2. Anti-infection
  3. Bacterial Antibiotic
  4. Hordenine

Hordenine  (Synonyms: Ordenina; Peyocactine)

Cat. No.: HY-N0113 Purity: 99.88%
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Hordenine, an alkaloid found in plants, inhibits melanogenesis by suppression of cyclic adenosine monophosphate (cAMP) production.

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

Hordenine Chemical Structure

Hordenine Chemical Structure

CAS No. : 539-15-1

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10 mM * 1 mL in DMSO
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Based on 1 publication(s) in Google Scholar

Other Forms of Hordenine:

Hordenine Related Antibodies

Top Publications Citing Use of Products

1 Publications Citing Use of MCE Hordenine

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  • Biological Activity

  • Purity & Documentation

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Description

Hordenine, an alkaloid found in plants, inhibits melanogenesis by suppression of cyclic adenosine monophosphate (cAMP) production[1].

In Vitro

Hordenine (50 and 100 μM, 5 days) reduces both melanin content and tyrosinase activity in human epidermal melanocytes[1].
Hordenine (500 μM, 2 weeks) decreases melanin pigmentation in reconstructed epidermis[1].
Hordenine (50 and 100 μM, 5 days) decreases cAMP production and inhibits the expression of CREB phosphorylation and MITF in human epidermal melanocytes[1].
Hordenine (50 and 100 μM, 5 days) inhibits the expression of melanogenesis-related proteins, tyrosinase, tyrosinase-related protein (TRP)-1 and TRP-2.[1]

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

Hordenine Related Antibodies

Western Blot Analysis[1]

Cell Line: Human epidermal melanocytes
Concentration: 0, 0.5, 5, 50, 100 μM
Incubation Time: 5 days
Result: Inhibited the expression of CREB phosphorylation and MITF.
Molecular Weight

165.23

Formula

C10H15NO
CAS No.
Appearance

Solid

Color

Off-white to light yellow

SMILES

OC1=CC=C(CCN(C)C)C=C1
Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.
Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 2 years
-20°C 1 year
Solvent & Solubility
In Vitro: 

DMSO : 250 mg/mL (1513.04 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 6.0522 mL 30.2609 mL 60.5217 mL
5 mM 1.2104 mL 6.0522 mL 12.1043 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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

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  • 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: ≥ 6.25 mg/mL (37.83 mM); Clear solution

    This protocol yields a clear solution of ≥ 6.25 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (62.5 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.
  • Protocol 2

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

    Solubility: ≥ 6.25 mg/mL (37.83 mM); Clear solution

    This protocol yields a clear solution of ≥ 6.25 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (62.5 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).
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 6.0522 mL 30.2608 mL 60.5217 mL 151.3042 mL
5 mM 1.2104 mL 6.0522 mL 12.1043 mL 30.2608 mL
10 mM 0.6052 mL 3.0261 mL 6.0522 mL 15.1304 mL
15 mM 0.4035 mL 2.0174 mL 4.0348 mL 10.0869 mL
20 mM 0.3026 mL 1.5130 mL 3.0261 mL 7.5652 mL
25 mM 0.2421 mL 1.2104 mL 2.4209 mL 6.0522 mL
30 mM 0.2017 mL 1.0087 mL 2.0174 mL 5.0435 mL
40 mM 0.1513 mL 0.7565 mL 1.5130 mL 3.7826 mL
50 mM 0.1210 mL 0.6052 mL 1.2104 mL 3.0261 mL
60 mM 0.1009 mL 0.5043 mL 1.0087 mL 2.5217 mL
80 mM 0.0757 mL 0.3783 mL 0.7565 mL 1.8913 mL
100 mM 0.0605 mL 0.3026 mL 0.6052 mL 1.5130 mL
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Hordenine 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:

Hordenine539-15-1Ordenina PeyocactineBacterialAntibioticInhibitorinhibitorinhibit

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