 24 h) suppresses cell proliferation, induces G2/M cell cycle arrest, autophagy and apoptosis in bladder cancer cells[2].
Actein (0-20 μM, 24 h) potentiates ROS generation and JNK phosphorylation and suppresses AKT pathway in BIU-87 and T24 cells[2].
Actein (10 nM and 10 μM, 5-10 min) increases calcium release into the cytoplasm of breast cancer cells and colon cancer cells[3].
Actein (0-40 μg/mL, 48 h) inhibits the NF-κB and MEK pathways by decreasing the level of IKKβ protein in 293T (null) and 293T (NF-κB) cells[3].

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

Cell Viability Assay[1]

Cell Line: SNU-216 and AGS gastric cancer cell lines
Concentration: 0-30 µM
Incubation Time: 24 h
Result: Exhibited a strong inhibitory effect on gastric cancer cell proliferation in a dose-dependent manner combined with TRAIL in gastric cancer cells.

Immunofluorescence[2]

Cell Line: BIU-87 and T24 cells
Concentration: 0-20 μM
Incubation Time: 24 h
Result: Exhibited dose-increased levels of oxidation-sensitive red fluorescence, indicating the elevation of ROS in BIU-87 and T24 cells.

Western Blot Analysis[1]

Cell Line: SNU-216 and AGS gastric cancer cell lines
Concentration: 0-30 µM
Incubation Time: 24 h
Result: Dose-dependently reduced the AKT/mTOR and JAK2/STAT3 activity, while p38 and JNK were highly phosphorylated in BIU-87 and T24 cells.

Western Blot Analysis[3]

Cell Line: 293T (null) and 293T (NF-κB) cells
Concentration: 0-40 μg/mL
Incubation Time: 48 h
Result: Decreased the level of IKKβ protein in a dose dependent manner in 293T (null) and 293T (NF-κB) cells.
Molecular Weight

676.83

Formula

C37H56O11

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

C[C@]12[C@@]3([H])[C@@]4(C[C@@H](OC(C)=O)[C@@]1([C@]5([H])[C@](O[C@]6([C@H]7[C@]([C@@H](O)O6)(C)O7)C[C@H]5C)([H])C2)C)[C@@]8([C@@](C(C)([C@@H](O[C@@]9([H])[C@@H]([C@H]([C@H](O)CO9)O)O)CC8)C)([H])CC3)C4

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 : 100 mg/mL (147.75 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 1.4775 mL 7.3874 mL 14.7748 mL
5 mM 0.2955 mL 1.4775 mL 2.9550 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
=
Concentration
×
Volume
×
Molecular Weight *

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

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

×
Volume (start)

V1

=
Concentration (final)

C2

×
Volume (final)

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% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: ≥ 2.5 mg/mL (3.69 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

    Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
  • Protocol 2

    Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

    Solubility: ≥ 2.5 mg/mL (3.69 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

    Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
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: 99.25%

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 1.4775 mL 7.3874 mL 14.7748 mL 36.9369 mL
5 mM 0.2955 mL 1.4775 mL 2.9550 mL 7.3874 mL
10 mM 0.1477 mL 0.7387 mL 1.4775 mL 3.6937 mL
15 mM 0.0985 mL 0.4925 mL 0.9850 mL 2.4625 mL
20 mM 0.0739 mL 0.3694 mL 0.7387 mL 1.8468 mL
25 mM 0.0591 mL 0.2955 mL 0.5910 mL 1.4775 mL
30 mM 0.0492 mL 0.2462 mL 0.4925 mL 1.2312 mL
40 mM 0.0369 mL 0.1847 mL 0.3694 mL 0.9234 mL
50 mM 0.0295 mL 0.1477 mL 0.2955 mL 0.7387 mL
60 mM 0.0246 mL 0.1231 mL 0.2462 mL 0.6156 mL
80 mM 0.0185 mL 0.0923 mL 0.1847 mL 0.4617 mL
100 mM 0.0148 mL 0.0739 mL 0.1477 mL 0.3694 mL
  • No file chosen (Maximum size is: 1024 Kb)
  • If you have published this work, please enter the PubMed ID.
  • Your name will appear on the site.
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.

Your Recently Viewed Products:

Inquiry Online

Your information is safe with us. * Required Fields.

Product Name

 

Requested Quantity *

Applicant Name *

 

Salutation

Email Address *

 

Phone Number *

Department

 

Organization Name *

City

State

Country or Region *

     

Remarks

Bulk Inquiry

Inquiry Information

Product Name:
Actein
Cat. No.:
HY-N6872
Quantity:
MCE Japan Authorized Agent: