1. Natural Products
  2. Plants Terpenoids
  3. Zingiberaceae Diterpenoids
  4. Hedychium yunnanense Gagnep.
  5. Hedychenone

Hedychenone (compound 3) is a labdane diterpene. Hedychenone can be isolated from the rhizomes of Hedychium yunnanense. Hedychenone against HeLa cell with IC50 value of 9.76 μg/ml.

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

Hedychenone

Hedychenone Chemical Structure

CAS No. : 56324-54-0

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Based on 1 publication(s) in Google Scholar

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  • Biological Activity

  • Purity & Documentation

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Description

Hedychenone (compound 3) is a labdane diterpene. Hedychenone can be isolated from the rhizomes of Hedychium yunnanense. Hedychenone against HeLa cell with IC50 value of 9.76 μg/ml.

Cellular Effect
Cell Line Type Value Description References
A-375 IC50
21.13 μg/mL
Compound: Hedychenone
Cytotoxicity against human A375 cells after 24 hrs
Cytotoxicity against human A375 cells after 24 hrs
[PMID: 20303755]
A549 IC50
33.12 μg/mL
Compound: Hedychenone
Cytotoxicity against human A549 cells after 24 hrs
Cytotoxicity against human A549 cells after 24 hrs
[PMID: 20303755]
A549 GI50
7.4 μM
Compound: 7
Growth inhibition of human A549 cells by Sulforhodamine B assay
Growth inhibition of human A549 cells by Sulforhodamine B assay
[PMID: 21106458]
CHO IC50
8.2 μg/mL
Compound: Hedychenone
Cytotoxicity against CHO cells after 24 hrs
Cytotoxicity against CHO cells after 24 hrs
[PMID: 20303755]
HeLa GI50
63.2 μM
Compound: 7
Growth inhibition of human HeLa cells by Sulforhodamine B assay
Growth inhibition of human HeLa cells by Sulforhodamine B assay
[PMID: 21106458]
HL-60 IC50
17.68 μg/mL
Compound: Hedychenone
Cytotoxicity against human HL60 cells after 24 hrs
Cytotoxicity against human HL60 cells after 24 hrs
[PMID: 20303755]
MCF7 GI50
14.9 μM
Compound: 7
Growth inhibition of human MCF7 cells by Sulforhodamine B assay
Growth inhibition of human MCF7 cells by Sulforhodamine B assay
[PMID: 21106458]
MCF7 IC50
19.41 μg/mL
Compound: Hedychenone
Cytotoxicity against human MCF7 cells after 24 hrs
Cytotoxicity against human MCF7 cells after 24 hrs
[PMID: 20303755]
SK-N-SH GI50
11.6 μM
Compound: 7
Growth inhibition of human SK-N-SH cells by Sulforhodamine B assay
Growth inhibition of human SK-N-SH cells by Sulforhodamine B assay
[PMID: 21106458]
Molecular Weight

298.42

Formula

C20H26O2

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

C[C@@]12[C@](C(C=C([C@@H]2/C=C/C3=COC=C3)C)=O)([H])C(C)(CCC1)C

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

-20°C, protect from light

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

Solvent & Solubility
In Vitro: 

DMSO : 50 mg/mL (167.55 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 3.3510 mL 16.7549 mL 33.5098 mL
5 mM 0.6702 mL 3.3510 mL 6.7020 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)

V1

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Concentration (final)

C2

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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: ≥ 1.25 mg/mL (4.19 mM); Clear solution

    This protocol yields a clear solution of ≥ 1.25 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (12.5 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.
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
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 3.3510 mL 16.7549 mL 33.5098 mL 83.7745 mL
5 mM 0.6702 mL 3.3510 mL 6.7020 mL 16.7549 mL
10 mM 0.3351 mL 1.6755 mL 3.3510 mL 8.3775 mL
15 mM 0.2234 mL 1.1170 mL 2.2340 mL 5.5850 mL
20 mM 0.1675 mL 0.8377 mL 1.6755 mL 4.1887 mL
25 mM 0.1340 mL 0.6702 mL 1.3404 mL 3.3510 mL
30 mM 0.1117 mL 0.5585 mL 1.1170 mL 2.7925 mL
40 mM 0.0838 mL 0.4189 mL 0.8377 mL 2.0944 mL
50 mM 0.0670 mL 0.3351 mL 0.6702 mL 1.6755 mL
60 mM 0.0558 mL 0.2792 mL 0.5585 mL 1.3962 mL
80 mM 0.0419 mL 0.2094 mL 0.4189 mL 1.0472 mL
100 mM 0.0335 mL 0.1675 mL 0.3351 mL 0.8377 mL
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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.

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Hedychenone
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