Spathulenol [6750-60-3]

Cat# HY-N1205-1mg

Size : 1mg

Brand : MedChemExpress


Description

Spathulenol is isolated from Aristolochia yunnanensis, and has antioxidant, anti-inflammatory, antiproliferative and antimycobacterial activities. Spathulenol shows a high antioxidant activity with an IC50 of 85.60 μg/mL in the DPPH system[1].

Cellular Effect
Cell Line Type Value Description References
A-431 ED50
>20 μg/mL
Compound: (+)-Spathulenol
Cytotoxicity against human A431 cells
Cytotoxicity against human A431 cells
[PMID: 1517737]
BC1 cell line ED50
>20 μg/mL
Compound: (+)-Spathulenol
Cytotoxicity against human BC1 cells
Cytotoxicity against human BC1 cells
[PMID: 1517737]
BC1 cell line ED50
>20 μg/mL
Compound: spathulenol
Cytotoxicity against human BC1 cells
Cytotoxicity against human BC1 cells
[PMID: 7931367]
Col2 ED50
>20 μg/mL
Compound: (+)-Spathulenol
Cytotoxicity against human Col2 cells
Cytotoxicity against human Col2 cells
[PMID: 1517737]
Col2 ED50
>20 μg/mL
Compound: spathulenol
Cytotoxicity against human Col2 cells
Cytotoxicity against human Col2 cells
[PMID: 7931367]
HT-1080 ED50
>20 μg/mL
Compound: (+)-Spathulenol
Cytotoxicity against human HT1080 cells
Cytotoxicity against human HT1080 cells
[PMID: 1517737]
HT-1080 ED50
>20 μg/mL
Compound: spathulenol
Cytotoxicity against human HT1080 cells
Cytotoxicity against human HT1080 cells
[PMID: 7931367]
KB ED50
>20 μg/mL
Compound: (+)-Spathulenol
Cytotoxicity against human KB cells
Cytotoxicity against human KB cells
[PMID: 1517737]
KB ED50
>20 μg/mL
Compound: spathulenol
Cytotoxicity against human KB cells
Cytotoxicity against human KB cells
[PMID: 7931367]
KB-V1 ED50
>20 μg/mL
Compound: (+)-Spathulenol
Cytotoxicity against human vinblastine-resistant KBV1 cells
Cytotoxicity against human vinblastine-resistant KBV1 cells
[PMID: 1517737]
KB-V1 ED50
>20 μg/mL
Compound: spathulenol
Cytotoxicity against human KBV1 cells
Cytotoxicity against human KBV1 cells
[PMID: 7931367]
LNCaP ED50
>20 μg/mL
Compound: (+)-Spathulenol
Cytotoxicity against human LNCAP cells
Cytotoxicity against human LNCAP cells
[PMID: 1517737]
Lu1 ED50
>20 μg/mL
Compound: (+)-Spathulenol
Cytotoxicity against human Lu1 cells
Cytotoxicity against human Lu1 cells
[PMID: 1517737]
Lu1 ED50
>20 μg/mL
Compound: spathulenol
Cytotoxicity against human Lu1 cells
Cytotoxicity against human Lu1 cells
[PMID: 7931367]
P388 ED50
>20 μg/mL
Compound: (+)-Spathulenol
Cytotoxicity against mouse P388 cells
Cytotoxicity against mouse P388 cells
[PMID: 1517737]
P388 ED50
>20 μg/mL
Compound: spathulenol
Cytotoxicity against mouse P388 cells
Cytotoxicity against mouse P388 cells
[PMID: 7931367]
SK-MEL-2 ED50
>20 μg/mL
Compound: (+)-Spathulenol
Cytotoxicity against human SK-MEL-2 cells
Cytotoxicity against human SK-MEL-2 cells
[PMID: 1517737]
SK-MEL-2 ED50
6.3 μg/mL
Compound: spathulenol
Cytotoxicity against human SK-MEL-2 cells
Cytotoxicity against human SK-MEL-2 cells
[PMID: 7931367]
ZR-75-1 ED50
>20 μg/mL
Compound: (+)-Spathulenol
Cytotoxicity against human ZR-75-1 cells
Cytotoxicity against human ZR-75-1 cells
[PMID: 1517737]
In Vitro

Spathulenol exhibits a high antioxidant activity s in the DPPH and MDA system, exhibits significant DPPH free radical activity, with IC50 values of 85.60 μg/mL[1].

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

Solvent & Solubility
In Vitro: 

DMSO : 100 mg/mL (453.82 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 4.5382 mL 22.6912 mL 45.3823 mL
5 mM 0.9076 mL 4.5382 mL 9.0765 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.

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 (11.35 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 (11.35 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.
Purity & Documentation
References

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